Lan-ying Qin

发表

Sulfonamido-aryl ethers as bradykinin B1 receptor antagonists.

S. Bevan, H. Gstach, Viral Patel, 2009, Bioorganic & medicinal chemistry letters.

Synthesis of (3,4-dimethoxyphenoxy)alkylamino acetamides as orexin-2 receptor antagonists.

M. Webb, I. Henderson, J. Saunders, 2008, Bioorganic & medicinal chemistry letters.

Solid-phase synthesis of 1,2,5-trisubstituted imidazolidin-4-ones

Yan Xu, A. Metzger, I. Henderson, 2009 .

Solid-phase synthesis of N-9-substituted 2,8-diaminopurines

A. Metzger, I. Henderson, G. Ahmed, 2006 .

Discovery and SAR of pyrrolo[2,1-f][1,2,4]triazin-4-amines as potent and selective PI3Kδ inhibitors.

C. Weigelt, M. Poss, J. Sack, 2016, Bioorganic & medicinal chemistry letters.

Identification of highly potent and selective PI3Kδ inhibitors.

G. Schieven, C. Weigelt, M. Poss, 2017, Bioorganic & medicinal chemistry letters.

Identification of a Potent, Selective, and Efficacious Phosphatidylinositol 3-Kinase δ (PI3Kδ) Inhibitor for the Treatment of Immunological Disorders.

K. McIntyre, Sidney Pitt, G. Schieven, 2017, Journal of medicinal chemistry.

Discovery of 7-(3-(piperazin-1-yl)phenyl)pyrrolo[2,1-f][1,2,4]triazin-4-amine derivatives as highly potent and selective PI3Kδ inhibitors.

C. Weigelt, M. Poss, J. Sack, 2017, Bioorganic & medicinal chemistry letters.

Synthesis and SAR studies of trisubstituted purinones as potent and selective adenosine A2A receptor antagonists.

I. Henderson, Tara M Stauffer, B. Mcguinness, 2009, Bioorganic & medicinal chemistry letters.

Combined solution-phase and solid-phase synthesis of 2-amino-7,8-dihydropteridin-6(5H)-ones

H. Gstach, J. Baldwin, A. Metzger, 2009 .

Cyclic dinucleotides as anticancer agents

B. Fink, Yufen Zhao, Dharmpal S. Dodd, 2018 .

Substituted benzyloxytricyclic compounds as retinoic acid-related orphan receptor gamma t (RORγt) agonists.

Zhuyin Li, C. Weigelt, B. Fink, 2020, Bioorganic & medicinal chemistry letters.