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Record Information

Version

5.0

Status

Detected and Quantified

Creation Date

2005-11-16 15:48:42 UTC

Update Date

2022-03-07 02:49:02 UTC

HMDB ID

HMDB0000430

Secondary Accession Numbers

HMDB00430

Metabolite Identification

Common Name

24,25-Dihydroxyvitamin D

Description

24,25-Dihydroxyvitamin D (24R,25(OH)2D3) circulates in blood at concentrations about 1000 times higher than 1alpha,25(OH)2D3. 24-Hydroxylase is present in the proximal convoluted tubule cells of the kidney and in virtual all target cells of 1alpha,25(OH)2D3. Interestingly, 1alpha,25(OH)2D3 is a very strong inducer of 24-hydroxylase activity and 24R,25(OH)2D3 formation. Also parathyroid hormone (PTH) regulates 24-hydroxylase activity but in a tissue specific manner, i.e. inhibitory in the kidney while a synergistic effect together with 1alpha,25(OH)2D3 is observed in osteoblasts. Generally, 24-hydroxylation has been considered the first step in the degradation pathway of 1alpha,25(OH)2D3 and 25-(OH)D3. However, through the past decades data have accumulated that 24R,25(OH)2D3 is not merely a degradation product but has effects on its own. Classic studies have demonstrated the significance of 24R,25(OH)2D3 for normal chicken egg hatchability and calcium and phosphorus homeostasis. More recently it became apparent that 24R,25(OH)2D3 also has distinct effects on cartilage in particular the resting zone cells. 24R,25(OH)2D3 stimulates osteocalcin synthesis in human osteoblasts. 24R,25(OH)2D3 plays a role in bone metabolism but that it acts in concert with 1alpha,25(OH)2D3 to obtain an optimal effect. (PMID: 11179746 ).

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

24,25-Dihydroxyvitamin D.mol
  Mrv1652304202019422D          

 31 33  0  0  0  0            999 V2000
   -2.7493   -2.8669    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3349   -3.5802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5099   -3.5780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3387   -2.1491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5137   -2.1491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1012   -1.4346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2762   -1.4346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1363   -0.7201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9594   -0.7168    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5130   -1.3284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2658   -0.9909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1774   -0.1706    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7890    0.3831    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6153    1.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1987    1.7729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9851    2.5698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1883    2.7833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3914    2.9969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9747    1.9864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5743    0.1302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3700   -0.0013    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8531    0.6675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9555    0.7121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1305    0.7099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2800   -0.0057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0993   -2.8624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2743   -2.8624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5743   -2.8669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5685    3.1532    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4018    3.5802    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6258   -1.4714    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  1  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 13 20  1  1  0  0  0
 12 21  1  0  0  0  0
  9 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  8 25  1  0  0  0  0
  3 26  1  0  0  0  0
  5 26  1  0  0  0  0
 26 27  2  0  0  0  0
  1 28  1  1  0  0  0
 16 29  1  0  0  0  0
 17 30  1  0  0  0  0
  9 31  1  6  0  0  0
M  END

HMDB0000430
     RDKit          3D
24,25-Dihydroxyvitamin D
 74 76  0  0  0  0  0  0  0  0999 V2000
   -4.9586    1.8417   -0.7420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6642    0.8114   -0.2744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8507    1.0092    0.6379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7078   -0.2631    0.5998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6733   -0.8490   -0.8170 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.8064    0.2619   -1.6813 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3338   -1.4932   -1.1014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2936   -0.5495   -0.6377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9998   -0.8456   -0.4927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9917    0.0657   -0.0011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7338   -0.3401    0.0412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3922   -1.6869   -0.4090 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0455   -1.9720   -0.5582 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0255   -1.0066    0.0061 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6527    0.4171   -0.1855 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3446    0.6005   -1.6467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7046    0.5452    0.5448 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0025    2.0043    0.3632 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3598    2.6494    0.3413 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3670    1.4801    0.4690 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6760    1.9966    0.1842 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8929    2.5263   -1.2347 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9102    1.4650    0.8059 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2549    0.0344    0.5830 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5830   -0.3288    1.2650 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5214   -0.1230    2.6208 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9568   -1.7547    0.9869 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3589   -2.0180    1.4919 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9988   -1.9722   -0.5308 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0538   -2.6646    1.5049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2731    2.8236   -0.4334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1562    1.7045   -1.4115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4266    1.8882    0.3341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4660    1.0957    1.6712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7416    0.0525    0.8063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3847   -0.9917    1.3461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5131   -1.5433   -0.9110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4450    0.0517   -2.5849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2770   -2.4734   -0.5850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2702   -1.7052   -2.1832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7144   -1.8478   -0.7656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1864    1.0646    0.4033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8754   -1.8207   -1.4267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9146   -2.4710    0.2095 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2953   -2.2071   -1.6382 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2532   -2.9632   -0.0497 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9682   -1.1893   -0.5891 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2368   -1.2800    1.0595 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3603    1.6263   -2.0010 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0282   -0.0782   -2.2261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6730    0.1999   -1.8198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4854    0.3920    1.6282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6298    2.3670    1.2016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5638    2.1451   -0.5695 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4578    3.3398    1.2021 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4835    3.1220   -0.6284 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3161    1.2662    1.5894 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6227    3.0610    0.7164 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7679    1.7389   -1.9941 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3048    3.4381   -1.4494 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9625    2.8323   -1.2708 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9292    1.7233    1.9172 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8334    2.0386    0.4582 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1819   -0.3132   -0.4373 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5090   -0.5605    1.1932 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3898    0.3152    0.8541 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8617   -0.8792    3.1599 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8467   -2.7623    0.8174 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3558   -2.3667    2.5455 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9959   -1.1066    1.4302 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0438   -2.3586   -0.9020 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2369   -0.9976   -1.0387 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7944   -2.6863   -0.7832 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0720   -3.5258    1.0217 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  6
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 27 30  1  0
  8  2  1  0
 17 11  1  0
 20 15  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  1
  6 38  1  0
  7 39  1  0
  7 40  1  0
  9 41  1  0
 10 42  1  0
 12 43  1  0
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 13 46  1  0
 14 47  1  0
 14 48  1  0
 16 49  1  0
 16 50  1  0
 16 51  1  0
 17 52  1  1
 18 53  1  0
 18 54  1  0
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 21 58  1  1
 22 59  1  0
 22 60  1  0
 22 61  1  0
 23 62  1  0
 23 63  1  0
 24 64  1  0
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 25 66  1  0
 26 67  1  0
 28 68  1  0
 28 69  1  0
 28 70  1  0
 29 71  1  0
 29 72  1  0
 29 73  1  0
 30 74  1  0
M  END

24,25-Dihydroxyvitamin D.mol
  Mrv1652304202019422D          

 31 33  0  0  0  0            999 V2000
   -2.7493   -2.8669    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3349   -3.5802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5099   -3.5780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3387   -2.1491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5137   -2.1491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1012   -1.4346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2762   -1.4346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1363   -0.7201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9594   -0.7168    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5130   -1.3284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2658   -0.9909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1774   -0.1706    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7890    0.3831    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6153    1.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1987    1.7729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9851    2.5698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1883    2.7833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3914    2.9969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9747    1.9864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5743    0.1302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3700   -0.0013    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8531    0.6675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9555    0.7121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1305    0.7099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2800   -0.0057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0993   -2.8624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2743   -2.8624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5743   -2.8669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5685    3.1532    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4018    3.5802    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6258   -1.4714    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  1  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 13 20  1  1  0  0  0
 12 21  1  0  0  0  0
  9 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  8 25  1  0  0  0  0
  3 26  1  0  0  0  0
  5 26  1  0  0  0  0
 26 27  2  0  0  0  0
  1 28  1  1  0  0  0
 16 29  1  0  0  0  0
 17 30  1  0  0  0  0
  9 31  1  6  0  0  0
M  END
> <DATABASE_ID>
HMDB0000430

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@@]12CC[C@H]([C@H](C)CCC(O)C(C)(C)O)[C@@]1(C)CCC\C2=C/C=C1/C[C@H](O)CCC1=C

> <INCHI_IDENTIFIER>
InChI=1S/C27H44O3/c1-18-8-12-22(28)17-21(18)11-10-20-7-6-16-27(5)23(13-14-24(20)27)19(2)9-15-25(29)26(3,4)30/h10-11,19,22-25,28-30H,1,6-9,12-17H2,2-5H3/b20-10+,21-11-/t19-,22-,23-,24+,25?,27-/m1/s1

> <INCHI_KEY>
FCKJYANJHNLEEP-OIMXRAFZSA-N

> <FORMULA>
C27H44O3

> <MOLECULAR_WEIGHT>
416.6365

> <EXACT_MASS>
416.329045274

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
50.979796762510205

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(6R)-6-[(1R,3aS,4E,7aR)-4-{2-[(1Z,5R)-5-hydroxy-2-methylidenecyclohexylidene]ethylidene}-7a-methyl-octahydro-1H-inden-1-yl]-2-methylheptane-2,3-diol

> <ALOGPS_LOGP>
5.47

> <JCHEM_LOGP>
4.579442462666668

> <ALOGPS_LOGS>
-4.69

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.325111733971049

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.849642780244135

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3184890847799178

> <JCHEM_POLAR_SURFACE_AREA>
60.69

> <JCHEM_REFRACTIVITY>
126.4221

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.44e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
24,25-dihydroxyvitamin

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0000430
     RDKit          3D
24,25-Dihydroxyvitamin D
 74 76  0  0  0  0  0  0  0  0999 V2000
   -4.9586    1.8417   -0.7420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6642    0.8114   -0.2744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8507    1.0092    0.6379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7078   -0.2631    0.5998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6733   -0.8490   -0.8170 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.8064    0.2619   -1.6813 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3338   -1.4932   -1.1014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2936   -0.5495   -0.6377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9998   -0.8456   -0.4927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9917    0.0657   -0.0011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7338   -0.3401    0.0412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3922   -1.6869   -0.4090 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0455   -1.9720   -0.5582 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0255   -1.0066    0.0061 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6527    0.4171   -0.1855 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3446    0.6005   -1.6467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7046    0.5452    0.5448 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0025    2.0043    0.3632 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3598    2.6494    0.3413 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3670    1.4801    0.4690 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6760    1.9966    0.1842 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8929    2.5263   -1.2347 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9102    1.4650    0.8059 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2549    0.0344    0.5830 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5830   -0.3288    1.2650 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5214   -0.1230    2.6208 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9568   -1.7547    0.9869 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3589   -2.0180    1.4919 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9988   -1.9722   -0.5308 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0538   -2.6646    1.5049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2731    2.8236   -0.4334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1562    1.7045   -1.4115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4266    1.8882    0.3341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4660    1.0957    1.6712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7416    0.0525    0.8063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3847   -0.9917    1.3461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5131   -1.5433   -0.9110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4450    0.0517   -2.5849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2770   -2.4734   -0.5850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2702   -1.7052   -2.1832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7144   -1.8478   -0.7656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1864    1.0646    0.4033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8754   -1.8207   -1.4267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9146   -2.4710    0.2095 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2953   -2.2071   -1.6382 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2532   -2.9632   -0.0497 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9682   -1.1893   -0.5891 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2368   -1.2800    1.0595 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3603    1.6263   -2.0010 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0282   -0.0782   -2.2261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6730    0.1999   -1.8198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4854    0.3920    1.6282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6298    2.3670    1.2016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5638    2.1451   -0.5695 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4578    3.3398    1.2021 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4835    3.1220   -0.6284 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3161    1.2662    1.5894 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6227    3.0610    0.7164 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7679    1.7389   -1.9941 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3048    3.4381   -1.4494 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9625    2.8323   -1.2708 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9292    1.7233    1.9172 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8334    2.0386    0.4582 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1819   -0.3132   -0.4373 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5090   -0.5605    1.1932 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3898    0.3152    0.8541 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8617   -0.8792    3.1599 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8467   -2.7623    0.8174 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3558   -2.3667    2.5455 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9959   -1.1066    1.4302 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0438   -2.3586   -0.9020 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2369   -0.9976   -1.0387 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7944   -2.6863   -0.7832 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0720   -3.5258    1.0217 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  6
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 27 30  1  0
  8  2  1  0
 17 11  1  0
 20 15  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  1
  6 38  1  0
  7 39  1  0
  7 40  1  0
  9 41  1  0
 10 42  1  0
 12 43  1  0
 12 44  1  0
 13 45  1  0
 13 46  1  0
 14 47  1  0
 14 48  1  0
 16 49  1  0
 16 50  1  0
 16 51  1  0
 17 52  1  1
 18 53  1  0
 18 54  1  0
 19 55  1  0
 19 56  1  0
 20 57  1  1
 21 58  1  1
 22 59  1  0
 22 60  1  0
 22 61  1  0
 23 62  1  0
 23 63  1  0
 24 64  1  0
 24 65  1  0
 25 66  1  0
 26 67  1  0
 28 68  1  0
 28 69  1  0
 28 70  1  0
 29 71  1  0
 29 72  1  0
 29 73  1  0
 30 74  1  0
M  END

HEADER    PROTEIN                                 20-APR-20   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: 24,25-Dihydroxyvitamin D.mol                      
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-20         0                                  
HETATM    1  C   UNK     0      -5.132  -5.352   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.358  -6.683   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.818  -6.679   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.366  -4.012   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.826  -4.012   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.056  -2.678   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.516  -2.678   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.254  -1.344   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.791  -1.338   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.824  -2.480   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.229  -1.850   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.064  -0.318   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.206   0.715   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.882   2.221   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.971   3.309   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.572   4.797   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.085   5.195   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.597   5.594   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.686   3.708   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.672   0.243   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.557  -0.002   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.459   1.246   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.784   1.329   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.244   1.325   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.523  -0.011   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -2.052  -5.343   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.512  -5.343   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -6.672  -5.352   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       6.661   5.886   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       4.483   6.683   0.000  0.00  0.00           O+0
HETATM   31  H   UNK     0       1.168  -2.747   0.000  0.00  0.00           H+0
CONECT    1    2    4   28                                                  
CONECT    2    1    3                                                       
CONECT    3    2   26                                                       
CONECT    4    1    5                                                       
CONECT    5    4    6   26                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   25                                                  
CONECT    9    8   10   21   31                                             
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   21                                                  
CONECT   13   12   14   20                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   29                                                  
CONECT   17   16   18   19   30                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   13                                                            
CONECT   21   12    9   22   23                                             
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24    8                                                       
CONECT   26    3    5   27                                                  
CONECT   27   26                                                            
CONECT   28    1                                                            
CONECT   29   16                                                            
CONECT   30   17                                                            
CONECT   31    9                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

COMPND    HMDB0000430
HETATM    1  C1  UNL     1      -4.959   1.842  -0.742  1.00  0.00           C  
HETATM    2  C2  UNL     1      -5.664   0.811  -0.274  1.00  0.00           C  
HETATM    3  C3  UNL     1      -6.851   1.009   0.638  1.00  0.00           C  
HETATM    4  C4  UNL     1      -7.708  -0.263   0.600  1.00  0.00           C  
HETATM    5  C5  UNL     1      -7.673  -0.849  -0.817  1.00  0.00           C  
HETATM    6  O1  UNL     1      -7.806   0.262  -1.681  1.00  0.00           O  
HETATM    7  C6  UNL     1      -6.334  -1.493  -1.101  1.00  0.00           C  
HETATM    8  C7  UNL     1      -5.294  -0.550  -0.638  1.00  0.00           C  
HETATM    9  C8  UNL     1      -4.000  -0.846  -0.493  1.00  0.00           C  
HETATM   10  C9  UNL     1      -2.992   0.066  -0.001  1.00  0.00           C  
HETATM   11  C10 UNL     1      -1.734  -0.340   0.041  1.00  0.00           C  
HETATM   12  C11 UNL     1      -1.392  -1.687  -0.409  1.00  0.00           C  
HETATM   13  C12 UNL     1       0.045  -1.972  -0.558  1.00  0.00           C  
HETATM   14  C13 UNL     1       1.026  -1.007   0.006  1.00  0.00           C  
HETATM   15  C14 UNL     1       0.653   0.417  -0.186  1.00  0.00           C  
HETATM   16  C15 UNL     1       0.345   0.601  -1.647  1.00  0.00           C  
HETATM   17  C16 UNL     1      -0.705   0.545   0.545  1.00  0.00           C  
HETATM   18  C17 UNL     1      -1.003   2.004   0.363  1.00  0.00           C  
HETATM   19  C18 UNL     1       0.360   2.649   0.341  1.00  0.00           C  
HETATM   20  C19 UNL     1       1.367   1.480   0.469  1.00  0.00           C  
HETATM   21  C20 UNL     1       2.676   1.997   0.184  1.00  0.00           C  
HETATM   22  C21 UNL     1       2.893   2.526  -1.235  1.00  0.00           C  
HETATM   23  C22 UNL     1       3.910   1.465   0.806  1.00  0.00           C  
HETATM   24  C23 UNL     1       4.255   0.034   0.583  1.00  0.00           C  
HETATM   25  C24 UNL     1       5.583  -0.329   1.265  1.00  0.00           C  
HETATM   26  O2  UNL     1       5.521  -0.123   2.621  1.00  0.00           O  
HETATM   27  C25 UNL     1       5.957  -1.755   0.987  1.00  0.00           C  
HETATM   28  C26 UNL     1       7.359  -2.018   1.492  1.00  0.00           C  
HETATM   29  C27 UNL     1       5.999  -1.972  -0.531  1.00  0.00           C  
HETATM   30  O3  UNL     1       5.054  -2.665   1.505  1.00  0.00           O  
HETATM   31  H1  UNL     1      -5.273   2.824  -0.433  1.00  0.00           H  
HETATM   32  H2  UNL     1      -4.156   1.704  -1.411  1.00  0.00           H  
HETATM   33  H3  UNL     1      -7.427   1.888   0.334  1.00  0.00           H  
HETATM   34  H4  UNL     1      -6.466   1.096   1.671  1.00  0.00           H  
HETATM   35  H5  UNL     1      -8.742   0.052   0.806  1.00  0.00           H  
HETATM   36  H6  UNL     1      -7.385  -0.992   1.346  1.00  0.00           H  
HETATM   37  H7  UNL     1      -8.513  -1.543  -0.911  1.00  0.00           H  
HETATM   38  H8  UNL     1      -7.445   0.052  -2.585  1.00  0.00           H  
HETATM   39  H9  UNL     1      -6.277  -2.473  -0.585  1.00  0.00           H  
HETATM   40  H10 UNL     1      -6.270  -1.705  -2.183  1.00  0.00           H  
HETATM   41  H11 UNL     1      -3.714  -1.848  -0.766  1.00  0.00           H  
HETATM   42  H12 UNL     1      -3.186   1.065   0.403  1.00  0.00           H  
HETATM   43  H13 UNL     1      -1.875  -1.821  -1.427  1.00  0.00           H  
HETATM   44  H14 UNL     1      -1.915  -2.471   0.209  1.00  0.00           H  
HETATM   45  H15 UNL     1       0.295  -2.207  -1.638  1.00  0.00           H  
HETATM   46  H16 UNL     1       0.253  -2.963  -0.050  1.00  0.00           H  
HETATM   47  H17 UNL     1       1.968  -1.189  -0.589  1.00  0.00           H  
HETATM   48  H18 UNL     1       1.237  -1.280   1.060  1.00  0.00           H  
HETATM   49  H19 UNL     1       0.360   1.626  -2.001  1.00  0.00           H  
HETATM   50  H20 UNL     1       1.028  -0.078  -2.226  1.00  0.00           H  
HETATM   51  H21 UNL     1      -0.673   0.200  -1.820  1.00  0.00           H  
HETATM   52  H22 UNL     1      -0.485   0.392   1.628  1.00  0.00           H  
HETATM   53  H23 UNL     1      -1.630   2.367   1.202  1.00  0.00           H  
HETATM   54  H24 UNL     1      -1.564   2.145  -0.570  1.00  0.00           H  
HETATM   55  H25 UNL     1       0.458   3.340   1.202  1.00  0.00           H  
HETATM   56  H26 UNL     1       0.484   3.122  -0.628  1.00  0.00           H  
HETATM   57  H27 UNL     1       1.316   1.266   1.589  1.00  0.00           H  
HETATM   58  H28 UNL     1       2.623   3.061   0.716  1.00  0.00           H  
HETATM   59  H29 UNL     1       2.768   1.739  -1.994  1.00  0.00           H  
HETATM   60  H30 UNL     1       2.305   3.438  -1.449  1.00  0.00           H  
HETATM   61  H31 UNL     1       3.962   2.832  -1.271  1.00  0.00           H  
HETATM   62  H32 UNL     1       3.929   1.723   1.917  1.00  0.00           H  
HETATM   63  H33 UNL     1       4.833   2.039   0.458  1.00  0.00           H  
HETATM   64  H34 UNL     1       4.182  -0.313  -0.437  1.00  0.00           H  
HETATM   65  H35 UNL     1       3.509  -0.561   1.193  1.00  0.00           H  
HETATM   66  H36 UNL     1       6.390   0.315   0.854  1.00  0.00           H  
HETATM   67  H37 UNL     1       5.862  -0.879   3.160  1.00  0.00           H  
HETATM   68  H38 UNL     1       7.847  -2.762   0.817  1.00  0.00           H  
HETATM   69  H39 UNL     1       7.356  -2.367   2.546  1.00  0.00           H  
HETATM   70  H40 UNL     1       7.996  -1.107   1.430  1.00  0.00           H  
HETATM   71  H41 UNL     1       5.044  -2.359  -0.902  1.00  0.00           H  
HETATM   72  H42 UNL     1       6.237  -0.998  -1.039  1.00  0.00           H  
HETATM   73  H43 UNL     1       6.794  -2.686  -0.783  1.00  0.00           H  
HETATM   74  H44 UNL     1       5.072  -3.526   1.022  1.00  0.00           H  
CONECT    1    2    2   31   32
CONECT    2    3    8
CONECT    3    4   33   34
CONECT    4    5   35   36
CONECT    5    6    7   37
CONECT    6   38
CONECT    7    8   39   40
CONECT    8    9    9
CONECT    9   10   41
CONECT   10   11   11   42
CONECT   11   12   17
CONECT   12   13   43   44
CONECT   13   14   45   46
CONECT   14   15   47   48
CONECT   15   16   17   20
CONECT   16   49   50   51
CONECT   17   18   52
CONECT   18   19   53   54
CONECT   19   20   55   56
CONECT   20   21   57
CONECT   21   22   23   58
CONECT   22   59   60   61
CONECT   23   24   62   63
CONECT   24   25   64   65
CONECT   25   26   27   66
CONECT   26   67
CONECT   27   28   29   30
CONECT   28   68   69   70
CONECT   29   71   72   73
CONECT   30   74
END

HMDB0000430
     RDKit          3D
24,25-Dihydroxyvitamin D
 74 76  0  0  0  0  0  0  0  0999 V2000
   -4.9586    1.8417   -0.7420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6642    0.8114   -0.2744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8507    1.0092    0.6379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7078   -0.2631    0.5998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6733   -0.8490   -0.8170 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.8064    0.2619   -1.6813 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3338   -1.4932   -1.1014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2936   -0.5495   -0.6377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9998   -0.8456   -0.4927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9917    0.0657   -0.0011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7338   -0.3401    0.0412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3922   -1.6869   -0.4090 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0455   -1.9720   -0.5582 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0255   -1.0066    0.0061 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6527    0.4171   -0.1855 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3446    0.6005   -1.6467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7046    0.5452    0.5448 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0025    2.0043    0.3632 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3598    2.6494    0.3413 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3670    1.4801    0.4690 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6760    1.9966    0.1842 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8929    2.5263   -1.2347 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9102    1.4650    0.8059 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2549    0.0344    0.5830 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5830   -0.3288    1.2650 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5214   -0.1230    2.6208 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9568   -1.7547    0.9869 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3589   -2.0180    1.4919 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9988   -1.9722   -0.5308 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0538   -2.6646    1.5049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2731    2.8236   -0.4334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1562    1.7045   -1.4115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4266    1.8882    0.3341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4660    1.0957    1.6712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7416    0.0525    0.8063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3847   -0.9917    1.3461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5131   -1.5433   -0.9110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4450    0.0517   -2.5849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2770   -2.4734   -0.5850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2702   -1.7052   -2.1832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7144   -1.8478   -0.7656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1864    1.0646    0.4033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8754   -1.8207   -1.4267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9146   -2.4710    0.2095 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2953   -2.2071   -1.6382 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2532   -2.9632   -0.0497 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9682   -1.1893   -0.5891 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2368   -1.2800    1.0595 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3603    1.6263   -2.0010 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0282   -0.0782   -2.2261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6730    0.1999   -1.8198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4854    0.3920    1.6282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6298    2.3670    1.2016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5638    2.1451   -0.5695 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4578    3.3398    1.2021 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4835    3.1220   -0.6284 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3161    1.2662    1.5894 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6227    3.0610    0.7164 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7679    1.7389   -1.9941 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3048    3.4381   -1.4494 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9625    2.8323   -1.2708 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9292    1.7233    1.9172 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8334    2.0386    0.4582 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1819   -0.3132   -0.4373 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5090   -0.5605    1.1932 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3898    0.3152    0.8541 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8617   -0.8792    3.1599 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8467   -2.7623    0.8174 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3558   -2.3667    2.5455 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9959   -1.1066    1.4302 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0438   -2.3586   -0.9020 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2369   -0.9976   -1.0387 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7944   -2.6863   -0.7832 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0720   -3.5258    1.0217 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  6
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 27 30  1  0
  8  2  1  0
 17 11  1  0
 20 15  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  1
  6 38  1  0
  7 39  1  0
  7 40  1  0
  9 41  1  0
 10 42  1  0
 12 43  1  0
 12 44  1  0
 13 45  1  0
 13 46  1  0
 14 47  1  0
 14 48  1  0
 16 49  1  0
 16 50  1  0
 16 51  1  0
 17 52  1  1
 18 53  1  0
 18 54  1  0
 19 55  1  0
 19 56  1  0
 20 57  1  1
 21 58  1  1
 22 59  1  0
 22 60  1  0
 22 61  1  0
 23 62  1  0
 23 63  1  0
 24 64  1  0
 24 65  1  0
 25 66  1  0
 26 67  1  0
 28 68  1  0
 28 69  1  0
 28 70  1  0
 29 71  1  0
 29 72  1  0
 29 73  1  0
 30 74  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(3b,5Z,7E)-9,10-Secocholesta-5,7,10(19)-triene-3,24,25-triol	HMDB
24,25-Dihydroxycholecalciferol	HMDB
24,25-Dihydroxyvitamin	HMDB
24,25-Dihydroxyvitamin D3	HMDB
24-Hydroxycalcidiol	HMDB
Vitamin D	HMDB
24,25 Dihydroxyvitamin D3	HMDB
(24R)-24,25-Dihydroxyvitamin D3	HMDB
24,25-Dihydroxyvitamin D 3, (3beta,5Z,7E,24R)-isomer	HMDB
24,25 Dihydroxycholecalciferol	HMDB
Dihydroxyvitamin D3, 24,25	HMDB
24R,25-Dihydroxycholecalciferol	HMDB
24,25 Dihydroxyvitamin D 3	HMDB
24,25-Dihydroxyvitamin D 3	HMDB
24,25-Dihydroxy-vitamin D	HMDB

Chemical Formula

C₂₇H₄₄O₃

Average Molecular Weight

416.6365

Monoisotopic Molecular Weight

416.329045274

IUPAC Name

(6R)-6-[(1R,3aS,4E,7aR)-4-{2-[(1Z,5R)-5-hydroxy-2-methylidenecyclohexylidene]ethylidene}-7a-methyl-octahydro-1H-inden-1-yl]-2-methylheptane-2,3-diol

Traditional Name

24,25-dihydroxyvitamin

CAS Registry Number

40013-87-4

SMILES

C[C@H](CCC(O)C(C)(C)O)[C@H]1CC[C@@]2([H])\C(CCC[C@]12C)=C\C=C1\C[C@H](O)CCC1=C

InChI Identifier

InChI=1S/C27H44O3/c1-18-8-12-22(28)17-21(18)11-10-20-7-6-16-27(5)23(13-14-24(20)27)19(2)9-15-25(29)26(3,4)30/h10-11,19,22-25,28-30H,1,6-9,12-17H2,2-5H3/b20-10+,21-11-/t19-,22-,23-,24+,25?,27-/m1/s1

InChI Key

FCKJYANJHNLEEP-OIMXRAFZSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as vitamin d and derivatives. Vitamin D and derivatives are compounds containing a secosteroid backbone, usually secoergostane or secocholestane.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Vitamin D and derivatives

Direct Parent

Vitamin D and derivatives

Alternative Parents

Substituents

Triterpenoid
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Non-excretory biofluid

Blood (PMID: 227368)

Cellular substructure

Membrane (HMDB: HMDB0000430)
Extracellular (HMDB: HMDB0000430)

Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)
Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Equine

Horse (FooDB: FOOD00378)

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.0084 g/L	ALOGPS
logP	5.47	ALOGPS
logP	4.58	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	13.85	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	60.69 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	126.42 m³·mol⁻¹	ChemAxon
Polarizability	50.98 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	198.918	31661259
DarkChem	[M-H]-	193.265	31661259
AllCCS	[M+H]+	208.427	32859911
AllCCS	[M-H]-	206.774	32859911
DeepCCS	[M-2H]-	236.923	30932474
DeepCCS	[M+Na]+	212.16	30932474
AllCCS	[M+H]+	208.4	32859911
AllCCS	[M+H-H2O]+	206.3	32859911
AllCCS	[M+NH4]+	210.4	32859911
AllCCS	[M+Na]+	210.9	32859911
AllCCS	[M-H]-	206.8	32859911
AllCCS	[M+Na-2H]-	208.9	32859911
AllCCS	[M+HCOO]-	211.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
24,25-Dihydroxyvitamin D	C[C@H](CCC(O)C(C)(C)O)[C@H]1CC[C@@]2([H])\C(CCC[C@]12C)=C\C=C1\C[C@H](O)CCC1=C	3678.4	Standard polar	33892256
24,25-Dihydroxyvitamin D	C[C@H](CCC(O)C(C)(C)O)[C@H]1CC[C@@]2([H])\C(CCC[C@]12C)=C\C=C1\C[C@H](O)CCC1=C	3406.2	Standard non polar	33892256
24,25-Dihydroxyvitamin D	C[C@H](CCC(O)C(C)(C)O)[C@H]1CC[C@@]2([H])\C(CCC[C@]12C)=C\C=C1\C[C@H](O)CCC1=C	3558.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
24,25-Dihydroxyvitamin D,1TMS,isomer #1	C=C1CC[C@@H](O)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O[Si](C)(C)C)C(C)(C)O	3466.2	Semi standard non polar	33892256
24,25-Dihydroxyvitamin D,1TMS,isomer #2	C=C1CC[C@@H](O)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O)C(C)(C)O[Si](C)(C)C	3499.0	Semi standard non polar	33892256
24,25-Dihydroxyvitamin D,1TMS,isomer #3	C=C1CC[C@@H](O[Si](C)(C)C)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O)C(C)(C)O	3440.1	Semi standard non polar	33892256
24,25-Dihydroxyvitamin D,2TMS,isomer #1	C=C1CC[C@@H](O[Si](C)(C)C)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O[Si](C)(C)C)C(C)(C)O	3410.9	Semi standard non polar	33892256
24,25-Dihydroxyvitamin D,2TMS,isomer #2	C=C1CC[C@@H](O)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O[Si](C)(C)C)C(C)(C)O[Si](C)(C)C	3503.0	Semi standard non polar	33892256
24,25-Dihydroxyvitamin D,2TMS,isomer #3	C=C1CC[C@@H](O[Si](C)(C)C)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O)C(C)(C)O[Si](C)(C)C	3466.2	Semi standard non polar	33892256
24,25-Dihydroxyvitamin D,3TMS,isomer #1	C=C1CC[C@@H](O[Si](C)(C)C)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O[Si](C)(C)C)C(C)(C)O[Si](C)(C)C	3461.8	Semi standard non polar	33892256
24,25-Dihydroxyvitamin D,1TBDMS,isomer #1	C=C1CC[C@@H](O)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)O	3710.0	Semi standard non polar	33892256
24,25-Dihydroxyvitamin D,1TBDMS,isomer #2	C=C1CC[C@@H](O)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O)C(C)(C)O[Si](C)(C)C(C)(C)C	3730.6	Semi standard non polar	33892256
24,25-Dihydroxyvitamin D,1TBDMS,isomer #3	C=C1CC[C@@H](O[Si](C)(C)C(C)(C)C)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O)C(C)(C)O	3638.8	Semi standard non polar	33892256
24,25-Dihydroxyvitamin D,2TBDMS,isomer #1	C=C1CC[C@@H](O[Si](C)(C)C(C)(C)C)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)O	3879.5	Semi standard non polar	33892256
24,25-Dihydroxyvitamin D,2TBDMS,isomer #2	C=C1CC[C@@H](O)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)O[Si](C)(C)C(C)(C)C	3978.0	Semi standard non polar	33892256
24,25-Dihydroxyvitamin D,2TBDMS,isomer #3	C=C1CC[C@@H](O[Si](C)(C)C(C)(C)C)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O)C(C)(C)O[Si](C)(C)C(C)(C)C	3914.5	Semi standard non polar	33892256
24,25-Dihydroxyvitamin D,3TBDMS,isomer #1	C=C1CC[C@@H](O[Si](C)(C)C(C)(C)C)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)O[Si](C)(C)C(C)(C)C	4179.5	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 24,25-Dihydroxyvitamin D GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4i-7029200000-c84dd427774a8bd55bf4	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 24,25-Dihydroxyvitamin D GC-MS (3 TMS) - 70eV, Positive	splash10-014i-1312049000-f6115b14a152464f5e1b	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 24,25-Dihydroxyvitamin D GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 24,25-Dihydroxyvitamin D GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 24,25-Dihydroxyvitamin D GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 24,25-Dihydroxyvitamin D GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 24,25-Dihydroxyvitamin D GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 24,25-Dihydroxyvitamin D GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 24,25-Dihydroxyvitamin D GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 24,25-Dihydroxyvitamin D GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 24,25-Dihydroxyvitamin D GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 24,25-Dihydroxyvitamin D GC-MS (TBDMS_1_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 24,25-Dihydroxyvitamin D GC-MS (TBDMS_2_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 24,25-Dihydroxyvitamin D GC-MS (TBDMS_2_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 24,25-Dihydroxyvitamin D GC-MS (TBDMS_2_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 24,25-Dihydroxyvitamin D GC-MS (TBDMS_3_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24,25-Dihydroxyvitamin D 10V, Positive-QTOF	splash10-00l2-0119200000-7bcd78fea8093a8230ae	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24,25-Dihydroxyvitamin D 20V, Positive-QTOF	splash10-0a5a-2369100000-04f3fb5d7d655a9ce470	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24,25-Dihydroxyvitamin D 40V, Positive-QTOF	splash10-0zgi-4389100000-269c6b355710e7dcd9b8	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24,25-Dihydroxyvitamin D 10V, Negative-QTOF	splash10-014i-0004900000-7bbe3ea5eae60b2a2059	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24,25-Dihydroxyvitamin D 20V, Negative-QTOF	splash10-05mk-0009300000-4137913e2e1e7271894c	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24,25-Dihydroxyvitamin D 40V, Negative-QTOF	splash10-0079-9006000000-b2d6915fde38c349870a	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24,25-Dihydroxyvitamin D 10V, Positive-QTOF	splash10-00lr-0439300000-d0f3435842264a17a15a	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24,25-Dihydroxyvitamin D 20V, Positive-QTOF	splash10-00rx-4579100000-2ffe9e7393dd492716a0	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24,25-Dihydroxyvitamin D 40V, Positive-QTOF	splash10-0avi-2960000000-4329739a1dba4656972b	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24,25-Dihydroxyvitamin D 10V, Negative-QTOF	splash10-014j-0007900000-764d7cf399a810ff092c	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24,25-Dihydroxyvitamin D 20V, Negative-QTOF	splash10-0671-3109300000-5c39962acfb73b3f737d	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 24,25-Dihydroxyvitamin D 40V, Negative-QTOF	splash10-01ri-2129300000-7f78982c59e2cf08742c	2021-09-23	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane (predicted from logP)

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected and Quantified	0.0043 +/- 0.0014 uM	Newborn (0-30 days old)	Both	Normal	Geigy Scientific ...	details
Blood	Detected and Quantified	0.0079 +/- 0.0031 uM	Children (1-13 years old)	Both	Normal	Geigy Scientific ...	details
Blood	Detected and Quantified	0.005 +/- 0.0012 uM	Adult (>18 years old)	Both	Normal	Geigy Scientific ...	details
Blood	Detected and Quantified	0.0084 +/- 0.0033 uM	Adult (>18 years old)	Both	Normal	227368	details

Abnormal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected and Quantified	0.0045 +/- 0.0031 uM	Adult (>18 years old)	Male	Anephrism	227368	details

Associated Disorders and Diseases

Disease References

Anephric patients
Shepard RM, Horst RL, Hamstra AJ, DeLuca HF: Determination of vitamin D and its metabolites in plasma from normal and anephric man. Biochem J. 1979 Jul 15;182(1):55-69. [PubMed:227368 ]

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB112199

KNApSAcK ID

Not Available

Chemspider ID

17215953

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

5419

PubChem Compound

12895043

PDB ID

Not Available

ChEBI ID

89324

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Ron M, Menczel J, Schwartz L, Palti Z, Kidroni G: Vitamin D3 metabolites in amniotic fluid in relation with maternal and fetal sera in term pregnancies. J Perinat Med. 1987;15(3):282-90. [PubMed:3501463 ]
Imawari M, Kozawa K, Yoshida T, Osuga T: A simple and sensitive assay for 25-hydroxyvitamin D, 24,25-dihydroxyvitamin D and 1,25-dihydroxyvitamin D in human serum. Clin Chim Acta. 1982 Sep 1;124(1):63-73. [PubMed:6982126 ]
Inaba M, Yukioka K, Furumitsu Y, Murano M, Goto H, Nishizawa Y, Morii H: Positive correlation between levels of IL-1 or IL-2 and 1,25(OH)2D/25-OH-D ratio in synovial fluid of patients with rheumatoid arthritis. Life Sci. 1997;61(10):977-85. [PubMed:9296336 ]
Traba ML, Babe M, de la Piedra C, Marin A: 24,25-dihydroxyvitamin D3 in serum: sample purification with Sep-Pak C-18 cartridges and liquid chromatography before protein-binding assay. Clin Chem. 1983 Oct;29(10):1806-7. [PubMed:6604593 ]
Coldwell RD, Trafford DJ, Makin HL, Varley MJ, Kirk DN: Specific estimation of 24,25-dihydroxyvitamin D in plasma by gas chromatography-mass spectrometry. Clin Chem. 1984 Jul;30(7):1193-8. [PubMed:6610503 ]
Guillemant S, Kremer R: [Radiocompetitive estimation of 25-hydroxyvitamin D in human serum (author's transl)]. Ann Biol Clin (Paris). 1978;36(6):491-6. [PubMed:749564 ]
Kumar R, Wiesner R, Scott M, Go VL: Physiology of 24,25-dihydroxyvitamin D3 in normal human subjects. Am J Physiol. 1982 Nov;243(5):E370-4. [PubMed:6753604 ]
Lazebnik R, Eisenberg Z, Lazebnik N, Spirer Z, Weisman Y: Vitamin D metabolites in amniotic fluid. J Clin Endocrinol Metab. 1983 Mar;56(3):632-4. [PubMed:6600461 ]
Mason RS, Lissner D, Grunstein HS, Posen S: A simplified assay for dihydroxylated vitamin D metabolites in human serum: application to hyper- and hypovitaminosis D. Clin Chem. 1980 Mar;26(3):444-50. [PubMed:6892691 ]
van Leeuwen JP, van den Bemd GJ, van Driel M, Buurman CJ, Pols HA: 24,25-Dihydroxyvitamin D(3) and bone metabolism. Steroids. 2001 Mar-May;66(3-5):375-80. [PubMed:11179746 ]

Showing metabocard for 24,25-Dihydroxyvitamin D (HMDB0000430)

MOL for HMDB0000430 (24,25-Dihydroxyvitamin D)

3D MOL for HMDB0000430 (24,25-Dihydroxyvitamin D)

3D SDF for HMDB0000430 (24,25-Dihydroxyvitamin D)

3D-SDF for HMDB0000430 (24,25-Dihydroxyvitamin D)

PDB for HMDB0000430 (24,25-Dihydroxyvitamin D)

3D PDB for HMDB0000430 (24,25-Dihydroxyvitamin D)

SMILES for HMDB0000430 (24,25-Dihydroxyvitamin D)

INCHI for HMDB0000430 (24,25-Dihydroxyvitamin D)

Structure for HMDB0000430 (24,25-Dihydroxyvitamin D)

3D Structure for HMDB0000430 (24,25-Dihydroxyvitamin D)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra