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- [1] Design, synthesis, and SAR studies of novel survivin inhibitors with potent antiproliferative propertiesABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2014, 248Xiao, Min论文数: 0 引用数: 0 h-index: 0机构: Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USA Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USAWang, Jin论文数: 0 引用数: 0 h-index: 0机构: Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USA Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USALu, Yan论文数: 0 引用数: 0 h-index: 0机构: Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USA Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USAMiller, Duane D.论文数: 0 引用数: 0 h-index: 0机构: Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USA Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USALi, Wei论文数: 0 引用数: 0 h-index: 0机构: Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USA Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USA
- [2] Design, synthesis, and studies of novel survivin inhibitorsABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2012, 243Chettiar, Somsundaram N.论文数: 0 引用数: 0 h-index: 0机构: Ohio State Univ, Coll Pharm, Div Med Chem & Pharmacognosy, Columbus, OH 43210 USA Ohio State Univ, Coll Pharm, Div Med Chem & Pharmacognosy, Columbus, OH 43210 USAPark, In-Hee论文数: 0 引用数: 0 h-index: 0机构: Ohio State Univ, Coll Pharm, Div Med Chem & Pharmacognosy, Columbus, OH 43210 USA Ohio State Univ, Coll Pharm, Div Med Chem & Pharmacognosy, Columbus, OH 43210 USACooley, James论文数: 0 引用数: 0 h-index: 0机构: Ohio State Univ, Coll Med, Dept Radiat Oncol, Columbus, OH 43210 USA Ohio State Univ, Coll Pharm, Div Med Chem & Pharmacognosy, Columbus, OH 43210 USABhasin, Deepak论文数: 0 引用数: 0 h-index: 0机构: Ohio State Univ, Coll Pharm, Div Med Chem & Pharmacognosy, Columbus, OH 43210 USA Ohio State Univ, Coll Pharm, Div Med Chem & Pharmacognosy, Columbus, OH 43210 USALi, Pui Kai论文数: 0 引用数: 0 h-index: 0机构: Ohio State Univ, Coll Pharm, Div Med Chem & Pharmacognosy, Columbus, OH 43210 USA Ohio State Univ, Coll Pharm, Div Med Chem & Pharmacognosy, Columbus, OH 43210 USAChakravarti, Arnab论文数: 0 引用数: 0 h-index: 0机构: Ohio State Univ, Coll Med, Dept Radiat Oncol, Columbus, OH 43210 USA Ohio State Univ, Coll Pharm, Div Med Chem & Pharmacognosy, Columbus, OH 43210 USANaduparambil, Jacob论文数: 0 引用数: 0 h-index: 0机构: Ohio State Univ, Coll Med, Dept Radiat Oncol, Columbus, OH 43210 USA Ohio State Univ, Coll Pharm, Div Med Chem & Pharmacognosy, Columbus, OH 43210 USALi, Chenglong论文数: 0 引用数: 0 h-index: 0机构: Ohio State Univ, Coll Pharm, Div Med Chem & Pharmacognosy, Columbus, OH 43210 USA Ohio State Univ, Coll Pharm, Div Med Chem & Pharmacognosy, Columbus, OH 43210 USA
- [3] Design, synthesis and SAR studies of novel tacrine derivatives as potent cholinesterase inhibitorsEUROPEAN JOURNAL OF MEDICINAL CHEMISTRY REPORTS, 2022, 6Dogga, Bhushanarao论文数: 0 引用数: 0 h-index: 0机构: Visvesvaraya Technol Univ, Dept Nanotechnol, CPGS Bangalore Reg, Bangalore 562101, India Syngene Int Ltd, Biocon Pk,Bommasandra 4Phase,Jigani Link Rd, Bangalore 560099, India Visvesvaraya Technol Univ, Dept Nanotechnol, CPGS Bangalore Reg, Bangalore 562101, IndiaReddy, Eeda Koti论文数: 0 引用数: 0 h-index: 0机构: Vignan Fdn Sci Technol & Res, Dept Chem, Guntur 522213, India Visvesvaraya Technol Univ, Dept Nanotechnol, CPGS Bangalore Reg, Bangalore 562101, IndiaSharanya, C. S.论文数: 0 引用数: 0 h-index: 0机构: Kannur Univ, Dept Biotechnol & Microbiol, Dr EK Janaki Ammal Campus, Kannur 670661, Kerala, India Rajagiri Coll Social Sci, Dept Biosci, Cochin 683104, India Visvesvaraya Technol Univ, Dept Nanotechnol, CPGS Bangalore Reg, Bangalore 562101, IndiaAbhithaj, J.论文数: 0 引用数: 0 h-index: 0机构: Kannur Univ, Dept Biotechnol & Microbiol, Dr EK Janaki Ammal Campus, Kannur 670661, Kerala, India Visvesvaraya Technol Univ, Dept Nanotechnol, CPGS Bangalore Reg, Bangalore 562101, IndiaArun, K. G.论文数: 0 引用数: 0 h-index: 0机构: Kannur Univ, Dept Biotechnol & Microbiol, Dr EK Janaki Ammal Campus, Kannur 670661, Kerala, India Visvesvaraya Technol Univ, Dept Nanotechnol, CPGS Bangalore Reg, Bangalore 562101, IndiaKumar, C. S. Ananda论文数: 0 引用数: 0 h-index: 0机构: Visvesvaraya Technol Univ, Dept Nanotechnol, CPGS Bangalore Reg, Bangalore 562101, India Visvesvaraya Technol Univ, Dept Nanotechnol, CPGS Bangalore Reg, Bangalore 562101, IndiaRangappa, K. S.论文数: 0 引用数: 0 h-index: 0机构: Univ Mysore, Inst Excellence, Mysuru 570006, India Visvesvaraya Technol Univ, Dept Nanotechnol, CPGS Bangalore Reg, Bangalore 562101, India
- [4] Design, Synthesis and SAR Studies of Novel and Potent Dipeptidyl Peptidase 4 InhibitorsCHINESE JOURNAL OF CHEMISTRY, 2021, 39 (01): : 115 - 120Luo, Na论文数: 0 引用数: 0 h-index: 0机构: East China Univ Sci & Technol, Shanghai Key Lab New Drug Design, Sch Pharm, 130 Meilong Rd, Shanghai 200237, Peoples R China East China Univ Sci & Technol, Shanghai Key Lab New Drug Design, Sch Pharm, 130 Meilong Rd, Shanghai 200237, Peoples R ChinaFang, Xiaoyu论文数: 0 引用数: 0 h-index: 0机构: East China Univ Sci & Technol, Shanghai Key Lab New Drug Design, Sch Pharm, 130 Meilong Rd, Shanghai 200237, Peoples R China East China Univ Sci & Technol, Shanghai Key Lab New Drug Design, Sch Pharm, 130 Meilong Rd, Shanghai 200237, Peoples R ChinaSu, Mingbo论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, 555 Zhuchongzhi Rd, Shanghai 201203, Peoples R China East China Univ Sci & Technol, Shanghai Key Lab New Drug Design, Sch Pharm, 130 Meilong Rd, Shanghai 200237, Peoples R ChinaZhang, Xinwen论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, 555 Zhuchongzhi Rd, Shanghai 201203, Peoples R China East China Univ Sci & Technol, Shanghai Key Lab New Drug Design, Sch Pharm, 130 Meilong Rd, Shanghai 200237, Peoples R ChinaLi, Dan论文数: 0 引用数: 0 h-index: 0机构: Shandong Biopolar Dichang Pharmaceut Co Ltd, RM2306,786 Linzi Ave, Zibo 255400, Shandong, Peoples R China East China Univ Sci & Technol, Shanghai Key Lab New Drug Design, Sch Pharm, 130 Meilong Rd, Shanghai 200237, Peoples R ChinaLi, Honglin论文数: 0 引用数: 0 h-index: 0机构: East China Univ Sci & Technol, Shanghai Key Lab New Drug Design, Sch Pharm, 130 Meilong Rd, Shanghai 200237, Peoples R China East China Univ Sci & Technol, Shanghai Key Lab New Drug Design, Sch Pharm, 130 Meilong Rd, Shanghai 200237, Peoples R ChinaLi, Shiliang论文数: 0 引用数: 0 h-index: 0机构: East China Univ Sci & Technol, Shanghai Key Lab New Drug Design, Sch Pharm, 130 Meilong Rd, Shanghai 200237, Peoples R China East China Univ Sci & Technol, Shanghai Key Lab New Drug Design, Sch Pharm, 130 Meilong Rd, Shanghai 200237, Peoples R ChinaZhao, Zhenjiang论文数: 0 引用数: 0 h-index: 0机构: East China Univ Sci & Technol, Shanghai Key Lab New Drug Design, Sch Pharm, 130 Meilong Rd, Shanghai 200237, Peoples R China East China Univ Sci & Technol, Shanghai Key Lab New Drug Design, Sch Pharm, 130 Meilong Rd, Shanghai 200237, Peoples R China
- [5] Design, Synthesis and Structure-Activity Relationship Studies of Novel Survivin Inhibitors with Potent Anti-Proliferative PropertiesPLOS ONE, 2015, 10 (06):Xiao, Min论文数: 0 引用数: 0 h-index: 0机构: Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USA Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USAWang, Jin论文数: 0 引用数: 0 h-index: 0机构: Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USA Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USALin, Zongtao论文数: 0 引用数: 0 h-index: 0机构: Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USA Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USALu, Yan论文数: 0 引用数: 0 h-index: 0机构: Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USA Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USALi, Zhenmei论文数: 0 引用数: 0 h-index: 0机构: St Jude Childrens Res Hosp, Dept Biol Struct, Memphis, TN 38105 USA Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USAWhite, Stephen W.论文数: 0 引用数: 0 h-index: 0机构: St Jude Childrens Res Hosp, Dept Biol Struct, Memphis, TN 38105 USA Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USAMiller, Duane D.论文数: 0 引用数: 0 h-index: 0机构: Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USA Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USALi, Wei论文数: 0 引用数: 0 h-index: 0机构: Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USA Univ Tennessee, Hlth Sci Ctr, Dept Pharmaceut Sci, Memphis, TN 38163 USA
- [6] Novel naphthalene derivatives as potent HCV NS5A inhibitors: Design, synthesis, SAR, and optimization studiesABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2014, 248Baskaran, Sam论文数: 0 引用数: 0 h-index: 0机构: GlaxoSmithKline, HCV DPU, Cary, NC 27519 USA GlaxoSmithKline, HCV DPU, Cary, NC 27519 USAKazmierski, Wieslaw论文数: 0 引用数: 0 h-index: 0机构: GlaxoSmithKline, HCV DPU, Cary, NC 27519 USA GlaxoSmithKline, HCV DPU, Cary, NC 27519 USADuan, Maosheng论文数: 0 引用数: 0 h-index: 0机构: GlaxoSmithKline, HCV DPU, Cary, NC 27519 USA GlaxoSmithKline, HCV DPU, Cary, NC 27519 USADickerson, Scott论文数: 0 引用数: 0 h-index: 0机构: GlaxoSmithKline, HCV DPU, Cary, NC 27519 USA GlaxoSmithKline, HCV DPU, Cary, NC 27519 USACooper, Joel论文数: 0 引用数: 0 h-index: 0机构: GlaxoSmithKline, HCV DPU, Cary, NC 27519 USA GlaxoSmithKline, HCV DPU, Cary, NC 27519 USAGrimes, Rick论文数: 0 引用数: 0 h-index: 0机构: GlaxoSmithKline, HCV DPU, Cary, NC 27519 USA GlaxoSmithKline, HCV DPU, Cary, NC 27519 USAWalker, Jill论文数: 0 引用数: 0 h-index: 0机构: GlaxoSmithKline, HCV DPU, Cary, NC 27519 USA GlaxoSmithKline, HCV DPU, Cary, NC 27519 USA
- [7] Design and Synthesis of Novel Dehydroepiandrosterone Analogues as Potent Antiproliferative AgentsMOLECULES, 2018, 23 (09):Huang, Xing论文数: 0 引用数: 0 h-index: 0机构: Yanbian Univ, Key Lab Nat Resources & Funct Mol Changbai Mt, Affiliated Minist Educ, Coll Pharm, Yanji 133002, Peoples R China Yanbian Univ, Key Lab Nat Resources & Funct Mol Changbai Mt, Affiliated Minist Educ, Coll Pharm, Yanji 133002, Peoples R ChinaShen, Qing-Kun论文数: 0 引用数: 0 h-index: 0机构: Yanbian Univ, Key Lab Nat Resources & Funct Mol Changbai Mt, Affiliated Minist Educ, Coll Pharm, Yanji 133002, Peoples R China Yanbian Univ, Key Lab Nat Resources & Funct Mol Changbai Mt, Affiliated Minist Educ, Coll Pharm, Yanji 133002, Peoples R ChinaZhang, Hong-Jian论文数: 0 引用数: 0 h-index: 0机构: Yanbian Univ, Key Lab Nat Resources & Funct Mol Changbai Mt, Affiliated Minist Educ, Coll Pharm, Yanji 133002, Peoples R China Yanbian Univ, Key Lab Nat Resources & Funct Mol Changbai Mt, Affiliated Minist Educ, Coll Pharm, Yanji 133002, Peoples R ChinaLi, Jia-Li论文数: 0 引用数: 0 h-index: 0机构: Yanbian Univ, Key Lab Nat Resources & Funct Mol Changbai Mt, Affiliated Minist Educ, Coll Pharm, Yanji 133002, Peoples R China Yanbian Univ, Key Lab Nat Resources & Funct Mol Changbai Mt, Affiliated Minist Educ, Coll Pharm, Yanji 133002, Peoples R ChinaTian, Yu-Shun论文数: 0 引用数: 0 h-index: 0机构: Yanbian Univ, Key Lab Nat Resources & Funct Mol Changbai Mt, Affiliated Minist Educ, Coll Pharm, Yanji 133002, Peoples R China Yanbian Univ, Key Lab Nat Resources & Funct Mol Changbai Mt, Affiliated Minist Educ, Coll Pharm, Yanji 133002, Peoples R ChinaQuan, Zhe-Shan论文数: 0 引用数: 0 h-index: 0机构: Yanbian Univ, Key Lab Nat Resources & Funct Mol Changbai Mt, Affiliated Minist Educ, Coll Pharm, Yanji 133002, Peoples R China Yanbian Univ, Key Lab Nat Resources & Funct Mol Changbai Mt, Affiliated Minist Educ, Coll Pharm, Yanji 133002, Peoples R China
- [8] A novel series of potent thrombin inhibitors: Chemistry and SAR studies.ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1997, 214 : 56 - MEDIAugelliSzafran, CE论文数: 0 引用数: 0 h-index: 0机构: WARNER LAMBERT PARKE DAVIS,PARKE DAVIS PHARMACEUT RES,DEPT MED CHEM,ANN ARBOR,MI 48105Bachand, B论文数: 0 引用数: 0 h-index: 0机构: WARNER LAMBERT PARKE DAVIS,PARKE DAVIS PHARMACEUT RES,DEPT MED CHEM,ANN ARBOR,MI 48105Berryman, KA论文数: 0 引用数: 0 h-index: 0机构: WARNER LAMBERT PARKE DAVIS,PARKE DAVIS PHARMACEUT RES,DEPT MED CHEM,ANN ARBOR,MI 48105Cai, CM论文数: 0 引用数: 0 h-index: 0机构: WARNER LAMBERT PARKE DAVIS,PARKE DAVIS PHARMACEUT RES,DEPT MED CHEM,ANN ARBOR,MI 48105Cody, WL论文数: 0 引用数: 0 h-index: 0机构: WARNER LAMBERT PARKE DAVIS,PARKE DAVIS PHARMACEUT RES,DEPT MED CHEM,ANN ARBOR,MI 48105Edmunds, JJ论文数: 0 引用数: 0 h-index: 0机构: WARNER LAMBERT PARKE DAVIS,PARKE DAVIS PHARMACEUT RES,DEPT MED CHEM,ANN ARBOR,MI 48105Holland, DR论文数: 0 引用数: 0 h-index: 0机构: WARNER LAMBERT PARKE DAVIS,PARKE DAVIS PHARMACEUT RES,DEPT MED CHEM,ANN ARBOR,MI 48105Jaen, JC论文数: 0 引用数: 0 h-index: 0机构: WARNER LAMBERT PARKE DAVIS,PARKE DAVIS PHARMACEUT RES,DEPT MED CHEM,ANN ARBOR,MI 48105Narasimhan, LS论文数: 0 引用数: 0 h-index: 0机构: WARNER LAMBERT PARKE DAVIS,PARKE DAVIS PHARMACEUT RES,DEPT MED CHEM,ANN ARBOR,MI 48105PenvoseYi, JR论文数: 0 引用数: 0 h-index: 0机构: WARNER LAMBERT PARKE DAVIS,PARKE DAVIS PHARMACEUT RES,DEPT MED CHEM,ANN ARBOR,MI 48105Plummer, JS论文数: 0 引用数: 0 h-index: 0机构: WARNER LAMBERT PARKE DAVIS,PARKE DAVIS PHARMACEUT RES,DEPT MED CHEM,ANN ARBOR,MI 48105Rapundalo, ST论文数: 0 引用数: 0 h-index: 0机构: WARNER LAMBERT PARKE DAVIS,PARKE DAVIS PHARMACEUT RES,DEPT MED CHEM,ANN ARBOR,MI 48105Rubin, JR论文数: 0 引用数: 0 h-index: 0机构: WARNER LAMBERT PARKE DAVIS,PARKE DAVIS PHARMACEUT RES,DEPT MED CHEM,ANN ARBOR,MI 48105Siddiqui, MA论文数: 0 引用数: 0 h-index: 0机构: WARNER LAMBERT PARKE DAVIS,PARKE DAVIS PHARMACEUT RES,DEPT MED CHEM,ANN ARBOR,MI 48105StDenis, Y论文数: 0 引用数: 0 h-index: 0机构: WARNER LAMBERT PARKE DAVIS,PARKE DAVIS PHARMACEUT RES,DEPT MED CHEM,ANN ARBOR,MI 48105Susser, A论文数: 0 引用数: 0 h-index: 0机构: WARNER LAMBERT PARKE DAVIS,PARKE DAVIS PHARMACEUT RES,DEPT MED CHEM,ANN ARBOR,MI 48105Doherty, AM论文数: 0 引用数: 0 h-index: 0机构: WARNER LAMBERT PARKE DAVIS,PARKE DAVIS PHARMACEUT RES,DEPT MED CHEM,ANN ARBOR,MI 48105
- [9] Design, synthesis and SAR of thienopyridines as potent CHK1 inhibitorsBIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2010, 20 (24) : 7216 - 7221Zhao, Lianyun论文数: 0 引用数: 0 h-index: 0机构: Merck Res Labs, Dept Chem, Cambridge, MA 02141 USA Merck Res Labs, Dept Chem, Cambridge, MA 02141 USAZhang, Yingxin论文数: 0 引用数: 0 h-index: 0机构: Merck Res Labs, Dept Chem, Cambridge, MA 02141 USA Merck Res Labs, Dept Chem, Cambridge, MA 02141 USADai, Chaoyang论文数: 0 引用数: 0 h-index: 0机构: Merck Res Labs, Dept Chem, Cambridge, MA 02141 USA Merck Res Labs, Dept Chem, Cambridge, MA 02141 USAGuzi, Timothy论文数: 0 引用数: 0 h-index: 0机构: Merck Res Labs, Dept Chem, Cambridge, MA 02141 USA Merck Res Labs, Dept Chem, Cambridge, MA 02141 USAWiswell, Derek论文数: 0 引用数: 0 h-index: 0机构: Merck Res Labs, Palo Alto, CA 94304 USA Merck Res Labs, Dept Chem, Cambridge, MA 02141 USASeghezzi, Wolfgang论文数: 0 引用数: 0 h-index: 0机构: Merck Res Labs, Palo Alto, CA 94304 USA Merck Res Labs, Dept Chem, Cambridge, MA 02141 USAParry, David论文数: 0 引用数: 0 h-index: 0机构: Merck Res Labs, Palo Alto, CA 94304 USA Merck Res Labs, Dept Chem, Cambridge, MA 02141 USAFischmann, Thierry论文数: 0 引用数: 0 h-index: 0机构: Merck Res Labs, Drug Design Dept, Kenilworth, NJ 07033 USA Merck Res Labs, Dept Chem, Cambridge, MA 02141 USASiddiqui, M. Arshad论文数: 0 引用数: 0 h-index: 0机构: Merck Res Labs, Dept Chem, Cambridge, MA 02141 USA Merck Res Labs, Dept Chem, Cambridge, MA 02141 USA
- [10] Design, Synthesis and SAR Studies of NAD Analogues as Potent Inhibitors towards CD38 NADaseMOLECULES, 2014, 19 (10) : 15754 - 15767Wang, Shengjun论文数: 0 引用数: 0 h-index: 0机构: 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 ChinaZhu, Wenjie论文数: 0 引用数: 0 h-index: 0机构: Peking Univ, Shenzhen Grad Sch, Sch Chem Biol & Biotechnol, Shenzhen 518052, Peoples R China Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R ChinaWang, Xuan论文数: 0 引用数: 0 h-index: 0机构: 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 ChinaLi, Jianguo论文数: 0 引用数: 0 h-index: 0机构: 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 ChinaZhang, Kehui论文数: 0 引用数: 0 h-index: 0机构: 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 ChinaZhang, Liangren论文数: 0 引用数: 0 h-index: 0机构: 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 ChinaZhao, Yong-Juan论文数: 0 引用数: 0 h-index: 0机构: Peking Univ, Shenzhen Grad Sch, Sch Chem Biol & Biotechnol, Shenzhen 518052, Peoples R China Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R ChinaLee, Hon Cheung论文数: 0 引用数: 0 h-index: 0机构: Peking Univ, Shenzhen Grad Sch, Sch Chem Biol & Biotechnol, Shenzhen 518052, Peoples R China Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R ChinaZhang, Lihe论文数: 0 引用数: 0 h-index: 0机构: 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