Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C13H10ClNO2 |
| Molecular Weight | 247.677 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=C(C=C(Cl)C=C1)C(=O)NC2=CC=CC=C2
InChI
InChIKey=KGYNGVVNFRUOOZ-UHFFFAOYSA-N
InChI=1S/C13H10ClNO2/c14-9-6-7-12(16)11(8-9)13(17)15-10-4-2-1-3-5-10/h1-8,16H,(H,15,17)
| Molecular Formula | C13H10ClNO2 |
| Molecular Weight | 247.677 |
| 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 |
|---|---|---|
| Relationship between the structure and antimycobacterial activity of substituted salicylanilides. | 2003 Mar |
|
| Antimycobacterial assessment of Salicylanilide benzoates including multidrug-resistant tuberculosis strains. | 2012 Oct 31 |
|
| Salicylanilide derivatives block Mycobacterium tuberculosis through inhibition of isocitrate lyase and methionine aminopeptidase. | 2012 Sep |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:11:54 GMT 2023
by
admin
on
Fri Dec 15 15:11:54 GMT 2023
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| Record UNII |
QI22Q9QE3I
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| Record Status |
Validated (UNII)
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| Record Version |
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