A. Namil

发表

New thiazolo[3,2-a]pyrimidine derivatives, synthesis and structure-activity relationships

G. Leclerc, E. Jeanneau‐Nicolle, M. Benoit‐Guyod, 1992 .

Novel esters and amides of nonsteroidal antiinflammatory carboxylic acids as antioxidants and antiproliferative agents.

M. Hellberg, T. L. Kessler, J. C. Nixon, 1999, Journal of medicinal chemistry.

A STUDY OF THE ENHANCED CORNEAL PENETRATION OF MOXIFLOXACIN

J. May, M. Hellberg, J. Liao, 2004 .

Syntheses and molecular structures of 3-N, N-di-n-propylamino-2-chromanones as new analogues of dopamine.

E. Nicolle, C. Coulombeau, G. Leclerc, 1995, Bioorganic & medicinal chemistry.

Quaternary ammonium substituted thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxides: Potential membrane-impermeable inhibitors of carbonic anhydrase.

A. Dantanarayana, J. May, Hwang-Hsing Chen, 2006, Bioorganic & Medicinal Chemistry.

A small-molecule inhibitor of C5 complement protein

M. Schirle, Mitsunori Kato, G. Michaud, 2019, Nature Chemical Biology.

Synthesis of 4-N,N-dialkylaminoethyl-2-indolones as potential dopamine agonists

G. Leclerc, M. Benoit‐Guyod, A. Namil, 1995 .

Synthesis of 4‐N,N‐Dialkylaminoethyl‐2‐indolones as Potential Dopamine Agonists.

G. Leclerc, M. Benoit‐Guyod, A. Namil, 1996 .

In vivo optimization of 2,3-diaminopyrazine Rho Kinase inhibitors for the treatment of glaucoma.

N. Sharif, Byron Li, I. Pang, 2014, Bioorganic & medicinal chemistry letters.