N. Subasinghe

发表

A novel series of N-(azetidin-3-yl)-2-(heteroarylamino)acetamide CCR2 antagonists.

E. Opas, Z. Sui, Dana L. Johnson, 2013, Bioorganic & medicinal chemistry letters.

Design and synthesis of 4,5-disubstituted-thiophene-2-amidines as potent urokinase inhibitors.

R. DesJarlais, J. Spurlino, C. Illig, 2002, Bioorganic & medicinal chemistry letters.

Carboxylic acid bioisosteres acylsulfonamides, acylsulfamides, and sulfonylureas as novel antagonists of the CXCR2 receptor.

B. Tomczuk, D. Ryan, Shuyuan Zhao, 2008, Bioorganic & medicinal chemistry letters.

The discovery of novel cyclohexylamide CCR2 antagonists.

C. Molloy, E. Opas, Z. Sui, 2011, Bioorganic & medicinal chemistry letters.

Discovery and SAR of novel tetrahydropyrrolo[3,4-c]pyrazoles as inhibitors of the N-type calcium channel.

Z. Sui, M. Brandt, C. M. Flores, 2014, Bioorganic & medicinal chemistry letters.

Synthesis of thiophene-2-carboxamidines containing 2-aminothiazoles and their biological evaluation as urokinase inhibitors.

R. DesJarlais, J. Spurlino, C. Illig, 2001, Bioorganic & medicinal chemistry letters.

Structure-based design, synthesis and SAR of a novel series of thiopheneamidine urokinase plasminogen activator inhibitors.

R. DesJarlais, J. Spurlino, C. Illig, 2001, Bioorganic & medicinal chemistry letters.

An efficient and high yield method for the N-tert-butoxycarbonyl protection of sterically hindered amino acids

Rodney L. Johnson, N. Subasinghe, Ehab Khalil, 1996 .

Synthesis of acyclic and dehydroaspartic acid analogues of Ac-Asp-Glu-OH and their inhibition of rat brain N-acetylated alpha-linked acidic dipeptidase (NAALA dipeptidase).

M. Schulte, R. J. Roon, R. Johnson, 1990, Journal of medicinal chemistry.

Stereospecific synthesis of 2-substituted bicyclic thiazolidine lactams

Rodney L. Johnson, N. Subasinghe, Ehab Khalil, 1997 .

A novel series of potent and selective small molecule inhibitors of the complement component C1s.

R. DesJarlais, J. Spurlino, C. Illig, 2004, Bioorganic & medicinal chemistry letters.

Discovery and optimization of a novel series of pyrazolyltetrahydropyran N-type calcium channel (Cav 2.2) blockers for the treatment of pain.

Z. Sui, M. Brandt, C. M. Flores, 2018, Bioorganic & medicinal chemistry letters.

Bicyclic thiazolidine lactam peptidomimetics of the dopamine receptor modulating peptide Pro-Leu-Gly-NH2.

R. J. Bontems, E. McIntee, R. Johnson, 1993, Journal of medicinal chemistry.

Design and synthesis of polyethylene glycol-modified biphenylsulfonyl-thiophene-carboxamidine inhibitors of the complement component C1s.

B. Tomczuk, C. Molloy, R. Bone, 2012, Bioorganic & medicinal chemistry letters.

Biphenylsulfonyl-thiophene-carboxamidine inhibitors of the complement component C1s.

B. Tomczuk, R. DesJarlais, Hui-Sheng Huang, 2008, Bioorganic & medicinal chemistry letters.

A novel series of arylsulfonylthiophene-2-carboxamidine inhibitors of the complement component C1s.

B. Tomczuk, R. DesJarlais, Hui-Sheng Huang, 2006, Bioorganic & medicinal chemistry letters.

A novel series of pyrazolylpiperidine N-type calcium channel blockers.

Z. Sui, M. Brandt, C. M. Flores, 2012, Bioorganic & medicinal chemistry letters.