| Cat. No. |
Product Name |
Information |
| PC-22005 |
Davelizomib
Proteasome inhibitor
|
Davelizomib is a proteasome inhibitor with antineoplastic effect. |
| PC-49521 |
WZ-1831
β5c inhibitor
|
WZ-1831 is a potent and highly selective inhibitor of human constitutive proteasome chymotryptic activity (β5c) with IC50 of 10 nM, >500-fold selectivity over β5i (IC50=7.1 uM). |
| PC-47062 |
TXS-8
Rpn6 binder
|
TXS-8 is a specific, small molecule binder of Rpn-6 with KD of 14 uM, Rpn-6 is a subunit of the 19S regulatory particle (RP) of 26s proteasome. |
| PC-72569 |
CBK006377
UPS inhibitor
|
CBK006377 (CBK77) is a small molecule inhibitor of the ubiquitin-proteasome system (UPS) with EC50 of 4.3 uM in MelJuSo Ub-YFP cells (6h treatment). |
| PC-72402 |
M3258
LMP7 inhibitor
|
M3258 (M 3258) is a potent, reversible, highly selective and orally acitve LMP7 inhibitor with cellular IC50 of 4.1 nM. |
| PC-35491 |
TCH-165
Proteasome modulator
|
TCH-165 is a specific small molecule modulator of proteasome assembly, regulates the dynamic equilibrium between the 20S and 26S proteasome complexes, favoring 20S-mediated protein degradation. |
| PC-43439 |
MG-132
Proteasome inhibitor
|
MG-132 (Z-Leu-leu-leu-al, Zlllal) is a potent, reversible, and cell-permeable proteasome inhibitor with IC50 of 0.1 and 1.2 μM for the inhibition of proteasome and calpain, respectively. |
| PC-43393 |
ONX-0914
LMP7 inhibitor
|
ONX-0914 (PR-957) is a potent, selective inhibitor of the chymotrypsin-like subunit of immunoproteasome LMP7 with IC80 <100 nM, 20- to 40-fold more selective over β5 or LMP2. |
| PC-43371 |
Celastrol
PRDX1 inhibitor, 20S proteasome inhibitor
|
Celastrol (Tripterin) is an active compound extracted from Chinese medicine Thunder of God Vine, is a potent proteasome inhibitor, preferentially inhibits the chymotrypsin-like activity of 20S proteasome with IC50 of 2.5 uM. |
| PC-42948 |
PI-1840
Proteasome inhibitor
|
PI-1840 is a potent, selective, noncovalent, reversible inhibitor for proteasome chymotrypsin-like (CT-L) activity with IC50 of 27 nM, shows no effect on trypsin-like and peptidylglutamyl peptide hydrolyzing activities (IC50>100 uM). |
| PC-42896 |
Oprozomib
Proteasome inhibitor
|
Oprozomib (ONX-0912, PR-047) is a potent, orally bioavailable proteasome inhibitor that inhibits chymotrypsin-like (CT-L) activity of 20S proteasome β5/LMP7 with IC50 of 36/82 nM. |
| PC-61352 |
o-Phenanthroline
Rpn11 inhibitor
|
o-Phenanthroline is a selective inhibitor of 26S proteasome subunit Rpn11 with IC50 of 10±2 uM. |
