39538-31-3Relevant academic research and scientific papers
Novel matrix metalloproteinase inhibitors: Generation of lead compounds by the in silico fragment-based approach
Takahashi, Kanji,Ikura, Masahiro,Habashita, Hiromu,Nishizaki, Minoru,Sugiura, Tsuneyuki,Yamamoto, Shingo,Nakatani, Shingo,Ogawa, Koji,Ohno, Hiroyuki,Nakai, Hisao,Toda, Masaaki
, p. 4527 - 4543 (2007/10/03)
Generation of structurally new matrix metalloproteinase inhibitors was successfully carried out using an in silico technique. In order to identify the small fragment interacting with residues in the S1′ pocket of MMP-1 through hydrogen bonds, we performed in silico screening using the LUDI program. As a result, acetyl-l-alanyl-(N-methyl)amide (Ac-l-Ala-NHMe) was selected to link with another fragment, hydroxamic acid that interacted with catalytic zinc. By this approach, the l-glutamic acid derivative 2b was discovered to be a new type of matrix metalloproteinase inhibitor. Further transformation to reduce its peptidic nature and improve activity yielded nonpeptidic lead compounds as inhibitors of MMP-1, -2, -3, and -9.
A synthetic approach to diaryl ethers using the Robinson annulation
Feng, Xianqi,Edstrom, Eric D.
, p. 99 - 105 (2007/10/03)
An alternative synthetic approach to diaryl ethers has been developed. In the key transformation, Robinson annulation of nonracemic aldehydes 16a,b, derived from L-glutamic acid 5-methyl ester and phenoxymethylvinyl ketone, provided α-phenoxyenones 17a,b.
