Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T40255 |
VCP/p97 inhibitor-1
VCP/p97 inhibitor-1 |
||
VCP/p97 inhibitor-1, a highly effective compound, inhibits VCP/p97 (also known as Cdc48, CDC-48, or Ter94) with an IC 50 of 54.7 nM. This inhibitor induces a disruption in protein homeostasis and interferes with the degradation process of misfolded polypeptides by the ubiquitin-proteasome system (UPS). | |||
T18871 |
VCP-Eribulin
|
Others | Others |
VCP-Eribulin, an Eribulin-based drug for antibody conjugates[1], combines the VCP (ADCs linker) with Eribulin, a distinct microtubule inhibitor used in cancer treatments[2]. | |||
T18278 |
Mal-PEG2-VCP-Eribulin
|
Others | Others |
Mal-PEG2-VCP-Eribulin is a chemotherapeutic compound comprising an antibody-drug conjugate (ADC) linker (Mal-PEG2-VCP) and the microtubule inhibitor Eribulin[1]. This compound uniquely targets microtubules, offering a novel approach to cancer treatment. Eribulin is specifically utilized in creating targeted Eribulin-based drugs for antibody conjugates[1]. | |||
T18279 |
Mal-PEG2-VCP-NB
|
Others | Others |
Mal-PEG2-VCP-NB is a nonclaevable ADC linker containing a Maleimide group, 2-unit PEG and a VCP NB. | |||
T70421 | VCP746 | ||
VCP-746 is a potent adenosine A2B receptor agonist that stimulates anti-fibrotic signalling. VCP746 reduces hypertrophy in a rat neonatal cardiac myocyte model. VCP746 is a hybrid molecule consisting of an adenosine moiety linked to an adenosine A1 receptor (A1AR) allosteric modulator moiety. At the A1AR, VCP746 mediated cardioprotection in the absence of haemodynamic side effects such as bradycardia. | |||
T3535 |
ML240
|
p97 | Ubiquitination |
ML240 是一种选择性的 ATP 竞争性 p97 抑制剂,IC50值为 100 nM。 | |||
T1853 |
NMS-873
|
p97 | Ubiquitination |
NMS873 是一种有效的选择性变构 VCP/p97 抑制剂,IC50值为 30 nM。 | |||
T9008 |
NPD8733
|
Others | Others |
NPD8733 是癌细胞增强的成纤维细胞迁移抑制剂。它是与多种细胞活动 (AAA+) 蛋白家族相关的 ATP 酶的成员,能够与含 valosin 的蛋白 (VCP)/p97特异性结合,对癌症疾病具有潜在的研究价值。 | |||
T1969 |
DBEQ
JRF 12 |
Apoptosis; p97; Autophagy | Apoptosis; Autophagy; Ubiquitination |
DBEQ (JRF 12) 是一种选择性的,ATP 竞争性p97抑制剂,对 p97(wt) 和 p97(C522A) 的IC50值分别为 1.5 μM 和 1.6 μM,也可抑制Vps4,IC50值为 11.5 μM。 | |||
T6796 |
CB-5083
CB5083,CB 5083 |
p97 | Ubiquitination |
CB-5083 是一种有效的、选择性的、可口服的 p97 AAA ATPase 抑制剂,IC50为 11 nM。 | |||
T4684 |
ML241 hydrochloride
|
p97 | Ubiquitination |
ML241 hydrochloride 是一种有效且选择性的 p97 ATPase 抑制剂,IC50值为 100 nM。 | |||
T29112 |
VPC171
(2-氨基-4-(3-(三氟甲基)苯基)噻吩-3-基)(苯基)甲酮,VPC 171,VPC-171 |
Adenosine Receptor | GPCR/G Protein; Neuroscience |
VPC171 是一种新型腺苷 A1 受体正变构调节剂 (PAM)。 | |||
T71930 |
aPKC-I
|
||
aPKC-I is an inhibitor of atypical protein kinase C (aPKC ) which inhibits both PKCζ and PKCι with high specificity and prevents VEGF-induced endothelial permeability in cell culture and in vivo, thereby blocking ischemia-reperfusion (IR)-induced permeability. | |||
T31567 |
Doxorubicin-MVCP
MC-Val-Cit-PAB-Doxorubicin,MC-Val-Cit-PAB-Dox |
||
Doxorubicin-MVCP (MC-Val-Cit-PAB-Doxorubicin) is a Doxorubicin derivative with an MC-Val-Cit-PAB linker. | |||
T33861 | Paclitaxel-MVCP | ||
Paclitaxel-MVCP ( MC-val-cit-pab-paclitaxel )is a paclitaxel derivative with an MC-Val-Cit-PAB linker, which can be used for the preparation of Paclitaxel conjugates for drug delivery and nanomedicine research. | |||
T12236 |
NMS-859
ZINC169324353 |
Others | Others |
NMS-859 是一种有效的含 valosin 蛋白 (VCP)/p97 的共价抑制剂,在细胞中存在 60 μM 和 1 mM ATP 的情况下,对野生型 VCP 的 IC50 分别为 0.37 μM 和 0.36 μM。 | |||
T62148 |
NW 1028
|
||
NW 1028 是一种 VCP/p97 的有效抑制剂。NW 1028 能够选择性作用于 p97 的 ND1L 结构域,抑制依赖于 p97 的报告基因的降解。NW 1028 能够良好的结合 ND1L (Kd: 100 nM) 和全长 p97 (Kd: 285 nM)。NW 1028 对细胞有丝分裂纺锤体具有调节作用。 | |||
T36570 |
KUS121
|
||
KUS121 is a valosin-containing protein (VCP) modulator that inhibits VCP ATPase activity (IC50= 330 nM).1It inhibits cell death, ATP depletion, and upregulation of C/EBP-homologous protein (CHOP) induced by tunicamycin, an inducer of ER stress, in HeLa cells when used at concentrations of 20, 50, and 50 μM, respectively. KUS121 (100 μM) inhibits ATP depletion and cell death induced by oxygen-glucose deprivation (OGD) in rat primary cortical neurons in anin vitromodel of cerebral ischemia.2It red... |