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
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)
| 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
| Title | Date | PubMed |
|---|---|---|
| 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 |
|
| Synthesis and ex vivo evaluation of carbon-11 labelled N-(4-methoxybenzyl)-N'-(5-nitro-1,3-thiazol-2-yl)urea ([11C]AR-A014418): a radiolabelled glycogen synthase kinase-3beta specific inhibitor for PET studies. | 2005 Dec 1 |
|
| N-(4-Meth-oxy-phen-yl)-N'-(5-nitro-1,3-thia-zol-2-yl)urea. | 2010 Aug 18 |
|
| Biological activity of modified and exchanged 2-amino-5-nitrothiazole amide analogues of nitazoxanide. | 2010 Jun 15 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 04:48:02 GMT 2023
by
admin
on
Sat Dec 16 04:48:02 GMT 2023
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| Record UNII |
1GR77A37Z5
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| Record Status |
Validated (UNII)
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| Record Version |
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WHO-VATC |
QP51AX16
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NCI_THESAURUS |
C277
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C76409
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8486
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m1723
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300000033070
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C034870
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1665683
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DTXSID6020066
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