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Clemastine is an antihistamine and anticholinergic. Unlike loratadine or fexofenadine, clemastine is a sedating antihistamine, however it exhibits fewer side effects than most of the widely used antihistamines. It is also classified as an antipruritic.
Clentiazem is a calcium channel blocker. It is a chloride derivative of diltiazem.
Climazolam is a drug which is an imidazobenzodiazepine derivative developed by Hoffman-LaRoche. It is similar in structure to triazolam, and is used in veterinary medicine for anaesthetising animals.
Climbazole is a topical antifungal agent commonly used in the treatment of human fungal skin infections such as dandruff and eczema. It has shown a high in vitro and in vivo efficacy against Pityrosporum ovale that appears to play an important role in the pathogenesis of dandruff. It may cause localized irritation of the skin with symptoms including redness, rashes and itching.
Clioquinol is an antifungal drug and antiprotozoal drug. It is neurotoxic in large doses. Clioquinol is a member of a family of drugs called hydroxyquinolines which inhibit certain enzymes related to DNA replication. Clioquinol is a constituent of the prescription medicine Vioform, which is a topical antifungal treatment. It is also used in the form of a cream in the treatment of inflammatory skin disorders.
Clobutinol is a cough suppressant. It was recently determined to cause cardiac arrhythmia in some patients. Recent studies have indicated that clobutinol has the potential to prolong the QT interval.
Clodantoin is a drug used in gynecology.
Clofedanol is a centrally-acting cough suppressant used in the treatment of dry cough. It has local anesthetic and antihistamine properties, and may have anticholinergic effects at high doses. It was approved for OTC status in 1987 by the FDA OTC monograph process and its safety and efficacy data are limited.
Clofibrate is a fibrate. It is a lipid lowering agent used for controlling the high cholesterol and triacylglyceride level in the blood. It increases lipoprotein lipase activity to promote the conversion of VLDL to LDL, and hence reduce the level of VLDL. It is proved that it can increase the level of HDL as well. It can induce SIADH, syndrome of inappropriate secretion of antidiuretic hormone ADH (vasopressin).
Clominorex is a centrally acting sympathomimetic which is related to other drugs such as aminorex and pemoline. It was developed as an appetite suppressant.
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