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Details

Stereochemistry ACHIRAL
Molecular Formula C9H9NO
Molecular Weight 147.1739
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 5-METHOXYINDOLE

SMILES

COC1=CC2=C(NC=C2)C=C1

InChI

InChIKey=DWAQDRSOVMLGRQ-UHFFFAOYSA-N
InChI=1S/C9H9NO/c1-11-8-2-3-9-7(6-8)4-5-10-9/h2-6,10H,1H3

HIDE SMILES / InChI

Molecular Formula C9H9NO
Molecular Weight 147.1739
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
A simple procedure for synthesis of roxindole, a dopamine D2-receptor agonist.
2001 Jul
Daily variation in the concentration of 5-methoxytryptophol and melatonin in the duck pineal gland and plasma.
2002 May
Daily variation in the concentration of melatonin and 5-methoxytryptophol in the goose pineal gland, retina, and plasma.
2003 Dec
Generation of new protein kinase inhibitors utilizing cytochrome p450 mutant enzymes for indigoid synthesis.
2004 Jun 3
Indole ring oxidation by activated leukocytes prevents the production of hypochlorous acid.
2005 Nov
Simultaneous liquid chromatographic measurement of melatonin and related indoles through post-column electrochemical demethylation and fluorescence derivatization.
2006 Feb
Nucleophilic reactivities of indoles.
2006 Nov 24
Biological targets for isatin and its analogues: Implications for therapy.
2007 Jun
Functional expression and comparative characterization of nine murine cytochromes P450 by fluorescent inhibition screening.
2008 Jul
The 5-HT3B subunit confers spontaneous channel opening and altered ligand properties of the 5-HT3 receptor.
2008 Mar 14
4-Des-oxy-4β-[(5-meth-oxy-1H-indol-3-yl)oxalylamino]podophyllotoxin methanol solvate.
2008 Nov 13
The synthesis of 2- and 3-aryl indoles and 1,3,4,5-tetrahydropyrano[4,3-b]indoles and their antibacterial and antifungal activity.
2009 Sep 1
Optimization of the interligand Overhauser effect for fragment linking: application to inhibitor discovery against Mycobacterium tuberculosis pantothenate synthetase.
2010 Apr 7
Rotationally resolved electronic spectroscopy of 5-methoxyindole.
2010 Jul 14
5-Meth-oxy-1-(3,4,5-trimethoxy-phen-yl)-1H-indole.
2010 Jun 16
Mechanism for the direct synthesis of tryptophan from indole and serine: a useful NMR technique for the detection of a reactive intermediate in the reaction mixture.
2010 Oct
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:12:22 GMT 2023
Edited
by admin
on Fri Dec 15 19:12:22 GMT 2023
Record UNII
DQM3AS43PQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
5-METHOXYINDOLE
Systematic Name English
INDOLE, 5-METHOXY-
Systematic Name English
INDOL-5-YL METHYL ETHER
Systematic Name English
NSC-521752
Code English
5-METHOXY-1H-INDOLE
Systematic Name English
1H-INDOLE, 5-METHOXY-
Systematic Name English
FEMEDOL
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID80143424
Created by admin on Fri Dec 15 19:12:22 GMT 2023 , Edited by admin on Fri Dec 15 19:12:22 GMT 2023
PRIMARY
CAS
1006-94-6
Created by admin on Fri Dec 15 19:12:22 GMT 2023 , Edited by admin on Fri Dec 15 19:12:22 GMT 2023
PRIMARY
FDA UNII
DQM3AS43PQ
Created by admin on Fri Dec 15 19:12:22 GMT 2023 , Edited by admin on Fri Dec 15 19:12:22 GMT 2023
PRIMARY
NSC
521752
Created by admin on Fri Dec 15 19:12:22 GMT 2023 , Edited by admin on Fri Dec 15 19:12:22 GMT 2023
PRIMARY
PUBCHEM
13872
Created by admin on Fri Dec 15 19:12:22 GMT 2023 , Edited by admin on Fri Dec 15 19:12:22 GMT 2023
PRIMARY
ECHA (EC/EINECS)
213-745-3
Created by admin on Fri Dec 15 19:12:22 GMT 2023 , Edited by admin on Fri Dec 15 19:12:22 GMT 2023
PRIMARY