John S. Sack - Concepedia

Author

John S. Sack

Bristol-Myers Squibb (United States)ORCID

Also Known As

J. S. Sack, J. Sack, J.S. SACK, J.S. Sack, John S Sack, John S. Sack, John Sack, John S. Sack, Sack, John S.

136

Publications

5.9K

Citations

H-Index

Concepts

All Affiliations

Bristol-Myers Squibb (United States)Bristol-Myers Squibb (Germany)Biocon (India)Bristol-Myers Squibb (India)Howard Hughes Medical Institute

About

John S. Sack is an author at Bristol-Myers Squibb (United States) specializing in medicine, biochemistry, and drug discovery.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	31	57	4.6K
2	Biochemistry	27	42	3.5K
3	Natural Sciences	25	39	2.3K
4	Engineering	2	2	368
5	Health Sciences	2	2	380

John S. Sack

Publications

5.7K

Citations

H-Index

Page 1

	Year	Citations
Three-dimensional structure of calmodulin Y.S. Babu, John S. Sack, Trevor J. Greenhough, Nature Crystal StructureBiochemistryThree-dimensional StructureStructure ElucidationConformational Study	1985	1K
Crystallographic structures of the ligand-binding domains of the androgen receptor and its T877A mutant complexed with the natural agonist dihydrotestosterone John S. Sack, Kevin Kish, Chihuei Wang, Proceedings of the National Academy of Sciences	2001	483
CHAIN — A crystallographic modeling program John S. Sack Journal of Molecular Graphics Crystal StructureEngineeringMolecular BiologyStructural BiologyComputational Chemistry	1988	339
Discovery of <i>N</i>-(4-(2-Amino-3-chloropyridin-4-yloxy)-3-fluorophenyl)-4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxamide (BMS-777607), a Selective and Orally Efficacious Inhibitor of the Met Kinase Superfamily Gretchen M. Schroeder, Yongmi An, Zhen‐Wei Cai, Journal of Medicinal Chemistry Orally Efficacious InhibitorDrug TargetPharmacotherapyPharmaceutical ChemistryTumor Biology	2009	276
<i>N</i>-(Cycloalkylamino)acyl-2-aminothiazole Inhibitors of Cyclin-Dependent Kinase 2. <i>N</i>-[5-[[[5-(1,1-Dimethylethyl)-2-oxazolyl]methyl]thio]-2-thiazolyl]-4- piperidinecarboxamide (BMS-387032), a Highly Efficacious and Selective Antitumor Agent Raj N. Misra, Hai‐Yun Xiao, Kyoung S. Kim, Journal of Medicinal Chemistry Chemoprevention StrategyImmunologyPharmacotherapyCdk2/cyce IcPharmaceutical Chemistry	2004	251
Periplasmic binding protein structure and function John S. Sack, Mark A. Saper, Florante A. Quiocho Journal of Molecular Biology Protein FunctionBiochemistryProtein AssemblyProtein FoldingNatural Sciences	1989	234
Location of Amino Acid Residues in Human Deoxy Hemoglobin John S. Sack, Lawrence C. Andrews, Karen A. Magnus, Hemoglobin Periodic Surface StructuresPossible ContactBiochemistryProtein FoldingNatural Sciences	1978	178
Discovery of Aminothiazole Inhibitors of Cyclin-Dependent Kinase 2: Synthesis, X-ray Crystallographic Analysis, and Biological Activities Kyoung Soon Kim, S. David Kimball, Raj N. Misra, Journal of Medicinal Chemistry Combinatorial ChemistryDrug TargetCdk2 ProteinCompound 14Heterocycle Chemistry	2002	156
Pharmacological and X-Ray Structural Characterization of a Novel Selective Androgen Receptor Modulator: Potent Hyperanabolic Stimulation of Skeletal Muscle with Hypostimulation of Prostate in Rats Jacek Ostrowski, Joyce E. Kuhns, John A. Lupisella, Endocrinology Observed Tissue SelectivityPharmacotherapyPotent Hyperanabolic StimulationSkeletal MusclePotent Oral Activity	2006	129
STRUCTURE OF A RECOMBINANT CALMODULIN FROM DROSOPHILA MELANOGASTER REFINED AT 2.2-ANGSTROMS RESOLUTION Denise Taylor, John S. Sack, John F. Maune,	1991	125

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