Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Randall W. Steinkampf"'
Autor:
Wayne Klohs, Denise L. Driscoll, Aneesa M. Amar, Wilbur R. Leopold, H. D. Hollis Showalter, Brian G. Hartl, William L. Elliott, Bill J. Roberts, Stacey L. Boushelle, Andrew M. Thompson, Randall W. Steinkampf, Connolly Cleo, Patrick W. Vincent, William A. Denny, James M. Hamby, Sandra J. Patmore, Alan J. Kraker
Publikováno v:
Journal of Medicinal Chemistry. 43:4200-4211
A series of 3-aryl-1,6-naphthyridine-2,7-diamines and related 2-ureas were prepared and evaluated as inhibitors of the FGF receptor-1 tyrosine kinase. Condensation of 4,6-diaminonicotinaldehyde and substituted phenylacetonitriles gave intermediate na
Autor:
Jean Veith, Barbara W. Henderson, Mel C. Schroeder, Adam B. Sumlin, Denise Driscoll, Paula J. Pera, Wayne D. Klohs, Amarnath Sharma, Sylvester Klutchko, Charles J. Dimitroff, Randall W. Steinkampf, Ralph J. Bernacki, Thomas J. Dougherty
Publikováno v:
Investigational New Drugs. 17:121-135
Angiogenesis, the formation of new blood vessels from an existing vasculature, is requisite for tumor growth. It entails intercellular coordination of endothelial and tumor cells through angiogenic growth factor signaling. Interruption of these event
Publikováno v:
European Journal of Cancer. 32:311-315
Stout and colleagues [ Proc Am Assoc Cancer Res 1993, 34, p. 298] previously reported that both hydrocortisone and tamoxifen increased the free fraction of suramin in human plasma. We examined several corticosteroids as well as tamoxifen for their ef
Publikováno v:
International Journal of Cancer. 62:636-642
The mechanism of action of the novel anti-cancer compound CI-994 was studied in C26 murine colon tumor and HCT-8 human colon adenocarcinoma cells. Treatment of either cell line resulted in the specific loss of a 16-kDa phosphoprotein in a time- and c
Autor:
William A. Denny, Alan J. Kraker, Jeff B. Smaill, Gordon W. Rewcastle, Brian D. Palmer, Ellen Myra Dobrusin, Randall W. Steinkampf, Charles W. Moore
Publikováno v:
ChemInform. 36
A series of 2-anilino-6-phenylpyrido[2,3-d]pyrimidin-7(8H)-ones were synthesized and evaluated for their inhibitory properties against the non-receptor kinase c-Src and the G2/M checkpoint kinase Wee1. Overall, the compounds were 10-100-fold more pot
Autor:
Patrick W. Vincent, Aneesa M. Amar, Gina H. Lu, Diane H. Boschelli, James M. Nelson, Hussein Hallak, Sylvester Klutchko, Donald J. Dykes, Laura A. Bradford, Panek Rl, Chad L. Stoner, Wayne D. Klohs, James M. Hamby, Brian G. Hartl, H. D. Hollis Showalter, Randall W. Steinkampf, Alan J. Kraker, Annette M. Doherty, Billy J. Roberts, Cynthia Shen, William L. Elliott, Terry C. Major, Tawny K. Dahring, Zhipei Wu, Denise L. Driscoll
Publikováno v:
Journal of medicinal chemistry. 41(17)
While engaged in therapeutic intervention against a number of proliferative diseases, we have discovered the 2-aminopyrido[2, 3-d]pyrimidin-7(8H)-ones as a novel class of potent, broadly active tyrosine kinase (TK) inhibitors. An efficient route was
Evaluation of galactosyltransferase isoenzyme II in a human colon carcinoma-derived cell line, HCT-8
Publikováno v:
European Journal of Cancer and Clinical Oncology. 22:205-210
Polyacrylamide gel electrophoresis of galactosyltransferase (GT) extracted from a human colon adenocarcinoma cell line, HCT-8, demonstrated the presence of two peaks of activity: a slow-moving peak, referred to as GT-II, and a more anodally migrating
Publikováno v:
The American Journal of Tropical Medicine and Hygiene. 33:526-533
The duration of protection from blood-stage malarial challenge following single injections of pyrimethamine pamoate was assessed in mice and monkeys. This duration was dose-related and ranged from several weeks in mice to over 4 months in the monkeys
Autor:
Amie E. Mertus, Randall W. Steinkampf, Josefino B. Tunac, Max S. Wicha, Wilbur R. Leopold, Wayne Daniel Klohs
Publikováno v:
JNCI: Journal of the National Cancer Institute.
Proline analogues such as cis-4-hydroxy-L-proline (CHP) and L-azetidine-2-carboxylic acid (A2C) were tested for their antitumor activity in tissue culture and in vivo. In culture, CHP specifically inhibited those tumor cells that synthesized basement