Zobrazeno 1 - 10
of 23
pro vyhledávání: '"D L DeCamp"'
Autor:
W. J. Howe, W. T. Lowther, J. O. Hui, W. G. Tarpley, D. E. Emmert, Chetana Rao, A G Tomasselli, John H. Kinner, V. S. Bradford, D. L. Alexander, Tomi K. Sawyer, B.M. Dunna, Robert A. Conradi, D. L. Decamp, Clark W. Smith, Allen W. Harrison, Charles S. Craik, James Michael Tustin, T. J. Mcquade, Robert L. Heinrikson, Y. Z. Zhang, Philip S. Burton, Jed F. Fisher, Roger A. Poorman, Joseph B. Moon, Jackson B. Hester, D J Staples, L. Liu, P. E. Scarborough, Maggiora Linda Louise
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 3:819-824
The structure-activity relationships and pharmacophore modeling aspects of a series of HIV PR inhibitors modified at the N- and/or C-terminus of the dipeptide isostere ChaΨ[CH(OH)CH2]Val (Cha, cyclohexylalanine) are reported. The HIV PR binding affi
Autor:
Zhihua Sui, Paul R. Ortiz de Montellano, James J. De Voss, D. L. Decamp, Charles S. Craik, Jia Li
Publikováno v:
Synthesis. 1993:803-808
Haloperidol ketals and ethanedithioketals of interest as HIV-1 protease inhibitors were synthesized by addition of organolithium and organomagnesium reagents to ketone precursors already containing the ketal or thioketal functionality. Addition of Gr
Autor:
Myoung Seo Koo, D. L. Decamp, Rafael Salto, Jeanne L. Lucich, Stephen B. Kahl, Lilia M. Babé, Charles S. Craik
Publikováno v:
ChemInform. 24
Autor:
L. Liu, Alexander Wlodawer, Tomi K. Sawyer, D. L. Decamp, Robert L. Heinrikson, K. O'connell, Ben M. Dunn, Joseph B. Moon, Jackson B. Hester, D J Staples, Mariusz Jaskolski, Jennifer L. Harris, Roger A. Poorman, Heinrich J. Schostarez, Clark W. Smith, A G Tomasselli, J. O. Hui, Charles S. Craik, W. J. Howe, W. T. Lowther
Publikováno v:
ChemInform. 24
Autor:
W. J. Howe, W. T. Lowther, A G Tomasselli, D. E. Emmert, D J Staples, Jackson B. Hester, W. G. Tarpley, J. O. Hui, Ben M. Dunn, John H. Kinner, Robert L. Heinrikson, Y. Z. Zhang, Tomi K. Sawyer, Charles S. Craik, D. L. Decamp, James Michael Tustin, T. J. Mcquade, D. L. Alexander, Allen W. Harrison, P. E. Scarborough, Robert A. Conradi, Jed F. Fisher, Roger A. Poorman, Philip S. Burton, Maggiora Linda Louise, V. S. Bradford, Joseph B. Moon, L. Liu, Clark W. Smith, Chetana Rao
Publikováno v:
ChemInform. 26
Publikováno v:
Journal of Biological Chemistry. 265:13890-13898
A synthetic DNA fragment encoding a protease precursor of the human immunodeficiency virus type 2 (HIV2) was cloned and expressed in bacteria and yeast. A recombinant plasmid encoding a hybrid polypeptide consisting of human superoxide dismutase and
Autor:
W. J. Howe, Robert L. Heinrikson, Carol A. Bannow, J. O. Hui, A G Tomasselli, D L DeCamp, I M Reardon, C S Craik, D J Staples, Tomi K. Sawyer
Publikováno v:
Journal of Biological Chemistry. 265:14675-14683
Highly purified, recombinant preparations of the virally encoded proteases from human immunodeficiency viruses (HIV) 1 and 2 have been compared relative to 1) their specificities toward non-viral protein and synthetic peptide substrates, and 2) their
Receptor-recognized forms of alpha 2-macroglobulin (alpha 2M*) bind to two macrophage receptors: an endocytic receptor, the low density lipoprotein receptor-related protein/alpha 2M receptor (LRP/alpha 2MR), and a G protein-coupled receptor, the alph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6eaf7d017e3bf8514c64a6d26f94ced5
https://europepmc.org/articles/PMC507171/
https://europepmc.org/articles/PMC507171/
Autor:
Lilia M. Babé, Paul R. Ortiz de Montellano, James J. De Voss, Charles S. Craik, Rafael Salto, D. L. Decamp, Zhihua Sui
Publikováno v:
Journal of medicinal chemistry. 37(5)
The proteases expressed by the HIV-1 and HIV-2 viruses process the polyproteins encoded by the viral genomes into the mature proteins required for virion replication and assembly. Eight analogs of haloperidol have been synthesized that cause time-dep
Autor:
E, Rutenber, E B, Fauman, R J, Keenan, S, Fong, P S, Furth, P R, Ortiz de Montellano, E, Meng, I D, Kuntz, D L, DeCamp, R, Salto
Publikováno v:
The Journal of biological chemistry. 268(21)
A stable, non-peptide inhibitor of the protease from type 1 human immunodeficiency virus has been developed, and the stereochemistry of binding defined through crystallographic three-dimensional structure determination. The initial compound, haloperi