Mei Su

发表

Discovery of a novel class of 2-ureido thiophene carboxamide checkpoint kinase inhibitors.

V. Oza, P. Lyne, J. Janetka, 2008, Bioorganic & medicinal chemistry letters.

Identification of amidoheteroaryls as potent inhibitors of mutant (V600E) B-Raf kinase with in vivo activity.

David A. Scott, P. Lyne, L. Drew, 2009, Bioorganic & medicinal chemistry letters.

Structure-Cytotoxicity Relationships of Analogues of N14-Desacetoxytubulysin H.

V. Bedian, Fengjiang Wang, A. Kamal, 2016, Journal of medicinal chemistry.

Synthetic studies toward the construction of the cis-decalin portion of superstolides A and B. Application of a sequential double michael reaction and an anionic oxy-Cope rearrangement.

Wensheng Yu, Mei Su, Zhendong Jin, 2005, Organic letters.

In vitro and in vivo evaluation of 6-aminopyrazolyl-pyridine-3-carbonitriles as JAK2 kinase inhibitors.

David A. Scott, M. Lamb, Hai‐Jun Zhang, 2011, Bioorganic & medicinal chemistry letters.

Discovery of 5-chloro-N2-[(1S)-1-(5-fluoropyrimidin-2-yl)ethyl]-N4-(5-methyl-1H-pyrazol-3-yl)pyrimidine-2,4-diamine (AZD1480) as a novel inhibitor of the Jak/Stat pathway.

Jon Read, Mei Su, Minwei Ye, 2011, Journal of medicinal chemistry.

Negishi Coupling between α-Alkyl(aryl)thio Vinyl Zinc Chloride and α-Bromo Vinyl Ether: A Convergent Synthesis of 2-Alkoxy-3-alkyl(aryl)thiobuta-1,3-dienes1

Wensheng Yu, Mei Su, Ying Kang, 2002 .

Discovery of 1-methyl-1H-imidazole derivatives as potent Jak2 inhibitors.

Mei Su, Minwei Ye, C. Chuaqui, 2014, Journal of medicinal chemistry.

Discovery of checkpoint kinase inhibitor (S)-5-(3-fluorophenyl)-N-(piperidin-3-yl)-3-ureidothiophene-2-carboxamide (AZD7762) by structure-based design and optimization of thiophenecarboxamide ureas.

J. Breed, V. Oza, P. Lyne, 2012, Journal of medicinal chemistry.

Discovery of pyrazol-3-ylamino pyrazines as novel JAK2 inhibitors.

M. Lamb, Audrey M Davies, M. Zinda, 2009, Bioorganic & medicinal chemistry letters.

A stereoselective synthesis of α-halo vinyl sulfides and their applications in organic synthesis☆

Wensheng Yu, Mei Su, Zhendong Jin, 2001 .

Towards the next generation of dual Bcl-2/Bcl-xL inhibitors.

Kate F. Byth, Prasenjit Mukherjee, J. Saeh, 2014, Bioorganic & medicinal chemistry letters.

Synthesis and evaluation of triazolones as checkpoint kinase 1 inhibitors.

Jon Read, Mei Su, J. Breed, 2012, Bioorganic & medicinal chemistry letters.

Discovery of a novel class of triazolones as checkpoint kinase inhibitors--hit to lead exploration.

J. Breed, V. Oza, P. Lyne, 2010, Bioorganic & medicinal chemistry letters.

A highly selective synthesis of (Z)-α,β-unsaturated ketones

Wensheng Yu, Mei Su, Zhendong Jin, 1999 .

Discovery of a novel class of 2-ureido thiophene carboxamide checkpoint kinase inhibitors.

P. Lyne, J. Janetka, S. Ashwell, 2008, Bioorganic & medicinal chemistry letters.