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Biological and Environmental Research Ontology
Last uploaded:
December 23, 2022
| Id | http://purl.obolibrary.org/obo/NCIT_C1135
http://purl.obolibrary.org/obo/NCIT_C1135
|
|---|---|
| Preferred Name | Indole-3-Carbinol |
| Definitions |
A naturally occurring, orally available cleavage product of the glucosinolate glucobrassicanin, a natural compound present in a wide variety of plant food substances including members of the family Cruciferae with antioxidant and potential chemopreventive properties. Indole-3-carbinol scavenges free radicals and induces various hepatic cytochrome P450 monooxygenases. Specifically, this agent induces the hepatic monooxygenase cytochrome P4501A1 (CYP1A1), resulting in increased 2-hydroxylation of estrogens and increased production of the chemoprotective estrogen 2-hydroxyestrone.
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | A naturally occurring, orally available cleavage product of the glucosinolate glucobrassicanin, a natural compound present in a wide variety of plant food substances including members of the family Cruciferae with antioxidant and potential chemopreventive properties. Indole-3-carbinol scavenges free radicals and induces various hepatic cytochrome P450 monooxygenases. Specifically, this agent induces the hepatic monooxygenase cytochrome P4501A1 (CYP1A1), resulting in increased 2-hydroxylation of estrogens and increased production of the chemoprotective estrogen 2-hydroxyestrone. |
|---|---|
| prefLabel | Indole-3-Carbinol
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| label | Indole-3-Carbinol
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| CHEBI_ID | CHEBI:24814
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| PDQ_Closed_Trial_Search_ID | 38058
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| code | C1135
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| prefixIRI | NCIT:C1135
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| in_subset |
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| Display_Name | Indole-3-Carbinol
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| Preferred_Name | Indole-3-Carbinol
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| FDA_UNII_Code | C11E72455F
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| Contributing_Source |
CRCH
CTRP
FDA
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| Chemical_Formula | C9H9NO
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| Maps_To | Indole-3-Carbinol
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| CAS_Registry | 700-06-1
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| NCI_Drug_Dictionary_ID | 38058
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| Legacy Concept Name | Indole-3-Carbinol
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| type | |
| ALT_DEFINITION | An indole with a carbinol group (-C2OH) attached at the 3 position of the pyrrole ring. The chemical structure is C1=CC=C2C(=C1)C(=CN2)CO.
A substance that is being studied as a cancer prevention drug. It is found in cruciferous vegetables.
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| Is_Value_For_GDC_Property | |
| subClassOf | |
| PDQ_Open_Trial_Search_ID | 38058
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| Semantic_Type |
Organic Chemical
Pharmacologic Substance
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| UMLS_CUI | C0063491
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