Anderson PS - Search Results

1

NMR and molecular modeling characterization of RGD containing peptides.

Bogusky MJ, Naylor AM, Pitzenberger SM, Nutt RF, Brady SF, Colton CD, Sisko JT, Anderson PS, Veber DF. Bogusky MJ, et al. Among authors: anderson ps. Int J Pept Protein Res. 1992 Jan;39(1):63-76. doi: 10.1111/j.1399-3011.1992.tb01557.x. Int J Pept Protein Res. 1992. PMID: 1634331

2

Cyclopsychotride A, a biologically active, 31-residue cyclic peptide isolated from Psychotria longipes.

Witherup KM, Bogusky MJ, Anderson PS, Ramjit H, Ransom RW, Wood T, Sardana M. Witherup KM, et al. Among authors: anderson ps. J Nat Prod. 1994 Dec;57(12):1619-25. doi: 10.1021/np50114a002. J Nat Prod. 1994. PMID: 7714530

3

Methods for drug discovery: development of potent, selective, orally effective cholecystokinin antagonists.

Evans BE, Rittle KE, Bock MG, DiPardo RM, Freidinger RM, Whitter WL, Lundell GF, Veber DF, Anderson PS, Chang RS, et al. Evans BE, et al. Among authors: anderson ps. J Med Chem. 1988 Dec;31(12):2235-46. doi: 10.1021/jm00120a002. J Med Chem. 1988. PMID: 2848124

4

Non-peptide fibrinogen receptor antagonists. 7. Design and synthesis of a potent, orally active fibrinogen receptor antagonist.

Duggan ME, Naylor-Olsen AM, Perkins JJ, Anderson PS, Chang CT, Cook JJ, Gould RJ, Ihle NC, Hartman GD, Lynch JJ, et al. Duggan ME, et al. Among authors: anderson ps. J Med Chem. 1995 Aug 18;38(17):3332-41. doi: 10.1021/jm00017a017. J Med Chem. 1995. PMID: 7650686

5

Design of potent, orally effective, nonpeptidal antagonists of the peptide hormone cholecystokinin.

Evans BE, Bock MG, Rittle KE, DiPardo RM, Whitter WL, Veber DF, Anderson PS, Freidinger RM. Evans BE, et al. Among authors: anderson ps. Proc Natl Acad Sci U S A. 1986 Jul;83(13):4918-22. doi: 10.1073/pnas.83.13.4918. Proc Natl Acad Sci U S A. 1986. PMID: 3014519 Free PMC article.

6

1-((7,7-Dimethyl-2(S)-(2(S)-amino-4-(methylsulfonyl)butyramido)bicyclo [2.2.1]-heptan-1(S)-yl)methyl)sulfonyl)-4-(2-methylphenyl)piperaz ine (L-368,899): an orally bioavailable, non-peptide oxytocin antagonist with potential utility for managing preterm labor.

Williams PD, Anderson PS, Ball RG, Bock MG, Carroll L, Chiu SH, Clineschmidt BV, Culberson JC, Erb JM, Evans BE, et al. Williams PD, et al. Among authors: anderson ps. J Med Chem. 1994 Mar 4;37(5):565-71. doi: 10.1021/jm00031a004. J Med Chem. 1994. PMID: 8126695

7

Benzocycloalkyl amines as novel C-termini for HIV protease inhibitors.

Lyle TA, Wiscount CM, Guare JP, Thompson WJ, Anderson PS, Darke PL, Zugay ZA, Emini EA, Schleif WA, Qunitero JC, et al. Lyle TA, et al. Among authors: anderson ps. J Med Chem. 1991 Mar;34(3):1228-30. doi: 10.1021/jm00107a051. J Med Chem. 1991. PMID: 2002466 No abstract available.

8

A structurally unique, potent, and selective oxytocin antagonist derived from Streptomyces silvensis.

Pettibone DJ, Clineschmidt BV, Anderson PS, Freidinger RM, Lundell GF, Koupal LR, Schwartz CD, Williamson JM, Goetz MA, Hensens OD, et al. Pettibone DJ, et al. Among authors: anderson ps. Endocrinology. 1989 Jul;125(1):217-22. doi: 10.1210/endo-125-1-217. Endocrinology. 1989. PMID: 2544402

9

Structure-based design of HIV-1 protease inhibitors: replacement of two amides and a 10 pi-aromatic system by a fused bis-tetrahydrofuran.

Ghosh AK, Thompson WJ, Fitzgerald PM, Culberson JC, Axel MG, McKee SP, Huff JR, Anderson PS. Ghosh AK, et al. Among authors: anderson ps. J Med Chem. 1994 Aug 5;37(16):2506-8. doi: 10.1021/jm00042a002. J Med Chem. 1994. PMID: 8057296 No abstract available.

10

HIV-1 protease inhibitors: synthesis and biological evaluation of glycopeptidemimetics.

Ghosh AK, McKee SP, Sanders WM, Darke PL, Zugay JA, Emini EA, Schleif WA, Quintero JC, Huff JR, Anderson PS. Ghosh AK, et al. Among authors: anderson ps. Drug Des Discov. 1993;10(1):77-88. Drug Des Discov. 1993. PMID: 8399995

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