HYDROXYHEXAMIDE

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C15H22N2O4S
Molecular Weight	326.411
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of HYDROXYHEXAMIDE

Structure Search

SMILES

CC(O)C1=CC=C(C=C1)S(=O)(=O)NC(=O)NC2CCCCC2

InChI

InChIKey=VQDAEOYLIBGCHE-UHFFFAOYSA-N

InChI=1S/C15H22N2O4S/c1-11(18)12-7-9-14(10-8-12)22(20,21)17-15(19)16-13-5-3-2-4-6-13/h7-11,13,18H,2-6H2,1H3,(H2,16,17,19)

HIDE SMILES / InChI

Molecular Formula	C15H22N2O4S
Molecular Weight	326.411
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Approval Year

PubMed

PubMed

Title	Date	PubMed
Hypoglycemic effect of S(-)-hydroxyhexamide, a major metabolite of acetohexamide, and its enantiomer R(+)-hydroxyhexamide.	2001-09-07	11693275

Substance Class	Chemical Created by `admin` on `Mon Mar 31 17:34:40 GMT 2025` Edited by `admin` on `Mon Mar 31 17:34:40 GMT 2025`
Record UNII	F3F26TZ9HN
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

HYDROXYHEXAMIDE

Common Name

English

(±)-HYDROXYHEXAMIDE

Preferred Name

English

BENZENESULFONAMIDE, N-((CYCLOHEXYLAMINO)CARBONYL)-4-(1-HYDROXYETHYL)-

Systematic Name

English

1-CYCLOHEXYL-3-((P-(1-HYDROXYETHYL)-PHENYL)SULFONYL)UREA

Common Name

English

Code System Code Type Description

CAS

3168-01-2

Created by admin on Mon Mar 31 17:34:40 GMT 2025 , Edited by admin on Mon Mar 31 17:34:40 GMT 2025

PRIMARY

FDA UNII

F3F26TZ9HN

Created by admin on Mon Mar 31 17:34:40 GMT 2025 , Edited by admin on Mon Mar 31 17:34:40 GMT 2025

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PUBCHEM

18497

Created by admin on Mon Mar 31 17:34:40 GMT 2025 , Edited by admin on Mon Mar 31 17:34:40 GMT 2025

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ChEMBL

CHEMBL2105052

Created by admin on Mon Mar 31 17:34:40 GMT 2025 , Edited by admin on Mon Mar 31 17:34:40 GMT 2025

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SMS_ID

300000020231

Created by admin on Mon Mar 31 17:34:40 GMT 2025 , Edited by admin on Mon Mar 31 17:34:40 GMT 2025

PRIMARY

EPA CompTox

DTXSID50953633

Created by admin on Mon Mar 31 17:34:40 GMT 2025 , Edited by admin on Mon Mar 31 17:34:40 GMT 2025

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MESH

C020362

Created by admin on Mon Mar 31 17:34:40 GMT 2025 , Edited by admin on Mon Mar 31 17:34:40 GMT 2025

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