U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C9H9N
Molecular Weight 131.1745
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-METHYLINDOLE

SMILES

CC1=C2C=CNC2=CC=C1

InChI

InChIKey=PZOUSPYUWWUPPK-UHFFFAOYSA-N
InChI=1S/C9H9N/c1-7-3-2-4-9-8(7)5-6-10-9/h2-6,10H,1H3

HIDE SMILES / InChI

Molecular Formula C9H9N
Molecular Weight 131.1745
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis and pharmacological evaluation of some 6-substituted 7-methyl-1,4-dioxa-7-azaspiro[4.5]decanes as potential dopamine agonists.
1986 Aug
DNA mediated charge transport: characterization of a DNA radical localized at an artificial nucleic acid base.
2002 Aug 7
Key labeling technologies to tackle sizeable problems in RNA structural biology.
2008 Jun
Use of 4-methylindole or 7-methyl-DL-tryptophan in a transformant selection system based on the feedback-insensitive anthranilate synthase alpha-subunit of tobacco (ASA2).
2008 Mar
Tobacco plastid transformation using the feedback-insensitive anthranilate synthase [alpha]-subunit of tobacco (ASA2) as a new selectable marker.
2009
An odorant receptor from the southern house mosquito Culex pipiens quinquefasciatus sensitive to oviposition attractants.
2010 Apr 8
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:07:13 GMT 2023
Edited
by admin
on Fri Dec 15 18:07:13 GMT 2023
Record UNII
3338387XEA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-METHYLINDOLE
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID20167043
Created by admin on Fri Dec 15 18:07:13 GMT 2023 , Edited by admin on Fri Dec 15 18:07:13 GMT 2023
PRIMARY
ECHA (EC/EINECS)
240-262-5
Created by admin on Fri Dec 15 18:07:13 GMT 2023 , Edited by admin on Fri Dec 15 18:07:13 GMT 2023
PRIMARY
CAS
16096-32-5
Created by admin on Fri Dec 15 18:07:13 GMT 2023 , Edited by admin on Fri Dec 15 18:07:13 GMT 2023
PRIMARY
FDA UNII
3338387XEA
Created by admin on Fri Dec 15 18:07:13 GMT 2023 , Edited by admin on Fri Dec 15 18:07:13 GMT 2023
PRIMARY
PUBCHEM
85282
Created by admin on Fri Dec 15 18:07:13 GMT 2023 , Edited by admin on Fri Dec 15 18:07:13 GMT 2023
PRIMARY