Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Manuel Zancanella"'
Autor:
Gwenaella Rescourio, Ana Z. Gonzalez, Salman Jabri, Brian Belmontes, Gordon Moody, Doug Whittington, Xin Huang, Sean Caenepeel, Mario Cardozo, Alan C. Cheng, David Chow, Hannah Dou, Adrie Jones, Ron C. Kelly, Yihong Li, Mike Lizarzaburu, Mei-Chu Lo, Rommel Mallari, Cesar Meleza, Yosup Rew, Scott Simonovich, Daqing Sun, Simon Turcotte, Xuelei Yan, Simon G. Wong, Evelyn Yanez, Manuel Zancanella, Jonathan Houze, Julio C. Medina, Paul E. Hughes, Sean P. Brown
Publikováno v:
Journal of Medicinal Chemistry. 62:10258-10271
Overexpression of the antiapoptotic protein Mcl-1 provides a survival advantage to some cancer cells, making inhibition of this protein an attractive therapeutic target for the treatment of certain types of tumors. Herein, we report our efforts towar
Autor:
Jia-Nan Gong, Angela Coxon, Sean Caenepeel, Cyril H. Benes, Andrew W. Roberts, Tao Osgood, Donia M Moujalled, Elaina Cajulis, Andrew H. Wei, Regina K. Egan, Mario G. Cardozo, Pedro J. Beltran, Liusheng Zhu, Marc Vimolratana, Sean P. Brown, Brian Lucas, Xin Huang, Gordon Moody, Paul E. Hughes, David C.S. Huang, Giovanna Pomilio, Joshua Taygerly, Jan Sun, Danny Chui, Leszek Poppe, Jude Canon, Douglas A. Whittington, Yunxiao Li, Manuel Zancanella, Nick A. Paras, Joseph McClanaghan, Xianghong Wang, Alan C. Cheng, Kathleen S. Keegan, Jonathan B. Houze, Leah J. Damon, Patricia Greninger, Brian Belmontes
Publikováno v:
Cancer discovery. 8(12)
The prosurvival BCL2 family member MCL1 is frequently dysregulated in cancer. To overcome the significant challenges associated with inhibition of MCL1 protein–protein interactions, we rigorously applied small-molecule conformational restriction, w
Autor:
Piotr Cieplak, Gil Ma, Robyn D. Richardson, Jeffrey W. Smith, Yatsandra Oyola, Daniel Romo, Lynn M. Knowles, Manuel Zancanella
Publikováno v:
Journal of Medicinal Chemistry. 51:5285-5296
Fatty acid synthase (FAS) is necessary for growth and survival of tumor cells and is a promising drug target for oncology. Here, we report on the syntheses and activity of novel inhibitors of the thioesterase domain of FAS. Using the structure of orl
Autor:
Manuel Zancanella, Daniel Romo
Publikováno v:
Organic Letters. 10:3685-3688
A facile synthesis of the trans-fused azabicyclo[3.3.0]octane core of palau'amine and related pyrrole-imidazole alkaloids is described. Following gamma-lactam cleavage with concomitant epimerization at C12 of a previously reported tricycle, a facile
Autor:
Rodney P. Feazell, John Brannon Gary, Jason A. Kautz, Kevin K. Klausmeyer, Ching Wah Wong, Manuel Zancanella
Publikováno v:
Acta Crystallographica Section E Structure Reports Online. 60:m532-m534
Publikováno v:
ChemInform. 42
The pyrrole-2-aminoimidazole (P-2-AI) alkaloids are a growing family of marine alkaloids, now numbering well over 150 members, with high topographical and biological information content. Their intriguing structural complexity, rich and compact stereo
Autor:
Daniel Romo, Jeffrey W. Smith, Gil Ma, Robyn D. Richardson, Yatsandra Oyola, Manuel Zancanella
Publikováno v:
Organic letters. 8(20)
Concise syntheses of orlistat (Xenical), a two-carbon transposed orlistat derivative, and valilactone are described that employ the tandem Mukaiyama aldol-lactonization (TMAL) process as a key step. This process allows facile modification of the alph
Autor:
Robyn D. Richardson, Gil Ma, Yatsandra Oyola, Manuel Zancanella, Lynn M. Knowles, Piotr Cieplak, Daniel Romo, Jeffrey W. Smith
Publikováno v:
Journal of Medicinal Chemistry; Jul2008, Vol. 51 Issue 17, p5285-5296, 12p