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Details

Stereochemistry ABSOLUTE
Molecular Formula 2C27H44N10O12.3H2O4S
Molecular Weight 1695.632
Optical Activity UNSPECIFIED
Defined Stereocenters 30 / 30
E/Z Centers 2
Charge 0

SHOW SMILES / InChI
Structure of STREPTONICOZID

SMILES

OS(O)(=O)=O.OS(O)(=O)=O.OS(O)(=O)=O.[H][C@@]4(O[C@H]1[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](NC(N)=N)[C@@H](O)[C@@H]2NC(N)=N)O[C@@H](C)[C@]1(O)\C=N\NC(=O)C3=CC=NC=C3)O[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]4NC.[H][C@@]8(O[C@H]5[C@H](O[C@H]6[C@H](O)[C@@H](O)[C@H](NC(N)=N)[C@@H](O)[C@@H]6NC(N)=N)O[C@@H](C)[C@]5(O)\C=N\NC(=O)C7=CC=NC=C7)O[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]8NC

InChI

InChIKey=OIOSFHRAQVHZRE-BZROWGSASA-N
InChI=1S/2C27H44N10O12.3H2O4S/c2*1-9-27(45,8-34-37-22(44)10-3-5-33-6-4-10)21(49-23-14(32-2)18(42)15(39)11(7-38)47-23)24(46-9)48-20-13(36-26(30)31)16(40)12(35-25(28)29)17(41)19(20)43;3*1-5(2,3)4/h2*3-6,8-9,11-21,23-24,32,38-43,45H,7H2,1-2H3,(H,37,44)(H4,28,29,35)(H4,30,31,36);3*(H2,1,2,3,4)/b2*34-8+;;;/t2*9-,11-,12+,13-,14-,15-,16+,17-,18-,19+,20+,21-,23-,24-,27+;;;/m00.../s1

HIDE SMILES / InChI
Streptoniazid is a streptomycin derivative patented by Societe des usines chimiques de Rhone-Poulenc as antibiotic effective against tuberculosis.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Clinical and biological study of streptoniazid].
1954
The intermittent use of streptomycin and isoniazid singly and together in murine leprosy.
1955 Dec
Patents

Patents

Name Type Language
STREPTONICOZID
MI   USAN  
USAN  
Official Name English
4-PYRIDINECARBOXYLIC ACID HYDRAZIDE, HYDRAZONE WITH O-2-DEOXY-2-(METHYLAMINO)-.ALPHA.-L-GLUCOPYRANOSYL-(1->2)-O-5-DEOXY-3-C-FORMYL-.ALPHA.-L-LYXOFURANOSYL-(1->4)-N,N-BIS(AMINOIMINOMETHYL)-D-STREPTAMINE SULFATE (2:3) (SALT)
Systematic Name English
STREPTONIAZID SULFATE
Common Name English
STREPTOHYDRAZID
Brand Name English
STRAZIDE
Brand Name English
STREPTONICOZID [USAN]
Common Name English
Isonicotinic acid hydrazide, hydrazone with streptomycin, sulfate (2:3)
Common Name English
STREPTONICOZID [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C280
Created by admin on Fri Dec 15 15:36:59 GMT 2023 , Edited by admin on Fri Dec 15 15:36:59 GMT 2023
Code System Code Type Description
ECHA (EC/EINECS)
227-128-1
Created by admin on Fri Dec 15 15:36:59 GMT 2023 , Edited by admin on Fri Dec 15 15:36:59 GMT 2023
PRIMARY
CAS
5667-71-0
Created by admin on Fri Dec 15 15:36:59 GMT 2023 , Edited by admin on Fri Dec 15 15:36:59 GMT 2023
PRIMARY
FDA UNII
20R578ZX2B
Created by admin on Fri Dec 15 15:36:59 GMT 2023 , Edited by admin on Fri Dec 15 15:36:59 GMT 2023
PRIMARY
MESH
C009328
Created by admin on Fri Dec 15 15:36:59 GMT 2023 , Edited by admin on Fri Dec 15 15:36:59 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110590
Created by admin on Fri Dec 15 15:36:59 GMT 2023 , Edited by admin on Fri Dec 15 15:36:59 GMT 2023
PRIMARY
MERCK INDEX
m937
Created by admin on Fri Dec 15 15:36:59 GMT 2023 , Edited by admin on Fri Dec 15 15:36:59 GMT 2023
PRIMARY Merck Index
PUBCHEM
70695622
Created by admin on Fri Dec 15 15:36:59 GMT 2023 , Edited by admin on Fri Dec 15 15:36:59 GMT 2023
PRIMARY
CAS
7430-90-2
Created by admin on Fri Dec 15 15:36:59 GMT 2023 , Edited by admin on Fri Dec 15 15:36:59 GMT 2023
NON-SPECIFIC STOICHIOMETRY
NCI_THESAURUS
C152438
Created by admin on Fri Dec 15 15:36:59 GMT 2023 , Edited by admin on Fri Dec 15 15:36:59 GMT 2023
PRIMARY