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Cat. No. Product Name Information
PC-60966

UK-101

LMP2 inhibitor

UK-101 is a potent, specific immunoproteasome β1i (LMP2) subunit inhibitor with IC50 of 104 nM, 144- and 10-fold selectivity over β1c and β5 subunit respectivey.
PC-60965

PR-825

Proteasome β5 inhibitor

PR-825 is a potent, specific immunoproteasome β5 subunit inhibitor.
PC-60964

PR-893

Proteasome inhibitor

PR-893 is a potent, specific immunoproteasome β5 subunit inhibitor with IC50 of 17 nM, 21-fold and 13-fold selectivity for β5 over LMP7 and LMP2 subunits, respecitvely.
PC-60963

PR-924

LMP7 inhibitor

PR-924 is a potent, specific immunoproteasome LMP7 subunit inhibitor with IC50 of 25 nM, >100-fold selectivity over β5c, β1i, β1c, β2i and β2c subunits (IC50>3 uM).
PC-60962

KZR-504

LMP2 inhibitor

KZR-504 (KZR504) is a potent, highly selective inhibitor of immunoproteasome low molecular polypeptide-2 (LMP2) subunit with IC50 of 51 nM.
PC-60898

Capzimin

Rpn11 inhibitor

Capzimin (Rpn11 inhibitor 3027) is a derivative of 8TQ, and potent and specific inhibitor of proteasome isopeptidase Rpn11 (PSMD14) with IC50 of 0.34 uM, >7-fold improved potency over 8TQ (quinoline-8-thiol).
PC-60476

FV-162

Proteasome inhibitor

FV-162 is a potent, orally bioavailable, irreversible proteasome inhibitor with potent antimyeloma activity (IC50<60 nM).
PC-42596

Ixazomib

Proteasome inhibitor

Ixazomib (MLN2238) is a potent, selective, orally bioavailable proteasome inhibitor with IC50 of 3.4 nM.
PC-42595

MLN9708

Proteasome inhibitor

Ixazomib citrate (MLN9708) is a potent, selective, orally bioavailable proteasome inhibitor with IC50 of 3.4 nM.
PC-42470

Bortezomib

Proteasome inhibitor

Bortezomib (PS341) is a potent, selective, competitive, orally active Proteasome inhibitor with Ki of 0.6 nM for 20S Proteasome.
PC-42597

Delanzomib

Proteasome inhibitor

Delanzomib (CEP18770) is a potent, orally active proteasome inhibitor with IC50 of 3.8 nM against chymotrypsin-like proteasome activity.
PC-42598

Carfilzomib

Proteasome inhibitor

Carfilzomib (PR-171) is a potent, highly selective inhibitor chymotrypsin-like activity of proteasome with IC50 of 6 nM.

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