Home   >  
Protease/Metabolic Enzyme
  • Protease/Metabolic Enzyme
  • Cell Cycle/DNA Damage

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products






Raw Materials


Chemical Structure Cat. No. Product Name CAS No.
MKT-077 Chemical Structure
BCP30211 MKT-077 147366-41-4
MKT-077 is an inhibitor of mitochondrial hsp70 family member mortalin (mot-2), causing the selective death of cancer cells.
KNK437 Chemical Structure
BCP28527 KNK437 218924-25-5
KNK437 is a HSP inhibitor, and inhibits the induction of HSP105, HSP70, and HSP40.
PU-WS13 Chemical Structure
BCP27901 PU-WS13 1454619-14-7
PU-WS13 is a selective Grp94 inhibitor, with an EC50 of 0.22 μM.
NMS-E973 Chemical Structure
BCP29502 NMS-E973 1253584-84-7
NMS-E973 is a novel, selective and potent inhibitor of heat shock protein 90 (Hsp90).
Gamitrinib Chemical Structure
BCP24917 Gamitrinib 1131626-46-4
G-TPP is a mitochondria-targeted Hsp90 inhibitor that increases cell death in HeLa and MCF7 cells, consistently inhibits cell death induced by oxidative stress and mitochondrial dysfunction induced by PINK1 mutation in mouse embryonic fibroblast cells and DA cell models such as SH-SY5Y and SN4741 cells.
MPC3100 Chemical Structure
BCP06949 MPC3100 958025-66-6
MPC-3100 is a n orally bioavailable, synthetic, second-generation small-molecule inhibitor of heat shock protein 90 (Hsp90) with potential antineoplastic activity.
Teprenone Chemical Structure
BCP11723 Teprenone 6809-52-5
Geranylgeranylacetone can induce expression of HSP70, HSPB8, and HSPB1.
KRIBB11 Chemical Structure
BCP19297 KRIBB11 342639-96-7
KRIBB11 is an inhibitor of Heat shock factor 1 (HSF1), with IC50 of 1.2 μM.
Retaspimycin Chemical Structure
BCP06481 Retaspimycin 857402-23-4
Retaspimycin hydrochloride is the hydrochloride salt of a small-molecule inhibitor of heat shock protein 90 (HSP90) with antiproliferative and antineoplastic activities.
AEG-3482 Chemical Structure
BCP01890 AEG-3482 63735-71-7
AEG 3482 is a cell-permeable imidazothiadiazole compound that activates cellular transcription factor HSF1 by binding to HSP90 and disrupting its association with HSF1.
123下一页末页共 36 条记录 1 / 4 页