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Chemical Structure Cat. No. Product Name CAS No.
EOAI3402143 Chemical Structure
BCP32727 EOAI3402143 1699750-95-2
EOAI3402143 is a deubiquitinase (DUB) inhibitor, which inhibits dose-dependently inhibits Usp9x/Usp24 and Usp5.
FT-671 Chemical Structure
BCP31908 FT-671 1959551-26-8
FT671 is a potent and selective USP7 inhibitor with high affinity and specificity in vitro and within human cells.
SJB3-019A Chemical Structure
BCP31485 SJB3-019A 2070015-29-9
SJB3-019A is a USP1 inhibitor.
GNE-6640 Chemical Structure
BCP31358 GNE-6640 2009273-67-8
GNE-6640 is a novel selective USP7 inhibitor, inducing tumor cell death. GNE-6640 enhances cytotoxicity with chemotherapeutic agents and targeted compounds, including PIM kinase inhibitors.
USP25 and 28 inhibitor AZ-2 Chemical Structure
BCP31313 USP25 and 28 inhibitor AZ-2 2165322-95-0
USP25 and 28 inhibitor AZ-2 is a potent, selective, dual USP25/28 inhibitor with IC50 of 0.9/0.9 uM, respectively.
USP25 and 28 inhibitor AZ-3 Chemical Structure
BCP31314 USP25 and 28 inhibitor AZ-3 AZ-3
USP25 and 28 inhibitor AZ-1 Chemical Structure
BCP31311 USP25 and 28 inhibitor AZ-1 2165322-94-9
AZ1 is a dual inhibitor of the USP25/28 deubiquitinating enzyme subfamily.
6-Thioguanine Chemical Structure
BCP27718 6-Thioguanine 154-42-7
Thioguanine is an antineoplastic compound which also has antimetabolite action. The drug is used in the therapy of acute leukemia.
TCID Chemical Structure
BCP29983 TCID 30675-13-9
TCID is a DUB inhibitor for ubiquitin C-terminal hydrolase L3 with IC50 of 0.6 μM, 125-fold selective to L1.
HBX 41108 Chemical Structure
BCP08394 HBX 41108 924296-39-9
HBX 41108 is an Inhibitor of ubiquitin-specific protease (USP) 7 activity (IC50 = 424 nM).
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