目录号 | 产品详情 | 靶点 | |
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T6107 | DUB Autophagy | ||
IU1 是一种可逆的特异性人类 USP14 蛋白酶体抑制剂,可以穿透细胞,IC50为 4.7 μM。 | |||
T8464 | Apoptosis DUB | ||
RA-9 是一种高选择性蛋白酶体相关的 DUBs 抑制剂,具有良好的毒性和抗癌活性。它阻断泛素依赖性蛋白降解而不影响 20S 蛋白酶体蛋白水解活性。它诱导卵巢癌细胞内质网应激反应,选择性诱导卵巢癌细胞株和供体原代培养细胞凋亡。 | |||
T8553 | Others | ||
BC-1471 是STAM 结合蛋白(STAMBP)去泛素酶抑制剂。BC-1471 抑制 NALP7(NACHT, LRR 和 PYD 结构域蛋白 7)的炎症小体活性。 | |||
T6300 | Apoptosis JAK Bcr-Abl DUB Autophagy | ||
Degrasyn (WP1130) 是一种可渗透细胞的去泛素化酶(DUB)抑制剂,直接抑制USP9x,USP5,USP14和UCH37的DUB 活性。 它减弱抗细胞凋亡蛋白Bcr-Abl 和JAK2。 | |||
T7678 | DUB | ||
SJB2-043 是一种 USP1-UAF1 的抑制剂 ,IC50值 544 nM。 | |||
T6925 | DUB | ||
P005091 (P5091) 是一种选择性有效的泛素特异性蛋白酶7(USP7)抑制剂,EC50值为 4.2 μM。 | |||
T4338 | DUB | ||
USP7/USP47 inhibitor (USP7/47 inhibitor-1) 是一种选择性泛素特异性蛋白酶 7/47 抑制剂,EC50值分别为 0.42 μM 和 1.0 μM。 | |||
T11464 | SARS-CoV DUB | ||
GRL0617 是一种选择性和竞争性的 SARS-CoVPLpro 和去泛素酶非共价抑制剂,其 IC50值为 0.6 μM,Ki 值为 0.49 μM. | |||
T9217 | DUB | ||
USP7-IN-8 (GNE-6776) 是一种选择性泛素特异性蛋白酶 7 (USP7) 抑制剂,IC50 为 1.4 μM。它具有抗癌作用。 | |||
T1932 | Apoptosis DUB | ||
B-AP15 (NSC-687852) 是 26S 蛋白酶体的去泛素化酶 Usp14 和 UCHL5 的选择性抑制剂。 它阻断 26S 蛋白酶体的去泛素化活性。 |
目录号 | 产品名/同用名 | 种属 | 表达系统 | ||
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TMPY-03011 | USP46 Protein, Human, Mouse, Recombinant | Human,Mouse | Baculovirus-Insect Cells | ||
USP46 belongs to the peptidase C19 family, USP12/USP46 subfamily. Deubiquitinating enzymes (DUBs) are a large group of proteases which are also commonly referred to as deubiquitinating peptidases, deubiquitinating isopeptidases, deubiquitinases, ubiquitin proteases, ubiquitin hydrolyases, ubiquitin isopeptidases, or Dubs. They regulate ubiquitin-dependent metabolic pathways by cleaving ubiquitin-protein bonds. They also may act as negative and positive regulators of the ubiquitin system. Besides ubiquitin recycling, they are also involved in processing of ubiquitin precursors, in proofreading of protein ubiquitination and in disassembly of inhibitory ubiquitin chains. USP46 is a deubiquitinating enzyme that plays a role in behavior, possibly by regulating GABA action. It may act by mediating the deubiquitination of GAD1/GAD67. USP46 has almost no deubiquitinating activity by itself and requires the interaction with WDR48 to have high activity and it is not involved in deubiquitination of monoubiquitinated FANCD2.
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TMPY-02522 | OTUB2 Protein, Human, Recombinant (His) | Human | E. coli | ||
Otubain 2 (OTUB2) is a member of DUBs that belong to the ovarian tumour (OTU) superfamily of proteins which consists of a five-stranded β-sheet sandwiched in between a small helical amino-terminal region consisting of α1 and α2, and a large helical region comprised of α3-α10. Like other DUBs, otubain 2 (OTUB2) cleaves proteins precisely at the ubiquitin-protein bond so that ubiquitylation process can be reversed and regulated. Otubain 2 (OTUB2)'s active-site cleft is sterically occluded by a novel loop conformation resulting in an oxyanion hole, which consists uniquely of backbone amides. Furthermore, the residues that orient and stabilize the active-site histidine of otubain 2 (OTUB2) are different from other cysteine proteases. This reorganization of the active-site topology provides a possible explanation for the low turnover and substrate specificity of the otubains.
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TMPY-02974 | USP46 Protein, Human, Mouse, Recombinant (SUMO) | Human,Mouse | Baculovirus-Insect Cells | ||
USP46 belongs to the peptidase C19 family, USP12/USP46 subfamily. Deubiquitinating enzymes (DUBs) are a large group of proteases which are also commonly referred to as deubiquitinating peptidases, deubiquitinating isopeptidases, deubiquitinases, ubiquitin proteases, ubiquitin hydrolyases, ubiquitin isopeptidases, or Dubs. They regulate ubiquitin-dependent metabolic pathways by cleaving ubiquitin-protein bonds. They also may act as negative and positive regulators of the ubiquitin system. Besides ubiquitin recycling, they are also involved in processing of ubiquitin precursors, in proofreading of protein ubiquitination and in disassembly of inhibitory ubiquitin chains. USP46 is a deubiquitinating enzyme that plays a role in behavior, possibly by regulating GABA action. It may act by mediating the deubiquitination of GAD1/GAD67. USP46 has almost no deubiquitinating activity by itself and requires the interaction with WDR48 to have high activity and it is not involved in deubiquitination of monoubiquitinated FANCD2.
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