| Weight | 300.833 g/mol |
|---|---|
| Formula | C18H21ClN2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
chlorcyclizine (82-93-9)
chlorcycline · chlorocyclizin · Histachlorazine
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- Sigma-Aldrich - chlorcyclizine81.40 - 328.50 USD
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- STIMULATORY EFFECT OF CHLORCYCLIZINE ON BARBITURATE METABOLISM (Journal of Pharmacology and Experimental Therapeutics, 1961)
- STUDIES ON THE EFFECT OF CHLORCYCLIZINE AND OTHER DRUGS ON THE TOXICITY OF SEVERAL ORGANOPHOSPHATE ANTICHOLINESTERASES (Journal of Pharmacology and Experimental Therapeutics, 1964)
- N-OXIDE FORMATION: A NEW ROUTE FOR INACTIVATION OF THE ANTIHISTAMINIC CHLORCYCLIZINE (Journal of Pharmacology and Experimental Therapeutics, 1967)
- PHYSIOLOGICAL DISTRIBUTION AND METABOLIC INACTIVATION OF CHLORCYCLIZINE AND CYCLIZINE. (Journal of Pharmacology and Experimental Therapeutics, 1965)
- Chlorcyclizine induction of cleft palate in the rat: Degradation of palatal glycosaminoglycans (Teratology, 1978)
- Repurposing of the antihistamine chlorcyclizine and related compounds for treatment of hepatitis C virus infection (Science Translational Medicine, 2015)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - chlorcycline
- chlorocyclizin
- Histachlorazine
-
SMILESCN1CCN(CC1)C(C2=CC=CC=C2)C3=CC=C(C=C3)Cl
-
InChIKeyWFNAKBGANONZEQ-UHFFFAOYSA-N
- Pubchem - chlorcyclizine
- Wikipedia - chlorcyclizine
Chlorcyclizine (Di-Paralene, Mantadil, Pruresidine, Trihistan) is a first-generation antihistamine of the diphenylmethylpiperazine group marketed in the United States and certain other countries. It is used primarily to treat allergy symptoms such as rhinitis, urticaria, and pruritus, and may also be used as an antiemetic. In addition to its antihistamine effects, chlorcyclizine also has some anticholinergic, antiserotonergic, and local anesthetic properties.
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chlorcyclizine
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