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Miconazole is an imidazole antifungal agent, commonly applied topically to the skin or to mucus membranes to cure fungal infections. It works by inhibiting the synthesis of ergosterol, a critical component of fungal cell membranes. It can also be used against certain species of Leishmania protozoa which are a type of unicellular parasite that also contain ergosterol in their cell membranes. In addition to its antifungal and antiparasitic actions, it also has some limited antibacterial properties. It is also used in Ektachrome film developing.

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Mizoribine is an immunosuppresive drug. The compound was first observed in Tokyo, Japan, in 1971. It is a natural product, first isolated from the mould Eupenicillium brefeldianum.

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Morclofone is a cough suppressant.

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Moxonidine is a new generation centrally acting antihypertensive drug licensed for the treatment of mild to moderate essential hypertension. It may have a role when thiazides, beta-blockers, ACE inhibitors and calcium channel blockers are not appropriate or have failed to control blood pressure. In addition, it demonstrates favourable effects on parameters of the insulin resistance syndrome, apparently independent of blood pressure reduction.

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Muzolimine is a diuretic.

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Nafimidone is an anticonvulsant drug of the imidazole class. It contains a naphthyl group.


Nalbuphine is a semi-synthetic opioid used commercially as an analgesic. It is noteworthy in part for the fact that at low dosages, it is found much more effective by women than by men, and may even increase pain in men, leading to its discontinuation in the UK in 2003. It is a semi-synthetic narcotic agonist-antagonist analgesic of the phenanthrene series.


Nalorphine an early antagonist of most depressant and stimulatory effects of morphine and related narcotic analgesics; precipitates severe withdrawal symptoms in morphine addicts, and counteracts the respiratory depression produced by morphine and related compounds; when administered in the absence of narcotics, nalorphine has mildly analgesic and respiratory depressant effects in nonaddicts; superseded by naloxone hydrochoride.It is used as an antagonist to morphine and related narcotics and in the diagnosis of narcotic addiction.

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Naloxazone is an irreversible μ opioid receptor antagonist which is selective for the μ1 receptor subtype. It produces very long lasting antagonist effects as it forms a covalent bond to the active site of the mu-opioid receptor, thus making it impossible for the molecule to unbind and blocking the receptor permanently until the receptor is recycled by endocytosis.

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