2-AMINO-3,6-DIHYDRO-3-METHYL-7H-IMIDAZO(4,5-F)QUINOLINE-7-ONE

CN1C(N)=NC2=C1C=CC3=C2C=CC(=O)N3

InChIKey=RRWYTKOWRFCKBO-UHFFFAOYSA-N

InChI=1S/C11H10N4O/c1-15-8-4-3-7-6(2-5-9(16)13-7)10(8)14-11(15)12/h2-5H,1H3,(H2,12,14)(H,13,16)

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

PubMed

Title	Date	PubMed
Metabolism of 2-amino-3-methylimidazo[4,5-f]quinoline in the male rat.	1989-06	2792966
Conversion of IQ, a dietary pyrolysis carcinogen to a direct-acting mutagen by normal intestinal bacteria of humans.	1988-11	3200256
Anaerobic metabolism of 2-amino-3-methyl-3H-imidazo[4,5-f]quinoline (IQ) by human fecal flora.	1987-03	3821779

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:48:51 GMT 2025` Edited by `admin` on `Mon Mar 31 21:48:51 GMT 2025`
Record UNII	5MNN6P93EM
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

2-AMINO-3,6-DIHYDRO-3-METHYL-7H-IMIDAZO(4,5-F)QUINOLINE-7-ONE

Systematic Name

English

7-HYDROXY-IQ

Preferred Name

English

7H-IMIDAZO(4,5-F)QUINOLIN-7-ONE, 3,6-DIHYDRO-2-AMINO-3-METHYL-

Systematic Name

English

Code System Code Type Description

EPA CompTox

DTXSID70148367

Created by admin on Mon Mar 31 21:48:51 GMT 2025 , Edited by admin on Mon Mar 31 21:48:51 GMT 2025

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CAS

108043-88-5

Created by admin on Mon Mar 31 21:48:51 GMT 2025 , Edited by admin on Mon Mar 31 21:48:51 GMT 2025

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FDA UNII

5MNN6P93EM

Created by admin on Mon Mar 31 21:48:51 GMT 2025 , Edited by admin on Mon Mar 31 21:48:51 GMT 2025

PRIMARY

PUBCHEM

115222

Created by admin on Mon Mar 31 21:48:51 GMT 2025 , Edited by admin on Mon Mar 31 21:48:51 GMT 2025

PRIMARY