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Chemical Structure Cat. No. Product Name CAS No.
CFI-402257 Chemical Structure
 BCP31204 CFI-402257 1610759-22-2
CFI-402257 is a highly selective and orally bioavailable TTK/Mps1 inhibitor with an IC50 of 1.7 nM for TTK in vitro. CFI-402257 has anti-cancer activity.
Denibulin Chemical Structure
 BCP21548 Denibulin 284019-34-7
Denibulin is a small molecular vascular disrupting agent (VDA), with potential antimitotic and antineoplastic activities. Denibulin selectively targets and reversibly binds to the colchicine-binding site on tubulin and inhibits microtubule assembly.
CCT241533 Chemical Structure
 BCP21396 CCT241533 1262849-73-9
CCT241533 is a potent and selective Inhibitor of CHK2 that potentiates the cytotoxicity of PARP inhibitors.
Carmofur Chemical Structure
 BCP21373 Carmofur 61422-45-5
Carmofur is a derivative of fluorouracil, an antimetabolite used as an antineoplastic agent.
SIS-17 Chemical Structure
 BCP31156 SIS-17 2374313-54-7
SIS17 is a mammalian histone deacetylase 11 (HDAC 11) inhibitor with an IC50 value of 0.83 μM, inhibits the demyristoylation HDAC11 substrate, serine hydroxymethyl transferase 2, without inhibiting other HDACs.
Fluorodeoxyuridylate Chemical Structure
 BCP31154 Fluorodeoxyuridylate 134-46-3
5-fluorodeoxyuridine monophosphate is a pyrimidine 2'-deoxyribonucleoside 5'-monophosphate.
Cyano Temozolomide Chemical Structure
 BCP22927 Cyano Temozolomide 287964-59-4
Temozolomide is an oral DNA alkylating agent used to treat some brain cancers.
Pioditazone hydrochloride Chemical Structure
 BCP22942 Pioditazone hydrochloride 112529-15-4
Pioglitazone hydrochloride is a potent and selective PPARγ agonist with EC50s of 0.93 and 0.99 μM for human and mouse PPARγ, respectively.
JG98 Chemical Structure
 BCP31061 JG98 1456551-16-8
JG-98, an allosteric heat shock protein 70 (Hsp70) inhibitor, which binds tightly to a conserved site on Hsp70 and disrupts the Hsp70-Bag3 interaction.
Alvespimycin HCl Chemical Structure
 BCP22705 Alvespimycin HCl 467214-21-7
Alvespimycin hydrochloride is a potent inhibitor of Hsp90, binding to Hsp90 with EC50 of 62±29 nM.
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