Indole-3-carbinol (I3C, C9H9NO) is produced by the breakdown of the glucosinolate glucobrassicin, which can be found at relatively high levels in cruciferous vegetables such as broccoli, cabbage, cauliflower, brussels sprouts, collard greens and kale. It is also available in dietary supplements. Indole-3-carbinol is the subject of on-going biomedical research into its possible anticarcinogenic, antioxidant, and anti-atherogenic effects. Research on indole-3-carbinol has been conducted primarily using laboratory animals and cultured cells. Limited and inconclusive human studies have been reported. A recent review of the biomedical research literature found that "evidence of an inverse association between cruciferous vegetable intake and breast or prostate cancer in humans is limited and inconsistent" and "larger randomized controlled trials are needed" to determine if supplemental indole-3-carbinol has health benefits. |
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InChI=1S/C15H20O4/c1- 10(7- 13(17) 18) 5- 6- 15(19) 11(2) 8- 12(16) 9- 14(15,3) 4/h5- 8,19H,9H2,1- 4H3,(H,17,18) /b6- 5+,10- 7- /t15- /m1/s1 |
JLIDBLDQVAYHNE-YKALOCIXSA-N |
CC(\C=C\[C@@]1(O)C(C)=CC(=O)CC1(C)C)=C\C(O)=O |
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Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
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plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
plant hormone
A plant growth regulator that modulates the formation of stems, leaves and flowers, as well as the development and ripening of fruit. The term includes endogenous and non-endogenous compounds (e.g. active compounds produced by bacteria on the leaf surface) as well as semi-synthetic and fully synthetic compounds.
abscisic acid receptor agonist
An agonist that binds to and activates abscisic acid receptors.
(via 2-cis-abscisic acid )
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View more via ChEBI Ontology
(2Z,4E)- 5- [(1S)- 1- hydroxy- 2,6,6- trimethyl- 4- oxocyclohex- 2- en- 1- yl]- 3- methylpenta- 2,4- dienoic acid
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(+)-(S)-ABA
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ChEBI
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(+)-Abscisic acid
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KEGG COMPOUND
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(+)-S-ABA
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ChEBI
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(7E,9Z)-(6S)-6-hydroxy-3-oxo-11-apo-ε-caroten-11-oic acid
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JCBN
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(S)-(+)-abscisic acid
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ChemIDplus
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2-cis,4-trans-abscisic acid
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ChemIDplus
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ABA
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ChemIDplus
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Abscisic acid
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KEGG COMPOUND
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abscisin II
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ChemIDplus
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21293-29-8
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CAS Registry Number
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KEGG COMPOUND
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21293-29-8
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CAS Registry Number
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ChemIDplus
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2130328
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Reaxys Registry Number
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Reaxys
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4190247
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Beilstein Registry Number
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Beilstein
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10915053
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PubMed citation
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ChEMBL
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12114582
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PubMed citation
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Europe PMC
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16169217
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PubMed citation
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ChEMBL
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17582774
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PubMed citation
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ChEMBL
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17741533
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PubMed citation
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Europe PMC
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19898420
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PubMed citation
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Europe PMC
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19956245
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PubMed citation
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Europe PMC
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