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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.
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.
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.
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.
Codorphone is an opioid analgesic drug. It is an analogue of hydrocodone substituted with an 8-ethyl group and an N-cyclopropylmethyl group. It is a mixed agonist-antagonist at the μ-opioid receptor, and is slightly more potent than codeine in analgesic effects but associated with somewhat greater side effects.
Colchicine is a toxic natural product and secondary metabolite, originally extracted from plants of the genus Colchicum. It was used originally to treat rheumatic complaints, especially gout, and still finds use for these purposes today despite dosing issues concerning its toxicity. It was also prescribed for its cathartic and emetic effects. Its present medicinal use is in the treatment of gout and familial Mediterranean fever; it can also be used as initial treatment for pericarditis and preventing recurrences of the condition. It is a common medication used in the treatment of Behcet's disease. It is also being investigated for its use as an anti-cancer drug. In neurons, axoplasmic transport is disrupted by colchicine.
Cordycepin is a derivative of the nucleoside adenosine, differing from the latter by the absence of oxygen in the 3' position of its ribose part. It was initially extracted from fungi of genus Cordyceps, but is now produced synthetically. It has interesting properties as a anti-tumor, anti-fungal, anti-viral agent, since it has the ability to inhibit some protein kinases. As an anti-tumor agent, researchers stated that it has the capacity to reduce the growth of ascites tumor cells in the Ehrlich mice with cervical cell carcinoma and Lewis lung cancer.
Crizotinib is an anaplastic lymphoma kinase inhibitor of the aminopyridine chemical series. It is currently undergoing clinical trials testing its safety and efficacy in treating several forms of cancer, particularly non-small cell lung carcinoma, anaplastic large cell lymphoma, neuroblastoma, and other advanced solid tumors in both adults and children.
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