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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=CC=CC=C12

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
Structure-activity relationship for bromoindole carbaldehydes: effects on the sea urchin embryo cell cycle.
2001 Mar
1,2-bis(1H-indol-3-yl)ethane-1,2-dione, an indole alkaloid from the marine sponge Smenospongia sp.
2002 Apr
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
Peroxynitrite scavenging activities of aromatic compounds isolated from Konnyaku, Amorphophallus konjac K.Koch.
2002 Jun
Complete and remarkable reversal of chemoselectivity in [4 + 2] cycloadditions involving electron-poor indoles as dienophiles. Diels-Alder versus hetero-Diels-Alder processes.
2003 Oct 17
Pharmacokinetics and tissue disposition of indole-3-carbinol and its acid condensation products after oral administration to mice.
2004 Aug 1
(Z)-3-(1H-Indol-3-yl)-2-(3-thienyl)acrylonitrile and (Z)-3-[1-(4-tert-butylbenzyl)-1H-indol-3-yl]-2-(3-thienyl)acrylonitrile.
2005 Feb
Hymeniacidon perleve associated bioactive bacterium pseudomonas sp. NJ6-3-1.
2005 Jan-Feb
Aldehyde oxidase (AO) in the root nodules of Lupinus albus and Medicago truncatula: identification of AO in meristematic and infection zones.
2005 May
Enantioselective total syntheses of welwitindolinone A and fischerindoles I and G.
2005 Nov 9
Molecular characterization of the gallate dioxygenase from Pseudomonas putida KT2440. The prototype of a new subgroup of extradiol dioxygenases.
2005 Oct 21
Rapid access to the Welwitindolinone alkaloid skeleton by cyclization of indolecarboxaldehyde substituted cyclohexanones.
2005 Sep 15
[Studies on chemical constituents in root of Isatis indigotica].
2007 Apr
Anticancer activity evaluation of kuanoniamines A and C isolated from the marine sponge Oceanapia sagittaria, collected from the Gulf of Thailand.
2007 Apr 17
Compounds from Wedelia chinensis synergistically suppress androgen activity and growth in prostate cancer cells.
2007 Dec
Amorphane sesquiterpenes from a marine Streptomyces sp.
2007 Feb
Synthesis, characterization and biological activity of Schiff base analogues of indole-3-carboxaldehyde.
2008 Jan
Highly sensitive feature detection for high resolution LC/MS.
2008 Nov 28
N'-[(E)-3-Indol-3-ylmethyl-ene]isonicotino-hydrazide monohydrate.
2009 Jul 18
An efficient one-step synthesis of heterobiaryl pyrazolo[3,4-b]pyridines via indole ring opening.
2009 Nov 19
An expeditious I2-catalyzed entry into 6H-indolo[2,3-b]quinoline system of cryptotackieine.
2009 Nov 6
Structure and biological evaluation of novel cytotoxic sterol glycosides from the marine red alga Peyssonnelia sp.
2010 Dec 1
A novel role for Arabidopsis mitochondrial ABC transporter ATM3 in molybdenum cofactor biosynthesis.
2010 Feb
Secondary metabolites of Volvariella bombycina and their inhibitory effects on melanogenesis.
2010 Jan
Identification of antibacterial and antifungal pharmacophore sites for potent bacteria and fungi inhibition: indolenyl sulfonamide derivatives.
2010 Mar
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 Sat Dec 16 06:50:18 UTC 2023
Edited
by admin
on Sat Dec 16 06:50:18 UTC 2023
Record UNII
7FN04C32UO
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
INDOLE-3-CARBOXALDEHYDE
Systematic Name English
INDOLE-3-CARBALDEHYDE
Systematic Name English
1H-INDOLE-3-CARBOXALDEHYDE
Systematic Name English
3-INDOLYLFORMALDEHYDE
Systematic Name English
NSC-10118
Code English
3-FORMYLINDOLE
Systematic Name English
Code System Code Type Description
NSC
10118
Created by admin on Sat Dec 16 06:50:18 UTC 2023 , Edited by admin on Sat Dec 16 06:50:18 UTC 2023
PRIMARY
CHEBI
28238
Created by admin on Sat Dec 16 06:50:18 UTC 2023 , Edited by admin on Sat Dec 16 06:50:18 UTC 2023
PRIMARY
EPA CompTox
DTXSID5060069
Created by admin on Sat Dec 16 06:50:18 UTC 2023 , Edited by admin on Sat Dec 16 06:50:18 UTC 2023
PRIMARY
ECHA (EC/EINECS)
207-665-8
Created by admin on Sat Dec 16 06:50:18 UTC 2023 , Edited by admin on Sat Dec 16 06:50:18 UTC 2023
PRIMARY
FDA UNII
7FN04C32UO
Created by admin on Sat Dec 16 06:50:18 UTC 2023 , Edited by admin on Sat Dec 16 06:50:18 UTC 2023
PRIMARY
CAS
487-89-8
Created by admin on Sat Dec 16 06:50:18 UTC 2023 , Edited by admin on Sat Dec 16 06:50:18 UTC 2023
PRIMARY
WIKIPEDIA
Indole-3-carboxaldehyde
Created by admin on Sat Dec 16 06:50:18 UTC 2023 , Edited by admin on Sat Dec 16 06:50:18 UTC 2023
PRIMARY
PUBCHEM
10256
Created by admin on Sat Dec 16 06:50:18 UTC 2023 , Edited by admin on Sat Dec 16 06:50:18 UTC 2023
PRIMARY
SMS_ID
300000027812
Created by admin on Sat Dec 16 06:50:18 UTC 2023 , Edited by admin on Sat Dec 16 06:50:18 UTC 2023
PRIMARY
Related Record Type Details
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