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Details

Stereochemistry ACHIRAL
Molecular Formula C3H3N3O2S
Molecular Weight 145.14
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-AMINO-5-NITROTHIAZOLE

SMILES

NC1=NC=C(S1)[N+]([O-])=O

InChI

InChIKey=MIHADVKEHAFNPG-UHFFFAOYSA-N
InChI=1S/C3H3N3O2S/c4-3-5-1-2(9-3)6(7)8/h1H,(H2,4,5)

HIDE SMILES / InChI

Molecular Formula C3H3N3O2S
Molecular Weight 145.14
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Bioassay of 2-amino-5-nitrothiazole for possible carcinogenicity.
1978
2-Amino-5-nitrothiazole monoethanol solvate: triply-interwoven hydrogen-bonded sheets containing centrosymmetric R2 2(8) and RR10 10(38) rings.
2004 Jan
Cryptobia iubilans infection in juvenile discus.
2004 May 15
N-(4-Meth-oxy-phen-yl)-N'-(5-nitro-1,3-thia-zol-2-yl)urea.
2010 Aug 18
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 04:48:02 GMT 2023
Edited
by admin
on Sat Dec 16 04:48:02 GMT 2023
Record UNII
1GR77A37Z5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-AMINO-5-NITROTHIAZOLE
HSDB   MI  
Systematic Name English
2-AMINO-5-NITROTHIAZOLE [IARC]
Common Name English
NSC-4
Code English
2-AMINO-5-NITROTHIAZOLE [MI]
Common Name English
NITAZOXANIDE RELATED COMPOUND A
USP-RS  
Common Name English
ENHEPTIN
Brand Name English
AMINONITROTHIAZOL
Systematic Name English
NITAZOXANIDE RELATED COMPOUND A [USP-RS]
Common Name English
2-AMINO-5-NITROTHIAZOL
Systematic Name English
5-NITRO-2-THIAZOLAMINE
Systematic Name English
2-AMINO-5-NITROTHIAZOLE [HSDB]
Common Name English
Classification Tree Code System Code
WHO-VATC QP51AX16
Created by admin on Sat Dec 16 04:48:02 GMT 2023 , Edited by admin on Sat Dec 16 04:48:02 GMT 2023
NCI_THESAURUS C277
Created by admin on Sat Dec 16 04:48:02 GMT 2023 , Edited by admin on Sat Dec 16 04:48:02 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C76409
Created by admin on Sat Dec 16 04:48:02 GMT 2023 , Edited by admin on Sat Dec 16 04:48:02 GMT 2023
PRIMARY
PUBCHEM
8486
Created by admin on Sat Dec 16 04:48:02 GMT 2023 , Edited by admin on Sat Dec 16 04:48:02 GMT 2023
PRIMARY
MERCK INDEX
m1723
Created by admin on Sat Dec 16 04:48:02 GMT 2023 , Edited by admin on Sat Dec 16 04:48:02 GMT 2023
PRIMARY Merck Index
SMS_ID
300000033070
Created by admin on Sat Dec 16 04:48:02 GMT 2023 , Edited by admin on Sat Dec 16 04:48:02 GMT 2023
PRIMARY
MESH
C034870
Created by admin on Sat Dec 16 04:48:02 GMT 2023 , Edited by admin on Sat Dec 16 04:48:02 GMT 2023
PRIMARY
RXCUI
1665683
Created by admin on Sat Dec 16 04:48:02 GMT 2023 , Edited by admin on Sat Dec 16 04:48:02 GMT 2023
PRIMARY RxNorm
CAS
121-66-4
Created by admin on Sat Dec 16 04:48:02 GMT 2023 , Edited by admin on Sat Dec 16 04:48:02 GMT 2023
PRIMARY
NSC
4
Created by admin on Sat Dec 16 04:48:02 GMT 2023 , Edited by admin on Sat Dec 16 04:48:02 GMT 2023
PRIMARY
RS_ITEM_NUM
1463971
Created by admin on Sat Dec 16 04:48:02 GMT 2023 , Edited by admin on Sat Dec 16 04:48:02 GMT 2023
PRIMARY
FDA UNII
1GR77A37Z5
Created by admin on Sat Dec 16 04:48:02 GMT 2023 , Edited by admin on Sat Dec 16 04:48:02 GMT 2023
PRIMARY
ECHA (EC/EINECS)
204-490-9
Created by admin on Sat Dec 16 04:48:02 GMT 2023 , Edited by admin on Sat Dec 16 04:48:02 GMT 2023
PRIMARY
EPA CompTox
DTXSID6020066
Created by admin on Sat Dec 16 04:48:02 GMT 2023 , Edited by admin on Sat Dec 16 04:48:02 GMT 2023
PRIMARY
DAILYMED
1GR77A37Z5
Created by admin on Sat Dec 16 04:48:02 GMT 2023 , Edited by admin on Sat Dec 16 04:48:02 GMT 2023
PRIMARY
HSDB
4022
Created by admin on Sat Dec 16 04:48:02 GMT 2023 , Edited by admin on Sat Dec 16 04:48:02 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY