| Weight | 343.898 g/mol |
|---|---|
| Formula | C21H26ClNO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 6 |
clemastine (15686-51-8)
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- Risk of developing life-threatening ventricular arrhythmia associated with terfenadine in comparison with over-the-counter antihistamines, ibuprofen and clemastine (American Journal of Cardiology, 1994)
- Evaluation ofin vivo parameters of drug metabolizing enzyme activity in man after administration of clemastine, phenobarbital or placebo (European Journal of Clinical Pharmacology, 1975)
- A comparison of triprolidine and clemastine on histamine antagonism and performance tests in man: Implications for the mechanism of drug induced drowsiness (European Journal of Clinical Pharmacology, 1975)
- Inhibition of idiosyncratic reactions to aspirin in asthmatic patients by clemastine. (Thorax, 1979)
- Randomized Controlled Trial of Clemastine Fumarate for Treatment of Experimental Rhinovirus Colds (Clinical Infectious Diseases, 1996)
- Effects of mizolastine and clemastine on actual driving and psychomotor performance in healthy volunteers (European Journal of Clinical Pharmacology, 1994)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C1=CC=CC=C1)(C2=CC=C(C=C2)Cl)OCCC3CCCN3C
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InChIKeyYNNUSGIPVFPVBX-UHFFFAOYSA-N
- Pubchem - clemastine
- Wikipedia - clemastine
Clemastine, also known as meclastin, is an antihistamine and anticholinergic. Unlike loratadine or fexofenadine, clemastine is a sedating antihistamine; however, it exhibits fewer other side effects than most of the widely used antihistamines. Clemastine is also classified as an antipruritic (i.e., it stops itching).
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