Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H8N4O4S3 |
| Molecular Weight | 320.369 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NS(=O)(=O)C1=NN=C(NS(=O)(=O)C2=CC=CC=C2)S1
InChI
InChIKey=PWDGTQXZLNDOKS-UHFFFAOYSA-N
InChI=1S/C8H8N4O4S3/c9-18(13,14)8-11-10-7(17-8)12-19(15,16)6-4-2-1-3-5-6/h1-5H,(H,10,12)(H2,9,13,14)
| Molecular Formula | C8H8N4O4S3 |
| Molecular Weight | 320.369 |
| 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 |
|---|---|---|
| Carbonic anhydrase inhibitors. Inhibition of the transmembrane isozyme XII with sulfonamides-a new target for the design of antitumor and antiglaucoma drugs? | 2005 Feb 15 |
|
| Carbonic anhydrase inhibitors: cloning, characterization, and inhibition studies of the cytosolic isozyme III with sulfonamides. | 2007 Dec 1 |
|
| T tubules and surface membranes provide equally effective pathways of carbonic anhydrase-facilitated lactic acid transport in skeletal muscle. | 2010 Dec 13 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 16 23:54:56 UTC 2022
by
admin
on
Fri Dec 16 23:54:56 UTC 2022
|
| Record UNII |
FC5AAH89R5
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
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Common Name | English | ||
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Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C29577
Created by
admin on Fri Dec 16 23:54:56 UTC 2022 , Edited by admin on Fri Dec 16 23:54:56 UTC 2022
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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C96537
Created by
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DTXSID10187356
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3368-13-6
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DB07050
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FC5AAH89R5
Created by
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18794
Created by
admin on Fri Dec 16 23:54:56 UTC 2022 , Edited by admin on Fri Dec 16 23:54:56 UTC 2022
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PRIMARY |