T5461 |
GNE-6640
|
2009273-67-8
|
99.59%
|
|
GNE-6640 is a non-covalent inhibitor targeting ubiquitin specific peptidase 7 (USP7), exhibiting IC50 values of 0.75 μM for full-length USP7, 0.43 μM for the USP...
|
T15604 |
IU1-47
|
670270-31-2
|
99.55%
|
|
IU1-47 is an effective and specific USP14 inhibitor (IC50: 0.6 μM). IU1-47 causes tau elimination in cultured neurons. IU1-47 inhibits IsoT/USP5 (IC50: 20 μM).
|
T60130 |
USP5-IN-1
|
|
99.53%
|
|
USP5-IN-1 (compound 64) is a potent deubiquitinase USP5 inhibitor, which binds to the USP5 ZnF-UBD with a KD of 2.8 μM and is selective over nine proteins contai...
|
T60039 |
KSQ-4279
|
2446480-97-1
|
99.43%
|
|
KSQ-4279 (USP1-IN-1) is an inhibitor of USP1 and PARP.KSQ-4279 has anticancer activity and is used in the study of non-small cell lung cancer, osteosarcoma, ovar...
|
T77763 |
Wu-5
|
2630378-05-9
|
99.29%
|
|
Wu-5 is a potent USP10 inhibitor that inhibits FLT3 and AMPK pathways, promoting the breakdown of FLT3-ITD and inducing apoptosis.
|
T67873 |
USP8-IN-3
|
2477651-10-6
|
99.18%
|
|
USP8-IN-3 is a potent inhibitor of the deubiquitinating enzymes USP7 and USP8, with IC50 of 4.0 μM against USP8D. USP8-IN-3 inhibited the proliferation of GH3 an...
|
T21527 |
HBX 41108
|
924296-39-9
|
99.13%
|
|
HBX 41108 (HBX-41108) is a non-competitive, reversible inhibitor of USP7 with an IC50 of 424nM. HBX 41108 inhibited deubiquitination of p53 mediated by USP7 in a...
|
T36682 |
USP30 inhibitor 18
|
2242582-40-5
|
99.03%
|
|
USP30 inhibitor 18 is a selective USP30 inhibitor with an IC50 of 0.02 μM. USP30 inhibitor 18 increases protein ubiquitination and accelerates mitophagy[1].
[1]....
|
T67876 |
USP8-IN-2
|
2477651-11-7
|
98.83%
|
|
USP8-IN-2 is a potent inhibitor of the deubiquitinating enzymes USP7 and USP8, with an IC50 of 4.0 μM against USP8D. USP8-IN-2 is a potential compound for the tr...
|
T9122 |
XL177A
|
2417089-74-6
|
98.75%
|
|
XL177A is a selective irreversible USP7 inhibitor(IC50 : 0.34 nM). XL177A elicits cancer cell killing through a p53-dependent mechanism.
|
T13268 |
USP7-IN-1
|
1381291-36-6
|
98.70%
|
|
USP7-IN-1 is a selective and reversible ubiquitin-specific protease 7 (USP7) inhibitor (IC50 = 77 μM).
|
T11111 |
DUB-IN-2
|
924296-19-5
|
98.53%
|
|
Dub-in-2, with an IC50 value of 0.28 for USP8, is an effective deubiquitinase inhibitor.
|
T4338 |
USP7/USP47 inhibitor
|
1247825-37-1
|
98.5%
|
|
USP7/USP47 inhibitor (USP7/47 inhibitor-1) is a selective ubiquitin-specific protease 7/47 (USP7/USP47) inhibitor, with EC50s of 0.42 μM and 1.0 μM, respectively...
|
T9375 |
IU1-248
|
2307472-03-1
|
98.49%
|
|
IU1-248 is a derivative of IU1. IU1-248 is a potent and selective USP14 inhibitor with an IC50 of 0.83 μM[1].
|
T9217 |
USP7-IN-8
|
2009273-60-1
|
98.48%
|
|
Benzamide, 4-[6-amino-4-ethyl-5-(4-hydroxyphenyl)-3-pyridinyl]-N-methyl- is a selective ubiquitin-specific protease 7 (USP7) inhibitor with an IC50 of 1.4 μM. US...
|
T72784 |
OTUB1/USP8-IN-1
|
2858800-98-1
|
98.47%
|
|
OTUB1/USP8-IN-1 is a potent OTUB1/USP8 inhibitor with potential anticancer activity, with IC50 values of 0.17 and 0.28 nM for OTUB1 and USP8, respectively.OTUB1/...
|
T2424 |
P 22077
|
1247819-59-5
|
98.42%
|
|
P 22077 (P22077) is an inhibitor of ubiquitin-specific protease USP7 with EC50 of 8.6 μM. It also inhibits the closely related USP47.
|
T3089 |
6-Thioguanine
|
154-42-7
|
98.34%
|
|
6-Thioguanine (2-Amino-6-purinethiol) is an antineoplastic compound which also has antimetabolite action. The drug is used in the therapy of acute leukemia.
|
T73151 |
USP22-IN-1
|
309735-96-4
|
98.2%
|
|
USP22-IN-1 is a ubiquitin-specific peptidase 22 (USP22) inhibitor that can be used to treat proliferative diseases or cancer.
|
T11209 |
EOAI3402143
|
1699750-95-2
|
98.09%
|
|
EOAI3402143 inhibits Usp9x and Usp24 activity, increases tumor cell apoptosis. EOAI3402143 phenocopies the FAS induction and apoptotic sensitization of Usp5 knoc...
|