(5-CHLORO-6-((6-METHYLPYRIDIN-3-YL)AMINO)PYRIDIN-3-YL)-((2R)-2-ETHYLPIPERIDIN-1-YL)METHANONE

CC[C@@H]1CCCCN1C(=O)C2=CC(Cl)=C(NC3=CC=C(C)N=C3)N=C2

InChIKey=QABUURICQJOWID-MRXNPFEDSA-N

InChI=1S/C19H23ClN4O/c1-3-16-6-4-5-9-24(16)19(25)14-10-17(20)18(22-11-14)23-15-8-7-13(2)21-12-15/h7-8,10-12,16H,3-6,9H2,1-2H3,(H,22,23)/t16-/m1/s1

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	1 / 1
E/Z Centers	0
Optical Activity	UNSPECIFIED

PubMed

Title	Date	PubMed
Piperidyl amides as novel, potent and orally active mGlu5 receptor antagonists with anxiolytic-like activity.	2010-01-01	19931453

Substance Class	Chemical Created by `admin` on `Mon Mar 31 22:39:22 GMT 2025` Edited by `admin` on `Mon Mar 31 22:39:22 GMT 2025`
Record UNII	J5PMS063XX
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

METHANONE, (5-CHLORO-6-((6-METHYL-3-PYRIDINYL)AMINO)-3-PYRIDINYL)((2R)-2-ETHYL-1-PIPERIDINYL)-

Preferred Name

English

(5-CHLORO-6-((6-METHYLPYRIDIN-3-YL)AMINO)PYRIDIN-3-YL)-((2R)-2-ETHYLPIPERIDIN-1-YL)METHANONE

Systematic Name

English

Code System Code Type Description

PUBCHEM

23725699

Created by admin on Mon Mar 31 22:39:22 GMT 2025 , Edited by admin on Mon Mar 31 22:39:22 GMT 2025

PRIMARY

CAS

942510-68-1

Created by admin on Mon Mar 31 22:39:22 GMT 2025 , Edited by admin on Mon Mar 31 22:39:22 GMT 2025

PRIMARY

FDA UNII

J5PMS063XX

Created by admin on Mon Mar 31 22:39:22 GMT 2025 , Edited by admin on Mon Mar 31 22:39:22 GMT 2025

PRIMARY