5.31088

VCP Inhibitor III, NMS-873

• 別名: VCP Inhibitor III, NMS-873, 3-(3-(Cyclopentylthio)-5-((2-methyl-4ʹ-(methylsulfonyl)biphenyl-4-yloxy)methyl)-4H-1,2,4-triazol-4-yl)pyridine, 3-(3-Cyclopentylsulfanyl-5-(4ʹ-methanesulfonyl-2-methyl-biphenyl-4-yloxymethyl)-[1,2,4]triazol-4-yl)-pyridine, Valosin-containing Protein Inhibitor III, p97 Inhibitor III, ERAD Inhibitor III, NMS873
• 実験式（ヒル表記法）: C₂₇H₂₈N₄O₃S₂
• CAS番号: 1418013-75-8
• 分子量: 520.67
• MDL番号: MFCD28009371
• UNSPSCコード: 12352200

特性

• アッセイ: ≥98% (HPLC)
• 品質水準: 100
• 形状: powder
• メーカー／製品名: Calbiochem^®
• 保管条件: OK to freeze; protect from light
• 色: light beige
• 保管温度: 2-8°C
• InChI: 1S/C27H28N4O3S2/c1-19-16-22(11-14-25(19)20-9-12-24(13-10-20)36(2,32)33)34-18-26-29-30-27(35-23-7-3-4-8-23)31(26)21-6-5-15-28-17-21/h5-6,9-17,23H,3-4,7-8,18H2,1-2H3
• InChI Key: UJGTUKMAJVCBIS-UHFFFAOYSA-N

詳細

詳細

A cell-permeable triazolylpyridine compound that potently inhibits VCP ATPase activity in a non-ATP-competitive manner (IC₅₀/[ATP] = 20 nM/1 mM & 30 nM/60 µM; [wt hVCP] = 10 nM) via an allosteric mechanism where the inhibitor targets the lateral tunnel formed by the D1 & D2 domains of one VCP protomer together with the D1 from the adjacent VCP molecule in the hexamer, effectively locking the protomer in a rigid conformation and thereby preventing the release of bound ADP for successful propagation of interprotomer ATP hydrolysis cycle, while being ineffective against a panel of 53 kinases or the ATPase activities of 4 other AAA (ATPase Associated with diverse/various cellular Activities) ATPases (NSF, SPATAS, VPS4B, and cdc6) and Hsp90 (by <15% at 10 µM). In agreement with siRNA-mediated VCP knockdown, NMS-873 is shown to prevent VCP from extracting ubiquitinated client proteins, including cyclin E & Mcl-1, for proteasomal degradation, resulting in cellular UPR (unfold protein response) activation, autophagy induction, and eventual apoptosis in HCT-116 cultures in a dose- and time-dependent manner (0.5 to 5 µM; 8 to 72 h). Anti-cancer studies using a panel of 40 various hematological and solid tumor lines reveal wide-spread sensitivities to NMS-873-induced killings (IC₅₀ from 80 nM to 2 µM), differing in degrees than those observed with the proteasome inhibitor Bortezomib (Cat. No. Cat. No. 504314). Exhibits high clearance and low bioavailability in in vivo studies.

A cell-permeable triazolylpyridine compound that potently inhibits VCP ATPase activity in a non-ATP-competitive manner (IC₅₀/[ATP] = 20 nM/1 mM & 30 nM/60 µM; [wt hVCP] = 10 nM) via an allosteric mechanism where the inhibitor targets the lateral tunnel formed by the D1 & D2 domains of one VCP protomer together with the D1 from the adjacent VCP molecule in the hexamer, effectively locking the protomer in a rigid conformation and thereby preventing the release of bound ADP for successful propagation of interprotomer ATP hydrolysis cycle, while being ineffective against a panel of 53 kinases or the ATPase activities of 4 other AAA (ATPase Associated with diverse/various cellular Activities) ATPases (NSF, SPATAS, VPS4B, and cdc6) and Hsp90 (by <15% at 10 µM). In agreement with siRNA-mediated VCP knockdown, NMS-873 is shown to prevent VCP from extracting ubiquitinated client proteins, including cyclin E & Mcl-1, for proteasomal degradation, resulting in cellular UPR (unfold protein response) activation, autophagy induction, and eventual apoptosis in HCT-116 cultures in a dose- and time-dependent manner (0.5 to 5 µM; 8 to 72 h). Anti-cancer studies using a panel of 40 various hematological and solid tumor lines reveal wide-spread sensitivities to NMS-873-induced killings (IC₅₀ from 80 nM to 2 µM), differing in degrees than those observed with the proteasome inhibitor Bortezomib (Cat. No. Cat. No. 504314). Exhibits high clearance and low bioavailability in in vivo studies.

Please note that the molecular weight for this compound is batch-specific due to variable water content.

生物化学的／生理学的作用

Cell permeable: yes

Primary Target
VCP

Reversible: yes

包装

Packaged under inert gas

警告

Toxicity: Standard Handling (A)

再構成

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C.

その他情報

Magnaghi, P., et al. 2013. Nat. Chem. Biol.9, 548.
Polucci, P., et al. 2013. J. Med. Chem.56, 437.

法的情報

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

安全性情報

• 保管分類コード: 11 - Combustible Solids
• WGK: WGK 3
• 引火点(°F): Not applicable
• 引火点(℃): Not applicable