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Bumadizone is a non-steroidal anti-inflammatory drug.


Bupranolol is a non-selective beta blocker without intrinsic sympathomimetic activity, but with strong membrane stabilizing activity. Its potency is similar to propranolol. It can be used to treat hypertension and tachycardia.


Burimamide is an antagonist at the H2 and H3 histamine receptors. It is a thiourea derivative. It was first developed by scientists at Smith, Kline & French in their intent to develop a histamine antagonist for the treatment of peptic ulcers.


Butenafine is only found in individuals that have used or taken this drug. It is a synthetic benzylamine antifungal agent. It has been suggested that butenafine, like allylamines, interferes with sterol biosynthesis (especially ergosterol) by inhibiting squalene monooxygenase, an enzyme responsible for converting squalene to 2,3-oxydo squalene.

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Butaxamine is a β2-selective beta blocker. Its primary use is in experimental situations in which blockade of β2 receptors is necessary to determine the activity of the drug. It has no common clinical use.


CELEMIN 5S is specially designed to meet the varied protein requirements of critically ill patients. CELEMIN 5S contains all essential & non-essential Amino acids. It is insulin independent source of carbohydrate "sorbitol.

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CH 5424802

CH5424802 is a potent, selective and orally bioavailable Anaplastic Lymphoma Kinase (ALK) Inhibitor capable of blocking the resistant gatekeeper mutant.

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CHIR-99021is a glycogen synthase kinase 3β (GSK3β) inhibitor that has antiproliferative activity in vitro and in vivo.

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Canertinib is an experimental drug candidate for the treatment of cancer. It is an irreversible tyrosine-kinase inhibitor with activity against EGFR.

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Cannabinol is a psychoactive substance cannabinoid found in Cannabis sativa and Cannabis indica or afghanica. It is also a metabolite of tetrahydrocannabinol. It acts as a weak agonist of the CB1 and CB2 receptors, with lower affinity in comparison to tetrahydrocannabinol.

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