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Bioavailable Acyl-CoA. Cholesterol Acyltransferase Inhibitor with Anti-peroxidative Activity. Synthesis and Biological Activity of Novel Indolinyl Amide and Urea Derivatives.

机译：生物可利用的acyl-coa。胆固醇酰基转移酶抑制剂具有抗过氧化活性。新型吲哚基酰胺和脲衍生物的合成与生物活性。

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Shoji KAMIYA; Hiroaki SHIRAHASE; Akihisa YOSHIMI; Shohei NAKAMURA; Mamoru KANDA; Hiroshi MATSUI; Masayasu KASAI; Kenji TAKAHASHI; Kazuyoshi KURAHASHI;
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1. Bioavailable acyl-CoA: cholesterol acyltransferase inhibitor with anti-peroxidative activity: synthesis and biological activity of novel indolinyl amide and urea derivatives. [J] . Kamiya S, Shirahase H, Yoshimi A, Chemical and Pharmaceutical Bulletin . 2000,第6期

机译：可生物利用的酰基辅酶A：具有抗过氧化活性的胆固醇酰基转移酶抑制剂：新型吲哚基酰胺和尿素衍生物的合成和生物活性。
2. Synthesis and biological activity of novel 4-phenyl-1,8-naphthyridin-2(1H)-on-3-yl ureas: potent acyl-CoA:cholesterol acyltransferase inhibitor with improved aqueous solubility. [J] . Ban H, Muraoka M, Ioriya K, Bioorganic and Medicinal Chemistry Letters . 2006,第1期

机译：新型4-苯基-1,8-萘啶-2（1H）-on-3-基脲的合成和生物活性：强水溶性的酰基辅酶A：胆固醇酰基转移酶抑制剂。
3. Potent quinoxaline-based inhibitors of PDGF receptor tyrosine kinase activity. Part 2: the synthesis and biological activities of RPR127963 an orally bioavailable inhibitor. [J] . He W, Myers MR, Hanney B, Bioorganic and Medicinal Chemistry Letters . 2003,第18期

机译：基于强喹喔啉的PDGF受体酪氨酸激酶活性抑制剂。第2部分：口服生物利用抑制剂RPR127963的合成和生物学活性。
4. Synthesis, characterization of some new l,3-oxazine-4-one derivatives containing 1,3,4-oxadiazole and 1,3,4-thiadiazole moiety with screening some of their biological activity. [C] . Raneen Hashim Rida, Maysoon Tariq Tawfiq International Scientific Conference on Pure Sciences, Brilliant Creativity and Renewed Building . 2019

机译：合成，表征一些含有1,3,4-二唑和1,3,4-噻二唑部分的一些新的L，3-氧嗪-4-一种衍生物，其具有筛选其一些生物活性。
5. Design, synthesis and biological evaluation of benzamide and phenyltetrazole derivatives with amide and urea linkers as BCRP inhibitors [D] . Gujarati, Nehaben A. 2017

机译：以酰胺和脲连接基作为BCRP抑制剂的苯甲酰胺和苯基四唑衍生物的设计，合成和生物学评估
6. Substituted Amides of Pyrazine-2-carboxylic acids: Synthesis and Biological Activity. [O] . Martin Dolezal, Miroslav Miletin, Jiri Kunes, 2002

机译：吡嗪-2-羧酸的取代酰胺：合成与生物活性。
7. Enantioselective Synthesis of the Key Intermediate of the Acyl-CoA. Cholesterol Acyltransferase (ACAT) Inhibitor (R-106578) Using 2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl (BINAP)-Ru(OAc)2 as a Catalyst. [O] . Masayuki MURAKAMI, Keijiro KOBAYASHI, Koichi HIRAI 2000

机译：酰基CoA键中间体对映选择性合成。胆固醇酰基转移酶（ACAT）抑制剂（R-106578）使用2,2'-BIS（二苯基膦基）-1,1'-二苯甲基（Binap）-Ru（OAC）2作为催化剂。

Bioavailable Acyl-CoA. Cholesterol Acyltransferase Inhibitor with Anti-peroxidative Activity. Synthesis and Biological Activity of Novel Indolinyl Amide and Urea Derivatives.

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