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

Details

Stereochemistry ABSOLUTE
Molecular Formula C27H44N10O12
Molecular Weight 700.6981
Optical Activity UNSPECIFIED
Defined Stereocenters 15 / 15
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of STREPTONIAZID

SMILES

[H][C@@]2(O[C@H]1[C@H](O)[C@@H](O)[C@H](NC(N)=N)[C@@H](O)[C@@H]1NC(N)=N)O[C@@H](C)[C@](O)(C=NNC(=O)C3=CC=NC=C3)[C@H]2O[C@]4([H])O[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]4NC

InChI

InChIKey=JCBKYEIGGFKWPQ-HKWRBIJSSA-N
InChI=1S/C27H44N10O12/c1-9-27(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/h3-6,8-9,11-21,23-24,32,38-43,45H,7H2,1-2H3,(H,37,44)(H4,28,29,35)(H4,30,31,36)/b34-8+/t9-,11-,12+,13-,14-,15-,16+,17-,18-,19+,20+,21-,23-,24-,27+/m0/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
STREPTONIAZID
INN   WHO-DD  
INN  
Official Name English
NSC-77675
Code English
Streptoniazid [WHO-DD]
Common Name English
ISONICOTINIC ACID HYDRAZIDE, HYDRAZONE WITH STREPTOMYCIN
Common Name English
D-STREPTAMINE, O-2-DEOXY-2-(METHYLAMINO)-.ALPHA.-L-GLUCOPYRANOSYL-(1-2)-O-5-DEOXY-3-C-(((4-PYRIDINYLCARBONYL)HYDRAZONO)METHYL)-.ALPHA.-L-LYXOFURANOSYL-(1-4)-N1,N3-BIS(AMINOIMINOMETHYL)-
Common Name English
ESTREPTONIAZID
Common Name English
streptoniazid [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C280
Created by admin on Fri Dec 15 18:28:13 GMT 2023 , Edited by admin on Fri Dec 15 18:28:13 GMT 2023
Code System Code Type Description
NSC
77675
Created by admin on Fri Dec 15 18:28:13 GMT 2023 , Edited by admin on Fri Dec 15 18:28:13 GMT 2023
PRIMARY
EVMPD
SUB10657MIG
Created by admin on Fri Dec 15 18:28:13 GMT 2023 , Edited by admin on Fri Dec 15 18:28:13 GMT 2023
PRIMARY
FDA UNII
IAB9JFQ8U2
Created by admin on Fri Dec 15 18:28:13 GMT 2023 , Edited by admin on Fri Dec 15 18:28:13 GMT 2023
PRIMARY
EPA CompTox
DTXSID001017016
Created by admin on Fri Dec 15 18:28:13 GMT 2023 , Edited by admin on Fri Dec 15 18:28:13 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110590
Created by admin on Fri Dec 15 18:28:13 GMT 2023 , Edited by admin on Fri Dec 15 18:28:13 GMT 2023
PRIMARY
NCI_THESAURUS
C152437
Created by admin on Fri Dec 15 18:28:13 GMT 2023 , Edited by admin on Fri Dec 15 18:28:13 GMT 2023
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INN
286
Created by admin on Fri Dec 15 18:28:13 GMT 2023 , Edited by admin on Fri Dec 15 18:28:13 GMT 2023
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CAS
4480-58-4
Created by admin on Fri Dec 15 18:28:13 GMT 2023 , Edited by admin on Fri Dec 15 18:28:13 GMT 2023
PRIMARY
PUBCHEM
91617807
Created by admin on Fri Dec 15 18:28:13 GMT 2023 , Edited by admin on Fri Dec 15 18:28:13 GMT 2023
PRIMARY
SMS_ID
100000083484
Created by admin on Fri Dec 15 18:28:13 GMT 2023 , Edited by admin on Fri Dec 15 18:28:13 GMT 2023
PRIMARY