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Cat. No. Product Name Information
PC-61633

CCT018159

DDX39B inhibitor, Hsp90 inhibitor

CCT018159 is al potent inhibitor of Hsp90 ATPase activity with IC50 of 7.1 uM, also inhibits the ATPase activity of R-loop unwinding helicase DDX39B (UAP56).
PC-61302

HSF1A

HSF1 activator

HSF1A is a small molecule human HSF1 (heat shock transcription factor 1) activator, also interacts with components of the TRiC/CCT complex.
PC-61250

KW-2478

HSP90 inhibitor

KW-2478 (KW2478) is a novel potent Hsp90 inhibitor with IC50 of 3.8 nM (Hsp90α), exhibits antitumor activities both in vitro and in vivo.
PC-70363

Hsp90α inhibitor A17

Hsp90α/p23 inhibitor

Hsp90α inhibitor A17 is a potent Hsp90α/p23 interaction inhibitor with IC50 of 0.15 uM, more effective than CP-9 in degrading pAkt/total Akt and Raf-1.
PC-70362

CP-9

Hsp90α/p23 inhibitor

CP-9 is a potent Hsp90α/p23 interaction inhibitor with IC50 of 3.2 uM, 5-fold less potent for Hsp90β/p23 interaction (IC50=15.3 uM).
PC-70347

STA-2842

HSP90 inhibitor

STA-2842 (STA2842) is a highly specific inhibitor of HSP90 (IC50=135 nM, HSP90α) that competitively binds the N-terminal ATP pocket of HSP90.
PC-61032

4-Br-BnIm

Grp94 inhibitor

4-Br-BnIm is a potent, subtype-selective Grp94 inhibitor with Kd of 0.96 uM, 13-fold selectivity over Hsp90α.
PC-60683

SNX-0723

HSP90 inhibitor

SNX-0723 is a selective, brain-permeable, orally acitve small-molecule inhibitor of Hsp90 (IC50=14 nM) that inhibits alpha-synuclein oligomerization with EC50 of 48 nM.
PC-60670

PF04942847

HSP90 inhibitor

PF04942847 is an orally available, ATP-competitive, small-molecule inhibitor of HSP90 with Ki of 6 nM.
PC-60660

KU-32

HSP90 inhibitor, Hsp70 inducer

KU-32 is a novel, novobiocin-based, C-terminal inhibitor of Hsp90 and a potent inducer of Hsp70.
PC-60609

KU675

HSP90 inhibitor

KU675 is a second-generation C-terminal Hsp90 inhibitor with Kd of 191 and 726 uM for Hsp90α and Hsp90β, respectively.
PC-60607

Gedunin

HSP90 inhibitor

Gedunin is a natural tetranortriterpenoid compound that inhibits Hsp90 and induce the degradation of Hsp90-dependent client proteins.

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