About 7 results found for searched term "DUB-IN-3" (0.123 seconds)
Cat.No. | Name | Target |
---|---|---|
M13627 | DUB-IN-3 | Deubiquitinase |
DUB-IN-3 is a potent deubiquitinase (USP) enzyme inhibitor extracted from reference compound 22c with an IC50 of 0.56 μM for USP8. | ||
M2565 | PR-619 | Deubiquitinase |
2,6-Diamino-3,5-dithiocyanopyridine | ||
PR-619 is a broad-spectrum reversible DUB (deubiquitinating enzyme) inhibitor of USP2, USP4, USP5, USP7 and USP8 with an EC50 of 3-9 μM. PR-619 also induces endoplasmic reticulum stress and endoplasmic reticulum stress-associated apoptosis. | ||
M2890 | NSC 632839 | Others |
F6 | ||
NSC 632839 is not only a DUB inhibitor, but also a deSUMOylase inhibitor, it inhibits USP2, USP7, and SENP2 with IC50 of 45 μM, 37 μM, and 9.8 μM, respectively. | ||
M3052 | TCID | Deubiquitinase |
4,5,6,7-Tetrachloroindan-1,3-dione | ||
TCID is a DUB inhibitor for ubiquitin C-terminal hydrolase L3 with IC50 of 0.6 μM, 125-fold selective to L1. | ||
M8915 | Dubermatinib | TAM Receptor |
TP-0903 | ||
Dubermatinib (TP-0903) is a potent and selective AXL inhibitor with an IC50 value of 27 nM. | ||
M9871 | GSK2643943A | Deubiquitinase |
GSK2643943A is a deubiquitylating enzyme (DUB) inhibitor targeting USP20/Ub-Rho with an IC50 of 160 nM. GSK2643943A has anti-tumor efficacy and can be used for the research of oral squamous cell carcinoma (OSCC). | ||
M54656 | NJH-2-056 | Others |
NJH-2-056 is a deubiquitinase-targeting chimera (DUBTAC) linking EN523, a recruitment factor for OTUB1, to lumacaftor, a CFTR chaperone protein.NJH-2-056 can be used in cystic fibrosis-related studies. |
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