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Chemical Structure Cat. No. Product Name CAS No.
Fluoxymesterone Chemical Structure
 BCP10776 Fluoxymesterone 76-43-7
Fluoxymesterone is an Androgen. The mechanism of action of fluoxymesterone is as an Androgen Receptor Agonist. The chemical classification of fluoxymesterone is Androstanes.
Mestanolone Chemical Structure
 BCP10775 Mestanolone 521-11-9
Mestanolone is a 3-oxo-5alpha-steroid.
NITD-349 Chemical Structure
 BCP30168 NITD-349 1473450-62-2
NITD-349 is an MmpL3 inhibitor that shows highly potent anti-mycobacterial activity with MIC50 of 23 nM against virulent Mycobacterium tuberculosis H37Rv.
Cefpodoxime Chemical Structure
 BCP24250 Cefpodoxime 80210-62-4
Cefpodoxime is an oral third generation cephalosporin antibiotic. It is active against most Gram positive and Gram negative bacteria.
Cefpodoxime proxetil Chemical Structure
 BCP12056 Cefpodoxime proxetil 87239-81-4
Cefpodoxime Proxetil is an antibacterial with a broad spectrum, orally absorbed third generation cephalosporin, ester prodrug of the active free acid metabolite and Cefpodoxime.
Methocarbamol Chemical Structure
 BCP13801 Methocarbamol 532-03-6
Methocarbamol is a skeletal muscle relaxant. This compound is a carbamate of guaifenesin. Methocarbamol has been observed to bind to carbonic anhydrase I and II with 1000-fold more specificity for carbonic anhydrase I.
Fospropofol disodium Chemical Structure
 BCP12945 Fospropofol disodium 258516-87-9
Fospropofol Disodium is a short acting hypnotic/sedative/anesthetic agent.
Febrifugine Chemical Structure
 BCP15889 Febrifugine 24159-07-7
Febrifugine is a quinazolinone alkaloid originally isolated from D. febrifuga that has antimalarial activity.
Distigmine Bromide Chemical Structure
 BCP16582 Distigmine Bromide 15876-67-2
Distigmine Bromide is an acetylcholinesterase inhibitor used for the treatment of underactive neurogenic bladder and myasthenia gravis.
Shionone Chemical Structure
 BCP15275 Shionone 10376-48-4
Shionone is a tetracyclic triterpenoid that is perhydrochrysene which is substituted by methyl groups at positions 1, 4bbeta, 6aalpha, 8beta, 10abeta and 12a positions, by a 4-methylpent-3-enyl group at the 8alpha position, and with an oxo group at position 2. It is a tetracyclic triterpenoid and a cyclic terpene ketone.
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