beta-carotene (CHEBI:17579)

ChEBI > Main

CHEBI:17579 - β-carotene

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name	β-carotene

ChEBI ID	CHEBI:17579

ChEBI ASCII Name	beta-carotene

Definition	A cyclic carotene obtained by dimerisation of all-trans-retinol. A strongly-coloured red-orange pigment abundant in plants and fruit and the most active and important provitamin A carotenoid.

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

Secondary ChEBI IDs	CHEBI:40987, CHEBI:10355, CHEBI:12392, CHEBI:22834

Supplier Information	ChemicalBook:CB7358779, eMolecules:502826, ZINC000000388555

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__407451518070435__ initializing

getValue debug = null

getValue logLevel = null

getValue allowjavascript = null

AppletRegistry.checkIn(jmolApplet0_object__407451518070435__)

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:12392","platform":"J.awtjs2d.Platform","fullName":"jmolApplet0_object__407451518070435__","display":"jmolApplet0_canvas2d","signedApplet":"true","appletReadyCallback":"Jmol._readyCallback","statusListener":"[J.appletjs.Jmol.MyStatusListener object]","codeBase":"https://www.ebi.ac.uk/chebi/javascripts/jsmol/","syncId":"407451518070435","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__407451518070435__ 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 02070614483D

starting HoverWatcher_5

Time for openFile(

Marvin 02070614483D

96 97 0 0 0 0 999 V2000

9.4731 -5.5451 3.8925 C 0 0 2 0 0 0 0 0 0 0 0 0

10.9476 -6.0010 4.2086 C 0 0 0 0 0 0 0 0 0 0 0 0

11.0045 -7.4257 4.7950 C 0 0 0 0 0 0 0 0 0 0 0 0

10.3027 -8.3971 3.8241 C 0 0 0 0 0 0 0 0 0 0 0 0

9.0987 -7.9178 3.1319 C 0 0 0 0 0 0 0 0 0 0 0 0

8.7315 -6.5975 3.1145 C 0 0 0 0 0 0 0 0 0 0 0 0

7.6416 -6.2679 2.3326 C 0 0 0 0 0 0 0 0 0 0 0 0

6.5336 -5.5806 2.6596 C 0 0 0 0 0 0 0 0 0 0 0 0

5.4192 -5.4496 1.8807 C 0 0 0 0 0 0 0 0 0 0 0 0

4.9253 -4.2186 1.6115 C 0 0 0 0 0 0 0 0 0 0 0 0

3.7899 -3.9331 0.9099 C 0 0 0 0 0 0 0 0 0 0 0 0

8.3669 -8.9982 2.4392 C 0 0 0 0 0 0 0 0 0 0 0 0

9.6233 -4.1837 3.1246 C 0 0 0 0 0 0 0 0 0 0 0 0

8.7712 -5.2353 5.2634 C 0 0 0 0 0 0 0 0 0 0 0 0

4.7561 -6.6839 1.4456 C 0 0 0 0 0 0 0 0 0 0 0 0

3.0718 -2.7956 0.9947 C 0 0 0 0 0 0 0 0 0 0 0 0

1.8717 -2.4765 0.3747 C 0 0 0 0 0 0 0 0 0 0 0 0

1.4395 -1.1885 0.3911 C 0 0 0 0 0 0 0 0 0 0 0 0

0.2982 -0.6386 -0.1314 C 0 0 0 0 0 0 0 0 0 0 0 0

-0.0724 0.6531 -0.0233 C 0 0 0 0 0 0 0 0 0 0 0 0

-1.2317 1.2023 -0.5088 C 0 0 0 0 0 0 0 0 0 0 0 0

-1.7042 2.4713 -0.4010 C 0 0 0 0 0 0 0 0 0 0 0 0

-2.9184 2.8051 -0.9906 C 0 0 0 0 0 0 0 0 0 0 0 0

-3.4434 4.0286 -1.2212 C 0 0 0 0 0 0 0 0 0 0 0 0

-4.6756 4.3127 -1.7519 C 0 0 0 0 0 0 0 0 0 0 0 0

-5.3356 5.5008 -1.8398 C 0 0 0 0 0 0 0 0 0 0 0 0

-6.6058 5.5509 -2.4148 C 0 0 0 0 0 0 0 0 0 0 0 0

-7.3601 6.5960 -2.8253 C 0 0 0 0 0 0 0 0 0 0 0 0

-8.6596 6.7362 -3.3434 C 0 0 0 0 0 0 0 0 0 0 0 0

-9.2455 7.9827 -3.3553 C 0 0 0 0 0 0 0 0 0 0 0 0

-10.5862 8.2354 -3.9221 C 0 0 0 0 0 0 0 0 0 0 0 0

-11.5426 7.0354 -3.9994 C 0 0 0 0 0 0 0 0 0 0 0 0

-10.7614 5.8849 -4.6455 C 0 0 0 0 0 0 0 0 0 0 0 0

-9.4126 5.5379 -3.8880 C 0 0 1 0 0 0 0 0 0 0 0 0

1.0818 -3.5295 -0.2815 C 0 0 0 0 0 0 0 0 0 0 0 0

-0.9451 3.4951 0.3339 C 0 0 0 0 0 0 0 0 0 0 0 0

-4.7301 6.7316 -1.3088 C 0 0 0 0 0 0 0 0 0 0 0 0

-8.6973 9.2702 -2.8667 C 0 0 0 0 0 0 0 0 0 0 0 0

-8.5898 4.7711 -4.9872 C 0 0 0 0 0 0 0 0 0 0 0 0

-9.8299 4.5479 -2.7368 C 0 0 0 0 0 0 0 0 0 0 0 0

11.5564 -6.0024 3.2979 H 0 0 0 0 0 0 0 0 0 0 0 0

11.4538 -5.3242 4.9041 H 0 0 0 0 0 0 0 0 0 0 0 0

12.0412 -7.7340 4.9556 H 0 0 0 0 0 0 0 0 0 0 0 0

10.5151 -7.4593 5.7714 H 0 0 0 0 0 0 0 0 0 0 0 0

10.0997 -9.3051 4.4009 H 0 0 0 0 0 0 0 0 0 0 0 0

11.0240 -8.6700 3.0468 H 0 0 0 0 0 0 0 0 0 0 0 0

7.6569 -6.6213 1.4000 H 0 0 0 0 0 0 0 0 0 0 0 0

6.4665 -5.1587 3.5494 H 0 0 0 0 0 0 0 0 0 0 0 0

5.4187 -3.4288 1.9725 H 0 0 0 0 0 0 0 0 0 0 0 0

3.4617 -4.6391 0.2973 H 0 0 0 0 0 0 0 0 0 0 0 0

8.6963 -10.0152 2.6669 H 0 0 0 0 0 0 0 0 0 0 0 0

8.4600 -8.8868 1.3574 H 0 0 0 0 0 0 0 0 0 0 0 0

7.3086 -8.9732 2.7072 H 0 0 0 0 0 0 0 0 0 0 0 0

10.1179 -4.3204 2.1603 H 0 0 0 0 0 0 0 0 0 0 0 0

8.6625 -3.7055 2.9281 H 0 0 0 0 0 0 0 0 0 0 0 0

10.2103 -3.4564 3.6927 H 0 0 0 0 0 0 0 0 0 0 0 0

9.3940 -4.6105 5.9081 H 0 0 0 0 0 0 0 0 0 0 0 0

7.8443 -4.6758 5.1688 H 0 0 0 0 0 0 0 0 0 0 0 0

8.5348 -6.1435 5.8198 H 0 0 0 0 0 0 0 0 0 0 0 0

5.2397 -7.6079 1.7728 H 0 0 0 0 0 0 0 0 0 0 0 0

4.6945 -6.7324 0.3573 H 0 0 0 0 0 0 0 0 0 0 0 0

3.7457 -6.7177 1.8596 H 0 0 0 0 0 0 0 0 0 0 0 0

3.4666 -2.1088 1.6022 H 0 0 0 0 0 0 0 0 0 0 0 0

2.0240 -0.5244 0.8540 H 0 0 0 0 0 0 0 0 0 0 0 0

-0.3226 -1.2303 -0.6295 H 0 0 0 0 0 0 0 0 0 0 0 0

0.5613 1.2461 0.4568 H 0 0 0 0 0 0 0 0 0 0 0 0

-1.7976 0.5521 -1.0124 H 0 0 0 0 0 0 0 0 0 0 0 0

-3.4977 2.0489 -1.2877 H 0 0 0 0 0 0 0 0 0 0 0 0

-2.8773 4.8009 -0.9797 H 0 0 0 0 0 0 0 0 0 0 0 0

-5.1411 3.5081 -2.1143 H 0 0 0 0 0 0 0 0 0 0 0 0

-7.0226 4.6719 -2.5371 H 0 0 0 0 0 0 0 0 0 0 0 0

-6.8370 7.4218 -2.7442 H 0 0 0 0 0 0 0 0 0 0 0 0

-10.4426 8.6340 -4.9325 H 0 0 0 0 0 0 0 0 0 0 0 0

-11.1611 8.9959 -3.3806 H 0 0 0 0 0 0 0 0 0 0 0 0

-12.4155 7.2917 -4.6088 H 0 0 0 0 0 0 0 0 0 0 0 0

-11.9030 6.7606 -3.0050 H 0 0 0 0 0 0 0 0 0 0 0 0

-11.4426 5.0319 -4.7346 H 0 0 0 0 0 0 0 0 0 0 0 0

-10.5857 6.1948 -5.6824 H 0 0 0 0 0 0 0 0 0 0 0 0

0.0038 -3.3927 -0.2014 H 0 0 0 0 0 0 0 0 0 0 0 0

1.3526 -3.5786 -1.3381 H 0 0 0 0 0 0 0 0 0 0 0 0

1.2165 -4.5196 0.1561 H 0 0 0 0 0 0 0 0 0 0 0 0

-0.2491 3.9873 -0.3481 H 0 0 0 0 0 0 0 0 0 0 0 0

-0.3857 3.1140 1.1879 H 0 0 0 0 0 0 0 0 0 0 0 0

-1.5753 4.2548 0.7980 H 0 0 0 0 0 0 0 0 0 0 0 0

-5.4602 7.4566 -0.9465 H 0 0 0 0 0 0 0 0 0 0 0 0

-4.1246 7.2029 -2.0854 H 0 0 0 0 0 0 0 0 0 0 0 0

-4.1064 6.5786 -0.4275 H 0 0 0 0 0 0 0 0 0 0 0 0

-8.6225 9.9850 -3.6912 H 0 0 0 0 0 0 0 0 0 0 0 0

-9.3492 9.7038 -2.1037 H 0 0 0 0 0 0 0 0 0 0 0 0

-7.7224 9.2879 -2.3907 H 0 0 0 0 0 0 0 0 0 0 0 0

-7.6971 4.2706 -4.6238 H 0 0 0 0 0 0 0 0 0 0 0 0

-8.2626 5.4574 -5.7730 H 0 0 0 0 0 0 0 0 0 0 0 0

-9.1752 3.9811 -5.4661 H 0 0 0 0 0 0 0 0 0 0 0 0

-9.0161 4.0061 -2.2682 H 0 0 0 0 0 0 0 0 0 0 0 0

-10.4808 3.7442 -3.0887 H 0 0 0 0 0 0 0 0 0 0 0 0

-10.3544 5.0684 -1.9337 H 0 0 0 0 0 0 0 0 0 0 0 0

34 40 1 0 0 0 0

34 39 1 0 0 0 0

33 34 1 0 0 0 0

32 33 1 0 0 0 0

31 32 1 0 0 0 0

30 38 1 0 0 0 0

30 31 1 0 0 0 0

29 34 1 0 0 0 0

29 30 2 0 0 0 0

28 29 1 0 0 0 0

27 28 2 0 0 0 0

26 37 1 0 0 0 0

26 27 1 0 0 0 0

25 26 2 0 0 0 0

24 25 1 0 0 0 0

23 24 2 0 0 0 0

22 36 1 0 0 0 0

22 23 1 0 0 0 0

21 22 2 0 0 0 0

20 21 1 0 0 0 0

19 20 2 0 0 0 0

18 19 1 0 0 0 0

17 35 1 0 0 0 0

17 18 2 0 0 0 0

16 17 1 0 0 0 0

11 16 2 0 0 0 0

10 11 1 0 0 0 0

9 15 1 0 0 0 0

9 10 2 0 0 0 0

8 9 1 0 0 0 0

7 8 2 0 0 0 0

6 7 1 0 0 0 0

5 12 1 0 0 0 0

5 6 2 0 0 0 0

4 5 1 0 0 0 0

3 4 1 0 0 0 0

2 3 1 0 0 0 0

1 14 1 0 0 0 0

1 13 1 0 0 0 0

1 6 1 0 0 0 0

1 2 1 0 0 0 0

41 2 1 0 0 0 0

42 2 1 0 0 0 0

43 3 1 0 0 0 0

44 3 1 0 0 0 0

45 4 1 0 0 0 0

46 4 1 0 0 0 0

47 7 1 0 0 0 0

48 8 1 0 0 0 0

49 10 1 0 0 0 0

50 11 1 0 0 0 0

51 12 1 0 0 0 0

52 12 1 0 0 0 0

53 12 1 0 0 0 0

54 13 1 0 0 0 0

55 13 1 0 0 0 0

56 13 1 0 0 0 0

57 14 1 0 0 0 0

58 14 1 0 0 0 0

59 14 1 0 0 0 0

60 15 1 0 0 0 0

61 15 1 0 0 0 0

62 15 1 0 0 0 0

63 16 1 0 0 0 0

64 18 1 0 0 0 0

65 19 1 0 0 0 0

66 20 1 0 0 0 0

67 21 1 0 0 0 0

68 23 1 0 0 0 0

69 24 1 0 0 0 0

70 25 1 0 0 0 0

71 27 1 0 0 0 0

72 28 1 0 0 0 0

73 31 1 0 0 0 0

74 31 1 0 0 0 0

75 32 1 0 0 0 0

76 32 1 0 0 0 0

77 33 1 0 0 0 0

78 33 1 0 0 0 0

79 35 1 0 0 0 0

80 35 1 0 0 0 0

81 35 1 0 0 0 0

82 36 1 0 0 0 0

83 36 1 0 0 0 0

84 36 1 0 0 0 0

85 37 1 0 0 0 0

86 37 1 0 0 0 0

87 37 1 0 0 0 0

88 38 1 0 0 0 0

89 38 1 0 0 0 0

90 38 1 0 0 0 0

91 39 1 0 0 0 0

92 39 1 0 0 0 0

93 39 1 0 0 0 0

94 40 1 0 0 0 0

95 40 1 0 0 0 0

96 40 1 0 0 0 0

M END): 25 ms

reading 96 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

96 atoms created

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

Script completed

Jmol script terminated

Molfile expand

Wikipedia	License
3,4-Dihydroxyphenylacetic acid (DOPAC) is a metabolite of the neurotransmitter dopamine. Dopamine can be metabolized into one of three substances. One such substance is DOPAC. Another is 3-methoxytyramine (3-MT). Both of these substances are degraded to form homovanillic acid (HVA). Both degradations involve the enzymes monoamine oxidase (MAO) and catechol-O-methyl transferase (COMT), albeit in reverse order: MAO catalyzes dopamine to DOPAC, and COMT catalyzes DOPAC to HVA; whereas COMT catalyzes dopamine to 3-MT and MAO catalyzes 3-MT to HVA. The third metabolic end-product of dopamine is norepinephrine (noradrenaline). It can also be found in the bark of Eucalyptus globulus. This product has been synthesized (52% yield) from 4-hydroxyphenylacetic acid via aerobic biotransformation using whole cell cultures of Arthrobacter protophormiae.
Read full article at Wikipedia

Formula

C40H56

Net Charge

Average Mass

536.87264

Monoisotopic Mass

536.43820

InChI

InChI=1S/C40H56/c1-31(19-13-21-33(3)25-27-37-35(5)23-15-29-39(37,7)8)17-11-12-18-32(2)20-14-22-34(4)26-28-38-36(6)24-16-30-40(38,9)10/h11-14,17-22,25-28H,15-16,23-24,29-30H2,1-10H3/b12-11+,19-13+,20-14+,27-25+,28-26+,31-17+,32-18+,33-21+,34-22+

InChIKey

OENHQHLEOONYIE-JLTXGRSLSA-N

SMILES

CC(\C=C\C=C(C)\C=C\C1=C(C)CCCC1(C)C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CCCC1(C)C

Metabolite of Species	Details
Mus musculus (NCBI:txid10090)	Source: BioModels - MODEL1507180067 See: PubMed
Homo sapiens (NCBI:txid9606)	See: DOI

Roles Classification
Chemical Role(s):	antioxidant A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.

Biological Role(s):	mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). cofactor An organic molecule or ion (usually a metal ion) that is required by an enzyme for its activity. It may be attached either loosely (coenzyme) or tightly (prosthetic group). biological pigment An endogenous molecular entity that results in a colour of an organism as the consequence of the selective absorption of light. provitamin A A provitamin that can be converted into vitamin A by enzymes from animal tissues. plant metabolite Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms. human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). ferroptosis inhibitor Any substance that inhibits the process of ferroptosis (a type of programmed cell death dependent on iron and characterized by the accumulation of lipid peroxides) in organisms.

View more via ChEBI Ontology

ChEBI Ontology
Outgoing	β-carotene (CHEBI:17579) has role antioxidant (CHEBI:22586) β-carotene (CHEBI:17579) has role biological pigment (CHEBI:26130) β-carotene (CHEBI:17579) has role cofactor (CHEBI:23357) β-carotene (CHEBI:17579) has role ferroptosis inhibitor (CHEBI:173084) β-carotene (CHEBI:17579) has role human metabolite (CHEBI:77746) β-carotene (CHEBI:17579) has role mouse metabolite (CHEBI:75771) β-carotene (CHEBI:17579) has role plant metabolite (CHEBI:76924) β-carotene (CHEBI:17579) has role provitamin A (CHEBI:67200) β-carotene (CHEBI:17579) is a carotenoid β-end derivative (CHEBI:139120) β-carotene (CHEBI:17579) is a cyclic carotene (CHEBI:35163)

Incoming	β-carotene 5,6-epoxide (CHEBI:27793) has functional parent β-carotene (CHEBI:17579) 4,4-dihydroxy-all-trans-β-carotene (CHEBI:140678) has functional parent β-carotene (CHEBI:17579) 4-hydroxy-all-trans-β-carotene (CHEBI:140677) has functional parent β-carotene (CHEBI:17579) β-cryptoxanthin (CHEBI:10362) has parent hydride β-carotene (CHEBI:17579) 7,8-dihydro-β-carotene (CHEBI:80427) has parent hydride β-carotene (CHEBI:17579) meso-zeaxanthin (CHEBI:138919) has parent hydride β-carotene (CHEBI:17579) astacene (CHEBI:35327) has parent hydride β-carotene (CHEBI:17579) astaxanthin (CHEBI:40968) has parent hydride β-carotene (CHEBI:17579) canthaxanthin (CHEBI:3362) has parent hydride β-carotene (CHEBI:17579) echinenone (CHEBI:4746) has parent hydride β-carotene (CHEBI:17579) zeaxanthin (CHEBI:27547) has parent hydride β-carotene (CHEBI:17579)

IUPAC Name

β,β-carotene

Synonyms	Sources
1,1'-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaene-1,18-diyl]bis(2,6,6-trimethylcyclohexene)	ChEBI
all-trans-β-carotene	UniProt
all-trans-β-carotene	NIST Chemistry WebBook
beta-Carotene	KEGG COMPOUND
BETA-CAROTENE	PDBeChem
β-Karotin	ChEBI

Manual Xrefs	Databases
345	DrugCentral
BCR	PDBeChem
Beta_Carotene	Wikipedia
C00000919	KNApSAcK
C02094	KEGG COMPOUND
CPD1F-129	MetaCyc
D03101	KEGG DRUG
HMDB0000561	HMDB
LMPR01070000	LIPID MAPS
LMPR01070001	LIPID MAPS
MOL000093	COMe
View more database links

Registry Numbers	Types	Sources
1917416	Reaxys Registry Number	Reaxys
7235-40-7	CAS Registry Number	KEGG COMPOUND
7235-40-7	CAS Registry Number	ChemIDplus
7235-40-7	CAS Registry Number	NIST Chemistry WebBook

Citations	Types	Sources
11171227	PubMed citation	Europe PMC
11182771	PubMed citation	Europe PMC
11332447	PubMed citation	Europe PMC
11359610	PubMed citation	Europe PMC
11382814	PubMed citation	Europe PMC
11567548	PubMed citation	Europe PMC
11677037	PubMed citation	Europe PMC
11714348	PubMed citation	Europe PMC
11962062	PubMed citation	Europe PMC
12081834	PubMed citation	Europe PMC
12891827	PubMed citation	Europe PMC
14658721	PubMed citation	Europe PMC
14764912	PubMed citation	Europe PMC
14976384	PubMed citation	Europe PMC
14997360	PubMed citation	Europe PMC
15113067	PubMed citation	Europe PMC
15333155	PubMed citation	Europe PMC
15695449	PubMed citation	Europe PMC
15789045	PubMed citation	Europe PMC
15909543	PubMed citation	Europe PMC
15949680	PubMed citation	Europe PMC
15949683	PubMed citation	Europe PMC
16036331	PubMed citation	Europe PMC
16087476	PubMed citation	Europe PMC
16338959	PubMed citation	Europe PMC
16563447	PubMed citation	Europe PMC
17004738	PubMed citation	Europe PMC
17625873	PubMed citation	Europe PMC
17708644	PubMed citation	Europe PMC
17851775	PubMed citation	Europe PMC
18429004	PubMed citation	Europe PMC
18766464	PubMed citation	Europe PMC
18767554	PubMed citation	Europe PMC
18794175	PubMed citation	Europe PMC
19480350	PubMed citation	Europe PMC
19574250	PubMed citation	Europe PMC
19669835	PubMed citation	Europe PMC
19703237	PubMed citation	Europe PMC
19852884	PubMed citation	Europe PMC
19888275	PubMed citation	Europe PMC
19896667	PubMed citation	Europe PMC
19937581	PubMed citation	Europe PMC
20074992	PubMed citation	Europe PMC
20515074	PubMed citation	Europe PMC
22079732	PubMed citation	Europe PMC
22309480	PubMed citation	Europe PMC
22428124	PubMed citation	Europe PMC
22489215	PubMed citation	Europe PMC
22534340	PubMed citation	Europe PMC
22575730	PubMed citation	Europe PMC

Last Modified

27 July 2021

CHEBI:17579 - β-carotene

ChEBI is part of the ELIXIR infrastructure