X. Dai

发表

Discovery of Highly Potent and Selective IRAK1 Degraders to Probe Scaffolding Functions of IRAK1 in ABC DLBCL.

Jennifer D. Venable, J. Edwards, U. Philippar, 2021, Journal of medicinal chemistry.

5-Substituted-N-pyridazinylbenzamides as potent and selective LRRK2 inhibitors: Improved brain unbound fraction enables efficacy.

Zehong Wan, A. Reith, F. D. Tattersall, 2019, Bioorganic & medicinal chemistry letters.

Synthesis of NO–NSAID Dendritic Prodrugs via Passerini Reaction: New Approach to the Design of Dendrimer-drug Conjugates

D. Zhang-Negrerie, X. Dai, Yanhui Lu, 2013 .

Synthesis and some transformations of substituted 5,6-dihydro-4H-1,3-oxazines

A. Katritzky, X. Dai, R. Tack, 1993 .

Assessing IRAK4 Functions in ABC DLBCL by IRAK4 Kinase Inhibition and Protein Degradation.

J. Edwards, U. Philippar, R. Attar, 2020, Cell chemical biology.

Computational studies of the binding modes of A2A adenosine receptor antagonists

Qingzhi Gao, Jing Wei, X. Dai, 2007, Amino Acids.

An improved synthesis of a selective αvβ3-integrin antagonist cyclo(-RGDfK-)

X. Dai, Z. Su, Jun O. Liu, 2000 .

The Discovery of a Facile Access to the Synthesis of NSAID Dendritic Prodrugs

D. Zhang-Negrerie, X. Dai, Yanhui Lu, 2013 .

Discovery of 5-substituent-N-arylbenzamide derivatives as potent, selective and orally bioavailable LRRK2 inhibitors.

Zehong Wan, A. Reith, P. Bamborough, 2017, Bioorganic & medicinal chemistry letters.

Mild and Regioselective N-Alkylation of 2-Pyridones in Water

Ting-Hai Yang, Xichen Lin, X. Dai, 2015 .

Synthesis and Resolution of Quinazolinone Atropisomeric Phosphine Ligands(,).

X. Dai, S. Virgil, Audrey Wong, 1998, The Journal of organic chemistry.

Asymmetric allylic alkylation catalyzed by palladium complexes with atropisomeric quinazolinone phosphine ligands

X. Dai, S. Virgil, 1999 .

Bocdene and mocdene derivatives of catechols and catecholamines.

J. Vilarrasa, G. Shipps, X. Dai, 2001, Organic letters.

SYNTHESIS OF 2-HETEROSUBSTITUTED QUINAZOLINONE ATROPISOMERIC PHOSPHINE LIGANDS BY DIRECT LITHIATION OF A 2-UNSUBSTITUTED QUINAZOLINONE SYSTEM

X. Dai, S. Virgil, 1999 .

Synthesis and pharmacological effects of new, N‐substituted soft anticholinergics based on glycopyrrolate

N. Bodor, P. Buchwald, X. Dai, 2005, The Journal of pharmacy and pharmacology.

Bocdene and mocdene derivatives of catechols and catecholamines.

J. Vilarrasa, G. Shipps, X. Dai, 2001, Organic letters.

3D-Pharmacophore Models for Selective A2A and A2B Adenosine Receptor Antagonists

Jing Wei, Songqing Wang, Qingzhi Gao, 2007, J. Chem. Inf. Model..

Non-clinical immunogenicity, biodistribution and toxicology evaluation of a chimpanzee adenovirus-based COVID-19 vaccine in rat and rhesus macaque

Yong Yang, X. Tong, Wei Liu, 2022, Archives of Toxicology.

Discovery of a novel 2,3,11,11a-tetrahydro-1H-pyrazino[1,2-b]isoquinoline-1,4(6H)-dione series promoting neurogenesis of human neural progenitor cells.

Emiri T. Mandeville, K. Arai, E. Lo, 2015, Bioorganic & medicinal chemistry letters.

Pharmacological Characterization of JNJ-75276617, a Menin-KMT2A Inhibitor, As Targeted Treatment for KMT2A-Altered and NPM1-Mutant Acute Leukemia

Bie M. P. Verbist, U. Philippar, C. Drenberg, 2022, Blood.