J. Lanter

发表

Tetrazole‐Based Angiotensin II Type 1 (AT1) Antagonists for the Treatment of Heart Failure and Congestive Hypertension

B. Shook, E. Lawson, J. Lanter, 2013 .

A selective androgen receptor modulator that reduces prostate tumor size and prevents orchidectomy-induced bone loss in rats

Muh-Tsann Lai, G. Allan, S. Lundeen, 2007, The Journal of Steroid Biochemistry and Molecular Biology.

Direct dehydrative cross-coupling of tautomerizable heterocycles with alkynes via Pd/Cu-catalyzed phosphonium coupling.

Z. Sui, W. Murray, Fu‐An Kang, 2010, Chemical communications.

Discovery of a GPR40 Superagonist: The Impact of Aryl Propionic Acid α-Fluorination.

S. Meegalla, Hui-Sheng Huang, Brian Rady, 2018, ACS medicinal chemistry letters.

Targeting Enteropeptidase with Reversible Covalent Inhibitors To Achieve Metabolic Benefits

Jiejun Wu, M. Cummings, Xuqing Zhang, 2020, The Journal of Pharmacology and Experimental Therapeutics.

Conjugation of a peptide to an antibody engineered with free cysteines dramatically improves half-life and activity

R. Patch, S. Edavettal, Wenyu Li, 2020, mAbs.

Design, synthesis and SAR of a novel series of heterocyclic phenylpropanoic acids as GPR120 agonists.

Z. Sui, Xuqing Zhang, W. Murray, 2017, Bioorganic & medicinal chemistry letters.

A novel series of N-(azetidin-3-yl)-2-(heteroarylamino)acetamide CCR2 antagonists.

E. Opas, Z. Sui, Dana L. Johnson, 2013, Bioorganic & medicinal chemistry letters.

Overcoming hERG activity in the discovery of a series of 4-azetidinyl-1-aryl-cyclohexanes as CCR2 antagonists.

E. Opas, Z. Sui, Xuqing Zhang, 2011, Bioorganic & medicinal chemistry letters.

Discovery of Oxazoline Enhancers of Cellular Progranulin Release.

R. Hurst, D. Burnett, Xiaowen Peng, 2022, Bioorganic & medicinal chemistry letters.

The discovery of novel cyclohexylamide CCR2 antagonists.

C. Molloy, E. Opas, Z. Sui, 2011, Bioorganic & medicinal chemistry letters.

Structure-activity relationships of N-acyl pyrroloquinolone PDE-5 inhibitors.

Weiqin Jiang, Z. Sui, M. Macielag, 2004, Journal of medicinal chemistry.

Furoyl and benzofuroyl pyrroloquinolones as potent and selective PDE5 inhibitors for treatment of erectile dysfunction.

Weiqin Jiang, Z. Sui, M. Macielag, 2003, Journal of medicinal chemistry.

Single Stereodifferentiation Associated with Carbon Atom Insertion during the Oxonium Ion-Initiated Pinacol Rearrangement of Dihydrofuranyl and Dihydropyranyl Carbinols

L. Paquette, J. N. Johnston, J. Lanter, 1997 .

Asymmetric aza-Mannich reactions of sulfinimines: scope and application to the total synthesis of a bromopyrrole alkaloid.

Z. Sui, Xuqing Zhang, Hongfeng Chen, 2005, Organic letters.

1-Oxaspiro[4.4]nonan-6-ones. Synthetic access via oxonium ion technology, optical resolution, and conversion into enantiopure spirocyclic alpha,beta-butenolides.

D. Owen, L. Paquette, J. Lanter, 2001, The Journal of organic chemistry.

Silver(I) Perchlorate

J. Lanter, 2001 .

Synthesis of potent and tissue-selective androgen receptor modulators (SARMs): 2-(2,2,2)-Trifluoroethyl-benzimidazole scaffold.

G. Allan, S. Lundeen, Z. Sui, 2007, Bioorganic & medicinal chemistry letters.

β-Alkylthio indolyl carbinols: Potent nonsteroidal antiandrogens with oral efficacy in a prostate cancer model

Muh-Tsann Lai, G. Allan, R. Russell, 2007 .

The discovery of a potent orally efficacious indole androgen receptor antagonist through in vivo screening.

Weiqin Jiang, Muh-Tsann Lai, G. Allan, 2007, Bioorganic & medicinal chemistry letters.

A bioisosteric approach to the discovery of indole carbinol androgen receptor ligands.

Amy Musto, G. Allan, D. Hahn, 2006, Bioorganic & medicinal chemistry letters.

Resolution and Absolute Configurational Assignments to 1-Oxa- and 1-Thia-6-ketospiro[4,4]nonanyl Platforms

D. Owen, L. Paquette, F. Fabris, 2001 .

Synthesis and SAR of potent and selective androgen receptor antagonists: 5,6-Dichloro-benzimidazole derivatives.

G. Allan, S. Lundeen, Z. Sui, 2007, Bioorganic & medicinal chemistry letters.

Lab-Scale Preparation of a Novel Cyclopenta[b]furan Chemokine Receptor Antagonist

M. Reuman, R. Russell, Z. Sui, 2014 .

Intestinal serine protease inhibition increases FGF21 and improves metabolism in obese mice.

J. Lenhard, P. Hornby, Bhanu Singh, 2019, American journal of physiology. Gastrointestinal and liver physiology.

Discovery of a novel series of guanidinebenzoates as gut-restricted enteropeptidase and trypsin dual inhibitors for the treatment of metabolic syndrome.

M. Cummings, Xuqing Zhang, Weimei Sun, 2021, Bioorganic & Medicinal Chemistry Letters.

1104 - Intestinal Serine Protease Inhibition Increases Liver FGF21 Secretion in Diabetic Obese Mice

J. Lenhard, P. Hornby, J. Lanter, 2018 .

Synthesis of Potent and Tissue-Selective Androgen Receptor Modulators (SARMs): 2-(2,2,2)-Trifluoroethylbenzimidazole Scaffold.

G. Allan, S. Lundeen, J. Lanter, 2007 .

2-(2,2,2-Trifluoroethyl)-5,6-dichlorobenzimidazole derivatives as potent androgen receptor antagonists.

G. Allan, S. Lundeen, Z. Sui, 2007, Bioorganic & medicinal chemistry letters.

Recent advances in the development of selective androgen receptor modulators

Z. Sui, Xuqing Zhang, J. Lanter, 2009, Expert opinion on therapeutic patents.

Synthesis of Novel Pyrazolines via 1,3‐Dipolar Cycloadditions of Heterocyclic Isopropenes

Z. Sui, Xuqing Zhang, J. Lanter, 2007 .

Synthesis of Novel Pyrazolines via 1,3-Dipolar Cycloadditions of Heterocyclic Isopropenes.

Xuqing Zhang, J. Lanter, Sui Zhihua, 2007 .

Medicinal chemistry inspired fragment-based drug discovery.

Z. Sui, Xuqing Zhang, J. Lanter, 2011, Methods in enzymology.

Recentadvancesinthe developmentofselective androgenreceptormodulators

Z. Sui, Xuqing Zhang, J. Lanter, 2009 .