5.31088

VCP Inhibitor III, NMS-873

• Synonyme(s) : 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
• Formule empirique (notation de Hill): C₂₇H₂₈N₄O₃S₂
• Numéro CAS: 1418013-75-8
• Poids moléculaire : 520.67
• Numéro MDL: MFCD28009371
• Code UNSPSC : 12352200

Propriétés

• Pureté: ≥98% (HPLC)
• Niveau de qualité: 100
• Forme: powder
• Fabricant/nom de marque: Calbiochem^®
• Conditions de stockage: OK to freeze; protect from light
• Couleur: light beige
• Température de stockage: 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
• Clé InChI: UJGTUKMAJVCBIS-UHFFFAOYSA-N

Description

Description générale

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.

Actions biochimiques/physiologiques

Cell permeable: yes

Primary Target
VCP

Reversible: yes

Conditionnement

Packaged under inert gas

Avertissement

Toxicity: Standard Handling (A)

Reconstitution

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

Autres remarques

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

Informations légales

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

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable