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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.


Benzoic acid and its salts are used as a food preservative, represented by the E-numbers E210, E211, E212, and E213. Benzoic acid inhibits the growth of mold, yeast and some bacteria. Benzoic acid is a constituent of Whitfield's Ointment which is used for the treatment of fungal skin diseases such as tinea, ringworm, andathlete's foot. Benzoic acid is used to make a large number of chemicals. Benzoic acid is used as an dye intermediate. It is also used as an laboratory reagent.


Benzonatate is a non-opioid oral antitussive with effects that last from 6 to 8 hours. It was approved by the U.S. Food and Drug Administration (FDA) in 1958.

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Benzydamine is a locally-acting nonsteroidal anti-inflammatory drug with local anaesthetic and analgesic properties providing both rapid and extended pain relief as well as a significant anti-inflammatory treatment for the painful inflammatory conditions of the mouth and throat. It selectively binds to inflamed tissues and is virtually free of any adverse systemic effects.

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