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

Details

Stereochemistry ABSOLUTE
Molecular Formula C12H13N3O6
Molecular Weight 295.2481
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of GLYCONIAZIDE

SMILES

[H][C@@]1(OC(=O)[C@@H](O)[C@H]1O)[C@@H](O)\C=N\NC(=O)C2=CC=NC=C2

InChI

InChIKey=ZBRCAASZBMWIDA-QFPUCQTMSA-N
InChI=1S/C12H13N3O6/c16-7(10-8(17)9(18)12(20)21-10)5-14-15-11(19)6-1-3-13-4-2-6/h1-5,7-10,16-18H,(H,15,19)/b14-5+/t7-,8+,9-,10+/m0/s1

HIDE SMILES / InChI

Description

Glyconiazide is an antibacterial drug with high antitubercular activity in vitro as well as in vivo. The drug was reported to cause sensitive polyneuritis upon administration.

Approval Year

Unknown
139594
Patents

Patents

7790905
106
7927613
118
Name Type Language
GLYCONIAZIDE
MI   WHO-DD  
Common Name English
Glyconiazide [WHO-DD]
Common Name English
GLUCONIAZIDE
Common Name English
D-GLUCURONOLACTONE ISONICOTINYL HYDRAZONE
Common Name English
GLUCAZIDE
Common Name English
GALATONE
Common Name English
GATALONE
Brand Name English
MYCOBACTYL
Brand Name English
INH-G
Common Name English
NSC-27605
Code English
GLUCURONIC ACID, .GAMMA.-LACTONE, 1-((4-PYRIDINYLCARBONYL)HYDRAZONE)
Systematic Name English
GUIDAZIDE
Common Name English
HYDRONSAN
Brand Name English
GLUCURONIC ACID, .GAMMA.-LACTONE, 1-(ISONICOTINOYLHYDRAZONE), D-
Systematic Name English
GLYCONIAZIDE [MI]
Common Name English
GLURONAZIDE
Common Name English
ISONICOTINIC ACID, HYDRAZIDE, HYDRAZONE WITH D-GLUCURONIC ACID .GAMMA.-LACTONE
Systematic Name English
D-GLUCURONOLACTONE ISONICOTINOYLHYDRAZONE
Common Name English
GLURONAZID
Common Name English
Code System Code Type Description
MERCK INDEX
m5806
Created by admin on Sat Dec 16 08:43:05 GMT 2023 , Edited by admin on Sat Dec 16 08:43:05 GMT 2023
PRIMARY Merck Index
PUBCHEM
9571091
Created by admin on Sat Dec 16 08:43:05 GMT 2023 , Edited by admin on Sat Dec 16 08:43:05 GMT 2023
PRIMARY
FDA UNII
D71I145DMC
Created by admin on Sat Dec 16 08:43:05 GMT 2023 , Edited by admin on Sat Dec 16 08:43:05 GMT 2023
PRIMARY
NSC
27605
Created by admin on Sat Dec 16 08:43:05 GMT 2023 , Edited by admin on Sat Dec 16 08:43:05 GMT 2023
PRIMARY
CAS
3691-74-5
Created by admin on Sat Dec 16 08:43:05 GMT 2023 , Edited by admin on Sat Dec 16 08:43:05 GMT 2023
PRIMARY
EVMPD
SUB14000MIG
Created by admin on Sat Dec 16 08:43:05 GMT 2023 , Edited by admin on Sat Dec 16 08:43:05 GMT 2023
PRIMARY
EPA CompTox
DTXSID101031982
Created by admin on Sat Dec 16 08:43:05 GMT 2023 , Edited by admin on Sat Dec 16 08:43:05 GMT 2023
PRIMARY
ECHA (EC/EINECS)
223-005-1
Created by admin on Sat Dec 16 08:43:05 GMT 2023 , Edited by admin on Sat Dec 16 08:43:05 GMT 2023
PRIMARY
CAS
31046-10-3
Created by admin on Sat Dec 16 08:43:05 GMT 2023 , Edited by admin on Sat Dec 16 08:43:05 GMT 2023
SUPERSEDED
DRUG CENTRAL
3270
Created by admin on Sat Dec 16 08:43:05 GMT 2023 , Edited by admin on Sat Dec 16 08:43:05 GMT 2023
PRIMARY
SMS_ID
100000078198
Created by admin on Sat Dec 16 08:43:05 GMT 2023 , Edited by admin on Sat Dec 16 08:43:05 GMT 2023
PRIMARY
ACTIVE MOIETY
Structure of GLYCONIAZIDE
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966