机译:作为特定TRPM2抑制剂的新型ACA衍生物的发现,可减少体外和体内缺血性损伤
Peking Univ Sch Pharmaceut Sci State Key Lab Nat &
Biomimet Drugs Beijing 100191 Peoples R China;
Zhejiang Univ Dept Toxicol Sch Med Hangzhou 310058 Zhejiang Peoples R China;
Zhejiang Univ Dept Biophys Sch Med Hangzhou 310058 Peoples R China;
Peking Univ Sch Pharmaceut Sci State Key Lab Nat &
Biomimet Drugs Beijing 100191 Peoples R China;
Peking Univ Sch Pharmaceut Sci State Key Lab Nat &
Biomimet Drugs Beijing 100191 Peoples R China;
Zhejiang Univ Dept Biophys Sch Med Hangzhou 310058 Peoples R China;
Peking Univ Sch Pharmaceut Sci State Key Lab Nat &
Biomimet Drugs Beijing 100191 Peoples R China;
Peking Univ Sch Pharmaceut Sci State Key Lab Nat &
Biomimet Drugs Beijing 100191 Peoples R China;
Peking Univ Sch Pharmaceut Sci State Key Lab Nat &
Biomimet Drugs Beijing 100191 Peoples R China;
Zhejiang Univ Dept Biophys Sch Med Hangzhou 310058 Peoples R China;
Peking Univ Sch Pharmaceut Sci State Key Lab Nat &
Biomimet Drugs Beijing 100191 Peoples R China;
机译:新型钠氢交换剂Isoform-1抑制剂Zoniporide可减少体内和体外缺血性心肌损伤
机译:吡唑并[3,4-d]嘧啶衍生物的构效关系研究导致发现一种新型的多激酶抑制剂,该抑制剂可有效抑制FLT3和VEGFR2并评估其对体内外急性髓性白血病的活性
机译:单烷铵甘草酸注射对体内心肌缺血性损伤的心脏保护作用:L型钙通道抑制氧化应激和调节Ca 2+稳态的累积
机译:光动力影响在体内和体外模型中诱导缺血性耐受性
机译:免疫抑制剂mTOR抑制剂依维莫司和西罗莫司与钙调神经磷酸酶抑制剂环孢霉素和他克莫司联用的体内和体外比较肾毒性研究
机译:A11一种新型的二芳基酰基hydr衍生物可在体内和体外发挥抗缺血性损伤的神经保护作用
机译:作为特定TRPM2抑制剂的新型ACA衍生物的发现,可在体外和体内减少缺血性损伤
机译:哺乳动物组织中的胰蛋白酶样酶:取代异香豆素机制为基础的抑制剂,苯甲脒衍生物的底物特异性和Inhibitorypotency和精氨酸氟烷酮过渡态抑制剂