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- [31] Design and synthesis of novel pyrimidine analogs as highly selective, non-covalent BTK inhibitorsBIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2018, 28 (02) : 145 - 151Kawahata, Wataru论文数: 0 引用数: 0 h-index: 0机构: Carna Biosci Inc, Res & Dev, BMA, Chuo Ku, 3rd Floor,1-5-5 Minatojima Minamimachi, Kobe, Hyogo 6500047, Japan Carna Biosci Inc, Res & Dev, BMA, Chuo Ku, 3rd Floor,1-5-5 Minatojima Minamimachi, Kobe, Hyogo 6500047, JapanAsami, Tokiko论文数: 0 引用数: 0 h-index: 0机构: Carna Biosci Inc, Res & Dev, BMA, Chuo Ku, 3rd Floor,1-5-5 Minatojima Minamimachi, Kobe, Hyogo 6500047, Japan Carna Biosci Inc, Res & Dev, BMA, Chuo Ku, 3rd Floor,1-5-5 Minatojima Minamimachi, Kobe, Hyogo 6500047, JapanIrie, Takayuki论文数: 0 引用数: 0 h-index: 0机构: Carna Biosci Inc, Res & Dev, BMA, Chuo Ku, 3rd Floor,1-5-5 Minatojima Minamimachi, Kobe, Hyogo 6500047, Japan Carna Biosci Inc, Res & Dev, BMA, Chuo Ku, 3rd Floor,1-5-5 Minatojima Minamimachi, Kobe, Hyogo 6500047, JapanSawa, Masaaki论文数: 0 引用数: 0 h-index: 0机构: Carna Biosci Inc, Res & Dev, BMA, Chuo Ku, 3rd Floor,1-5-5 Minatojima Minamimachi, Kobe, Hyogo 6500047, Japan Carna Biosci Inc, Res & Dev, BMA, Chuo Ku, 3rd Floor,1-5-5 Minatojima Minamimachi, Kobe, Hyogo 6500047, Japan
- [32] Design and synthesis of novel α-MSH peptide analogs highly selective for the hMC4RUNDERSTANDING BIOLOGY USING PEPTIDES, 2006, : 629 - +Hruby, Victor J.论文数: 0 引用数: 0 h-index: 0机构: Univ Arizona, Dept Chem, Tucson, AZ 85721 USA Univ Arizona, Dept Chem, Tucson, AZ 85721 USAYing, Jinfa论文数: 0 引用数: 0 h-index: 0机构: Univ Arizona, Dept Chem, Tucson, AZ 85721 USA Univ Arizona, Dept Chem, Tucson, AZ 85721 USAGu, Xuyuan论文数: 0 引用数: 0 h-index: 0机构: Univ Arizona, Dept Chem, Tucson, AZ 85721 USA Univ Arizona, Dept Chem, Tucson, AZ 85721 USACai, Minying论文数: 0 引用数: 0 h-index: 0机构: Univ Arizona, Dept Chem, Tucson, AZ 85721 USA Univ Arizona, Dept Chem, Tucson, AZ 85721 USAVagner, Josef论文数: 0 引用数: 0 h-index: 0机构: Univ Arizona, Dept Chem, Tucson, AZ 85721 USA Univ Arizona, Dept Chem, Tucson, AZ 85721 USATrivedi, Dev B.论文数: 0 引用数: 0 h-index: 0机构: Univ Arizona, Dept Chem, Tucson, AZ 85721 USA Univ Arizona, Dept Chem, Tucson, AZ 85721 USAKover, Katalin E.论文数: 0 引用数: 0 h-index: 0机构: Univ Debrecen, Dept Chem, H-4010 Debrecen, Hungary Univ Arizona, Dept Chem, Tucson, AZ 85721 USA
- [33] Total Synthesis and Biological Evaluation of Pederin, Psymberin, and Highly Potent AnalogsJOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2011, 133 (41) : 16668 - 16679Wan, Shuangyi论文数: 0 引用数: 0 h-index: 0机构: Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USAWu, Fanghui论文数: 0 引用数: 0 h-index: 0机构: Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USARech, Jason C.论文数: 0 引用数: 0 h-index: 0机构: Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USAGreen, Michael E.论文数: 0 引用数: 0 h-index: 0机构: Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USABalachandran, Raghavan论文数: 0 引用数: 0 h-index: 0机构: Univ Pittsburgh, Dept Pharmaceut Sci, Pittsburgh, PA 15260 USA Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USAHorne, W. Seth论文数: 0 引用数: 0 h-index: 0机构: Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USADay, Billy W.论文数: 0 引用数: 0 h-index: 0机构: Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA Univ Pittsburgh, Dept Pharmaceut Sci, Pittsburgh, PA 15260 USA Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USAFloreancig, Paul E.论文数: 0 引用数: 0 h-index: 0机构: Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA
- [34] Design, Synthesis, and Pharmacological Evaluation of Highly Potent and Selective Dipeptidyl Peptidase-4 InhibitorsARCHIV DER PHARMAZIE, 2015, 348 (06) : 399 - 407Jiang, Tao论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R China Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R ChinaZhou, Yuren论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R China Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R ChinaZhu, Jianming论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R China Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R ChinaChen, Zhuxi论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R China Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R ChinaSun, Peng论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R China Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R ChinaZhang, Qiang论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R China Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R ChinaWang, Zhen论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R China Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R ChinaShao, Qiang论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R China Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R ChinaJiang, Xiangrui论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R China Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R ChinaLi, Bo论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R China Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R ChinaWang, Heyao论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R China Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R ChinaZhu, Weiliang论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R China Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R ChinaShen, Jingshan论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R China Chinese Acad Sci, Shanghai Inst Mat Med, Key Lab Receptor Res, Drug Discovery & Design Ctr, Shanghai 201203, Peoples R China
- [35] Design and Synthesis of C-19 Isosteviol Derivatives as Potent and Highly Selective Antiproliferative AgentsMOLECULES, 2019, 24 (01)Luan, Tian论文数: 0 引用数: 0 h-index: 0机构: Yanbian Univ, Coll Pharm, Affiliated Minist Educ, Key Lab Nat Resources & Funct Mol Changbai Mt, Yanji 133002, Peoples R China Yanbian Univ, Coll Pharm, Affiliated Minist Educ, Key Lab Nat Resources & Funct Mol Changbai Mt, Yanji 133002, Peoples R ChinaCao, Li-Hua论文数: 0 引用数: 0 h-index: 0机构: Yanbian Univ, Coll Med, Dept Pharmacol, Yanji 133002, Peoples R China Yanbian Univ, Coll Pharm, Affiliated Minist Educ, Key Lab Nat Resources & Funct Mol Changbai Mt, Yanji 133002, Peoples R ChinaDeng, Hao论文数: 0 引用数: 0 h-index: 0机构: Yanbian Univ, Coll Pharm, Affiliated Minist Educ, Key Lab Nat Resources & Funct Mol Changbai Mt, Yanji 133002, Peoples R China Yanbian Univ, Coll Pharm, Affiliated Minist Educ, Key Lab Nat Resources & Funct Mol Changbai Mt, Yanji 133002, Peoples R ChinaShen, Qing-Kun论文数: 0 引用数: 0 h-index: 0机构: Yanbian Univ, Coll Pharm, Affiliated Minist Educ, Key Lab Nat Resources & Funct Mol Changbai Mt, Yanji 133002, Peoples R China Yanbian Univ, Coll Pharm, Affiliated Minist Educ, Key Lab Nat Resources & Funct Mol Changbai Mt, Yanji 133002, Peoples R ChinaTian, Yu-Shun论文数: 0 引用数: 0 h-index: 0机构: Yanbian Univ, Coll Pharm, Affiliated Minist Educ, Key Lab Nat Resources & Funct Mol Changbai Mt, Yanji 133002, Peoples R China Yanbian Univ, Coll Pharm, Affiliated Minist Educ, Key Lab Nat Resources & Funct Mol Changbai Mt, Yanji 133002, Peoples R ChinaQuan, Zhe-Shan论文数: 0 引用数: 0 h-index: 0机构: Yanbian Univ, Coll Pharm, Affiliated Minist Educ, Key Lab Nat Resources & Funct Mol Changbai Mt, Yanji 133002, Peoples R China Yanbian Univ, Coll Pharm, Affiliated Minist Educ, Key Lab Nat Resources & Funct Mol Changbai Mt, Yanji 133002, Peoples R China
- [36] Design and synthesis of a potent, highly selective, orally bioavailable, retinoic acid receptor alpha agonistBIOORGANIC & MEDICINAL CHEMISTRY, 2018, 26 (04) : 798 - 814Clarke, Earl论文数: 0 引用数: 0 h-index: 0机构: Kings Coll London, Wolfson Ctr Age Related Dis, Neurosci Drug Discovery Unit, Guys Campus, London SE1 1UL, England Kings Coll London, Wolfson Ctr Age Related Dis, Neurosci Drug Discovery Unit, Guys Campus, London SE1 1UL, EnglandJarvis, Christopher I.论文数: 0 引用数: 0 h-index: 0机构: Kings Coll London, Wolfson Ctr Age Related Dis, Neurosci Drug Discovery Unit, Guys Campus, London SE1 1UL, England Kings Coll London, Wolfson Ctr Age Related Dis, Neurosci Drug Discovery Unit, Guys Campus, London SE1 1UL, EnglandGoncalves, Maria B.论文数: 0 引用数: 0 h-index: 0机构: Kings Coll London, Wolfson Ctr Age Related Dis, Neurosci Drug Discovery Unit, Guys Campus, London SE1 1UL, England Kings Coll London, Wolfson Ctr Age Related Dis, Neurosci Drug Discovery Unit, Guys Campus, London SE1 1UL, EnglandKalindjian, S. Barret论文数: 0 引用数: 0 h-index: 0机构: Kings Coll London, Wolfson Ctr Age Related Dis, Neurosci Drug Discovery Unit, Guys Campus, London SE1 1UL, England Kings Coll London, Wolfson Ctr Age Related Dis, Neurosci Drug Discovery Unit, Guys Campus, London SE1 1UL, EnglandAdams, David R.论文数: 0 引用数: 0 h-index: 0机构: Sygnature Discovery Ltd, Biocity, Pennyfoot St, Nottingham NG1 1GF, England Kings Coll London, Wolfson Ctr Age Related Dis, Neurosci Drug Discovery Unit, Guys Campus, London SE1 1UL, EnglandBrown, Jane T.论文数: 0 引用数: 0 h-index: 0机构: Sygnature Discovery Ltd, Biocity, Pennyfoot St, Nottingham NG1 1GF, England Kings Coll London, Wolfson Ctr Age Related Dis, Neurosci Drug Discovery Unit, Guys Campus, London SE1 1UL, EnglandShiers, Jason J.论文数: 0 引用数: 0 h-index: 0机构: Sygnature Discovery Ltd, Biocity, Pennyfoot St, Nottingham NG1 1GF, England Kings Coll London, Wolfson Ctr Age Related Dis, Neurosci Drug Discovery Unit, Guys Campus, London SE1 1UL, EnglandTaddei, David M. A.论文数: 0 引用数: 0 h-index: 0机构: Sygnature Discovery Ltd, Biocity, Pennyfoot St, Nottingham NG1 1GF, England Kings Coll London, Wolfson Ctr Age Related Dis, Neurosci Drug Discovery Unit, Guys Campus, London SE1 1UL, EnglandRavier, Elodie论文数: 0 引用数: 0 h-index: 0机构: Sygnature Discovery Ltd, Biocity, Pennyfoot St, Nottingham NG1 1GF, England Kings Coll London, Wolfson Ctr Age Related Dis, Neurosci Drug Discovery Unit, Guys Campus, London SE1 1UL, EnglandBarlow, Stephanie论文数: 0 引用数: 0 h-index: 0机构: Sygnature Discovery Ltd, Biocity, Pennyfoot St, Nottingham NG1 1GF, England Kings Coll London, Wolfson Ctr Age Related Dis, Neurosci Drug Discovery Unit, Guys Campus, London SE1 1UL, EnglandMiller, Iain论文数: 0 引用数: 0 h-index: 0机构: Sygnature Discovery Ltd, Biocity, Pennyfoot St, Nottingham NG1 1GF, England Kings Coll London, Wolfson Ctr Age Related Dis, Neurosci Drug Discovery Unit, Guys Campus, London SE1 1UL, EnglandSmith, Vanessa论文数: 0 引用数: 0 h-index: 0机构: Sygnature Discovery Ltd, Biocity, Pennyfoot St, Nottingham NG1 1GF, England Kings Coll London, Wolfson Ctr Age Related Dis, Neurosci Drug Discovery Unit, Guys Campus, London SE1 1UL, EnglandBorthwick, Alan D.论文数: 0 引用数: 0 h-index: 0机构: DrugMolDesign, 15 Temple Grove, London NW11 7UA, England Kings Coll London, Wolfson Ctr Age Related Dis, Neurosci Drug Discovery Unit, Guys Campus, London SE1 1UL, EnglandCorcoran, Jonathan P. T.论文数: 0 引用数: 0 h-index: 0机构: Kings Coll London, Wolfson Ctr Age Related Dis, Neurosci Drug Discovery Unit, Guys Campus, London SE1 1UL, England Kings Coll London, Wolfson Ctr Age Related Dis, Neurosci Drug Discovery Unit, Guys Campus, London SE1 1UL, England
- [37] SYNTHESIS AND BIOLOGICAL-ACTIVITY OF HIGHLY POTENT OCTAPEPTIDE ANALOGS OF SOMATOSTATINPROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (06) : 1896 - 1900CAI, RZ论文数: 0 引用数: 0 h-index: 0机构: VET ADM MED CTR,NEW ORLEANS,LA 70146 VET ADM MED CTR,NEW ORLEANS,LA 70146SZOKE, B论文数: 0 引用数: 0 h-index: 0机构: VET ADM MED CTR,NEW ORLEANS,LA 70146 VET ADM MED CTR,NEW ORLEANS,LA 70146LU, R论文数: 0 引用数: 0 h-index: 0机构: VET ADM MED CTR,NEW ORLEANS,LA 70146 VET ADM MED CTR,NEW ORLEANS,LA 70146FU, D论文数: 0 引用数: 0 h-index: 0机构: VET ADM MED CTR,NEW ORLEANS,LA 70146 VET ADM MED CTR,NEW ORLEANS,LA 70146REDDING, TW论文数: 0 引用数: 0 h-index: 0机构: VET ADM MED CTR,NEW ORLEANS,LA 70146 VET ADM MED CTR,NEW ORLEANS,LA 70146SCHALLY, AV论文数: 0 引用数: 0 h-index: 0机构: VET ADM MED CTR,NEW ORLEANS,LA 70146 VET ADM MED CTR,NEW ORLEANS,LA 70146
- [38] Synthesis of highly potent tubulysin analogs as payloads for targeting therapies of cancerABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2014, 248You, Fei论文数: 0 引用数: 0 h-index: 0机构: Endocyte Inc, W Lafayette, IN 47906 USA Endocyte Inc, W Lafayette, IN 47906 USAKleindl, Paul J.论文数: 0 引用数: 0 h-index: 0机构: Endocyte Inc, W Lafayette, IN 47906 USA Endocyte Inc, W Lafayette, IN 47906 USAWang, Kevin论文数: 0 引用数: 0 h-index: 0机构: Endocyte Inc, W Lafayette, IN 47906 USA Endocyte Inc, W Lafayette, IN 47906 USAQi, Longwu论文数: 0 引用数: 0 h-index: 0机构: Endocyte Inc, W Lafayette, IN 47906 USA Endocyte Inc, W Lafayette, IN 47906 USASanthapuram, Hari K.论文数: 0 引用数: 0 h-index: 0机构: Endocyte Inc, W Lafayette, IN 47906 USA Endocyte Inc, W Lafayette, IN 47906 USAHahn, Spencer J.论文数: 0 引用数: 0 h-index: 0机构: Endocyte Inc, W Lafayette, IN 47906 USA Endocyte Inc, W Lafayette, IN 47906 USAVaughn, Jeremy F.论文数: 0 引用数: 0 h-index: 0机构: Endocyte Inc, W Lafayette, IN 47906 USA Endocyte Inc, W Lafayette, IN 47906 USAParham, Garth L.论文数: 0 引用数: 0 h-index: 0机构: Endocyte Inc, W Lafayette, IN 47906 USA Endocyte Inc, W Lafayette, IN 47906 USAVetzel, Marilynn论文数: 0 引用数: 0 h-index: 0机构: Endocyte Inc, W Lafayette, IN 47906 USA Endocyte Inc, W Lafayette, IN 47906 USAReddy, Joseph A.论文数: 0 引用数: 0 h-index: 0机构: Endocyte Inc, W Lafayette, IN 47906 USA Endocyte Inc, W Lafayette, IN 47906 USALeamon, Christopher P.论文数: 0 引用数: 0 h-index: 0机构: Endocyte Inc, W Lafayette, IN 47906 USA Endocyte Inc, W Lafayette, IN 47906 USAVlahov, Iontcho R.论文数: 0 引用数: 0 h-index: 0机构: Endocyte Inc, W Lafayette, IN 47906 USA Endocyte Inc, W Lafayette, IN 47906 USA
- [39] Design and synthesis of highly potent and selective human peroxisome proliferator-activated receptor α agonistsBIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2007, 17 (16) : 4689 - 4693Yamazaki, Yukiyoshi论文数: 0 引用数: 0 h-index: 0机构: Kowa Co Ltd, Div Pharmaceut, Tokyo New Drug Res Labs 1, 2-17-43 Noguchicho, Tokyo 1890022, Japan Kowa Co Ltd, Div Pharmaceut, Tokyo New Drug Res Labs 1, 2-17-43 Noguchicho, Tokyo 1890022, JapanAbe, Kazutoyo论文数: 0 引用数: 0 h-index: 0机构: Kowa Co Ltd, Div Pharmaceut, Tokyo New Drug Res Labs 1, 2-17-43 Noguchicho, Tokyo 1890022, JapanTorna, Tsutornu论文数: 0 引用数: 0 h-index: 0机构: Kowa Co Ltd, Div Pharmaceut, Tokyo New Drug Res Labs 1, 2-17-43 Noguchicho, Tokyo 1890022, JapanNishikawa, Masahiro论文数: 0 引用数: 0 h-index: 0机构: Kowa Co Ltd, Div Pharmaceut, Tokyo New Drug Res Labs 1, 2-17-43 Noguchicho, Tokyo 1890022, JapanOzawa, Hidefurni论文数: 0 引用数: 0 h-index: 0机构: Kowa Co Ltd, Div Pharmaceut, Tokyo New Drug Res Labs 1, 2-17-43 Noguchicho, Tokyo 1890022, JapanOkuda, Ayurnu论文数: 0 引用数: 0 h-index: 0机构: Kowa Co Ltd, Div Pharmaceut, Tokyo New Drug Res Labs 1, 2-17-43 Noguchicho, Tokyo 1890022, JapanAraki, Takaaki论文数: 0 引用数: 0 h-index: 0机构: Kowa Co Ltd, Div Pharmaceut, Tokyo New Drug Res Labs 1, 2-17-43 Noguchicho, Tokyo 1890022, JapanOdaa, Soichi论文数: 0 引用数: 0 h-index: 0机构: Kowa Co Ltd, Div Pharmaceut, Tokyo New Drug Res Labs 1, 2-17-43 Noguchicho, Tokyo 1890022, JapanInoue, Keisuke论文数: 0 引用数: 0 h-index: 0机构: Kowa Co Ltd, Div Pharmaceut, Tokyo New Drug Res Labs 1, 2-17-43 Noguchicho, Tokyo 1890022, JapanShibuya, Kimiyuki论文数: 0 引用数: 0 h-index: 0机构: Kowa Co Ltd, Div Pharmaceut, Tokyo New Drug Res Labs 1, 2-17-43 Noguchicho, Tokyo 1890022, JapanStaels, Bart论文数: 0 引用数: 0 h-index: 0机构: Kowa Co Ltd, Div Pharmaceut, Tokyo New Drug Res Labs 1, 2-17-43 Noguchicho, Tokyo 1890022, JapanFruchart, Jean-Charles论文数: 0 引用数: 0 h-index: 0机构: Kowa Co Ltd, Div Pharmaceut, Tokyo New Drug Res Labs 1, 2-17-43 Noguchicho, Tokyo 1890022, Japan
- [40] Design and Synthesis of Potent and Highly Selective Orexin 1 Receptor Antagonists with a Morphinan Skeleton and Their PharmacologiesJOURNAL OF MEDICINAL CHEMISTRY, 2017, 60 (03) : 1018 - 1040Nagase, Hiroshi论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan Univ Tsukuba, Grad Sch Pure & Appl Sci, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058571, Japan Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, JapanYamamoto, Naoshi论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, JapanYata, Masahiro论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Grad Sch Pure & Appl Sci, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058571, Japan Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, JapanOhrui, Sayaka论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, JapanOkada, Takahiro论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Grad Sch Pure & Appl Sci, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058571, Japan Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, JapanSaitoh, Tsuyoshi论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, JapanKutsumura, Noriki论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, JapanNagumo, Yasuyuki论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, JapanIrukayama-Tomobe, Yoko论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, JapanIshikawa, Yukiko论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, JapanOgawa, Yasuhiro论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan论文数: 引用数: h-index:机构:Kuroda, Daisuke论文数: 0 引用数: 0 h-index: 0机构: Showa Univ, Sch Pharm, Shinagawa Ku, 1-5-8 Hatanodai, Tokyo 1428555, Japan Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, JapanWatanabe, Yurie论文数: 0 引用数: 0 h-index: 0机构: Showa Univ, Sch Pharm, Shinagawa Ku, 1-5-8 Hatanodai, Tokyo 1428555, Japan Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, JapanGouda, Hiroaki论文数: 0 引用数: 0 h-index: 0机构: Showa Univ, Sch Pharm, Shinagawa Ku, 1-5-8 Hatanodai, Tokyo 1428555, Japan Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, JapanYanagisawa, Masashi论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan