Home   >  
Cell Cycle/DNA Damage
  • Epigenetics
  >  
HDAC

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products

Antibodies

Peptides

Catalysts

Impurities

Intermediate

Raw Materials

HDAC

Chemical Structure Cat. No. Product Name CAS No.
Crotonoside Chemical Structure
BCP34471 Crotonoside 1818-71-9
Crotonoside is isolated from Chinese medicinal herb, Croton. Crotonoside inhibits FLT3 and HDAC3/6, exhibits selective inhibition in acute myeloid leukemia (AML) cells. Crotonoside could be a promising new lead compound for the treatment of AML.
Sinapic acid Chemical Structure
BCP25316 Sinapic acid 530-59-6
Sinapic acid is found in american cranberry. Sinapic acid is a common constituent of plants and fruit.
Valproic acid Chemical Structure
BCP33204 Valproic acid 99-66-1
Valproic acid is an inhibitor of histone deacetylase (HDAC) inhibitor, which has an anticancer effect. Valproic acid was shown to induce proliferation and enhance self-renewal of hematopoietic stem cells (HSC).
ACY-957 Chemical Structure
BCP25969 ACY-957 1609389-52-7
ACY-957 is an orally active and selective inhibitor of HDAC1 and HDAC2, with IC50s of 7 nM, 18 nM, and 1300 nM against HDAC1/2/3, respectively, and shows no inhibition on HDAC4/5/6/7/8/9.
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.
123下一頁末頁共 85 條記錄 1 / 9 頁 
0086-13720134139
福建36选7奖金 怎样打好麻将才能赢钱 浙江11选5走势图一定牛 快乐十分官方网 36棋牌新神兽规律 龙江麻将下载 微信捕鱼达人玩法与技巧 江西时时彩走势图300期 北京快三开奖时间调整 平码用加七算法 865棋牌靠谱865棋牌靠谱吗 天易棋牌揭秘赢技巧 谁有打麻将的微信群 福建麻将胡牌规则 河北河北快三走势图 pk10走势图杀码技巧 开心棋牌最新版本下载