Details
Stereochemistry | ACHIRAL |
Molecular Formula | C11H7N3O2 |
Molecular Weight | 213.1922 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=CN2C(C=NC3=CC=CC=C23)=N1
InChI
InChIKey=JVKYTWZLUFMIKS-UHFFFAOYSA-N
InChI=1S/C11H7N3O2/c15-11(16)8-6-14-9-4-2-1-3-7(9)12-5-10(14)13-8/h1-6H,(H,15,16)
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/2897466
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2897466
Dazoquinast is an imidazoquinoxaline derivative with antiallergic properties, developed by the British company Roussel Laboratories Ltd. Dazoquinast inhibited the IgE-mediated passive cutaneous anaphylaxis in rats passively sensitized to ovalbumen after intravenous and oral administration with ED50s of 0.073 and 0.13 mg/kg respectively.
Originator
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Synthesis and oral antiallergic activity of carboxylic acids derived from imidazo[2,1-c][1,4]benzoxazines, imidazo[1,2-a]quinolines, imidazo[1,2-a]quinoxalines, imidazo[1,2-a]quinoxalinones, pyrrolo[1,2-a]quinoxalinones, pyrrolo[2,3-a]quinoxalinones, and imidazo[2,1-b]benzothiazoles. | 1988 Jun |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2897466
ED50 in rats 0.073 mg/kg after intravenous and 0.13 mg/kg after oral administration.
Route of Administration:
Other
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C29712
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ACTIVE MOIETY