B. Jiang

发表

Characterisation of heteroatomic compounds in catalytic hydropyrolysates released from marine crude oil asphaltenes by ESI FT-ICR MS

Y. Zou, Yankuan Tian, B. Jiang, 2022, Organic Geochemistry.

Discovery of (3S,4S)-3-methyl-3-(4-fluorophenyl)-4-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxyprop-2-yl)phenyl)pyrrolidines as novel RORγt inverse agonists.

Michael A. Galella, D. Shen, C. Weigelt, 2020, Bioorganic & medicinal chemistry letters.

Poly[[aqua(μ-4,4′-bipyridyl-κ2 N:N′)bis(μ-formato-κ2 O:O′)iron(II)] tetrahydrate]

Zhilu Liu, B. Jiang, 2009, Acta crystallographica. Section E, Structure reports online.

Biologic-like In Vivo Efficacy with Small Molecule Inhibitors of TNFα Identified Using Scaffold Hopping and Structure-Based Drug Design Approaches.

D. Shuster, J. Macor, J. Yanchunas, 2020, Journal of medicinal chemistry.

Discovery of highly potent, selective, covalent inhibitors of JAK3.

S. Spergel, G. Schieven, J. Barrish, 2017, Bioorganic & medicinal chemistry letters.

Discovery of pyrrolo[1,2-b]pyridazine-3-carboxamides as Janus kinase (JAK) inhibitors.

David S. Nirschl, David S Nirschl, Sidney Pitt, 2014, Bioorganic & medicinal chemistry letters.

Improving the pharmacokinetic and CYP inhibition profiles of azaxanthene-based glucocorticoid receptor modulators-identification of (S)-5-(2-(9-fluoro-2-(4-(2-hydroxypropan-2-yl)phenyl)-5H-chromeno[2,3-b]pyridin-5-yl)-2-methylpropanamido)-N-(tetrahydro-2H-pyran-4-yl)-1,3,4-thiadiazole-2-carboxamide

Michael G. Yang, Michael A. Galella, K. McIntyre, 2015, Journal of medicinal chemistry.

2,4-Disubstituted piperidines as selective CC chemokine receptor 3 (CCR3) antagonists: synthesis and selectivity.

G. Trainor, M. Covington, C. Decicco, 2006, Bioorganic & medicinal chemistry letters.

Crystal structure of methyl (E)-N2-((3-methylquinolin-8-yl)sulfonyl)-Nω′-nitro-L-argininate - ethanol (1/1), C19H28N6O7S

Guo-Chun Zhou, B. Jiang, 2019 .

Identification of dihydroquinolizinone derivatives with cyclic ether moieties as new anti-HBV agents.

Hui-Min Song, Mingliang Liu, Kai Lv, 2022, European journal of medicinal chemistry.

Structure-based Discovery of Phenyl (3-Phenylpyrrolidin-3-yl)sulfones as Selective, Orally Active RORγt Inverse Agonists.

Michael A. Galella, D. Shuster, D. Shen, 2019, ACS medicinal chemistry letters.

Syntheses and biological activities of bis(3-indolyl)thiazoles, analogues of marine bis(indole)alkaloid nortopsentins.

X. Wan, B. Jiang, X. Gu, 1999, Bioorganic & medicinal chemistry letters.

Synthesis of novel analogues of marine indole alkaloids: mono(indolyl)-4-trifluoromethylpyridines and bis(indolyl)-4-trifluoromethylpyridines as potential anticancer agents.

B. Jiang, W. Xiong, C. G. Yang, 2001, Bioorganic & medicinal chemistry.

Discovery of low nanomolar non-hydroxamate inhibitors of tumor necrosis factor-alpha converting enzyme (TACE).

Soong-Hoon Kim, W. Pitts, M. Covington, 2007, Bioorganic & medicinal chemistry letters.

Design, synthesis and anti-TB and anti-bacterial activity of Ciprofloxacin derivatives containing N-(amino)piperazine moieties

Hui-Min Song, Mingliang Liu, Kai Lv, 2023, Medicinal Chemistry Research.

Discovery of novel 4(1H)-quinolone derivatives as potential antiproliferative and apoptosis inducing agents.

Linsheng Huang, Xuehua Deng, P. Zhou, 2017, Bioorganic & medicinal chemistry letters.

Identification of (6S)-cyclopropyl-6,7-dihydropyrazolo[1,5-a]pyrazine-5(4H)-carboxamines as new HBV capsid assembly modulators.

Jiandong Jiang, Mingliang Liu, Kai Lv, 2021, European journal of medicinal chemistry.

Discovery of potent and efficacious pyrrolopyridazines as dual JAK1/3 inhibitors.

K. McIntyre, Sidney Pitt, G. Schieven, 2017, Bioorganic & medicinal chemistry letters.

A diastereoselective synthesis of 2,4-disubstituted piperidines: scaffolds for drug discovery.

B. Jiang, B. Jiang, P. S. Watson, 2000, Organic letters.

Identification of dihydroquinolizinone derivatives with cyclic ether moieties as new anti-HBV agents.

Hui-Min Song, Mingliang Liu, Kai Lv, 2022, European journal of medicinal chemistry.