Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H7ClN2O3 |
| Molecular Weight | 262.649 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)C1=NC2=C(O1)C3=C(C=CC=N3)C(Cl)=C2
InChI
InChIKey=ZCRBUWNCWCWRGL-UHFFFAOYSA-N
InChI=1S/C12H7ClN2O3/c1-17-12(16)11-15-8-5-7(13)6-3-2-4-14-9(6)10(8)18-11/h2-5H,1H3
| Molecular Formula | C12H7ClN2O3 |
| Molecular Weight | 262.649 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Quazolast is an orally active mast cell stabilising agent which was in development with Rhône-Poulenc Rorer. In preclinical trials Quazolast was evaluated for efficacy against acid independent (alcohol, HCl), or dependent (aspirin, indomethacin) gastric damage in rats. Quazolasts gastroprotective profile was compared to that of ranitidine. Quazolast, in direct contrast to ranitidine, protected the rat gastric mucosa from acid-independent, but not acid-dependent gastric damage. Quazolast lacked antisecretory activity in rats; however, it did heal acetic acid induced gastric ulcers in this species. In clinical trials Quazolast was superior to placebo in protecting against nasal congestion and nasal itchiness after ragweed nasal challenge.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2221488
400 mg bid orally
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:49:07 GMT 2025
by
admin
on
Mon Mar 31 18:49:07 GMT 2025
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| Record UNII |
N8K2307472
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| Record Status |
Validated (UNII)
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| Record Version |
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NCI_THESAURUS |
C29714
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C046483
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CHEMBL23811
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U-96
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SUB10191MIG
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DTXSID10235366
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100000081082
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86048-40-0
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5894
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N8K2307472
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C80961
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24747
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| Related Record | Type | Details | ||
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