共 50 条
- [1] Design, Synthesis of Novel, Potent, Selective, Orally Bioavailable Adenosine A2A Receptor Antagonists and Their Biological Evaluation[J]. JOURNAL OF MEDICINAL CHEMISTRY, 2017, 60 (02) : 681 - 694Basu, Sujay论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaBarawkar, Dinesh A.论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaThorat, Sachin论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaShejul, Yogesh D.论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaPatel, Meena论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaNaykodi, Minakshi论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaJain, Vaibhav论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaSalve, Yogesh论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaPrasad, Vandna论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaChaudhary, Sumit论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaGhosh, Indraneel论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaBhat, Ganesh论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaQuraishi, Azfar论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaPatil, Harish论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaAnsari, Shariq论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaMenon, Suraj论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaUnadkat, Vishal论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaThakare, Rhishikesh论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaSeervi, Madhav S.论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaMeru, Ashwinkumar V.论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaDe, Siddhartha论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaBhamidipati, Ravi K.论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaRouduri, Sreekanth R.论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaPalle, Venkata P.论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaChug, Anita论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, IndiaMookhtiar, Kasim A.论文数: 0 引用数: 0 h-index: 0机构: Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India Advinus Therapeut Ltd, Drug Discovery Facil, Quantum Towers,Plot 9,Phase 1, Pune 411057, Maharashtra, India
- [2] Discovery of Pyridinone Derivatives as Potent, Selective, and Orally Bioavailable Adenosine A2A Receptor Antagonists for Cancer Immunotherapy[J]. JOURNAL OF MEDICINAL CHEMISTRY, 2023, 66 (07) : 4734 - 4754论文数: 引用数: h-index:机构:Ze, Shuyin论文数: 0 引用数: 0 h-index: 0机构: East China Normal Univ, Inst Biomed Sci, Shanghai Key Lab Regulatory Biol, Shanghai 200241, Peoples R China East China Normal Univ, Sch Life Sci, Shanghai 200241, Peoples R China Fudan Univ, Sch Pharm, Dept Med Chem, Shanghai 201203, Peoples R ChinaZhou, Ronghui论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Sch Pharm, Dept Med Chem, Shanghai 201203, Peoples R China Fudan Univ, Sch Pharm, Dept Med Chem, Shanghai 201203, Peoples R China论文数: 引用数: h-index:机构:Wang, Haojie论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Sch Pharm, Dept Med Chem, Shanghai 201203, Peoples R China Fudan Univ, Sch Pharm, Dept Med Chem, Shanghai 201203, Peoples R ChinaChai, Xiaolei论文数: 0 引用数: 0 h-index: 0机构: East China Normal Univ, Inst Biomed Sci, Shanghai Key Lab Regulatory Biol, Shanghai 200241, Peoples R China East China Normal Univ, Sch Life Sci, Shanghai 200241, Peoples R China Fudan Univ, Sch Pharm, Dept Med Chem, Shanghai 201203, Peoples R ChinaFang, Meimiao论文数: 0 引用数: 0 h-index: 0机构: East China Normal Univ, Inst Biomed Sci, Shanghai Key Lab Regulatory Biol, Shanghai 200241, Peoples R China East China Normal Univ, Sch Life Sci, Shanghai 200241, Peoples R China Fudan Univ, Sch Pharm, Dept Med Chem, Shanghai 201203, Peoples R ChinaLiu, Mingyao论文数: 0 引用数: 0 h-index: 0机构: East China Normal Univ, Inst Biomed Sci, Shanghai Key Lab Regulatory Biol, Shanghai 200241, Peoples R China East China Normal Univ, Sch Life Sci, Shanghai 200241, Peoples R China Fudan Univ, Sch Pharm, Dept Med Chem, Shanghai 201203, Peoples R China论文数: 引用数: h-index:机构:Lu, Weiqiang论文数: 0 引用数: 0 h-index: 0机构: East China Normal Univ, Inst Biomed Sci, Shanghai Key Lab Regulatory Biol, Shanghai 200241, Peoples R China East China Normal Univ, Sch Life Sci, Shanghai 200241, Peoples R China Fudan Univ, Sch Pharm, Dept Med Chem, Shanghai 201203, Peoples R ChinaXie, Qiong论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Sch Pharm, Dept Med Chem, Shanghai 201203, Peoples R China Fudan Univ, Sch Pharm, Dept Med Chem, Shanghai 201203, Peoples R China
- [3] Selective adenosine A2A receptor antagonists[J]. FARMACO, 2001, 56 (1-2): : 87 - 90Ongini, E论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Res Inst, I-20132 Milan, ItalyMonopoli, A论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Res Inst, I-20132 Milan, ItalyCacciari, B论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Res Inst, I-20132 Milan, ItalyBaraldi, PG论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Res Inst, I-20132 Milan, Italy
- [4] 8-Phenylethynylxanthines-highly potent and selective adenosine A2A receptor antagonists[J]. PURINERGIC SIGNALLING, 2012, 8 (01) : 140 - 140Zech, Amelie论文数: 0 引用数: 0 h-index: 0机构: Univ Bonn, Inst Pharmaceut, PharmaCtr Bonn, D-53121 Bonn, Germany Univ Bonn, Inst Pharmaceut, PharmaCtr Bonn, D-53121 Bonn, GermanyHockemeyer, Joerg论文数: 0 引用数: 0 h-index: 0机构: Univ Bonn, Inst Pharmaceut, PharmaCtr Bonn, D-53121 Bonn, Germany Univ Bonn, Inst Pharmaceut, PharmaCtr Bonn, D-53121 Bonn, GermanyTzvetkov, Nikolay论文数: 0 引用数: 0 h-index: 0机构: Univ Bonn, Inst Pharmaceut, PharmaCtr Bonn, D-53121 Bonn, Germany Univ Bonn, Inst Pharmaceut, PharmaCtr Bonn, D-53121 Bonn, GermanyKoese, Meryem论文数: 0 引用数: 0 h-index: 0机构: Univ Bonn, Inst Pharmaceut, PharmaCtr Bonn, D-53121 Bonn, Germany Univ Bonn, Inst Pharmaceut, PharmaCtr Bonn, D-53121 Bonn, GermanyRadjainia, Hamid论文数: 0 引用数: 0 h-index: 0机构: Univ Bonn, Inst Pharmaceut, PharmaCtr Bonn, D-53121 Bonn, Germany Univ Bonn, Inst Pharmaceut, PharmaCtr Bonn, D-53121 Bonn, GermanyMueller, Christa E.论文数: 0 引用数: 0 h-index: 0机构: Univ Bonn, Inst Pharmaceut, PharmaCtr Bonn, D-53121 Bonn, Germany Univ Bonn, Inst Pharmaceut, PharmaCtr Bonn, D-53121 Bonn, Germany
- [5] Biaryl and heteroaryl derivatives of SCH 58261 as potent and selective adenosine A2A receptor antagonists[J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2008, 18 (14) : 4199 - 4203Shah, Unmesh论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USA Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USABoyle, Craig D.论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USA Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USAChackalamannil, Samuel论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USA Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USANeustadt, Bernard R.论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USA Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USALindo, Neil论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USA Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USAGreenlee, William J.论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USA Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USAFoster, Carolyn论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USA Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USAArik, Leyla论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USA Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USAZhai, Ying论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USA Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USANg, Kwokei论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USA Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USAWang, Shiyong论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USA Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USAMonopoli, Angela论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USA Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USALachowicz, Jean E.论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USA Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USA
- [6] Isoquinoline Derivatives as Potent, Selective, and Orally Active CRTH2 Antagonists[J]. CHEMICAL & PHARMACEUTICAL BULLETIN, 2014, 62 (06) : 528 - 537Nishikawa-Shimono, Rie论文数: 0 引用数: 0 h-index: 0机构: Taisho Pharmaceut Co Ltd, Med Chem Labs, Kita Ku, Saitama 3319530, Japan Taisho Pharmaceut Co Ltd, Med Chem Labs, Kita Ku, Saitama 3319530, JapanSekiguchi, Yoshinori论文数: 0 引用数: 0 h-index: 0机构: Taisho Pharmaceut Co Ltd, Med Chem Labs, Kita Ku, Saitama 3319530, Japan Taisho Pharmaceut Co Ltd, Med Chem Labs, Kita Ku, Saitama 3319530, JapanKawamura, Madoka论文数: 0 引用数: 0 h-index: 0机构: Taisho Pharmaceut Co Ltd, Med Chem Labs, Kita Ku, Saitama 3319530, Japan Taisho Pharmaceut Co Ltd, Med Chem Labs, Kita Ku, Saitama 3319530, JapanWakasugi, Daisuke论文数: 0 引用数: 0 h-index: 0机构: Taisho Pharmaceut Co Ltd, Med Chem Labs, Kita Ku, Saitama 3319530, Japan Taisho Pharmaceut Co Ltd, Med Chem Labs, Kita Ku, Saitama 3319530, JapanKawanishi, Masahumi论文数: 0 引用数: 0 h-index: 0机构: Taisho Pharmaceut Co Ltd, Mol Funct & Pharmacol Labs, Kita Ku, Saitama 3319530, Japan Taisho Pharmaceut Co Ltd, Med Chem Labs, Kita Ku, Saitama 3319530, JapanWatanabe, Kazuhito论文数: 0 引用数: 0 h-index: 0机构: Taisho Pharmaceut Co Ltd, Mol Funct & Pharmacol Labs, Kita Ku, Saitama 3319530, Japan Taisho Pharmaceut Co Ltd, Med Chem Labs, Kita Ku, Saitama 3319530, JapanAsakura, Yumiko论文数: 0 引用数: 0 h-index: 0机构: Taisho Pharmaceut Co Ltd, Mol Funct & Pharmacol Labs, Kita Ku, Saitama 3319530, Japan Taisho Pharmaceut Co Ltd, Med Chem Labs, Kita Ku, Saitama 3319530, JapanTakaoka, Akiko论文数: 0 引用数: 0 h-index: 0机构: Taisho Pharmaceut Co Ltd, Mol Funct & Pharmacol Labs, Kita Ku, Saitama 3319530, Japan Taisho Pharmaceut Co Ltd, Med Chem Labs, Kita Ku, Saitama 3319530, JapanTakayama, Tetsuo论文数: 0 引用数: 0 h-index: 0机构: Taisho Pharmaceut Co Ltd, Med Chem Labs, Kita Ku, Saitama 3319530, Japan Taisho Pharmaceut Co Ltd, Med Chem Labs, Kita Ku, Saitama 3319530, Japan
- [7] POTENT, SELECTIVE, AND ORALLY ACTIVE CRTH2 ANTAGONISTS FOR ALLERGIC DISEASE[J]. INFLAMMATION RESEARCH, 2011, 60 : 284 - 284Burgess, L.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USAEberhardt, C.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USAWright, D.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USACook, A.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USACorrette, C.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USAHunt, K.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USAClark, C.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USARomoff, T.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USAKim, G.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USAMiknis, G.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USABoys, M.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USAKraser, C.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USAMoreno, D.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USADelisle, K.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USAGomez, A.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USAHayter, L.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USANeale, J.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USAGustafson, C.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USARhodes, S.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USAHingorani, G.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USAHartley, D.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USADoherty, G.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USAChantry, D.论文数: 0 引用数: 0 h-index: 0机构: ARRAY BIOPHARMA, Boulder, CO USA ARRAY BIOPHARMA, Boulder, CO USA
- [8] Novel triazolopyrazine, triazolopyrimidine, and triazolotriazine derivatives as potent and selective adenosine A2a receptor antagonists[J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2006, 231Kumaravel, Gnanasambandam论文数: 0 引用数: 0 h-index: 0机构: Biogen Idec, Cambridge Ctr 14, Dept Med Chem, Cambridge, MA 02142 USAEngber, Thomas论文数: 0 引用数: 0 h-index: 0机构: Biogen Idec, Cambridge Ctr 14, Dept Med Chem, Cambridge, MA 02142 USAVu, Chi B.论文数: 0 引用数: 0 h-index: 0机构: Biogen Idec, Cambridge Ctr 14, Dept Med Chem, Cambridge, MA 02142 USAPeng, Hairuo论文数: 0 引用数: 0 h-index: 0机构: Biogen Idec, Cambridge Ctr 14, Dept Med Chem, Cambridge, MA 02142 USADowling, James E.论文数: 0 引用数: 0 h-index: 0机构: Biogen Idec, Cambridge Ctr 14, Dept Med Chem, Cambridge, MA 02142 USAYao, Gang论文数: 0 引用数: 0 h-index: 0机构: Biogen Idec, Cambridge Ctr 14, Dept Med Chem, Cambridge, MA 02142 USAVessels, Jeffery T.论文数: 0 引用数: 0 h-index: 0机构: Biogen Idec, Cambridge Ctr 14, Dept Med Chem, Cambridge, MA 02142 USAScott, Daniel论文数: 0 引用数: 0 h-index: 0机构: Biogen Idec, Cambridge Ctr 14, Dept Med Chem, Cambridge, MA 02142 USAPetter, Russell C.论文数: 0 引用数: 0 h-index: 0机构: Biogen Idec, Cambridge Ctr 14, Dept Med Chem, Cambridge, MA 02142 USA
- [9] Biaryl and heteroaryl derivatives of SCH 58261 as potent and selective adenosine A2A receptor antagonists[J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2005, 230 : U2549 - U2550Shah, U论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, CNS CV Chem Res, Kenilworth, NJ 07033 USABoyle, CD论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, CNS CV Chem Res, Kenilworth, NJ 07033 USAChackalamannil, S论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, CNS CV Chem Res, Kenilworth, NJ 07033 USANeustadt, B论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, CNS CV Chem Res, Kenilworth, NJ 07033 USAFoster, C论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, CNS CV Chem Res, Kenilworth, NJ 07033 USAArik, L论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, CNS CV Chem Res, Kenilworth, NJ 07033 USAZhai, Y论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, CNS CV Chem Res, Kenilworth, NJ 07033 USALachowicz, JE论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, CNS CV Chem Res, Kenilworth, NJ 07033 USANg, K论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, CNS CV Chem Res, Kenilworth, NJ 07033 USAShiyong, W论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, CNS CV Chem Res, Kenilworth, NJ 07033 USAMonopoli, A论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, CNS CV Chem Res, Kenilworth, NJ 07033 USAOngini, E论文数: 0 引用数: 0 h-index: 0机构: Schering Plough Corp, CNS CV Chem Res, Kenilworth, NJ 07033 USA
- [10] Synthesis and SAR studies of trisubstituted purinones as potent and selective adenosine A2A receptor antagonists[J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2009, 19 (05) : 1399 - 1402Shao, Yuefei论文数: 0 引用数: 0 h-index: 0机构: Pharmacopeia Inc, Princeton, NJ 08543 USA Pharmacopeia Inc, Princeton, NJ 08543 USACole, Andrew G.论文数: 0 引用数: 0 h-index: 0机构: Pharmacopeia Inc, Princeton, NJ 08543 USA Pharmacopeia Inc, Princeton, NJ 08543 USABrescia, Marc-Raleigh论文数: 0 引用数: 0 h-index: 0机构: Pharmacopeia Inc, Princeton, NJ 08543 USA Pharmacopeia Inc, Princeton, NJ 08543 USAQin, Lan-Ying论文数: 0 引用数: 0 h-index: 0机构: Pharmacopeia Inc, Princeton, NJ 08543 USA Pharmacopeia Inc, Princeton, NJ 08543 USADuo, Jingqi论文数: 0 引用数: 0 h-index: 0机构: Pharmacopeia Inc, Princeton, NJ 08543 USA Pharmacopeia Inc, Princeton, NJ 08543 USAStauffer, Tara M.论文数: 0 引用数: 0 h-index: 0机构: Pharmacopeia Inc, Princeton, NJ 08543 USA Pharmacopeia Inc, Princeton, NJ 08543 USARokosz, Laura L.论文数: 0 引用数: 0 h-index: 0机构: Pharmacopeia Inc, Princeton, NJ 08543 USA Pharmacopeia Inc, Princeton, NJ 08543 USAMcGuinness, Brian F.论文数: 0 引用数: 0 h-index: 0机构: Pharmacopeia Inc, Princeton, NJ 08543 USA Pharmacopeia Inc, Princeton, NJ 08543 USAHenderson, Ian论文数: 0 引用数: 0 h-index: 0机构: Pharmacopeia Inc, Princeton, NJ 08543 USA Pharmacopeia Inc, Princeton, NJ 08543 USA