Anderson PS - Search Results

1

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

2

Benzodiazepine gastrin and brain cholecystokinin receptor ligands: L-365,260.

Bock MG, DiPardo RM, Evans BE, Rittle KE, Whitter WL, Veber DE, Anderson PS, Freidinger RM. Bock MG, et al. Among authors: anderson ps. J Med Chem. 1989 Jan;32(1):13-6. doi: 10.1021/jm00121a004. J Med Chem. 1989. PMID: 2909725 No abstract available.

3

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.

4

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

5

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

6

(+)- and (-)-3-Methoxycyproheptadine. A comparative evaluation of the antiserotonin, antihistaminic, anticholinergic, and orexigenic properties with cyproheptadine.

Remy DC, Rittle KE, Hunt CA, Anderson PS, Engelhardt EL, Clineschmidt BV, Scriabine A. Remy DC, et al. Among authors: anderson ps. J Med Chem. 1977 Dec;20(12):1681-4. doi: 10.1021/jm00222a031. J Med Chem. 1977. PMID: 592336

7

Synthesis of 4-substituted 2H-naphth[1,2-b]-1,4-oxazines, a new class of dopamine agonists.

Jones JH, Anderson PS, Baldwin JJ, Clineschmidt BV, McClure DE, Lundell GF, Randall WC, Martin GE, Williams M, Hirshfield JM, et al. Jones JH, et al. Among authors: anderson ps. J Med Chem. 1984 Dec;27(12):1607-13. doi: 10.1021/jm00378a014. J Med Chem. 1984. PMID: 6094811

8

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

9

Synthesis, assignment of absolute configuration, and receptor binding studies relevant to the neuroleptic activities of a series of chiral 3-substituted cyproheptadine atropisomers.

Randall WC, Anderson PS, Cresson EL, Hunt CA, Lyon TF, Rittle KE, Remy DC, Springer JP, Hirshfield JM, Hoogsteen K, Williams M, Risley EA, Totaro JA. Randall WC, et al. Among authors: anderson ps. J Med Chem. 1979 Oct;22(10):1222-30. doi: 10.1021/jm00196a014. J Med Chem. 1979. PMID: 41950 No abstract available.

10

Synthesis of (7R)-7H-indolo[3,4-gh][1,4]benzoxazines, a new class of D-heteroergolines with dopamine agonist activity.

Anderson PS, Baldwin JJ, McClure DE, Lundell GF, Jones JH, Randall WC, Martin GE, Williams M, Hirshfield JM, Clineschmidt BV, Lumma PK, Remy DC. Anderson PS, et al. J Med Chem. 1983 Mar;26(3):363-7. doi: 10.1021/jm00357a010. J Med Chem. 1983. PMID: 6298427

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