共 50 条
- [41] Design, synthesis and molecular docking of α,β-unsaturated cyclohexanone analogous of curcumin as potent EGFR inhibitors with antiproliferative activityBIOORGANIC & MEDICINAL CHEMISTRY, 2013, 21 (02) : 388 - 394Xu, Yun-YunCao, YiMa, HailkuoLi, Huan-QiuAo, Gui-Zhen
- [42] Design and synthesis of potent RSK inhibitorsBIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2018, 28 (19) : 3197 - 3201Jain, RamaMathur, MichelleLan, JiongCostales, AbranAtallah, GordanaRamurthy, SavithriSubramanian, SharadhaSetti, LinaFeucht, PaulWarne, BobDoyle, LauraBasham, StephenJefferson, Anne B.Appleton, Brent A.Lindvall, MikaShafer, Cynthia M.
- [43] Design, synthesis and anticancer properties of IsoCombretaQuinolines as potent tubulin assembly inhibitorsEUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2017, 127 : 1025 - 1034Khelifi, IlhemNaret, TimotheeRenko, DolorHamze, AbdallahBernadat, GuillaumeBignon, JeromeLenoir, ChristineDubois, JoelleBrion, Jean-DanielProvot, OlivierAlami, Mouad
- [44] Discovery of 2-pyrimidyl-5-amidothiophenes as potent inhibitors for AKT: Synthesis and SAR studiesBIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2006, 16 (16) : 4163 - 4168Lin, XiaodongMurray, Jeremy M.Rico, Alice C.Wang, Michael X.Chu, Daniel T.Zhou, YasheenDel Rosario, MerciKaufman, SusanMa, SylviaFang, EricCrawford, KennethJefferson, A. B.
- [45] Synthesis, SAR, and X-ray structure of novel potent DPPIV inhibitors: Oxadiazolyl ketonesBIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2007, 17 (15) : 4167 - 4172Koo, Ki DongKim, Min JungKim, SungsubKim, Kyoung-HeeHong, Sang YongHur, Gwong-CheungYim, Hyeon JooKim, Geun TaeHan, Hee OonKwon, O. HwanKwon, Tae SikKoh, Jong SungLee, Chang-Seok
- [46] Design, synthesis and SAR of bipyridine derivatives as potent and selective p38 kinase inhibitorsABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2005, 230 : U2724 - U2724Tadesse, SHong, FTTamayo, NLiao, LPowers, DYudor, YYYu, VWong, MHenkle, BMiddleton, SSyed, RHarvey, THungate, RDominguez, C
- [47] Synthesis and SAR of two potent series of novel and selective arylsulfonamides as inhibitors of matrix metalloproteinases.ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1997, 214 : 102 - MEDIPurchase, CFWhite, ADRoth, BDJohnson, LBaragi, VFinkel, MLaemont, KRenkiewicz, RRSchrier, DJHallak, HKindt, EKOrtwine, DF
- [48] Design, synthesis and biological evaluation of novel steroidal spiro-oxindoles as potent antiproliferative agentsJOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2014, 141 : 121 - 134Yu, BinShi, Xiao-JingQi, Ping-PingYu, De-QuanLiu, Hong-Min
- [49] Design, synthesis and biological studies of novel tubulin inhibitorsBIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2013, 23 (15) : 4465 - 4468Sun, YanjunPandit, BulbulChettiar, Somsundaram N.Etter, Jonathan P.Lewis, AndrewJohnsamuel, JayasekarLi, Pui-Kai
- [50] Design and synthesis of novel sialyltransferase inhibitors and their inhibition studiesABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2011, 241Nasi, RavindranathHsieh, MargaretKhieu, Nam HuanZou, WeiJennings, Harold J.