W. Pendergast

发表

Effect of digital rectal examination on serum prostate-specific antigen in a primary care setting. The Internal Medicine Clinic Research Consortium.

Jill, M. McNeil, R. Zeldin, 1995, Archives of internal medicine.

Destruction of WiDr multicellular tumor spheroids with the novel thymidylate synthase inhibitor 1843U89 at physiological thymidine concentrations

Gary K. Smith, S. Dickerson, W. Pendergast, 2004, Cancer Chemotherapy and Pharmacology.

Randomized trial of physician alerts for thromboprophylaxis after discharge.

S. Goldhaber, S. Stevens, T. Ortel, 2013, The American journal of medicine.

Synthesis and P2Y receptor activity of a series of uridine dinucleoside 5'-polyphosphates.

I. Sims, W. Pendergast, J. Douglass, 2001, Bioorganic & medicinal chemistry letters.

Structure–activity relationships of dinucleotides: Potent and selective agonists of P2Y receptors

J. Boyer, M. Picher, W. Pendergast, 2005, Purinergic Signalling.

The stable pyrimidines UDPbetaS and UTPgammaS discriminate between contractile cerebrovascular P2 receptors.

D. Erlinge, L. Edvinsson, M. Malmsjö, 2003, European journal of pharmacology.

The stable pyrimidines UDPβS and UTPγS discriminate between the P2 receptors that mediate vascular contraction and relaxation of the rat mesenteric artery

T. K. Harden, D. Erlinge, L. Edvinsson, 2000 .

Characterization of contractile P2 receptors in human coronary arteries by use of the stable pyrimidines uridine 5'-O-thiodiphosphate and uridine 5'-O-3-thiotriphosphate.

T. K. Harden, D. Erlinge, L. Edvinsson, 2000, The Journal of pharmacology and experimental therapeutics.

Potent P2Y6 receptor mediated contractions in human cerebral arteries

D. Erlinge, L. Edvinsson, M. Malmsjö, 2003, BMC pharmacology.

Syntheses of 8-aminoimidazo[4′,5′:5,6]pyrido[2,3-d]pyrimiciines: Linear tricyclic analogs of adenine

P. A. Harris, W. Pendergast, 1996 .

Benzo[f]quinazoline inhibitors of thymidylate synthase: methyleneamino-linked aroylglutamate derivatives.

R. Ferone, S. Dickerson, W. Pendergast, 1994, Journal of medicinal chemistry.

Benzoquinazoline inhibitors of thymidylate synthase: enzyme inhibitory activity and cytotoxicity of some sulfonamidobenzoylglutamate and related derivatives.

R. Ferone, S. Dickerson, W. Pendergast, 1993, Journal of medicinal chemistry.

Benzoquinazoline inhibitors of thymidylate synthase: enzyme inhibitory activity and cytotoxicity of some 3-amino- and 3-methylbenzo[f]quinazolin-1(2H)-ones.

R. Ferone, J. Humphreys, J. Kelly, 1993, Journal of medicinal chemistry.

V-Triazolo(4,5-d)pyrimidines (8-azapurines). XII. Cleavage of the pyrimidine ring in 8-azapurines by some active methylene reagents and eventual closure to give v-triazolo(4,5-b)pyridines.

A. Albert, W. Pendergast, 1973, Journal of the Chemical Society. Perkin transactions 1.

Syntheses of 8-Aminoimidazo(4′,5′:5,6)pyrido(2,3-d)pyrimidines: Linear Tricyclic Analogues of Adenine.

P. A. Harris, W. Pendergast, 1996 .

Cleavage of pyrimidines and fused pyrimidines by active methylene reagents with closure to give pyridine derivatives.

A. Albert, W. Pendergast, 1973, Journal of the Chemical Society. Perkin transactions 1.

Late orogenic alteration in the wall rocks of the Pegmont Pb-Zn deposit, Cloncurry District, Queensland, Australia

Patrick J. Williams, W. Pendergast, G. Dong, 1998 .

A highly stereospecific synthesis of (R)- and (S)-[2-3H]Glycine.

W. Pendergast, W. Armarego, B. A. Milloy, 1976, Journal of the Chemical Society. Perkin transactions 1.

Biochemical and cellular pharmacology of 1843U89, a novel benzoquinazoline inhibitor of thymidylate synthase.

R. Ferone, J. Humphreys, Gary K. Smith, 1993, Cancer research.

v-Triazolo[4,5-d]pyrimidines (8-azapurines). Part XIII. Reaction of 8-azapurines with bifunctional nucleophiles

A. Albert, W. Pendergast, 1973 .

Stable derivatives of 5,6,7,8-tetrahydropteridines

W. Pendergast, W. Hall, 1985 .

UDP acts as a growth factor for vascular smooth muscle cells by activation of P2Y(6) receptors.

C. Kuhn, D. Erlinge, L. Edvinsson, 2002, American journal of physiology. Heart and circulatory physiology.

Synthesis of some 7‐substituted‐2,4,8(1H,3H,7H)pyrimido[5,4‐d]pyrimidinetriones

W. Pendergast, W. Hall, 1986 .

The activity of alkyl phosphorylcholines and related derivatives against Leishmania donovani.

S. Croft, J. H. Chan, W. Pendergast, 1987, Biochemical pharmacology.

Synthesis of Some 7-Substituted-2,4,8(1H,3H,7H)Pyrimido(5,4-d)pyrimidinetriones.

W. Pendergast, W. Hall, 1987 .

Physician Alerts to Prevent Symptomatic Venous Thromboembolism in Hospitalized Patients

Marilyn D Paterno, Joseph O Jacobson, Samuel Z Goldhaber, 2009, Circulation.

The stable pyrimidines UDPbS and UTPgS discriminate between the P2 receptors that mediate vascular contraction and relaxation of the rat mesenteric artery

D. Erlinge, L. Edvinsson, M. Adner, 2022 .

ARD-353 [4-((2R,5S)-4-(R)-(4-Diethylcarbamoylphenyl)(3-hydroxyphenyl)methyl)-2,5-dimethylpiperazin-1-ylmethyl)benzoic Acid], A Novel Nonpeptide δ Receptor Agonist, Reduces Myocardial Infarct Size without Central Effects

Kwen-Jen Chang, G. Gross, Kwen-Jen Chang, 2006, Journal of Pharmacology and Experimental Therapeutics.

DPI-221 [4-((α-S)-α-((2S,5R)-2,5-Dimethyl-4-(3-fluorobenzyl)-1-piperazinyl)benzyl)-N,N-diethylbenzamide]: A Novel Nonpeptide δ Receptor Agonist Producing Increased Micturition Interval in Normal Rats

Jane P. Chang, Kwen-Jen Chang, J. Chang, 2005, Journal of Pharmacology and Experimental Therapeutics.

DPI-221 [4-((alpha-s)-alpha-((2s,5r)-2,5-dimethyl-4-(3-fluorobenzyl)-1-piperazinyl)benzyl)-N,N-diethylbenzamide]: a novel nonpeptide delta receptor agonist producing increased micturition interval in normal rats.

J. Chang, Kwen-Jen Chang, P. Gengo, 2005, The Journal of pharmacology and experimental therapeutics.

Some stable derivatives of 7,8-dihydropurines

W. Pendergast, W. Hall, 1990 .

V‐TRIAZOLO(4,5‐D)PYRIMIDINES (8‐AZAPURINES) PART 12, CLEAVAGE OF THE PYRIMIDINE RING IN 8‐AZAPURINES BY SOME ACTIVE METHYLENE REAGENTS AND EVENTUAL CLOSURE TO GIVE V‐TRIAZOLO(4,5‐B)PYRIDINES

A. Albert, W. Pendergast, 1973 .

Metabolism and transport of purinergic receptor agonists in rabbit conjunctival epithelial cells.

V. H. Lee, H. Gukasyan, W. Pendergast, 2000, Advances in experimental medicine and biology.

The stable pyrimidines UDPbetaS and UTPgammaS discriminate between the P2 receptors that mediate vascular contraction and relaxation of the rat mesenteric artery.

D. Erlinge, L. Edvinsson, M. Adner, 2000, British Journal of Pharmacology.

Metabolism and Transport of Purinergic Receptor Agonists in Rabbit Conjunctival Epithelial Cells

V. H. Lee, H. Gukasyan, W. Pendergast, 2002 .

4-Substituted Uridine 5′-Triphosphates as Agonists of the P2Y2 Purinergic Receptor

M. K. James, S. Siddiqi, W. Pendergast, 1997 .