Details
Stereochemistry | ACHIRAL |
Molecular Formula | C13H8N2O3 |
Molecular Weight | 240.2142 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=CC2=C(C=C1)N=C3C=CC=CN3C2=O
InChI
InChIKey=HMZDSBSMNLBGIW-UHFFFAOYSA-N
InChI=1S/C13H8N2O3/c16-12-9-7-8(13(17)18)4-5-10(9)14-11-3-1-2-6-15(11)12/h1-7H,(H,17,18)
Doqualast is an antiasthmatic and antiallergic agent. It has a mode of antiallergic action similar to that of disodium cromoglycate and inhibits antigen-induced mediator release by interfering with the calcium transport required for histamine secretion across the mast cell membrane. In rabbits, no embryotoxic or teratogenic effects of doqualast were observed. The concomitant use of doqualast and theophylline might cause drug interaction. Doqualast is thought to increase the blood free fraction of concomitantly used theophylline and to accelerate elimination of theophylline from blood.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: GO:0001821 Sources: https://www.ncbi.nlm.nih.gov/pubmed/2434111 |
PubMed
Title | Date | PubMed |
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Effects of the new antiallergic drug 11-oxo-11H-pyrido[2,1-b] quinazoline-2-carboxylic acid on immediate allergic reactions. | 1986 Nov |
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Immunopharmacological actions of the new antiallergic drug 11-oxo-11H-pyrido[2,1-b]quinazoline-2-carboxylic acid. Effects on type I hypersensitivity reactions in human leukocytes and in human and monkey lungs. | 1986 Nov |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3814221
Curator's Comment: Rats data
Single dose 50 mg/kg
Route of Administration:
Oral
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NCI_THESAURUS |
C29712
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ACTIVE MOIETY