(R)-1,2-distearoylphosphatidylethanolamine (CHEBI:47766)

ChEBI > Main

CHEBI:47766 - (R)-1,2-distearoylphosphatidylethanolamine

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name	(R)-1,2-distearoylphosphatidylethanolamine

ChEBI ID	CHEBI:47766

ChEBI ASCII Name	(R)-1,2-distearoylphosphatidylethanolamine

Definition	An optically active form of 1,2-distearoylphosphatidylethanolamine having (R)-configuration.

Stars	This entity has been manually annotated by the ChEBI Team.

Secondary ChEBI IDs	CHEBI:44886, CHEBI:47765

Supplier Information	ChemicalBook:CB9142109, eMolecules:507912, ZINC000032837870

Download	Molfile XML SDF

more structures >>

call loadScript javascripts\jsmol\core\package.js

call loadScript javascripts\jsmol\core\core.z.js -- required by ClazzNode

call loadScript javascripts\jsmol\J\awtjs2d\WebOutputChannel.js

Jmol JavaScript applet jmolApplet0_object__761988661292656__ initializing

getValue debug = null

getValue logLevel = null

getValue allowjavascript = null

AppletRegistry.checkIn(jmolApplet0_object__761988661292656__)

call loadScript javascripts\jsmol\core\corestate.z.js

viewerOptions:

{ "name":"jmolApplet0_object","applet":true,"documentBase":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:47766","platform":"J.awtjs2d.Platform","fullName":"jmolApplet0_object__761988661292656__","display":"jmolApplet0_canvas2d","signedApplet":"true","appletReadyCallback":"Jmol._readyCallback","statusListener":"[J.appletjs.Jmol.MyStatusListener object]","codeBase":"https://www.ebi.ac.uk/chebi/javascripts/jsmol/","syncId":"761988661292656","bgcolor":"#000" }

Jmol Version: 13.2.7 $Date: 2013-10-01 11:35:15 -0500 (Tue, 01 Oct 2013) $

java.vendor: j2s

java.version: 0.0

os.name: j2s

Access: ALL

memory: 0.0/0.0

processors available: 1

useCommandThread: false

appletId:jmolApplet0_object (signed)

starting HoverWatcher_1

getValue emulate = null

defaults = "Jmol"

getValue boxbgcolor = null

getValue bgcolor = #000

backgroundColor = "#000"

getValue ANIMFRAMECallback = null

getValue APPLETREADYCallback = Jmol._readyCallback

APPLETREADYCallback = "Jmol._readyCallback"

getValue ATOMMOVEDCallback = null

getValue CLICKCallback = null

getValue ECHOCallback = null

getValue ERRORCallback = null

getValue EVALCallback = null

getValue HOVERCallback = null

getValue LOADSTRUCTCallback = null

getValue MEASURECallback = null

getValue MESSAGECallback = null

getValue MINIMIZATIONCallback = null

getValue PICKCallback = null

getValue RESIZECallback = null

getValue SCRIPTCallback = null

getValue SYNCCallback = null

getValue STRUCTUREMODIFIEDCallback = null

getValue doTranslate = null

language=en_US

getValue popupMenu = null

getValue script = null

Jmol applet jmolApplet0_object__761988661292656__ ready

call loadScript javascripts\jsmol\core\corescript.z.js

call loadScript javascripts\jsmol\J\script\FileLoadThread.js

starting QueueThread0_2

script 1 started

starting HoverWatcher_3

starting HoverWatcher_4

The Resolver thinks Mol

Marvin 11120715453D

starting HoverWatcher_5

Time for openFile(

Marvin 11120715453D

133132 0 0 0 0 999 V2000

2.1961 3.0139 3.9432 P 0 0 2 0 0 0 0 0 0 0 0 0

1.6155 6.6132 1.6348 N 0 0 0 0 0 0 0 0 0 0 0 0

1.1957 1.7731 3.7145 O 0 0 0 0 0 0 0 0 0 0 0 0

2.1073 4.0144 2.6852 O 0 0 0 0 0 0 0 0 0 0 0 0

3.7032 2.4684 4.0895 O 0 0 0 0 0 0 0 0 0 0 0 0

1.8120 3.7372 5.1765 O 0 0 0 0 0 0 0 0 0 0 0 0

3.0125 5.0887 2.9461 C 0 0 0 0 0 0 0 0 0 0 0 0

2.9760 6.0805 1.7820 C 0 0 0 0 0 0 0 0 0 0 0 0

1.3202 0.9277 4.8588 C 0 0 0 0 0 0 0 0 0 0 0 0

0.3905 -0.2773 4.7042 C 0 0 1 0 0 0 0 0 0 0 0 0

-1.0559 0.2056 4.5824 C 0 0 0 0 0 0 0 0 0 0 0 0

-1.1818 1.0667 3.4200 O 0 0 0 0 0 0 0 0 0 0 0 0

-3.3347 1.3847 3.8061 O 0 0 0 0 0 0 0 0 0 0 0 0

-2.3701 1.6111 3.1136 C 0 0 0 0 0 0 0 0 0 0 0 0

-2.5012 2.5043 1.9076 C 0 0 0 0 0 0 0 0 0 0 0 0

-3.9469 2.9878 1.7854 C 0 0 0 0 0 0 0 0 0 0 0 0

-4.0803 3.8957 0.5608 C 0 0 0 0 0 0 0 0 0 0 0 0

-5.5267 4.3786 0.4391 C 0 0 0 0 0 0 0 0 0 0 0 0

-5.6598 5.2868 -0.7846 C 0 0 0 0 0 0 0 0 0 0 0 0

-7.1055 5.7704 -0.9068 C 0 0 0 0 0 0 0 0 0 0 0 0

-7.2382 6.6775 -2.1312 C 0 0 0 0 0 0 0 0 0 0 0 0

-8.6853 7.1612 -2.2531 C 0 0 0 0 0 0 0 0 0 0 0 0

-8.8187 8.0677 -3.4771 C 0 0 0 0 0 0 0 0 0 0 0 0

-10.2644 8.5526 -3.5999 C 0 0 0 0 0 0 0 0 0 0 0 0

-10.3978 9.4591 -4.8239 C 0 0 0 0 0 0 0 0 0 0 0 0

-11.8442 9.9434 -4.9462 C 0 0 0 0 0 0 0 0 0 0 0 0

-11.9776 10.8499 -6.1702 C 0 0 0 0 0 0 0 0 0 0 0 0

-13.4237 11.3346 -6.2916 C 0 0 0 0 0 0 0 0 0 0 0 0

-13.5567 12.2413 -7.5169 C 0 0 0 0 0 0 0 0 0 0 0 0

-15.0035 12.7254 -7.6379 C 0 0 0 0 0 0 0 0 0 0 0 0

-15.1365 13.6321 -8.8633 C 0 0 0 0 0 0 0 0 0 0 0 0

0.7539 -1.0203 3.5105 O 0 0 0 0 0 0 0 0 0 0 0 0

2.1672 -2.2844 4.6453 O 0 0 0 0 0 0 0 0 0 0 0 0

1.6566 -2.0102 3.5848 C 0 0 0 0 0 0 0 0 0 0 0 0

2.0348 -2.7804 2.3462 C 0 0 0 0 0 0 0 0 0 0 0 0

3.0742 -3.8446 2.7050 C 0 0 0 0 0 0 0 0 0 0 0 0

3.4576 -4.6275 1.4464 C 0 0 0 0 0 0 0 0 0 0 0 0

4.4971 -5.6903 1.8047 C 0 0 0 0 0 0 0 0 0 0 0 0

4.8810 -6.4725 0.5479 C 0 0 0 0 0 0 0 0 0 0 0 0

5.9211 -7.5361 0.9062 C 0 0 0 0 0 0 0 0 0 0 0 0

6.3041 -8.3179 -0.3516 C 0 0 0 0 0 0 0 0 0 0 0 0

7.3433 -9.3824 0.0063 C 0 0 0 0 0 0 0 0 0 0 0 0

7.7269 -10.1650 -1.2514 C 0 0 0 0 0 0 0 0 0 0 0 0

8.7671 -11.2285 -0.8931 C 0 0 0 0 0 0 0 0 0 0 0 0

9.1493 -12.0109 -2.1504 C 0 0 0 0 0 0 0 0 0 0 0 0

10.1892 -13.0749 -1.7930 C 0 0 0 0 0 0 0 0 0 0 0 0

10.5729 -13.8574 -3.0506 C 0 0 0 0 0 0 0 0 0 0 0 0

11.6123 -14.9216 -2.6919 C 0 0 0 0 0 0 0 0 0 0 0 0

11.9960 -15.7028 -3.9501 C 0 0 0 0 0 0 0 0 0 0 0 0

13.0352 -16.7673 -3.5922 C 0 0 0 0 0 0 0 0 0 0 0 0

13.4188 -17.5499 -4.8499 C 0 0 0 0 0 0 0 0 0 0 0 0

14.1593 -18.3069 -4.5949 H 0 0 0 0 0 0 0 0 0 0 0 0

12.5327 -18.0311 -5.2617 H 0 0 0 0 0 0 0 0 0 0 0 0

13.8378 -16.8663 -5.5892 H 0 0 0 0 0 0 0 0 0 0 0 0

13.9215 -16.2844 -3.1800 H 0 0 0 0 0 0 0 0 0 0 0 0

12.6175 -17.4497 -2.8537 H 0 0 0 0 0 0 0 0 0 0 0 0

11.1096 -16.1858 -4.3623 H 0 0 0 0 0 0 0 0 0 0 0 0

12.4143 -15.0198 -4.6890 H 0 0 0 0 0 0 0 0 0 0 0 0

12.4987 -14.4386 -2.2797 H 0 0 0 0 0 0 0 0 0 0 0 0

11.1940 -15.6032 -1.9535 H 0 0 0 0 0 0 0 0 0 0 0 0

9.6865 -14.3391 -3.4633 H 0 0 0 0 0 0 0 0 0 0 0 0

10.9912 -13.1745 -3.7896 H 0 0 0 0 0 0 0 0 0 0 0 0

11.0756 -12.5932 -1.3803 H 0 0 0 0 0 0 0 0 0 0 0 0

9.7709 -13.7578 -1.0540 H 0 0 0 0 0 0 0 0 0 0 0 0

8.2637 -12.4933 -2.5630 H 0 0 0 0 0 0 0 0 0 0 0 0

9.5691 -11.3281 -2.8897 H 0 0 0 0 0 0 0 0 0 0 0 0

9.6525 -10.7465 -0.4813 H 0 0 0 0 0 0 0 0 0 0 0 0

8.3487 -11.9115 -0.1541 H 0 0 0 0 0 0 0 0 0 0 0 0

6.8412 -10.6473 -1.6640 H 0 0 0 0 0 0 0 0 0 0 0 0

8.1453 -9.4820 -1.9903 H 0 0 0 0 0 0 0 0 0 0 0 0

8.2297 -8.9008 0.4190 H 0 0 0 0 0 0 0 0 0 0 0 0

6.9249 -10.0654 0.7452 H 0 0 0 0 0 0 0 0 0 0 0 0

5.4177 -8.8009 -0.7637 H 0 0 0 0 0 0 0 0 0 0 0 0

6.7224 -7.6363 -1.0900 H 0 0 0 0 0 0 0 0 0 0 0 0

6.8056 -7.0550 1.3175 H 0 0 0 0 0 0 0 0 0 0 0 0

5.5018 -8.2200 1.6447 H 0 0 0 0 0 0 0 0 0 0 0 0

3.9946 -6.9555 0.1357 H 0 0 0 0 0 0 0 0 0 0 0 0

5.2993 -5.7896 -0.1910 H 0 0 0 0 0 0 0 0 0 0 0 0

5.3841 -5.2081 2.2169 H 0 0 0 0 0 0 0 0 0 0 0 0

4.0787 -6.3733 2.5436 H 0 0 0 0 0 0 0 0 0 0 0 0

2.5718 -5.1084 1.0355 H 0 0 0 0 0 0 0 0 0 0 0 0

3.8762 -3.9442 0.7084 H 0 0 0 0 0 0 0 0 0 0 0 0

3.9604 -3.3620 3.1163 H 0 0 0 0 0 0 0 0 0 0 0 0

2.6559 -4.5275 3.4439 H 0 0 0 0 0 0 0 0 0 0 0 0

1.1484 -3.2634 1.9341 H 0 0 0 0 0 0 0 0 0 0 0 0

2.4531 -2.0975 1.6073 H 0 0 0 0 0 0 0 0 0 0 0 0

0.4848 -0.9234 5.5772 H 0 0 0 0 0 0 0 0 0 0 0 0

1.0468 1.4851 5.7539 H 0 0 0 0 0 0 0 0 0 0 0 0

2.3503 0.5831 4.9445 H 0 0 0 0 0 0 0 0 0 0 0 0

3.9133 2.0048 3.2666 H 0 0 0 0 0 0 0 0 0 0 0 0

2.7195 5.5956 3.8649 H 0 0 0 0 0 0 0 0 0 0 0 0

4.0230 4.6936 3.0555 H 0 0 0 0 0 0 0 0 0 0 0 0

3.6675 6.8996 1.9816 H 0 0 0 0 0 0 0 0 0 0 0 0

3.2704 5.5734 0.8628 H 0 0 0 0 0 0 0 0 0 0 0 0

1.6385 7.2589 0.8595 H 0 0 0 0 0 0 0 0 0 0 0 0

1.0318 5.8404 1.3507 H 0 0 0 0 0 0 0 0 0 0 0 0

-1.3284 0.7626 5.4785 H 0 0 0 0 0 0 0 0 0 0 0 0

-1.7178 -0.6530 4.4733 H 0 0 0 0 0 0 0 0 0 0 0 0

-2.2280 1.9466 1.0116 H 0 0 0 0 0 0 0 0 0 0 0 0

-1.8383 3.3625 2.0177 H 0 0 0 0 0 0 0 0 0 0 0 0

-4.2200 3.5456 2.6814 H 0 0 0 0 0 0 0 0 0 0 0 0

-4.6095 2.1300 1.6762 H 0 0 0 0 0 0 0 0 0 0 0 0

-3.8068 3.3383 -0.3343 H 0 0 0 0 0 0 0 0 0 0 0 0

-3.4181 4.7533 0.6714 H 0 0 0 0 0 0 0 0 0 0 0 0

-5.7998 4.9364 1.3351 H 0 0 0 0 0 0 0 0 0 0 0 0

-6.1893 3.5208 0.3299 H 0 0 0 0 0 0 0 0 0 0 0 0

-5.3866 4.7291 -1.6806 H 0 0 0 0 0 0 0 0 0 0 0 0

-4.9979 6.1441 -0.6750 H 0 0 0 0 0 0 0 0 0 0 0 0

-7.3789 6.3277 -0.0117 H 0 0 0 0 0 0 0 0 0 0 0 0

-7.7684 4.9122 -1.0169 H 0 0 0 0 0 0 0 0 0 0 0 0

-6.9664 6.1199 -3.0269 H 0 0 0 0 0 0 0 0 0 0 0 0

-6.5767 7.5359 -2.0208 H 0 0 0 0 0 0 0 0 0 0 0 0

-8.9585 7.7189 -1.3571 H 0 0 0 0 0 0 0 0 0 0 0 0

-9.3479 6.3033 -2.3623 H 0 0 0 0 0 0 0 0 0 0 0 0

-8.5455 7.5113 -4.3737 H 0 0 0 0 0 0 0 0 0 0 0 0

-8.1565 8.9267 -3.3671 H 0 0 0 0 0 0 0 0 0 0 0 0

-10.5376 9.1103 -2.7038 H 0 0 0 0 0 0 0 0 0 0 0 0

-10.9263 7.6940 -3.7090 H 0 0 0 0 0 0 0 0 0 0 0 0

-10.1253 8.9021 -5.7200 H 0 0 0 0 0 0 0 0 0 0 0 0

-9.7357 10.3181 -4.7139 H 0 0 0 0 0 0 0 0 0 0 0 0

-12.1174 10.5011 -4.0501 H 0 0 0 0 0 0 0 0 0 0 0 0

-12.5061 9.0848 -5.0553 H 0 0 0 0 0 0 0 0 0 0 0 0

-11.7038 10.2928 -7.0667 H 0 0 0 0 0 0 0 0 0 0 0 0

-11.3154 11.7089 -6.0602 H 0 0 0 0 0 0 0 0 0 0 0 0

-13.6958 11.8918 -5.3968 H 0 0 0 0 0 0 0 0 0 0 0 0

-14.0852 10.4762 -6.4020 H 0 0 0 0 0 0 0 0 0 0 0 0

-13.2836 11.6836 -8.4130 H 0 0 0 0 0 0 0 0 0 0 0 0

-12.8946 13.1002 -7.4069 H 0 0 0 0 0 0 0 0 0 0 0 0

-15.2763 13.2820 -6.7427 H 0 0 0 0 0 0 0 0 0 0 0 0

-15.6650 11.8670 -7.7483 H 0 0 0 0 0 0 0 0 0 0 0 0

-16.1662 13.9769 -8.9503 H 0 0 0 0 0 0 0 0 0 0 0 0

-14.4737 14.4903 -8.7532 H 0 0 0 0 0 0 0 0 0 0 0 0

-14.8627 13.0750 -9.7597 H 0 0 0 0 0 0 0 0 0 0 0 0

1 3 1 0 0 0 0

1 4 1 0 0 0 0

1 5 1 0 0 0 0

1 6 2 0 0 0 0

2 8 1 0 0 0 0

2 95 1 0 0 0 0

2 96 1 0 0 0 0

3 9 1 0 0 0 0

4 7 1 0 0 0 0

5 90 1 0 0 0 0

7 8 1 0 0 0 0

7 91 1 0 0 0 0

7 92 1 0 0 0 0

8 93 1 0 0 0 0

8 94 1 0 0 0 0

9 10 1 0 0 0 0

9 88 1 0 0 0 0

9 89 1 0 0 0 0

10 11 1 0 0 0 0

10 32 1 0 0 0 0

10 87 1 0 0 0 0

11 12 1 0 0 0 0

11 97 1 0 0 0 0

11 98 1 0 0 0 0

12 14 1 0 0 0 0

13 14 2 0 0 0 0

14 15 1 0 0 0 0

15 16 1 0 0 0 0

15 99 1 0 0 0 0

15100 1 0 0 0 0

16 17 1 0 0 0 0

16101 1 0 0 0 0

16102 1 0 0 0 0

17 18 1 0 0 0 0

17103 1 0 0 0 0

17104 1 0 0 0 0

18 19 1 0 0 0 0

18105 1 0 0 0 0

18106 1 0 0 0 0

19 20 1 0 0 0 0

19107 1 0 0 0 0

19108 1 0 0 0 0

20 21 1 0 0 0 0

20109 1 0 0 0 0

20110 1 0 0 0 0

21 22 1 0 0 0 0

21111 1 0 0 0 0

21112 1 0 0 0 0

22 23 1 0 0 0 0

22113 1 0 0 0 0

22114 1 0 0 0 0

23 24 1 0 0 0 0

23115 1 0 0 0 0

23116 1 0 0 0 0

24 25 1 0 0 0 0

24117 1 0 0 0 0

24118 1 0 0 0 0

25 26 1 0 0 0 0

25119 1 0 0 0 0

25120 1 0 0 0 0

26 27 1 0 0 0 0

26121 1 0 0 0 0

26122 1 0 0 0 0

27 28 1 0 0 0 0

27123 1 0 0 0 0

27124 1 0 0 0 0

28 29 1 0 0 0 0

28125 1 0 0 0 0

28126 1 0 0 0 0

29 30 1 0 0 0 0

29127 1 0 0 0 0

29128 1 0 0 0 0

30 31 1 0 0 0 0

30129 1 0 0 0 0

30130 1 0 0 0 0

31131 1 0 0 0 0

31132 1 0 0 0 0

31133 1 0 0 0 0

32 34 1 0 0 0 0

33 34 2 0 0 0 0

34 35 1 0 0 0 0

35 36 1 0 0 0 0

35 85 1 0 0 0 0

35 86 1 0 0 0 0

36 37 1 0 0 0 0

36 83 1 0 0 0 0

36 84 1 0 0 0 0

37 38 1 0 0 0 0

37 81 1 0 0 0 0

37 82 1 0 0 0 0

38 39 1 0 0 0 0

38 79 1 0 0 0 0

38 80 1 0 0 0 0

39 40 1 0 0 0 0

39 77 1 0 0 0 0

39 78 1 0 0 0 0

40 41 1 0 0 0 0

40 75 1 0 0 0 0

40 76 1 0 0 0 0

41 42 1 0 0 0 0

41 73 1 0 0 0 0

41 74 1 0 0 0 0

42 43 1 0 0 0 0

42 71 1 0 0 0 0

42 72 1 0 0 0 0

43 44 1 0 0 0 0

43 69 1 0 0 0 0

43 70 1 0 0 0 0

44 45 1 0 0 0 0

44 67 1 0 0 0 0

44 68 1 0 0 0 0

45 46 1 0 0 0 0

45 65 1 0 0 0 0

45 66 1 0 0 0 0

46 47 1 0 0 0 0

46 63 1 0 0 0 0

46 64 1 0 0 0 0

47 48 1 0 0 0 0

47 61 1 0 0 0 0

47 62 1 0 0 0 0

48 49 1 0 0 0 0

48 59 1 0 0 0 0

48 60 1 0 0 0 0

49 50 1 0 0 0 0

49 57 1 0 0 0 0

49 58 1 0 0 0 0

50 51 1 0 0 0 0

50 55 1 0 0 0 0

50 56 1 0 0 0 0

51 52 1 0 0 0 0

51 53 1 0 0 0 0

51 54 1 0 0 0 0

M END): 22 ms

reading 133 atoms

ModelSet: haveSymmetry:false haveUnitcells:false haveFractionalCoord:false

1 model in this collection. Use getProperty "modelInfo" or getProperty "auxiliaryInfo" to inspect them.

Default Van der Waals type for model set to Babel

133 atoms created

ModelSet: not autobonding; use forceAutobond=true to force automatic bond creation

Script completed

Jmol script terminated

Molfile expand

Formula

C41H82NO8P

Net Charge

Average Mass

748.06548

Monoisotopic Mass

747.57781

InChI

InChI=1S/C41H82NO8P/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-40(43)47-37-39(38-49-51(45,46)48-36-35-42)50-41(44)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h39H,3-38,42H2,1-2H3,(H,45,46)/t39-/m1/s1

InChIKey

LVNGJLRDBYCPGB-LDLOPFEMSA-N

SMILES

CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(=O)OCCN)OC(=O)CCCCCCCCCCCCCCCCC

Metabolite of Species	Details
Mus musculus (NCBI:txid10090)	See: MetaboLights Study

Roles Classification
Biological Role(s):	mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).

View more via ChEBI Ontology

ChEBI Ontology
Outgoing	(R)-1,2-distearoylphosphatidylethanolamine (CHEBI:47766) has role mouse metabolite (CHEBI:75771) (R)-1,2-distearoylphosphatidylethanolamine (CHEBI:47766) is a 1,2-distearoylphosphatidylethanolamine (CHEBI:47764) (R)-1,2-distearoylphosphatidylethanolamine (CHEBI:47766) is enantiomer of (S)-1,2-distearoylphosphatidylethanolamine (CHEBI:47767) (R)-1,2-distearoylphosphatidylethanolamine (CHEBI:47766) is tautomer of (R)-1,2-distearoylphosphatidylethanolamine zwitterion (CHEBI:39934)

Incoming	(S)-1,2-distearoylphosphatidylethanolamine (CHEBI:47767) is enantiomer of (R)-1,2-distearoylphosphatidylethanolamine (CHEBI:47766) (R)-1,2-distearoylphosphatidylethanolamine zwitterion (CHEBI:39934) is tautomer of (R)-1,2-distearoylphosphatidylethanolamine (CHEBI:47766)

IUPAC Name

(2R)-3-{[(2-aminoethoxy)(hydroxy)phosphoryl]oxy}propane-1,2-diyl dioctadecanoate

Synonyms	Sources
(R)-1-((((2-Aminoethoxy)hydroxyphosphinyl)oxy)methyl)ethane-1,2-diyl distearate	ChemIDplus
1,2-dioctadecanoyl-sn-glycero-3-phosphoethanolamine	LIPID MAPS
1,2-Distearoyl-sn-glycero-3-phosphoethanolamine	LIPID MAPS
DI-STEAROYL-3-SN-PHOSPHATIDYLETHANOLAMINE	PDBeChem
Distearoyl phosphatidylethanolamine	LIPID MAPS

Manual Xrefs	Databases
3PE	PDBeChem
LMGP02010097	LIPID MAPS
PEH	PDBeChem
View more database links

Registry Numbers	Types	Sources
1069-79-0	CAS Registry Number	ChemIDplus
1730641	Reaxys Registry Number	Reaxys

Citations

Cavalcanti LP, Tho I, Konovalov O, Fossheim S, Brandl M (2011)
Compressibility study of quaternary phospholipid blend monolayers.
Colloids and surfaces. B, Biointerfaces 85, 153-160 [PubMed:21397464]
[show Abstract]

Cressman S, Dobson I, Lee JB, Tam YY, Cullis PR (2009)
Synthesis of a labeled RGD-lipid, its incorporation into liposomal nanoparticles, and their trafficking in cultured endothelial cells.
Bioconjugate chemistry 20, 1404-1411 [PubMed:19534457]
[show Abstract]

Heger M, Salles II, van Vuure W, Hamelers IH, de Kroon AI, Deckmyn H, Beek JF (2009)
On the interaction of fluorophore-encapsulating PEGylated lecithin liposomes with hamster and human platelets.
Microvascular research 78, 57-66 [PubMed:19281828]
[show Abstract]

Qiu L, Jing N, Jin Y (2008)
Preparation and in vitro evaluation of liposomal chloroquine diphosphate loaded by a transmembrane pH-gradient method.
International journal of pharmaceutics 361, 56-63 [PubMed:18573626]
[show Abstract]

Rai S, Paliwal R, Vaidya B, Khatri K, Goyal AK, Gupta PN, Vyas SP (2008)
Targeted delivery of doxorubicin via estrone-appended liposomes.
Journal of drug targeting 16, 455-463 [PubMed:18604658]
[show Abstract]

Dynarowicz-Łatka P, Hac-Wydro K (2004)
Interactions between phosphatidylcholines and cholesterol in monolayers at the air/water interface.
Colloids and surfaces. B, Biointerfaces 37, 21-25 [PubMed:15450304]
[show Abstract]

Chou TH, Chen SC, Chu IM (2003)
Effect of composition on the stability of liposomal irinotecan prepared by a pH gradient method.
Journal of bioscience and bioengineering 95, 405-408 [PubMed:16233428]
[show Abstract]

Last Modified

21 November 2019

CHEBI:47766 - (R)-1,2-distearoylphosphatidylethanolamine

ChEBI is part of the ELIXIR infrastructure