A. Chen

发表

Allosteric modulation of A(3) adenosine receptors by a series of 3-(2-pyridinyl)isoquinoline derivatives.

K. Jacobson, A. IJzerman, C. Müller, 2001, Molecular pharmacology.

Constitutive activation of A(3) adenosine receptors by site-directed mutagenesis.

K. Jacobson, Zhang-Guo Gao, D. Barak, 2001, Biochemical and biophysical research communications.

Pharmacology of L-744,453, a novel nonpeptidyl endothelin antagonist.

W. Greenlee, D. Veber, P. Chakravarty, 1996, Life sciences.

Inhibition of human purine nucleoside phosphorylase by acyclic nucleosides and nucleotides.

J. D. Karkas, M. Maccoss, R. Tolman, 1987, Biochemical Pharmacology.

A highly potent, orally active imidazo[4,5-b]pyridine biphenylacylsulfonamide (MK-996; L-159,282): a new AT1-selective angiotensin II receptor antagonist.

R. Chang, V. J. Lotti, P. Chakravarty, 1994, Journal of medicinal chemistry.

Syntheses of all Four Possible Diastereomers of the Acyclonucleoside 9‐(1,3,4‐Trihydroxy‐2‐butoxymethyl)guanine from Carbohydrate Precursors.

M. Maccoss, R. Tolman, A. Chen, 1985 .

Synthesis of the chiral acyclonucleoside antiherpetic agent (S)-9-(2,3-dihydroxy-1-propoxymethyl)guanine

M. Maccoss, R. Tolman, A. Chen, 1985 .

The Synthesis and Preliminary Biological Evaluations of Selected Analogues of the Potent Broad-Spectrum Antiviral Agent Ganciclovir 1′,3′-Cyclic Monophosphate1 (2′-Nor-cGMP)

J. D. Karkas, M. Maccoss, R. Tolman, 1989 .

Cycloaddition reactions of cyclopropane-containing systems. III. Cycloaddition of alkenylidenecyclopropanes with 4-phenyl-1,2,4-triazoline-3,5-dione

G. Binsch, A. Chen, D. Pasto, 1973 .

Cycloaddition reactions of substituted vinylcyclopropanes with 4-phenyl-1,2,4-triazoline-3,5-dione and chlorosulfonylisocyanate

A. Chen, D. Pasto, 1973 .

Inhibition of the mammalian beta-lactamase renal dipeptidase (dehydropeptidase-I) by (Z)-2-(acylamino)-3-substituted-propenoic acids.

J. Springer, R. Brown, A. Chen, 1987, Journal of medicinal chemistry.

Neoceptor concept based on molecular complementarity in GPCRs: a mutant adenosine A(3) receptor with selectively enhanced affinity for amine-modified nucleosides.

K. Jacobson, S. van Calenbergh, Zhang-Guo Gao, 2001, Journal of medicinal chemistry.

THE FACILE SYNTHESIS OF 1- AND 2-ALKYLAZULENES BY THE REACTIONS OF 2H-CYCLOHEPTA[b]FURAN-2-ONES WITH ENAMINES OF ALDEHYDES AND ACYCLIC KETONES

A. Chen, K. Takase, M. Yasunami, 1980 .

SYNTHESIS OF AZULENE DERIVATIVES BY THE REACTIONS OF 2H-CYCLOHEPTA(B)FURAN-2-ONES WITH ENAMINES. IV. THE FACILE SYNTHESIS OF 1- AND 2-ALKYLAZULENES BY THE REACTIONS OF 2H-CYCLOHEPTA(B)FURAN-2-ONES WITH ENAMINES OF ALDEHYDES AND ACYCLI

A. Chen, K. Takase, P. W. Yang, 1980 .