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Chemical Structure Cat. No. Product Name CAS No.
CXD101 Chemical Structure
BCP24800 CXD101 934828-12-3
CXD101 is a potent, selective and orally active class I HDAC inhibitor with IC50s of 63 nM, 570 nM and 550 nM for HDAC1, HDAC2 and HDAC3, respectively. CXD101 has no activity against HDAC class II. CXD101 has antitumor activity.
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.
Remetinostat Chemical Structure
BCP30561 Remetinostat 946150-57-8
Remetinostat (SHP-141) is a hydroxamic acid-based inhibitor of histone deacetylase enzymes (HDAC) which is under development for the treatment of cutaneous T-cell lymphoma.
Corin Chemical Structure
BCP30529 Corin 1808113-09-8
Corin is a dual inhibitor of histone lysine specific demethylase (LSD1) and histone deacetylase (HDAC), with a Ki(inact) of 110 nM for LSD1 and an IC50 of 147 nM for HDAC1.
Tinostamustine hydrochloride Chemical Structure
BCP30456 Tinostamustine hydrochloride 1793059-58-1
Tinostamustine, also known as EDO-S101, is an alkylatlng histone-deacetylase inhibitor (HDACi) fusion molecule.
ACY-775 Chemical Structure
BCP30179 ACY-775 1375466-18-4
ACY-775 is a potent and selective inhibitor of the of histone deacetylase 6 (HDAC6) with an IC50 of 7.5 nM.
Divalproex sodium Chemical Structure
BCP12800 Divalproex sodium 76584-70-8
Divalproex Sodium, consisting of a compound of sodium valproate and valproic acid in a 1:1 molar relationship in an enteric coated form, is a HDAC inhibitor, used in the treatment for epilepsy.
HDAC-IN-6 Chemical Structure
BCP13267 HDAC-IN-6 1026295-98-6
HDAC-IN-6 is an HDAC inhibitor, targeting HDAC2, HDAC3, HDAC4, HDAC5, HDAC7, HDAC8, and HDAC9.
Apicidin Chemical Structure
BCP13245 Apicidin 183506-66-3
Apicidin, a natural fugal metabolite, is a selective inhibitor of HDAC.
TH34 Chemical Structure
BCP30033 TH34 2196203-96-8
TH34 is a potent HDAC6/8/10 inhibitor.
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