(Q1770257)

Gene Ontology release 2019-11-16

cellular response to indole-3-methanol

subject has role

reactant

1 reference

Gene Ontology release 2019-11-16

chemical structure

Indol-3-carbinol.svg
127 × 93; 7 KB

0 references

mass

147.068 dalton

1 reference

Indole-3-carbinol (English)

5 October 2016

chemical formula

C₉H₉NO

1 reference

Indole-3-carbinol (English)

19 November 2016

canonical SMILES

C1=CC=C2C(=C1)C(=CN2)CO

1 reference

Indole-3-carbinol (English)

19 November 2016

melting point

98.0 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

safety classification and labelling

NFPA 704: Standard System for the Identification of the Hazards of Materials for Emergency Response

no value

1 reference

imported from Wikimedia project

1 reference

Identification and Quantification of Indole-3-methanol in Etiolated Seedlings of Scots Pine (Pinus sylvestris L.).

Brassicaceae

1 reference

Indole-3-carbinol inhibits LPS-induced inflammatory response by blocking TRIF-dependent signaling pathway in macrophages

Haliclona oculata

1 reference

Oculatol, oculatolide, and A-nor sterols from the sponge Haliclona oculata

Brassica oleracea

2 references

High-performance liquid chromatographic analysis of anticarcinogenic indoles in Brassica oleracea

Bioavailability and new biomarkers of cruciferous sprouts consumption

Dalbergia

1 reference

Detection of abscisic acid, indole-3-acetic acid and indole-3-ethanol in seeds of Dalbergia dolichopetala

Leptosphaeria maculans

1 reference

The cruciferous phytoalexins rapalexin A, brussalexin A and erucalexin: Chemistry and metabolism in Leptosphaeria maculans

Brassica

3 references

N-Alkoxy derivatization of indole-3-carbinol increases the efficacy of the G1 cell cycle arrest and of I3C-specific regulation of cell cycle gene transcription and activity in human breast cancer cells

Indole-3-carbinol inhibits the expression of cyclin-dependent kinase-6 and induces a G1 cell cycle arrest of human breast cancer cells independent of estrogen receptor signaling.

Roles of SIRT1 and phosphoinositide 3-OH kinase/protein kinase C pathways in evodiamine-induced human melanoma A375-S2 cell death

radish

1 reference

Deciphering the Nutraceutical Potential of -A Comprehensive Overview

Picea abies

1 reference

Dynamics of indole-3-acetic acid during germination of Picea abies seeds

subject has role

anticarcinogens

1 reference

InChI=1S/C9H9NO/c11-6-7-5-10-9-4-2-1-3-8(7)9/h1-5,10-11H,6H2

Medical Subject Headings

15 March 2018

Indole-3-carbinol

0 references

Identifiers

InChI

1 reference

Indole-3-carbinol (English)

19 November 2016

2 references

Indole-3-carbinol (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

700-06-1

2 references

indole-3-carbinol (English)

19 November 2016

https://commonchemistry.cas.org/detail?cas_rn=700-06-1

9 April 2021

1 reference

Indole-3-carbidol (English)

19 November 2016

2 references

Indole-3-carbinol (English)

19 November 2016

Reaxys registry number

121323

1 reference

indole-3-methanol (English)

5 October 2016

Gmelin number

1603301

0 references

ChEBI ID

24814

mapping relation type

2 references

INDOLE-3-CARBINOL (English)

19 November 2016

International Chemical Identifier

InChI

InChI=1S/C9H9NO/c11-6-7-5-10-9-4-2-1-3-8(7)9/h1-5,10-11H,6H2

1 reference

INDOLE-3-CARBINOL (English)

19 November 2016

2 references

inferred from InChIKey

splash10-0fai-3900000000-456eeacfdc17f124472f

1 reference

MassBank accession ID

MSBNK-IPB_Halle-PB000515

0 references

MSBNK-IPB_Halle-PB000516

0 references

MSBNK-IPB_Halle-PB000517

0 references

SPLASH

0 references

splash10-004i-9200000000-43d8007af2a1b33116f9

0 references

splash10-00r5-2900000000-f67a34f5d6d03a911b8c

0 references

splash10-0006-9000000000-12f644dadc5182e9f9c6

0 references

splash10-03fr-9000000000-be1a2f6d844ca724831d

0 references

NMRShiftDB structure ID

20221552

1 reference

imported from Wikimedia project

RTECS number

NL9483000

1 reference

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

0 references

0 references

1 reference

indole-3-carbinol (English)

ECHA Substance Infocard ID

19 November 2016

100.010.762

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.010.762

27 December 2018

Guide to Pharmacology Ligand ID

3-hydroxymethylindole (English)

quotation

CAS no.: 700-06-1 (English)

10047

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

5 February 2021

1 reference

Medical Subject Headings

14 March 2018

1 reference

Human Metabolome Database ID

HMDB0005785

2 references

based on heuristic

inferred from InChIKey

KNApSAcK ID

C00041598

2 references

based on heuristic

inferred from InChIKey

2 references

indole-3-carbinol (English)

19 November 2016

PatientsLikeMe treatment ID

0 references

1 reference

indole-3-carbinol (English)

19 November 2016

0 references

1 reference

6 April 2020

1 reference

28 October 2013

Microsoft Academic ID

0 references

1 reference

indole-3-carbinol (English)