1404322-08-2Relevant academic research and scientific papers
Rational Design of Novel 1,3-Oxazine Based β-Secretase (BACE1) Inhibitors: Incorporation of a Double Bond to Reduce P-gp Efflux Leading to Robust Aβ Reduction in the Brain
Fuchino, Kouki,Mitsuoka, Yasunori,Masui, Moriyasu,Kurose, Noriyuki,Yoshida, Shuhei,Komano, Kazuo,Yamamoto, Takahiko,Ogawa, Masayoshi,Unemura, Chie,Hosono, Motoko,Ito, Hisanori,Sakaguchi, Gaku,Ando, Shigeru,Ohnishi, Shuichi,Kido, Yasuto,Fukushima, Tamio,Miyajima, Hirofumi,Hiroyama, Shuichi,Koyabu, Kiyotaka,Dhuyvetter, Deborah,Borghys, Herman,Gijsen, Harrie J.M.,Yamano, Yoshinori,Iso, Yasuyoshi,Kusakabe, Ken-Ichi
, p. 5122 - 5137 (2018/05/23)
Accumulation of Aβ peptides is a hallmark of Alzheimer's disease (AD) and is considered a causal factor in the pathogenesis of AD. β-Secretase (BACE1) is a key enzyme responsible for producing Aβ peptides, and thus agents that inhibit BACE1 should be bene
OXAZINE DERIVATIVES AND A PHARMACEUTICAL COMPOSITION FOR INHIBITING BACE1 CONTAINING THEM
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Paragraph 0198; 0207, (2014/03/24)
The present invention provides a compound of formula (I): wherein —X═ is —CR7═ or —N═,ring B is a substituted or unsubstituted carbocycle or a substituted or unsubstituted heterocycle,R1 is substituted or unsubstituted alkyl or the l
