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Details

Stereochemistry ACHIRAL
Molecular Formula C9H7NO
Molecular Weight 145.158
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of INDOLE-3-CARBOXALDEHYDE

SMILES

O=CC1=CNC2=C1C=CC=C2

InChI

InChIKey=OLNJUISKUQQNIM-UHFFFAOYSA-N
InChI=1S/C9H7NO/c11-6-7-5-10-9-4-2-1-3-8(7)9/h1-6,10H

HIDE SMILES / InChI

Molecular Formula C9H7NO
Molecular Weight 145.158
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Antimalarial agents from plants. III. Trichothecenes from Ficus fistulosa and Rhaphidophora decursiva.
2002 Dec
Isolation and identification of lateral bud growth inhibitor, indole-3-aldehyde, involved in apical dominance of pea seedlings.
2002 Dec
Fate of indole-3-carbinol in cultured human breast tumor cells.
2002 Feb
Pharmacokinetics and tissue disposition of indole-3-carbinol and its acid condensation products after oral administration to mice.
2004 Aug 1
Universally occurring phenylpropanoid and species-specific indolic metabolites in infected and uninfected Arabidopsis thaliana roots and leaves.
2004 Mar
Enantioselective total syntheses of welwitindolinone A and fischerindoles I and G.
2005 Nov 9
Anticancer activity evaluation of kuanoniamines A and C isolated from the marine sponge Oceanapia sagittaria, collected from the Gulf of Thailand.
2007 Apr 17
Monoindole alkaloids from a marine sponge Spongosorites sp.
2007 Jun 25
Benhamycin, novel alkaloid from terrestrial Streptomyces sp.
2007 Nov
Highly sensitive feature detection for high resolution LC/MS.
2008 Nov 28
A chromanone alkaloid from Derris ovalifolia stem.
2009
Synthesis, spectroscopic, and antimicrobial studies on bivalent zinc and mercury complexes of 2-formylpyridine thiosemicarbazone.
2009
Synthesis and assessment of 99mTc chelate-conjugated alendronate for development of specific radiopharmaceuticals.
2009 Apr
Formyl- and acetylindols: vibrational spectroscopy of an expectably pharmacologically active compound family.
2009 Dec
The multifunctional enzyme CYP71B15 (PHYTOALEXIN DEFICIENT3) converts cysteine-indole-3-acetonitrile to camalexin in the indole-3-acetonitrile metabolic network of Arabidopsis thaliana.
2009 Jun
[Production of biologically active substances of indol nature by bacteria of Azotobacter genus].
2009 May-Jun
Structure and biological evaluation of novel cytotoxic sterol glycosides from the marine red alga Peyssonnelia sp.
2010 Dec 1
Metabolomic, transcriptional, hormonal, and signaling cross-talk in superroot2.
2010 Jan
Cutaneous bacteria of the redback salamander prevent morbidity associated with a lethal disease.
2010 Jun 4
The activity pattern and gene expression profile of aldehyde oxidase during the development of Pisum sativum seeds.
2010 Nov
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:38:35 GMT 2025
Edited
by admin
on Mon Mar 31 21:38:35 GMT 2025
Record UNII
7FN04C32UO
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
INDOLE-3-CARBOXALDEHYDE
Systematic Name English
NSC-10118
Preferred Name English
INDOLE-3-CARBALDEHYDE
Systematic Name English
1H-INDOLE-3-CARBOXALDEHYDE
Systematic Name English
3-INDOLYLFORMALDEHYDE
Systematic Name English
3-FORMYLINDOLE
Systematic Name English
Code System Code Type Description
NSC
10118
Created by admin on Mon Mar 31 21:38:35 GMT 2025 , Edited by admin on Mon Mar 31 21:38:35 GMT 2025
PRIMARY
CHEBI
28238
Created by admin on Mon Mar 31 21:38:35 GMT 2025 , Edited by admin on Mon Mar 31 21:38:35 GMT 2025
PRIMARY
EPA CompTox
DTXSID5060069
Created by admin on Mon Mar 31 21:38:35 GMT 2025 , Edited by admin on Mon Mar 31 21:38:35 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-665-8
Created by admin on Mon Mar 31 21:38:35 GMT 2025 , Edited by admin on Mon Mar 31 21:38:35 GMT 2025
PRIMARY
FDA UNII
7FN04C32UO
Created by admin on Mon Mar 31 21:38:35 GMT 2025 , Edited by admin on Mon Mar 31 21:38:35 GMT 2025
PRIMARY
CAS
487-89-8
Created by admin on Mon Mar 31 21:38:35 GMT 2025 , Edited by admin on Mon Mar 31 21:38:35 GMT 2025
PRIMARY
WIKIPEDIA
Indole-3-carboxaldehyde
Created by admin on Mon Mar 31 21:38:35 GMT 2025 , Edited by admin on Mon Mar 31 21:38:35 GMT 2025
PRIMARY
PUBCHEM
10256
Created by admin on Mon Mar 31 21:38:35 GMT 2025 , Edited by admin on Mon Mar 31 21:38:35 GMT 2025
PRIMARY
SMS_ID
300000027812
Created by admin on Mon Mar 31 21:38:35 GMT 2025 , Edited by admin on Mon Mar 31 21:38:35 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> METABOLITE