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Flutamide is an oral nonsteroidal antiandrogen drug primarily used to treat prostate cancer. It competes with testosterone and its powerful metabolite, dihydrotestosterone (DHT) for binding to androgen receptors in the prostate gland.Flutamide may also be used to treat excess androgen levels in women-especially those with PolyCystic Ovarian Syndrome (PCOS).Flutamide is a nonsteroidal antiandrogen that blocks the action of both endogenous and exogenous testosterone by binding to the androgen receptor.

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Foretinib is an oral multikinase inhibitor targeting Met, RON, Axl, and vascular endothelial growth factor receptor. It inhibits HGF receptor family tyrosine kinases with an IC50 of 3 nM for Ron. Foretinib also inhibits KDR, Flt-1, and Flt-4 with IC50 of 0.9, 6.8 and 2.8 nM, respectively.

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Forskolin is a labdane diterpene that is produced by the Indian Coleus plant. Forskolin is commonly used to raise levels of cyclic AMP (cAMP) in the study and research of cell physiology. Forskolin resensitizes cell receptors by activating the enzyme adenylyl cyclase and increasing the intracellular levels of cAMP. Forskolin may be helpful to control the underlying cause of glaucoma.

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Fosazepam is a drug which is a benzodiazepine derivative. It has sedative and anxiolytic effects, and is a derivative of diazepam which has been substituted with a dimethylphosphoryl group to improve solubility in water. It has similar effects on sleep as other benzodiazepines. In a clinical trial it was reported that fosazepam lead to increased sleep duration with less broken sleep but sleep quality was worsened with suppressed deep sleep and increased light sleep.


Gepefrine is a cardiac stimulant drug.


Gidazepam is a drug which is an atypical benzodiazepine derivative. It is a selectively anxiolytic benzodiazepine. It also has therapeutic value in the management of certain cardiovascular disorders. It is a prodrug for its active metabolite 7-bromo-5-phenyl-1,2-di-hydro-3H-1,4- benzodiazepine-2-one. It is used as an antianxiety drug.

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Girisopam is a drug which is a 2,3-benzodiazepine derivative, related to tofisopam. It has selective anxiolytic action with no sedative, anticonvulsant or muscle relaxant effects.


Glipizide is an oral hypoglycemic agent which is rapidly absorbed and completely metabolized.The acute oral toxicity was extremely low in all species tested (LD50 greater than 4 g/kg). Overdosage of sulfonylureas including glipizide can produce hypoglycemia.

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Glyburide is an antidiabetic drug in a class of medications known as sulfonylureas, closely related to sulfa drugs. It was developed in 1966 in a cooperative study between Boehringer Mannheim and Hoechst. It is used in the treatment of type II diabetes. Additionally, recent research shows that glyburide improves outcome in animal stroke models by preventing brain swelling. A retrospective study showed that in type 2 diabetic patients already taking glyburide, there was improved NIH stroke scale scores on discharge compared to diabetic patients not taking glyburide.

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Goserelin is a synthetic hormone. In men, it stops the production of the hormone testosterone, which may stimulate the growth of cancer cells. In women, goserelin decreases the production of the hormone estradiol (which may stimulate the growth of cancer cells) to levels similar to a postmenopausal state. When the medication is stopped, hormone levels return to normal.Goserelin is a synthetic decapeptide analogue of LHRH. Goserelin acts as a potent inhibitor of pituitary gonadotropin secretion when administered in the biodegradable formulation. The result is sustained suppression of LH and serum testosterone levels.

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