S. Iwama

发表

X-ray crystal structure determination and molecular dynamics simulation of prophospholipase A2 inhibited by amide-type substrate analogues.

K. Tomoo, S. Katsumura, T. Ishida, 1997, Biochimica et biophysica acta.

Novel ligands lacking a positive charge for the δ- and μ-opioid receptors

Amos B. Smith, P. Schiller, C. Lemieux, 2000 .

An efficient synthesis of short-chain sphingomyelin analogs and their susceptibility to hydrolysis catalyzed by sphingomyelinase

S. Katsumura, K. Ikeda, S. Fujii, 1997 .

Highly Diastereoselective Synthesis of D-threo- and D-erythro-Sphingosine from Glycidol

S. Katsumura, S. Iwama, N. Yamamoto, 1995 .

New entry for asymmetric deoxyazasugar synthesis: syntheses of deoxymannojirimycin, deoxyaltrojirimycin and deoxygalactostatin

S. Katsumura, S. Iwama, T. Hakogi, 1999 .

Stereocontrolled synthesis of a potent agonist of group II metabotropic glutamate receptors, (+)-LY354740, and its related derivatives

T. Shinada, S. Iwama, K. Shimamoto, 2003 .

Novel and efficient transformation of α-amino nitrile to α-imino and α-amide nitriles in asymmetric Strecker synthesis

T. Shinada, S. Iwama, M. Kawasaki, 2001 .

Stereocontrolled synthesis of a sphingomyelin methylene analogue as a sphingomyelinase inhibitor.

S. Katsumura, S. Iwama, T. Hakogi, 2000, Organic letters.

Cyclic peptide formation catalyzed by an antibody ligase.

S. Benkovic, J. Liu, S. Iwama, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Design and synthesis of new secretory phospholipase A2 inhibitor of a phospholipid analog.

S. Katsumura, K. Ikeda, M. Segawa, 1998, Bioorganic & medicinal chemistry letters.

Synthesis of sphingomyelin carbon analogues as sphingomyelinase inhibitors.

S. Katsumura, K. Ikeda, S. Fujii, 2002, The Journal of organic chemistry.

pH dependence of the reaction rate of p-bromophenacyl bromide and of the binding constants of Ca2+ and an amide-type substrate analog to bovine pancreatic phospholipase A2.

S. Katsumura, K. Ikeda, S. Fujii, 1998, Archives of biochemistry and biophysics.

Novel ligands lacking a positive charge for the delta- and mu-opioid receptors.

P. Schiller, C. Lemieux, N. N. Chung, 2000, Journal of medicinal chemistry.

New phospholipase A2 inhibitor: synthesis and inhibition mechanism of oxazolidinone phospholipid analog.

S. Katsumura, K. Ikeda, S. Fujii, 1995, Bioorganic & medicinal chemistry.

Synthesis of oxazolidinone phospholipid analogue as a new inhibitor of phospholipase A2

S. Katsumura, K. Ikeda, S. Iwama, 1993 .

Design and synthesis of an aminopiperidine series of γ-secretase modulators.

S. Iwama, Tomonori Kobayashi, M. Tobe, 2014, Bioorganic & medicinal chemistry letters.

Discovery of a potent and selective alpha v beta 3 integrin antagonist with strong inhibitory activity against neointima formation in rat balloon injury model.

M. Notake, S. Iwama, Y. Honda, 2004, Bioorganic & medicinal chemistry letters.

A Novel αvβ3 Integrin Antagonist Suppresses Neointima Formation for More Than 4 Weeks After Balloon Injury in Rats

M. Notake, S. Iwama, Y. Honda, 2005 .

A New Route for Protected Amino Alcohols from (R)-Glycidol. Copper(I) Mediated Alkylation of 4-Tosyloxymethyl-2-oxazolidinone

S. Katsumura, S. Iwama, 1994 .

A New Route for Protected Amino Alcohols from (E)-Glycidol. Copper(I) Mediated Alkylation of 4-Tosyloxymethyl-2-oxazolidinone.

S. Katsumura, S. Iwama, 1995 .

Binding mode of phospholipase A2 with a new type of phospholipid analog having an oxazolidinone ring.

S. Katsumura, K. Ikeda, K. Hayashi, 1995, Journal of biochemistry.

Identification of 2-(2'-fluoro-[1,1'-biphenyl]-2-yl)acetamide as a Sodium Valproate-like broad spectrum anti-epileptic drug candidate.

S. Iwama, Y. Inoue, Tomoyuki Tanaka, 2019, Bioorganic & medicinal chemistry letters.

Roles of asp126 and asp156 in the enzyme function of sphingomyelinase from Bacillus cereus.

S. Katsumura, M. Tomita, K. Ikeda, 1999, Journal of biochemistry.