Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C13H10ClNO |
| Molecular Weight | 231.678 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC(=O)N(C1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=XNBKKRFABABBPM-UHFFFAOYSA-N
InChI=1S/C13H10ClNO/c14-13(16)15(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H
| Molecular Formula | C13H10ClNO |
| Molecular Weight | 231.678 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: GO:0004175 Sources: https://www.ncbi.nlm.nih.gov/pubmed/7032610 |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Carbonic anhydrase inhibitors. Inhibition of cytosolic isozymes I and II and transmembrane, cancer-associated isozyme IX with lipophilic sulfonamides. | 2003-08 |
|
| Antimycobacterial activity of 3,4-dichlorophenyl-ureas, N,N-diphenyl-ureas and related derivatives. | 2001-11 |
|
| [Isolation and comparative properties of serine proteinases of the microscopic fungi Trichoderma lignorum and Trichoderma koningii]. | 1981-11 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:45:51 GMT 2025
by
admin
on
Mon Mar 31 22:45:51 GMT 2025
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| Record UNII |
LJ209318B2
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| Record Status |
Validated (UNII)
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