首页> 外文OA文献 >Prostanoids and Related Compounds. VII. Synthesis and Inhibitory Activity of 1-Isoindolinone Derivatives Possessing Inhibitory Activity against Thromboxane A2 Analog (U-46619)-Induced Vasoconstriction.

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Prostanoids and Related Compounds. VII. Synthesis and Inhibitory Activity of 1-Isoindolinone Derivatives Possessing Inhibitory Activity against Thromboxane A2 Analog (U-46619)-Induced Vasoconstriction.

机译：前列腺素和相关化合物。 VII。具有抑制血栓素A2（U-46619）的抑制活性的1-异吲哚啉酮衍生物的合成和抑制活性 - 诱导血管收缩。

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Yoshiaki KATO; Masumi TAKEMOTO; Kazuo ACHIWA;
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年度 1999
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1. Prostanoids and related compounds. VII. Synthesis and inhibitory activity of 1-isoindolinone derivatives possessing inhibitory activity against thromboxane A2 analog (U-46619)-induced vasoconstriction. [J] . Kato Y, Takemoto M, Achiwa K Chemical and Pharmaceutical Bulletin . 1999,第4期

机译：前列腺素和相关化合物。七。具有对血栓烷A2类似物（U-46619）诱导的血管收缩具有抑制活性的1-异吲哚啉酮衍生物的合成和抑制活性。
2. Synthesis of [[(Benzenesulfonamido)alkyl]phenyl]alkanoic Acid Derivatives Containing Pyridyl or Imidazolyl Groups and Their Thromboxane A2 Receptor Antagonistic and Thromboxane A2 Synthase Inhibitory Activities [J] . Shunichiro Sakurai, Nobuo Ogawa, Tomio Suzuki, Chemical and Pharmaceutical Bulletin . 1996,第8期

机译：含吡啶基或咪唑基的[[（苯磺酰胺基）烷基]苯基]链烷酸衍生物的合成及其对血氧烷A2受体的拮抗作用及对血氧烷A2合酶的抑制活性
3. Modulation of Anti-Glomerular Basement Membrane Nephritis in Rats by ONO-1301, a Non-Prostanoid Prostaglandin I2 Mimetic Compound with Inhibitory Activity against Thromboxane A2 Synthase [J] . Kazumi Hayashi, Tadashi Nagamatsu, Tatsuya Oka, Japanese Journal of Pharmacology . 1997,第1期

机译：具有抗血栓素A2合酶活性的非前列腺素前列腺素I2模拟化合物ONO-1301对大鼠抗肾小球基底膜性肾炎的调节作用
4. Synthesis of uronic acid derivatives with unsaturated bond andtheir infection inhibitory activity against Japanese encephalitis virus [C] . Reo Kondo, Kazuya I.P.J.Hidari, Hirofumi Nakano 日本化学会春季年会 . 2020

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5. I. Comparison of translesion bypass of guanine-N2 monoadducts of mitomycin C and guanine -N7 monoadducts of 2,7-diaminomitosene by T7 exo-, Klenow exo-, eta and Klenow exo+ DNA polymerases. II. Structure-based design, synthesis, structure-conformation and structure -activity relationships studies of D-Phe-Pro-D-Arg-P1'-CONH2 tetrapeptides with inhibitory activity for thrombin. [D] . Clement, Cristina C. 2006

机译：I.通过T7 exo-，Klenow exo-，eta和Klenow exo + DNA聚合酶比较丝裂霉素C的鸟嘌呤-N2单加合物和2,7-二氨基光油的鸟嘌呤-N7单加合物的跨病变旁路。二。具有凝血酶抑制活性的D-Phe-Pro-D-Arg-P1'-CONH2四肽的基于结构的设计，合成，结构构象和结构-活性关系研究。
6. Design synthesis in vitro potent antiproliferative activity and kinase inhibitory effects of new triarylpyrazole derivatives possessing different heterocycle terminal moieties [O] . Mahmoud M. Gamal El-Din, Mohammed I. El-Gamal, Mohammed S. Abdel-Maksoud, 2019

机译：具有不同杂环末端部分的新三芳基吡唑衍生物的设计合成体外有效的抗增殖活性和激酶抑制作用
7. Prostanoids and Related Compounds. VI. Synthesis of Isoindolinone Derivatives Possessing Inhibitory Activity for Thromboxane A2 Analog (U-46619)-Induced Vasoconstriction. [O] . Yoshiaki KATO, Masumi TAKEMOTO, Kazuo ACHIWA 1993

机译：前列腺素和相关化合物。 VI。异吲哚啉酮衍生物的合成具有血栓素A2β-β-β-β-抗血管收缩的抑制活性。

Prostanoids and Related Compounds. VII. Synthesis and Inhibitory Activity of 1-Isoindolinone Derivatives Possessing Inhibitory Activity against Thromboxane A2 Analog (U-46619)-Induced Vasoconstriction.

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