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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).

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Clominorex is a centrally acting sympathomimetic which is related to other drugs such as aminorex and pemoline. It was developed as an appetite suppressant.


Clomifene is a selective estrogen receptor modulator that increases production of gonadotropins by inhibiting negative feedback on the hypothalamus. It is used mainly for ovarian stimulation in female infertility due to anovulation.

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Clonazepam is a benzodiazepine derivative having anticonvulsant, muscle relaxant, and very potent anxiolytic properties. It is a chlorinated derivative of nitrazepam and therefore a nitrobenzodiazepine. Benzodiazepines such as clonazepam have a fast onset of action and high effectiveness rate and low toxicity in overdose but have drawbacks due to adverse reactions including paradoxical effects, drowsiness, and cognitive impairment. Cognitive impairments can persist for at least 6 months after withdrawal of clonazepam; it is unclear whether full recovery of memory functions occurs.

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Cloprednol is a glucocorticoid. It is synthetic. It has been investigated for use in asthma.


Clorgyline is an irreversible and selective inhibitor of monoamine oxidase A that is used in scientific research. It is structurally related to pargyline.


Cloxazolam is a drug which is a benzodiazepine derivative. It is metabolised into the active metabolite chlordesmethyldiazepam. It possesses anxiolytic, anticonvulsant, hypnotic, sedative and skeletal muscle relaxant properties.

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Cobicistat is a licensed drug for use in the treatment of infection with the human immunodeficiency virus (HIV).cobicistat is of interest not for its anti-HIV properties, but rather its ability to inhibit liver enzymes that metabolize other medications used to treat HIV, notably elvitegravir, an HIV integrase inhibitor currently under investigation itself. Cobicistat is a component of the four-drug, fixed-dose combination HIV treatment elvitegravir/cobicistat/emtricitabine/tenofovir.Cobicistat is a potent inhibitor of cytochrome P450 3A enzymes, including the important CYP3A4 subtype. It also inhibits intestinal transport proteins, increasing the overall absorption of several HIV medications, including atazanavir, darunavir and tenofovir alafenamide fumarate.

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