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Guangyan Du
Guangyan Du
Dana-Farber Cancer Institute, Harvard Medical School
Dirección de correo verificada de dfci.harvard.edu
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Citado por
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Año
A Quantitative Tissue-Specific Landscape of Protein Redox Regulation during Aging
H Xiao, MP Jedrychowski, DK Schweppe, EL Huttlin, Q Yu, DE Heppner, ...
Cell, 2020
2592020
Small molecule degraders of the hepatitis C virus protease reduce susceptibility to resistance mutations
M de Wispelaere, G Du, KA Donovan, T Zhang, NA Eleuteri, JC Yuan, ...
Nature Communications 10 (1), 3468, 2019
1462019
A smart “off–on” gate for the in situ detection of hydrogen sulphide with Cu (II)-assisted europium emission
Z Liang, TH Tsoi, CF Chan, L Dai, Y Wu, G Du, L Zhu, CS Lee, WT Wong, ...
Chemical Science 7 (3), 2151-2156, 2016
632016
Selective degradation of GSPT1 by cereblon modulators identified via a focused combinatorial library
CE Powell, G Du, J Che, Z He, KA Donovan, H Yue, ES Wang, RP Nowak, ...
ACS Chemical Biology 15 (10), 2722-2730, 2020
582020
Specific covalent inhibition of MALT1 paracaspase suppresses B cell lymphoma growth
The Journal of Clinical Investigation, 2018
582018
Construction of the Tricyclic Furanochroman Skeleton of Phomactin A via the Prins/Conia-Ene Cascade Cyclization Approach
S Huang, G Du, CS Lee
The Journal of organic chemistry 76 (16), 6534-6541, 2011
492011
Leveraging compound promiscuity to identify targetable cysteines within the kinome
S Rao, D Gurbani, G Du, RA Everley, CM Browne, A Chaikuad, L Tan, ...
Cell chemical biology 26 (6), 818-829. e9, 2019
452019
Exploring the target scope of KEAP1 E3 ligase-based PROTACs
G Du, J Jiang, NJ Henning, N Safaee, E Koide, RP Nowak, KA Donovan, ...
Cell Chemical Biology 29 (10), 1470-1481. e31, 2022
372022
Structure-guided development of covalent TAK1 inhibitors
L Tan, D Gurbani, EL Weisberg, JC Hunter, L Li, DS Jones, SB Ficarro, ...
Bioorganic & medicinal chemistry 25 (3), 838-846, 2017
332017
Bioinspired total synthesis of (±)-Yezo’otogirin C
S He, W Yang, L Zhu, G Du, CS Lee
Organic letters 16 (2), 496-499, 2014
322014
Discovery of a potent degrader for fibroblast growth factor receptor 1/2
G Du, J Jiang, Q Wu, NJ Henning, KA Donovan, H Yue, J Che, W Lu, ...
Angewandte Chemie 133 (29), 16041-16047, 2021
292021
Structure-based design of a potent and selective covalent inhibitor for SRC kinase that targets a P-loop cysteine
G Du, S Rao, D Gurbani, NJ Henning, J Jiang, J Che, A Yang, SB Ficarro, ...
Journal of Medicinal Chemistry 63 (4), 1624-1641, 2020
242020
Studies of TAK1-centered polypharmacology with novel covalent TAK1 inhibitors
L Tan, D Gurbani, EL Weisberg, DS Jones, S Rao, WD Singer, ...
Bioorganic & medicinal chemistry 25 (4), 1320-1328, 2017
212017
A Bifunctional Lewis Acid Induced Cascade Cyclization to the Tricyclic Core of ent-Kaurenoids and Its Application to the Formal Synthesis of (±)-Platensimycin
L Zhu, Y Han, G Du, CS Lee
Organic letters 15 (3), 524-527, 2013
212013
Structure and Characterization of a Covalent Inhibitor of Src Kinase
D Gurbani, G Du, NJ Henning, S Rao, AK Bera, T Zhang, NS Gray, ...
Frontiers in Molecular Biosciences 7, 81, 2020
192020
Selective degradation-inducing probes for studying cereblon (CRBN) biology
CE Powell, G Du, JW Bushman, Z He, T Zhang, ES Fischer, NS Gray
RSC Medicinal Chemistry 12 (8), 1381-1390, 2021
182021
Syntheses of diverse natural products via dual-mode Lewis acid induced cascade cyclization reactions
G Du, G Wang, W Ma, Q Yang, W Bao, X Liang, L Zhu, CS Lee
Synlett 28 (12), 1394-1406, 2017
182017
Peptide-based covalent inhibitors of MALT1 paracaspase
JM Hatcher, G Du, L Fontán, I Us, Q Qiao, S Chennamadhavuni, J Shao, ...
Bioorganic & medicinal chemistry letters 29 (11), 1336-1339, 2019
172019
Formal Synthesis of (+)-Phomactin A
J Huang, W Bao, S Huang, W Yang, Z Lizhi, G Du, CS Lee
Organic letters 20 (23), 7466-7469, 2018
172018
Quinoline and thiazolopyridine allosteric inhibitors of MALT1
DA Scott, JM Hatcher, H Liu, M Fu, G Du, L Fontán, I Us, G Casalena, ...
Bioorganic & medicinal chemistry letters 29 (14), 1694-1698, 2019
162019
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