Jiewei Jiang

3-aroylmethylene-2,3,6,7-tetrahydro-1H-pyrazino[2,1-a]isoquinolin-4(11bH)-ones as potent Nrf2/ARE inducers in human cancer cells and AOM-DSS treated mice.

M. Zhang, R. Hu, Q. You, 2013, Journal of medicinal chemistry.

1,4‐Dihydropyridinebutyrolactone‐derived ring‐opened ester and amide analogs targeting BET bromodomains

J. Qi, E. Schönbrunn, G. Georg, 2022, Archiv der Pharmazie.

BRDT Inhibitors for Male Contraceptive Drug Discovery: Current Status

G. Georg, Zhenyuan Miao, Xianghong Guan, 2018 .

Synthesis and antibacterial evaluation of a novel series of 10-hydroxyl ketolide derivatives.

Ying Sun, Q. You, Haopeng Sun, 2013, Bioorganic & medicinal chemistry letters.

BET Bromodomain Inhibitors with One-Step Synthesis Discovered from Virtual Screen.

Gunda I Georg, William C K Pomerantz, Ernst Schönbrunn, 2017, Journal of medicinal chemistry.

6.beta.-[N,N-Bis(2-chloroethyl)amino]-17-(cyclopropylmethyl)-4,5.alpha.-epoxy-3,14-dihydroxymorphinan (chloranaltrexamine), a potent opioid receptor alkylating agent with ultralong narcotic antagonist activity

P. Portoghese, A. Takemori, Jiewei Jiang, 1978 .

Dihydropyridine Lactam Analogs Targeting BET Bromodomains

J. Qi, E. Schönbrunn, G. Georg, 2021, ChemMedChem.