| Weight | 290.41 g/mol |
|---|---|
| Formula | C20H22N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
AZATADINE (3964-81-6)
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- Syntheses of molecularly imprinted polymers: Molecular recognition of cyproheptadine using original print molecules and azatadine as dummy templates (Analytica Chimica Acta, 2009)
- Demonstration of Inhibition of Mediator Release From Human Mast Cells by Azatadine Base: In Vivo and In Vitro Evaluation (JAMA, 1986)
- The pharmacology of azatadine, a potential antiallergy drug (Inflammation Research, 1974)
- Fungal biotransformation of the antihistamine azatadine by Cunninghamella elegans. (Applied and Environmental Microbiology, 1996)
- Effects of azatadine maleate on subjective appraisal and psychomotor functions relevant to driving performance (Current Medical Research and Opinion, 1979)
- Comparison of the effects of azatadine maleate and terfenadine on human performance (1983)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCN1CCC(=C2C3=CC=CC=C3CCC4=C2N=CC=C4)CC1
-
InChIKeySEBMTIQKRHYNIT-UHFFFAOYSA-N
- Pubchem - AZATADINE
- Wikipedia - azatadine
Azatadine (Optimine) is a first-generation antihistamine and anticholinergic that was launched Schering-Plough in 1973. It was patented in 1967. It has been succeeded by other antihistamines and marketing approvals have been widely withdrawn.
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