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Azacitidine is a chemical analogue of the cytosine nucleoside used in DNA and RNA. It is only found in individuals that have used or taken this drug. It is a pyrimidine nucleoside analogue that inhibits DNA methyltransferase, impairing DNA methylation. It is also an antimetabolite of cytidine, incorporated primarily into RNA. Azacytidine has been used as an antineoplastic agent.

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Balsalazide is an anti-inflammatory drug used in the treatment of inflammatory bowel disease. It releases mesalazine in the large intestine. Its advantage over that drug in the treatment of ulcerative colitis is believed to be the delivery of the active agent past the small intestine to the large intestine, the active site of ulcerative colitis.

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Bambermycin is effective against gram-positive bacteria. It can inhibit the synthesis of bacterial cell wall , It reduces the thickness of the intestinal wall and thus increases the absorption of nutrients.


Barbigerone is one of a few pyranoisoflavones among several groups of isoflavones. It was first isolated from the seed of a leguminous plant Tephrosia barbigera; hence the name barbigerone. It has also been isolated from the medicinal plant Sarcolobus globosus. Barbigerone from S. globosus is validated to have significant antioxidant property. It exhibits profound antiplasmodial activity against the malarial parasite Plasmodium falciparum. It is also demonstrated that it has anti-cancer potential as it causes apoptosis of murine lung-cancer cells.


Baricitinib is an orally administered selective JAK1 and JAK2 inhibitor that is JAK3-sparing. Currently, baricitinib is in Phase II development as a treatment for rheumatoid arthritis and psoriasis.

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Batanopride is an antiemetic drug of the benzamide class which acts as a selective 5-HT3 receptor antagonist. It was trialled to reduce nausea during cancer chemotherapy, but was never approved for medical use due to dose-limiting side effects including hypotension and long QT syndrome.


Batoprazine is a drug of the phenylpiperazine class which has been described as a serenic or antiaggressive agent. It acts as a 5-HT1A and 5-HT1B receptor agonist. It is closely related to eltoprazine, fluprazine, and naphthylpiperazine, of which possess similar actions and effects.


Beauvericin is a cyclohexadepsipeptide mycotoxin which has insecticidal properties and which can induce apoptosis in mammalian cells. Beauvericin is produced by some entomo- and phytopathogenic Fusarium species.Beauvericin is a specific cholesterol acyltransferase inhibitor and is toxic to several human cell lines.It is a bioactive cyclodepsipeptide, which contains three D-a-hydroxy-isovaleryl and N-methyl-L-phenylalanyl residues in alternating sequence.

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Befloxatone is a selective monoamine oxidase inhibitor of type MAO-A.


Benserazide is a peripherally-acting aromatic L-amino acid decarboxylase inhibitor, which is unable to cross the blood-brain barrier. It is used in the management of Parkinson's disease in combination with L-DOPA as co-beneldopa. These combinations are also used for the treatment of restless legs syndrome.

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