Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C2H4N4O2S2 |
| Molecular Weight | 180.209 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=NN=C(S1)S(N)(=O)=O
InChI
InChIKey=VGMVBPQOACUDRU-UHFFFAOYSA-N
InChI=1S/C2H4N4O2S2/c3-1-5-6-2(9-1)10(4,7)8/h(H2,3,5)(H2,4,7,8)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Bile acid derivatives of 5-amino-1,3,4-thiadiazole-2-sulfonamide as new carbonic anhydrase inhibitors: synthesis and investigation of inhibition effects. | 2002 Aug |
|
| Carbonic anhydrase inhibitors. Inhibition of tumor-associated isozyme IX by halogenosulfanilamide and halogenophenylaminobenzolamide derivatives. | 2003 May 22 |
|
| Carbonic anhydrase inhibitors: Schiff's bases of aromatic and heterocyclic sulfonamides and their metal complexes. | 2004 Jun |
|
| Carbonic anhydrase inhibitors. Biphenylsulfonamides with inhibitory action towards the transmembrane, tumor-associated isozymes IX possess cytotoxic activity against human colon, lung and breast cancer cell lines. | 2009 Apr |
Patents
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F687N81LIZ
Created by
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14949-00-9
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1005048
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22979
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84724
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DTXSID10164324
Created by
admin on Fri Dec 15 17:35:35 GMT 2023 , Edited by admin on Fri Dec 15 17:35:35 GMT 2023
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SUBSTANCE RECORD
