ALLOSTERISM;
ANIMAL EXPERIMENT;
ANTIPROLIFERATIVE ACTIVITY;
AREA UNDER THE CURVE;
ARTICLE;
CELL MEMBRANE PERMEABILITY;
CONFORMATIONAL TRANSITION;
CONTROLLED STUDY;
DRUG BIOAVAILABILITY;
DRUG CLEARANCE;
DRUG DISTRIBUTION;
DRUG MECHANISM;
DRUG METABOLISM;
DRUG PENETRATION;
DRUG POTENCY;
DRUG SELECTIVITY;
DRUG SOLUBILITY;
DRUG SYNTHESIS;
DRUG TARGETING;
FEMALE;
FIRST PASS EFFECT;
HIGH THROUGHPUT SCREENING;
HUMAN;
HUMAN CELL;
MAXIMUM PLASMA CONCENTRATION;
MOUSE;
NONHUMAN;
SINGLE DRUG DOSE;
STRUCTURE ACTIVITY RELATION;
Molecular perspectives on p97-VCP: Progress in understanding its structure and diverse biological functions
Wang, Q.; Changcheng Song, C.; Li, C. H. Molecular perspectives on p97-VCP: progress in understanding its structure and diverse biological functions J. Struct. Biol. 2004, 146, 44-57
Improved structures of full-length p97, an AAA ATPase: Implications for mechanisms of nucleotide-dependent conformational change
Davies, J. M.; Brunger, A. T.; Weis, W. I. Improved structures of full-length p97, an AAA ATPase: implications for mechanisms of nucleotide-dependent conformational change Structure 2008, 16, 715-726
Targeted deletion of p97 (VCP/CDC48) in mouse results in early embryonic lethality
Muller, J. M.; Deinhardt, K.; Rosewell, I.; Warren, G.; Shima, D. T. Targeted deletion of p97 (VCP/CDC48) in mouse results in early embryonic lethality Biochem. Biophys. Res. Commun. 2007, 354, 459-65
Elevated Expression of Valosin-Containing Protein (p97) in Hepatocellular Carcinoma Is Correlated with Increased Incidence of Tumor Recurrence
Yamamoto, S.; Tomita, Y.; Nakamori, S.; Hoshida, Y.; Nagano, H.; Dono, K.; Umeshita, K.; Sakon, M.; Monden, M.; Aozasa., K. Elevated Expression of Valosin-Containing Protein (p97) in Hepatocellular Carcinoma Is Correlated With Increased Incidence of Tumor Recurrence J. Clin. Oncol. 2003, 21 (3) 447-452
Expression Level of Valosin-Containing Protein Is Strongly Associated with Progression and Prognosis of Gastric Carcinoma
Yamamoto, S.; Tomita, Y.; Hoshida, Y.; Takiguchi, S.; Fujiwara, Y.; Yasuda, T.; Yano, M.; Nakamori, S.; Sakon, M.; Monden, M.; Katsuyuki Aozasa, K. Expression Level of Valosin-Containing Protein Is Strongly Associated With Progression and Prognosis of Gastric Carcinoma J. Clin. Oncol. 2003, 21 (13) 2537-2544
The ERAD Inhibitor Eeyarestatin i Is a Bifunctional Compound with a Membrane-Binding Domain and a p97/VCP Inhibitory Group
Wang, Q.; Shinkre, B. A.; Lee, J.; Weniger, M. A.; Liu, Y.; Chen, W.; Wiestner, A.; Trenkle, W. C.; Ye, Y. The ERAD Inhibitor Eeyarestatin I Is a Bifunctional Compound with a Membrane-Binding Domain and a p97/VCP Inhibitory Group PLoS One 2010, 5 (11) e15479
Reversible inhibitor of p97, DBeQ, impairs both ubiquitin-dependent and autophagic protein clearance pathways
Choua, T.; Brownb, S. J.; Minondc, D.; Nordind, B. E.; Lie, K.; Jones, A. C.; Chasec, P.; Porubskye, P. R.; Stoltzf, B. M.; Schoenene, F. J.; Patricellid, M. P.; Hodderc, P.; Rosenb, H.; Deshaies, R. J. Reversible inhibitor of p97, DBeQ, impairs both ubiquitin-dependent and autophagic protein clearance pathways Proc. Natl. Acad. Sci. U. S. A. 2011, 108 (12) 4834-4839
2-Anilino-4-aryl-1,3-thiazole inhibitors of valosin-containing protein (VCP or p97)
Bursavich, M. G.; Parkera, D. P.; Willardsena, J. A.; Gaob, Z.; Davisb, T.; Ostaninb, K.; Robinsonb, R.; Petersonb, A.; Cimborab, D. M.; Zhub, J.; Richards, B. 2-Anilino-4-aryl-1,3-thiazole inhibitors of valosin-containing protein (VCP or p97) Bioorg. Med. Chem. Lett. 2010, 20 (5) 1677-1879
Interprotomer motion-transmission mechanism for the hexameric AAA ATPase p97
Li, G.; Huang, C.; Zhao, G.; Lennarz, W. J. Interprotomer motion-transmission mechanism for the hexameric AAA ATPase p97 Proc. Natl. Acad. Sci. U. S. A. 2012, 109, 3737-3741
Dynamic flexibility of the ATPase p97 is important for its interprotomer motion trasmission
Huang, C.; Li, G.; Lennarz, W. J. Dynamic flexibility of the ATPase p97 is important for its interprotomer motion trasmission Proc. Natl. Acad. Sci. U. S. A. 2012, 109 (25) 9792-9797
Synthesis of 5-aryl-2 H -tetrazole-2-acetic acids, and [(4-phenyl-5-aryl-4 H -1,2,4-triazol-3-yl)thio]acetic acids as possible superoxide scavengers and antiinflammatory agents
Maxwell, J. R.; Wasdahl, D. A.; Wolfson, A. C.; Stenberg, V. I. Synthesis of 5-aryl-2 H -tetrazole-2-acetic acids, and [(4-phenyl-5-aryl-4 H -1,2,4-triazol-3-yl)thio]acetic acids as possible superoxide scavengers and antiinflammatory agents J. Med. Chem. 1984, 27, 1565-1570
A convenient synthesis of 4,5-disubstituted 1,2,4-triazoles functionalized in position 3
Ivanova, N. V.; Sviridov, S. I.; Shorshnev, S. V.; Stepanov, A. E. A convenient synthesis of 4,5-disubstituted 1,2,4-triazoles functionalized in position 3 Synthesis 2006, 1, 156-160
Synthesis and in vitro antifungal and cytotoxicity evaluation of thiazolo-4 H -1,2,4-triazoles and 1,2,3-thiadiazolo-4 H -1,2,4-triazoles
Per Jalilian, A. R.; Sattari, S.; Bineshmarvasti, M.; Shafiee, A.; Daneshtalab, M. Synthesis and in vitro antifungal and cytotoxicity evaluation of thiazolo-4 H -1,2,4-triazoles and 1,2,3-thiadiazolo-4 H -1,2,4-triazoles Arch. Pharm. 2000, 333, 347-354
Synthesis of a non-heme template for attaching four peptides: An approach to artificial iron(II)-containing peroxidases
Heuvel, M.; Berg, T. A.; Kellog, R. M.; Choma, C. T.; Feringa, B. L. Synthesis of a non-heme template for attaching four peptides: an approach to artificial iron(II)-containing peroxidases J. Org. Chem. 2004, 69, 250-262
Discovery of 4,5-diphenyl-1,2,4-triazole derivatives as a novel class of selective antagonist for the human V1A receptor
Kakefuda, A.; Takeshi, S.; Takahiko, T.; Atsuo, T.; Shuichi, S.; Shin-ichi, T. Discovery of 4,5-diphenyl-1,2,4-triazole derivatives as a novel class of selective antagonist for the human V1A receptor Bioorg. Med. Chem. 2002, 10, 1905-1912
Synthesis and structure-activity relationships of carboxylated chalcones: A novel series of cysLT1 (LTD4) receptor antagonists
Zwaagstra, M. E.; Timmerman, H.; Tamura, M.; Tohma, T.; Wada, Y. Synthesis and structure-activity relationships of carboxylated chalcones: a novel series of cysLT1 (LTD4) receptor antagonists J. Med. Chem. 1997, 40, 1075-1089
Consecutive hydrogenation of benzaldehyde over Pd catalysts: Influence of supports and sulfur poisoning
Pinna, F.; Menegazzo, F.; Signoretto, M.; Canton, P.; Fagherazzi, G.; Perticone, N. Consecutive hydrogenation of benzaldehyde over Pd catalysts: influence of supports and sulfur poisoning Appl. Catal., A 2002, 219, 195-200
Structural and functional implications of phosphorylation and acetylation in the regulation of the AAA+ protein p97
Ewens, C. A.; Kloppsteck, P.; Förster, A.; Zhang, X.; Freemont, P. S. Structural and functional implications of phosphorylation and acetylation in the regulation of the AAA+ protein p97 Biochem. Cell Biol. 2010, 88, 41-48
The ATPase activity of purified CDC48p from Saccharomyces cerevisiae shows complex dependence on ATP-, ADP-, and NADH-concentrations and is completely inhibited by NEM
Fröhlich, K. U.; Fries, H. W.; Peters, J. M.; Mecke, D. The ATPase activity of purified CDC48p from Saccharomyces cerevisiae shows complex dependence on ATP-, ADP-, and NADH-concentrations and is completely inhibited by NEM Biochim. Biophys. Acta 1995, 1253, 25-32
Identification of 4,5-Dihydro-1 H -pyrazolo[4,3-h ]quinazoline Derivatives as a New Class of Orally and Selective Polo-Like Kinase 1 Inhibitors
Beria, I.; Ballinari, D.; Bertrand, J. A.; Borghi, D.; Bossi, R. T.; Brasca, M. G.; Cappella, P.; Caruso, M.; Ceccarelli, W.; Ciavolella, A.; Cristiani, C.; Croci, V.; De Ponti, A.; Fachin, G.; Ferguson, R. D.; Lansen, J.; Moll, J. K.; Pesenti, E.; Posteri, H.; Perego, R.; Rocchetti, M.; Storici, P.; Volpi, D.; Valsasina, B. Identification of 4,5-Dihydro-1 H -pyrazolo[4,3-h ]quinazoline Derivatives as a New Class of Orally and Selective Polo-Like Kinase 1 Inhibitors J. Med. Chem. 2010, 53, 3532-3551