Dianqing Sun
Dianqing Sun
University of Hawaii at Hilo
Verified email at - Homepage
Cited by
Cited by
Macrocyclic drugs and synthetic methodologies toward macrocycles
X Yu, D Sun
Molecules 18 (6), 6230-6268, 2013
Spectinamides: a new class of semisynthetic antituberculosis agents that overcome native drug efflux
RE Lee, JG Hurdle, J Liu, DF Bruhn, T Matt, MS Scherman, PK Vaddady, ...
Nature medicine 20 (2), 152-158, 2014
Recent synthetic developments and applications of the ullmann reaction. A review
H Lin, D Sun
Organic preparations and procedures international 45 (5), 341-394, 2013
The structure–activity relationship of urea derivatives as anti-tuberculosis agents
JR Brown, EJ North, JG Hurdle, C Morisseau, JS Scarborough, D Sun, ...
Bioorganic & medicinal chemistry 19 (18), 5585-5595, 2011
Discovery of novel isoxazolines as anti-tuberculosis agents
RP Tangallapally, D Sun, N Budha, REB Lee, AJM Lenaerts, B Meibohm, ...
Bioorganic & medicinal chemistry letters 17 (23), 6638-6642, 2007
Synthesis, structure–activity relationship studies, and antibacterial evaluation of 4-chromanones and chalcones, as well as olympicin A and derivatives
L Feng, MM Maddox, MZ Alam, LS Tsutsumi, G Narula, DF Bruhn, X Wu, ...
Journal of medicinal chemistry 57 (20), 8398-8420, 2014
Carbazole scaffold in medicinal chemistry and natural products: a review from 2010-2015
L S Tsutsumi, D GŁndisch, D Sun
Current Topics in Medicinal Chemistry 16 (11), 1290-1313, 2016
Identification of triazinoindol-benzimidazolones as nanomolar inhibitors of the Mycobacterium tuberculosis enzyme TDP-6-deoxy-d-xylo-4-hexopyranosid-4-ulose 3, 5-epimerase (RmlC)
S Sivendran, V Jones, D Sun, Y Wang, AE Grzegorzewicz, MS Scherman, ...
Bioorganic & medicinal chemistry 18 (2), 896-908, 2010
Synthesis, optimization and structure–activity relationships of 3, 5-disubstituted isoxazolines as new anti-tuberculosis agents
D Sun, RB Lee, RP Tangallapally, RE Lee
European journal of medicinal chemistry 44 (2), 460-472, 2009
Recent advances of natural and synthetic β-carbolines as anticancer agents
M Zhang, D Sun
Anti-Cancer Agents in Medicinal Chemistry (Formerly Current Medicinal†…, 2015
Progress in the discovery of treatments for C. difficile infection: a clinical and medicinal chemistry review
L S Tsutsumi, Y B Owusu, J G Hurdle, D Sun
Current topics in medicinal chemistry 14 (1), 152-175, 2014
Evaluation of flavonoid and resveratrol chemical libraries reveals abyssinone II as a promising antibacterial lead
D Sun, JG Hurdle, RE Lee, RE Lee, M Cushman, JM Pezzuto
ChemMedChem 7 (9), 1541, 2012
Total synthesis and structural revision of engelhardione
L Shen, D Sun
Tetrahedron letters 52 (35), 4570-4574, 2011
Solid-phase synthesis and biological evaluation of a uridinyl branched peptide urea library
D Sun, V Jones, EI Carson, REB Lee, MS Scherman, MR McNeil, RE Lee
Bioorganic & medicinal chemistry letters 17 (24), 6899-6904, 2007
Evaluation of analogs of reutericyclin as prospective candidates for treatment of staphylococcal skin infections
JG Hurdle, R Yendapally, D Sun, RE Lee
Antimicrobial agents and chemotherapy 53 (9), 4028-4031, 2009
The Fatty Acid Synthesis Protein Enoyl-ACP Reductase II (FabK) is a Target for Narrow-Spectrum Antibacterials for Clostridium difficile Infection
RKR Marreddy, X Wu, M Sapkota, AM Prior, JA Jones, D Sun, ...
ACS infectious diseases 5 (2), 208-217, 2018
Macrocycle-antibiotic hybrids: A path to clinical candidates
AS Surur, D Sun
Frontiers in Chemistry 9, 659845, 2021
Synthesis of 2-arylindole derivatives and evaluation as nitric oxide synthase and NFκB inhibitors
X Yu, EJ Park, TP Kondratyuk, JM Pezzuto, D Sun
Organic & biomolecular chemistry 10 (44), 8835-8847, 2012
Pharmacophore modeling, synthesis, and antibacterial evaluation of chalcones and derivatives
M Zhang, AM Prior, MM Maddox, WJ Shen, KE Hevener, DF Bruhn, ...
ACS omega 3 (12), 18343-18360, 2018
Structure-activity relationships and docking studies of synthetic 2-arylindole derivatives determined with aromatase and quinone reductase 1
AM Prior, X Yu, EJ Park, TP Kondratyuk, Y Lin, JM Pezzuto, D Sun
Bioorganic & medicinal chemistry letters 27 (24), 5393-5399, 2017
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