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

Details

Stereochemistry RACEMIC
Molecular Formula C8H16N6OS2
Molecular Weight 276.382
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 2
Charge 0

SHOW SMILES / InChI
Structure of GLOXAZONE

SMILES

CCOC(C)C(C=NNC(N)=S)=NNC(N)=S

InChI

InChIKey=ARIFZLJIERKKEL-UHFFFAOYSA-N
InChI=1S/C8H16N6OS2/c1-3-15-5(2)6(12-14-8(10)17)4-11-13-7(9)16/h4-5H,3H2,1-2H3,(H3,9,13,16)(H3,10,14,17)

HIDE SMILES / InChI

Molecular Formula C8H16N6OS2
Molecular Weight 276.382
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 2
Optical Activity ( + / - )

Gloxazone is a drug tested against anaplasmosis and cowdriosis, both tick-borne diseases. It was found to cause toxicity in the kidneys of rats and also had unacceptably high toxic levels in lactating cattle.

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:44:21 GMT 2023
Edited
by admin
on Fri Dec 15 18:44:21 GMT 2023
Record UNII
OP8B49OL1J
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GLOXAZONE
INN   USAN  
USAN   INN  
Official Name English
CONTRAPAR
Brand Name English
BW 356-C-61
Code English
3-Ethoxy-2-oxobutyraldehyde bis(thiosemicarbazone)
Systematic Name English
gloxazone [INN]
Common Name English
HYDRAZINECARBOTHIOAMIDE, 2,2'-(1-(1-ETHOXYETHYL)-1,2-ETHANEDIYLIDENE)BIS-
Systematic Name English
BW-356C61
Code English
GLOXAZONE [USAN]
Common Name English
BW-356-C-61
Code English
NSC-82116
Code English
(1-ETHOXYETHYL)GLYOXAL BIS(THIOSEMICARBAZONE)
Systematic Name English
KETHOXAL BIS(THIOSEMICARBAZONE) [MI]
Common Name English
KETHOXAL BIS(THIOSEMICARBAZONE)
MI  
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C28394
Created by admin on Fri Dec 15 18:44:21 GMT 2023 , Edited by admin on Fri Dec 15 18:44:21 GMT 2023
Code System Code Type Description
ECHA (EC/EINECS)
219-715-6
Created by admin on Fri Dec 15 18:44:21 GMT 2023 , Edited by admin on Fri Dec 15 18:44:21 GMT 2023
PRIMARY
MERCK INDEX
m6617
Created by admin on Fri Dec 15 18:44:21 GMT 2023 , Edited by admin on Fri Dec 15 18:44:21 GMT 2023
PRIMARY Merck Index
MESH
C072679
Created by admin on Fri Dec 15 18:44:21 GMT 2023 , Edited by admin on Fri Dec 15 18:44:21 GMT 2023
PRIMARY
CAS
2507-91-7
Created by admin on Fri Dec 15 18:44:21 GMT 2023 , Edited by admin on Fri Dec 15 18:44:21 GMT 2023
PRIMARY
NCI_THESAURUS
C76265
Created by admin on Fri Dec 15 18:44:21 GMT 2023 , Edited by admin on Fri Dec 15 18:44:21 GMT 2023
PRIMARY
ChEMBL
CHEMBL1981146
Created by admin on Fri Dec 15 18:44:21 GMT 2023 , Edited by admin on Fri Dec 15 18:44:21 GMT 2023
PRIMARY
PUBCHEM
6399216
Created by admin on Fri Dec 15 18:44:21 GMT 2023 , Edited by admin on Fri Dec 15 18:44:21 GMT 2023
PRIMARY
SMS_ID
100000084225
Created by admin on Fri Dec 15 18:44:21 GMT 2023 , Edited by admin on Fri Dec 15 18:44:21 GMT 2023
PRIMARY
EPA CompTox
DTXSID70862975
Created by admin on Fri Dec 15 18:44:21 GMT 2023 , Edited by admin on Fri Dec 15 18:44:21 GMT 2023
PRIMARY
INN
2473
Created by admin on Fri Dec 15 18:44:21 GMT 2023 , Edited by admin on Fri Dec 15 18:44:21 GMT 2023
PRIMARY
NSC
82116
Created by admin on Fri Dec 15 18:44:21 GMT 2023 , Edited by admin on Fri Dec 15 18:44:21 GMT 2023
PRIMARY
EVMPD
SUB07934MIG
Created by admin on Fri Dec 15 18:44:21 GMT 2023 , Edited by admin on Fri Dec 15 18:44:21 GMT 2023
PRIMARY
FDA UNII
OP8B49OL1J
Created by admin on Fri Dec 15 18:44:21 GMT 2023 , Edited by admin on Fri Dec 15 18:44:21 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY