J. Wetzel

发表

The alpha 1-adrenergic receptor that mediates smooth muscle contraction in human prostate has the pharmacological properties of the cloned human alpha 1c subtype.

T. Branchek, H. Lepor, E. Shapiro, 1994, Molecular pharmacology.

Characterization of specific binding of [125I]L-762,459, a selective alpha1A-adrenoceptor radioligand to rat and human tissues.

R. Chang, H. Burns, B. Francis, 1998, European journal of pharmacology.

MECHANISTIC STUDIES IN THE DEOXYGENATION OF PYRIDINE N-OXIDE: NEW 1,2 ELIMINATION

J. Hwu, J. Wetzel, 1985 .

General scope of 1,3-dioxolanation of .alpha.,.beta.-unsaturated aldehydes with 1,2-bis(trimethylsilyloxy)ethane and trimethylsilyl trifluoromethanesulfonate

J. Hwu, J. Robl, J. Wetzel, 1987 .

The trimethylsilyl cationic species as a bulky proton. Application to chemoselective dioxolanation

J. Hwu, J. Wetzel, 1985 .

Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 1. Structure-activity relationship in dihydropyrimidinones.

R. Chang, P. Kling, B. Lagu, 1999, Journal of medicinal chemistry.

Silicon-promoted ring contractions in the formation of carbocyclic spiro compounds. Total synthesis of (-)-solavetivone

J. Hwu, J. Wetzel, 1992 .

Design and Synthesis of Novel α1a Adrenoceptor-Selective Dihydropyridine Antagonists for the Treatment of Benign Prostatic Hyperplasia

R. Chang, T. Branchek, C. Forray, 1998 .

Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 4. Structure-activity relationship in the dihydropyrimidine series.

R. Chang, P. Kling, B. Lagu, 1999, Journal of medicinal chemistry.

De novo design of a novel oxazolidinone analogue as a potent and selective alpha1A adrenergic receptor antagonist with high oral bioavailability.

A. D. Rodrigues, R. Chang, B. Lagu, 2000, Journal of medicinal chemistry.

Comparison of the electronic effect and the steric influence between the 1,1,2,2,2-pentamethyldisilanyl and the trimethylsilyl groups

J. Hwu, R. Butcher, J. Wetzel, 1993 .

Calcium in liquid ammonia for the reduction of benzyl ethers. Mechanistic clues derived from chemoselectivity studies

J. Hwu, J. Wetzel, R. Barrans, 1986 .

Diversity in steroidogenesis of symbiotic microorganisms from planthoppers

K. Nakanishi, H. Noda, Y. Naya, 1992, Journal of Chemical Ecology.

Identification and Characterization of Two G Protein-coupled Receptors for Neuropeptide FF*

B. Borowsky, T. Branchek, J. A. Bonini, 2000, The Journal of Biological Chemistry.

Brachycephalic airway syndrome: management of post-operative respiratory complications in 248 dogs.

J. Wetzel, P. Moses, D. Cook, 2020, Australian veterinary journal.

Localization of mRNA and receptor binding sites for the alpha 1a-adrenoceptor subtype in the rat, monkey and human urinary bladder and prostate.

H. Lepor, P. Walden, E. Gustafson, 1997, The Journal of urology.

Localization of the alpha 1A-adrenoceptor in the human prostate.

H. Lepor, E. Shapiro, C. Forray, 1995, The Journal of urology.

Design and synthesis of novel dihydropyridine alpha-1a antagonists.

R. Chang, C. Forray, W. Wong, 1999, Bioorganic & medicinal chemistry letters.

Letter: Fragmentation Studies of Ergosterol. The Formation of the Fragment Ion at m/z 337

P. T. Kenny, J. Wetzel, 1995 .

Warfarin pharmacokinetics in the horse.

A. E. van den Bogaard, A. Muller, J. Wetzel, 1983, American journal of veterinary research.

Synthesis and structure-activity relationship of fluoro analogues of 8-{2-[4-(4-methoxyphenyl)piperazin-1yl]ethyl}-8-azaspiro[4.5]decane-7,9-dione as selective alpha(1d)-adrenergic receptor antagonists.

D. Craig, S. Noble, C. Gluchowski, 2005, Journal of medicinal chemistry.

Discovery of alpha 1a-adrenergic receptor antagonists based on the L-type Ca2+ channel antagonist niguldipine.

T. Branchek, L. Borden, C. Forray, 1995, Journal of medicinal chemistry.

Identification of a dihydropyridine as a potent alpha1a adrenoceptor-selective antagonist that inhibits phenylephrine-induced contraction of the human prostate.

T. Branchek, H. Lepor, P. Vaysse, 1998, Journal of medicinal chemistry.

Modeling and mutagenesis of the human alpha 1a-adrenoceptor: orientation and function of transmembrane helix V sidechains.

T. Branchek, H. Nakanishi, D. Craig, 1996, Receptors & channels.

Design and Synthesis of Novel α1a Adrenoceptor-Selective Antagonists. 2. Approaches To Eliminate Opioid Agonist Metabolites via Modification of Linker and 4-Methoxycarbonyl-4-phenylpiperidine Moiety1,2

M. Bock, R. Freidinger, B. Lagu, 1999 .