OXAZEPAM GLUCURONIDE

Details

Stereochemistry	EPIMERIC
Molecular Formula	C21H19ClN2O8
Molecular Weight	462.837
Optical Activity	UNSPECIFIED
Defined Stereocenters	5 / 6
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

O[C@@H]1[C@@H](O)[C@H](OC2N=C(C3=CC=CC=C3)C4=CC(Cl)=CC=C4NC2=O)O[C@@H]([C@H]1O)C(O)=O

InChI

InChIKey=FIKQKGFUBZQEBL-IFBJMGMISA-N

InChI=1S/C21H19ClN2O8/c22-10-6-7-12-11(8-10)13(9-4-2-1-3-5-9)24-19(18(28)23-12)32-21-16(27)14(25)15(26)17(31-21)20(29)30/h1-8,14-17,19,21,25-27H,(H,23,28)(H,29,30)/t14-,15-,16+,17-,19?,21-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C21H19ClN2O8
Molecular Weight	462.837
Charge	0
Count

Stereochemistry	EPIMERIC
Additional Stereochemistry	No
Defined Stereocenters	5 / 6
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

PubMed

Title	Date	PubMed
(S)oxazepam glucuronidation is inhibited by ketoprofen and other substrates of UGT2B7.	1995 Feb	7773302
Stereoselective conjugation of oxazepam by human UDP-glucuronosyltransferases (UGTs): S-oxazepam is glucuronidated by UGT2B15, while R-oxazepam is glucuronidated by UGT2B7 and UGT1A9.	2002 Nov	12386133

Substance Class	Chemical Created by `admin` on `Mon Mar 31 22:50:58 GMT 2025` Edited by `admin` on `Mon Mar 31 22:50:58 GMT 2025`
Record UNII	26IK2C76NO
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

OXAZEPAM GLUCURONIDE

Common Name

English

.BETA.-D-GLUCOPYRANOSIDURONIC ACID, 7-CHLORO-2,3-DIHYDRO-2-OXO-5-PHENYL-1H-1,4-BENZODIAZEPIN-3-YL

Preferred Name

English

Code System Code Type Description

EPA CompTox

DTXSID701028080

Created by admin on Mon Mar 31 22:50:58 GMT 2025 , Edited by admin on Mon Mar 31 22:50:58 GMT 2025

PRIMARY

CAS

6801-81-6

Created by admin on Mon Mar 31 22:50:58 GMT 2025 , Edited by admin on Mon Mar 31 22:50:58 GMT 2025

PRIMARY

FDA UNII

26IK2C76NO

Created by admin on Mon Mar 31 22:50:58 GMT 2025 , Edited by admin on Mon Mar 31 22:50:58 GMT 2025

PRIMARY

PUBCHEM

160870

Created by admin on Mon Mar 31 22:50:58 GMT 2025 , Edited by admin on Mon Mar 31 22:50:58 GMT 2025

PRIMARY

Related Record Type Details


					CHB1QD2QSS

TEMAZEPAM

PARENT -> METABOLITE INACTIVE