Citation: ZENG Ling-Xiao, LI Xin-Ran, JIN Hong-Wei, LIU Zhen-Ming, ZHANG Liang-Ren. Comparison of the Selectivity of Human Adenosine Receptor Anta nists Based on Structure and Pharmacophore Features[J]. Acta Physico-Chimica Sinica, ;2015, 31(8): 1584-1596. doi: 10.3866/PKU.WHXB201505253 shu

Comparison of the Selectivity of Human Adenosine Receptor Anta nists Based on Structure and Pharmacophore Features

  • Received Date: 17 April 2015
    Available Online: 25 May 2015

    Fund Project: 国家自然科学基金(21272017) (21272017)教育部博士点基金(20090001120049)资助项目 (20090001120049)

  • Adenosine receptors (ARs) are crucial therapeutic targets, and selective adenosine receptor anta nists are promising for numerous therapeutic applications. In this study, three dimensional models of human adenosine A1, A2B, and A3 receptors (A1AR, A2BAR, A3AR, respectively) were generated by homology modeling. In addition, pharmacophore models of the anta nists of four human adenosine receptor subtypes were developed using the LigandScout 3.12 program. Furthermore, Induced Fit Docking module of Schrödinger program was implemented to investigate receptor-ligand interactions. The results show that because of the subfamily-wide conservation of the core pocket residues, the ligand binding pockets of the three raw AR homology models are extremely similar, which poses challenges for subtype selective ligand recognition. However, the pharmacophore models of the four AR subtypes differ in pharmacophore features and spatial configuration, which are also consistent with previous site-directed mutagenesis studies. This indicates that binding site optimization is a crucial step in model generation, and the distributions for a set of pharmacophore features in ligand-based pharmacophore, including hydrogen bond acceptors, hydrogen bond donors, hydrophobic centroids, and aromatic rings, can reflect the position and direction characterization of hydrogen bonds and hydrophobic cavities, which aid identification and characterization of binding sites. This study may provide a significant theoretical foundation for further raw model optimization in homology modeling and discovery of novel selective human adenosine receptor anta nists.

  • 加载中
    1. [1]

      (1) Krishnan, A.; Almen, M. S.; Fredriksson, R.; Schioth, H. B. PLoS One 2012, 7 (1), e29817.

    2. [2]

      (2) Lappano, R.; Maggiolini, M. Nat. Rev. Drug Discov. 2011, 10 (1), 47. doi: 10.1038/nrd3320

    3. [3]

      (3) Liang, F.; Yue, J.; Wang, J.; Zhang, L.; Fan, R.; Zhang, H.; Zhang, Q. Med. Oncol. 2015, 32 (3), 49. doi: 10.1007/s12032-015-0486-1

    4. [4]

      (4) Overington, J. P.; Al-Lazikani, B.; Hopkins, A. L. Nat. Rev. Drug Discov. 2006, 5 (12), 993. doi: 10.1038/nrd2199

    5. [5]

      (5) Chen, J. F.; Eltzschig, H. K.; Fredholm, B. B. Nat. Rev. Drug Discov. 2013, 12 (4), 265. doi: 10.1038/nrd3955

    6. [6]

      (6) Ke, Y. R.; Jin, H. W.; Liu, Z. M.; Zhang, L. R. Acta Phys. -Chim. Sin. 2010, 26 (10), 2833. [柯艳蓉, 金宏威, 刘振明, 张亮仁. 物理化学学报, 2010, 26 (10), 2833.] doi: 10.3866/PKU.WHXB20100916

    7. [7]

      (7) Robeva, A. S.; Woodard, R. L.; Jin, X.; Gao, Z.; Bhattacharya, S.; Taylor, H. E.; Rosin, D. L.; Linden, J. Drug Develop. Res. 1996, 39 (3-4), 243.

    8. [8]

      (8) Fredholm, B. B.; AP, I. J.; Jacobson, K. A.; Klotz, K. N.; Linden, J. Pharmacol. Rev. 2001, 53 (4), 527.

    9. [9]

      (9) Jacobson, K. A.; Gao, Z. G. Nat. Rev. Drug Discov. 2006, 5 (3), 247. doi: 10.1038/nrd1983

    10. [10]

      (10) Sliwoski, G.; Kothiwale, S.; Meiler, J.; Lowe, E. W., Jr. Pharmacol. Rev. 2014, 66 (1), 334.

    11. [11]

      (11) Congreve, M.; Langmead, C. J.; Mason, J. S.; Marshall, F. H. J. Med. Chem. 2011, 54 (13), 4283. doi: 10.1021/jm200371q

    12. [12]

      (12) Costanzi, S. Methods Mol. Biol. 2012, 857, 259.

    13. [13]

      (13) Katritch, V.; Kufareva, I.; Abagyan, R. Neuropharmacology 2011, 60 (1), 108. doi: 10.1016/j.neuropharm.2010.07.009

    14. [14]

      (14) Güner, O. F. Pharmacophore Perception, Development, and Use in Drug Design; International University Line: San Die , 2000; Vol. 2.

    15. [15]

      (15) Khedkar, S. A.; Malde, A. K.; Coutinho, E. C.; Srivastava, S. Med. Chem. 2007, 3 (2), 187. doi: 10.2174/157340607780059521

    16. [16]

      (16) Liu, W.; Chun, E.; Thompson, A. A.; Chubukov, P.; Xu, F.; Katritch, V.; Han, G. W.; Roth, C. B.; Heitman, L. H.; Ijzerman, A P.; Cherezov, V.; Stevens, R. C. Science 2012, 337 (6091), 232. doi: 10.1126/science.1219218

    17. [17]

      (17) Boeckmann, B.; Bairoch, A.; Apweiler, R.; Blatter, M. C.; Estreicher, A.; Gasteiger, E.; Martin, M. J.; Michoud, K.; O'Donovan, C.; Phan, I.; Pilbout, S.; Schneider, M.Nucleic. Acids Res. 2003, 31 (1), 365. doi: 10.1093/nar/gkg095

    18. [18]

      (18) Discovery Studio 2.5, Release 2.5; Accelrys Software Inc.: San Die , 2009.

    19. [19]

      (19) Laskowski, R. A.; MacArthur, M. W.; Moss, D. S.; Thornton, J. M. J. Appl. Cystallogr. 1993, 26, 283. doi: 10.1107/S0021889892009944

    20. [20]

      (20) Lin, K. J.; Zhu, D. J.; Leng, Y. G.; You, Q. D. Acta Phys. -Chim. Sin. 2012, 28 (7), 1783. [林克江, 朱冬吉, 冷勇敢, 尤启冬. 物理化学学报, 2012, 28 (7), 1783.] doi: 10.3866/PKU.WHXB201204192

    21. [21]

      (21) Gaulton, A.; Bellis, L. J.; Bento, A. P.; Chambers, J.; Davies, M.; Hersey, A.; Light, Y.; McGlinchey, S.; Michalovich, D.; Al-Lazikani, B.; Overington, J. P. Nucleic. Acids Res. 2012, 40 (Database issue), D1100.

    22. [22]

      (22) Xia, J.; Jin, H.; Liu, Z.; Zhang, L.; Wang, X. S. J. Chem. Inf. Model. 2014, 54 (5), 1433. doi: 10.1021/ci500062f

    23. [23]

      (23) Xia, J.; Tilahun, E. L.; Reid, T. E.; Zhang, L.; Wang, X. S. Methods 2015, 71, 146. doi: 10.1016/j.ymeth.2014.11.015

    24. [24]

      (24) Qiao, K.; Zeng, L. X.; Jin, H. W.; Liu, Z. M.; Zhang, L. R. Acta Phys. -Chim. Sin. 2012, 28 (6), 1509. [乔康, 曾凌晓, 金宏威, 刘振明, 张亮仁. 物理化学学报, 2012, 28(6), 1509.] doi: 10.3866/PKU. WHXB201203272

    25. [25]

      (25) Wolber, G.; Langer, T. J. Chem. Inf. Model. 2005, 45 (1), 160. doi: 10.1021/ci049885e

    26. [26]

      (26) Schrödinger Suite 2013; Schrödinger, LLC: New York, 2013.

    27. [27]

      (27) Ballesteros, J. A.; Weinstein, H. Methods Neurosci. 1995, 25, 366.

    28. [28]

      (28) Kiesman, W. F.; Zhao, J.; Conlon, P. R.; Dowling, J. E.; Petter, R. C.; Lutterodt, F.; Jin, X.; Smits, G.; Fure, M.; Jayaraj, A.; Kim, J.; Sullivan, G.; Linden, J. J. Med. Chem. 2006, 49 (24), 7119.

    29. [29]

      (29) Giovannoni, M. P.; Vergelli, C.; Cilibrizzi, A.; Crocetti, L.; Biancalani, C.; Graziano, A.; Dal Piaz, V.; Loza, M. I.; Cadavid, M. I.; Diaz, J. L.; Gavalda, A. Bioorg. Med. Chem. 2010, 18 (22), 7890. doi: 10.1016/j.bmc.2010.09.043

    30. [30]

      (30) Chang, L. C.; Kuenzel, J. V.; Mulder-Krieger, T.; Westerhout, J.; Spangenberg, T.; Brussee, J.; Ijzerman, A. P. J. Med. Chem. 2007, 50 (4), 828. doi: 10.1021/jm0607956

    31. [31]

      (31) Scheiff, A. B.; Yerande, S. G.; El-Tayeb, A.; Li, W.; Inamdar, G. S.; Vasu, K. K.; Sudarsanam, V.; Muller, C. E. Bioorg. Med. Chem. 2010, 18 (6), 2195. doi: 10.1016/j.bmc. 2010.01.072

    32. [32]

      (32) Novellino, E.; Cosimelli, B.; Ehlardo, M.; Greco, G.; Iadanza, M.; Lavecchia, A.; Rimoli, M. G.; Sala, A.; Da Settimo, A.; Primofiore, G.; Da Settimo, F.; Taliani, S.; La Motta, C.; Klotz, K. N.; Tuscano, D.; Trincavelli, M. L.; Martini, C. J. Med. Chem. 2005, 48 (26), 8253.

    33. [33]

      (33) Mishra, C. B.; Barodia, S. K.; Prakash, A.; Kumar, J. B. S.; Luthra, P. M. Bioorg. Med. Chem. 2010, 18 (7), 2491. doi: 10.1016/j.bmc.2010.02.048

    34. [34]

      (34) Moorjani, M.; Zhang, X.; Chen, Y.; Lin, E.; Rueter, J. K.; Gross, R. S.; Lanier, M. C.; Tellew, J. E.; Williams, J. P.; Lechner, S. M.; Malany, S.; Santos, M.; Ekhlassi, P.; Castro-Palomino, J. C.; Crespo, M. I.; Prat, M.; Gual, S.; Diaz, J. L.; Saunders, J.; Slee, D. H. Bioorg. Med. Chem. Lett. 2008, 18 (4), 1269. doi: 10.1016/j.bmcl.2008.01.036

    35. [35]

      (35) Gillespie, R. J.; Cliffe, I. A.; Dawson, C. E.; Dourish, C. T.; Gaur, S.; Jordan, A. M.; Knight, A. R.; Lerpiniere, J.; Misra, A.; Pratt, R. M.; Roffey, J.; Stratton, G. C.; Upton, R.; Weiss, S. M.; Williamson, D. S. Bioorg. Med. Chem. Lett. 2008, 18 (9), 2924. doi: 10.1016/j.bmcl.2008.03.072

    36. [36]

      (36) Gillespie, R. J.; Cliffe, I. A.; Dawson, C. E.; Dourish, C. T.; Gaur, S.; Giles, P. R.; Jordan, A. M.; Knight, A. R.; Lawrence, A.; Lerpiniere, J.; Misra, A.; Pratt, R. M.; Todd, R. S.; Upton, R.; Weiss, S. M.; Williamson, D. S. Bioorg. Med. Chem. Lett. 2008, 18 (9), 2920. doi: 10.1016/j.bmcl.2008.03.076

    37. [37]

      (37) Gillespie, R. J.; Bamford, S. J.; Clay, A.; Gaur, S.; Haymes, T.; Jackson, P. S.; Jordan, A. M.; Klenke, B.; Leonardi, S.; Liu, J.; Mansell, H. L.; Ng, S.; Saadi, M.; Simmonite, H.; Stratton, G. C.; Todd, R. S.; Williamson, D. S.; Yule, I. A. Bioorg. Med. Chem. 2009, 17 (18), 6590. doi: 10.1016/j.bmc.2009.07.078

    38. [38]

      (38) Silverman, L. S.; Caldwell, J. P.; Greenlee, W. J.; Kisel f, E.; Matasi, J. J.; Tulshian, D. B.; Arik, L.; Foster, C.; Bertorelli, R.; Monopoli, A.; Ongini, E. Bioorg. Med. Chem. Lett. 2007, 17 (6), 1659. doi: 10.1016/j.bmcl.2006.12.104

    39. [39]

      (39) Firooznia, F.; Cheung, A. W.; Brinkman, J.; Grimsby, J.; Gubler, M. L.; Hamid, R.; Marcopulos, N.; Ramsey, G.; Tan, J.; Wen, Y.; Sarabu, R. Bioorg. Med. Chem. Lett. 2011, 21 (7), 1933. doi: 10.1016/j.bmcl.2011.02.053

    40. [40]

      (40) Cheung, A. W.; Brinkman, J.; Firooznia, F.; Flohr, A.; Grimsby, J.; Gubler, M. L.; Guertin, K.; Hamid, R.; Marcopulos, N.; Norcross, R. D.; Qi, L.; Ramsey, G.; Tan, J.; Wen, Y.; Sarabu, R. Bioorg. Med. Chem. Lett. 2010, 20 (14), 4140. doi: 10.1016/j.bmcl.2010.05.056

    41. [41]

      (41) Kalla, R. V.; Elzein, E.; Perry, T.; Li, X.; Palle, V.; Varkhedkar, V.; Gimbel, A.; Maa, T.; Zeng, D.; Zablocki, J. J. Med. Chem. 2006, 49 (12), 3682. doi: 10.1021/jm051268+

    42. [42]

      (42) Kim, Y. C.; Ji, X.; Melman, N.; Linden, J.; Jacobson, K. A. J. Med. Chem. 2000, 43 (6), 1165. doi: 10.1021/jm990421v

    43. [43]

      (43) Stefanachi, A.; Nicolotti, O.; Leonetti, F.; Cellamare, S.; Campagna, F.; Loza, M. I.; Brea, J. M.; Mazza, F.; Gavuzzo, E.; Carotti, A. Bioorg. Med. Chem. 2008, 16 (22), 9780. doi: 10.1016/j.bmc.2008.09.067

    44. [44]

      (44) Da Settimo, F.; Primofiore, G.; Taliani, S.; Marini, A. M.; La Motta, C.; Simorini, F.; Salerno, S.; Sergianni, V.; Tuccinardi, T.; Martinelli, A.; Cosimelli, B.; Greco, G.; Novellino, E.; Ciampi, O.; Trincavelli, M. L.; Martini, C. J. Med. Chem. 2007, 50 (23), 5676. doi: 10.1021/jm0708376

    45. [45]

      (45) Prie , E. M.; Kuenzel, J. V.; Ijzerman, A. P.; Camarasa, M. J.; Perez-Perez, M. J. J. Med. Chem. 2002, 45 (16), 3337. doi: 10.1021/jm0208469

    46. [46]

      (46) Melman, A.; Wang, B.; Joshi, B. V.; Gao, Z. G.; Castro, S.; Heller, C. L.; Kim, S. K.; Jeong, L. S.; Jacobson, K. A. Bioorg. Med. Chem. 2008, 16 (18), 8546. doi: 10.1016/j.bmc.2008.08.007

    47. [47]

      (47) Baraldi, P. G.; Cacciari, B.; Moro, S.; Spalluto, G.; Pastorin, G.; Da Ros, T.; Klotz, K. N.; Varani, K.; Gessi, S.; Borea, P. A. J. Med. Chem. 2002, 45 (4), 770. doi: 10.1021/jm0109614

    48. [48]

      (48) Colotta, V.; Catarzi, D.; Varano, F.; Capelli, F.; Lenzi, O.; Filacchioni, G.; Martini, C.; Trincavelli, L.; Ciampi, O.; Pugliese, A. M.; Pedata, F.; Schiesaro, A.; Morizzo, E.; Moro, S. J. Med. Chem. 2007, 50 (17), 4061. doi: 10.1021/jm070123v

    49. [49]

      (49) Jaakola, V. P.; Griffith, M. T.; Hanson, M. A.; Cherezov, V.; Chien, E. Y.; Lane, J. R.; Ijzerman, A. P.; Stevens, R. C. Science 2008, 322 (5905), 1211. doi: 10.1126/science.1164772

    50. [50]

      (50) Olah, M. E.; Ren, H.; Ostrowski, J.; Jacobson, K. A.; Stiles, G. L. J. Biol. Chem. 1992, 267 (15), 10764.

    51. [51]

      (51) Rivkees, S. A.; Barbhaiya, H.; Ijzerman, A. P. J. Biol. Chem. 1999, 274 (6), 3617. doi: 10.1074/jbc.274.6.3617

    52. [52]

      (52) Jaakola, V. P.; Lane, J. R.; Lin, J. Y.; Katritch, V.; Ijzerman, A. P.; Stevens, R. C. J. Biol. Chem. 2010, 285 (17), 13032. doi: 10.1074/jbc.M109.096974

    53. [53]

      (53) Cheng, F.; Xu, Z.; Liu, G.; Tang, Y. Eur. J. Med. Chem. 2010, 45 (8), 3459. doi: 10.1016/j.ejmech.2010.04.039

    54. [54]

      (54) Thimm, D.; Schiedel, A. C.; Sherbiny, F. F.; Hinz, S.; Hochheiser, K.; Bertarelli, D. C.; Maass, A.; Muller, C. E. Biochemistry-US 2013, 52 (4), 726. doi: 10.1021/bi3012065

    55. [55]

      (55) Ivanov, A. A.; Baskin, II.; Palyulin, V. A.; Piccagli, L.; Baraldi, P. G.; Zefirov, N. S. J. Med. Chem. 2005, 48 (22), 6813. doi: 10.1021/jm049418o

    56. [56]

      (56) Gao, Z. G.; Kim, S. K.; Biadatti, T.; Chen, W.; Lee, K.; Barak, D.; Kim, S. G.; Johnson, C. R.; Jacobson, K. A. J. Med. Chem. 2002, 45 (20), 4471. doi: 10.1021/jm020211+

    57. [57]

      (57) Muller, C. E.; Jacobson, K. A. BBA-Biomembranes 2011, 1808 (5), 1290. doi: 10.1016/j.bbamem.2010.12.017


  • 加载中
    1. [1]

      Weihan Zhang Menglu Wang Ankang Jia Wei Deng Shuxing Bai . 表面硫物种对钯-硫纳米片加氢性能的影响. Acta Physico-Chimica Sinica, 2024, 40(11): 2309043-. doi: 10.3866/PKU.WHXB202309043

    2. [2]

      Shihui Shi Haoyu Li Shaojie Han Yifan Yao Siqi Liu . Regioselectively Synthesis of Halogenated Arenes via Self-Assembly and Synergistic Catalysis Strategy. University Chemistry, 2024, 39(5): 336-344. doi: 10.3866/PKU.DXHX202312002

    3. [3]

      Yunhao Zhang Yinuo Wang Siran Wang Dazhen Xu . Progress in Selective Construction of Functional Aromatics from Nitrogenous Cycloalkanes. University Chemistry, 2024, 39(11): 136-145. doi: 10.3866/PKU.DXHX202401083

    4. [4]

      Peiran ZHAOYuqian LIUCheng HEChunying DUAN . A functionalized Eu3+ metal-organic framework for selective fluorescent detection of pyrene. Chinese Journal of Inorganic Chemistry, 2024, 40(4): 713-724. doi: 10.11862/CJIC.20230355

    5. [5]

      Xilin Zhao Xingyu Tu Zongxuan Li Rui Dong Bo Jiang Zhiwei Miao . Research Progress in Enantioselective Synthesis of Axial Chiral Compounds. University Chemistry, 2024, 39(11): 158-173. doi: 10.12461/PKU.DXHX202403106

    6. [6]

      Jiakun BAITing XULu ZHANGJiang PENGYuqiang LIJunhui JIA . A red-emitting fluorescent probe with a large Stokes shift for selective detection of hypochlorous acid. Chinese Journal of Inorganic Chemistry, 2024, 40(6): 1095-1104. doi: 10.11862/CJIC.20240002

    7. [7]

      Jie ZHAOSen LIUQikang YINXiaoqing LUZhaojie WANG . Theoretical calculation of selective adsorption and separation of CO2 by alkali metal modified naphthalene/naphthalenediyne. Chinese Journal of Inorganic Chemistry, 2024, 40(3): 515-522. doi: 10.11862/CJIC.20230385

    8. [8]

      Junjie Zhang Yue Wang Qiuhan Wu Ruquan Shen Han Liu Xinhua Duan . Preparation and Selective Separation of Lightweight Magnetic Molecularly Imprinted Polymers for Trace Tetracycline Detection in Milk. University Chemistry, 2024, 39(5): 251-257. doi: 10.3866/PKU.DXHX202311084

    9. [9]

      Yinuo Wang Siran Wang Yilong Zhao Dazhen Xu . Selective Synthesis of Diarylmethyl Anilines and Triarylmethanes via Multicomponent Reactions: Introduce a Comprehensive Experiment of Organic Chemistry. University Chemistry, 2024, 39(8): 324-330. doi: 10.3866/PKU.DXHX202401063

    10. [10]

      Jingzhao Cheng Shiyu Gao Bei Cheng Kai Yang Wang Wang Shaowen Cao . 4-氨基-1H-咪唑-5-甲腈修饰供体-受体型氮化碳光催化剂的构建及其高效光催化产氢研究. Acta Physico-Chimica Sinica, 2024, 40(11): 2406026-. doi: 10.3866/PKU.WHXB202406026

    11. [11]

      Shuang Yang Qun Wang Caiqin Miao Ziqi Geng Xinran Li Yang Li Xiaohong Wu . Ideological and Political Education Design for Research-Oriented Experimental Course of Highly Efficient Hydrogen Production from Water Electrolysis in Aerospace Perspective. University Chemistry, 2024, 39(11): 269-277. doi: 10.12461/PKU.DXHX202403044

    12. [12]

      Huan LIShengyan WANGLong ZhangYue CAOXiaohan YANGZiliang WANGWenjuan ZHUWenlei ZHUYang ZHOU . Growth mechanisms and application potentials of magic-size clusters of groups Ⅱ-Ⅵ semiconductors. Chinese Journal of Inorganic Chemistry, 2024, 40(8): 1425-1441. doi: 10.11862/CJIC.20240088

    13. [13]

      Xinyu Zhu Meili Pang . Application of Functional Group Addition Strategy in Organic Synthesis. University Chemistry, 2024, 39(3): 218-230. doi: 10.3866/PKU.DXHX202308106

    14. [14]

      Danqing Wu Jiajun Liu Tianyu Li Dazhen Xu Zhiwei Miao . Research Progress on the Simultaneous Construction of C—O and C—X Bonds via 1,2-Difunctionalization of Olefins through Radical Pathways. University Chemistry, 2024, 39(11): 146-157. doi: 10.12461/PKU.DXHX202403087

    15. [15]

      Lei Shi . Nucleophilicity and Electrophilicity of Radicals. University Chemistry, 2024, 39(11): 131-135. doi: 10.3866/PKU.DXHX202402018

    16. [16]

      Zhao Lu Hu Lv Qinzhuang Liu Zhongliao Wang . Modulating NH2 Lewis Basicity in CTF-NH2 through Donor-Acceptor Groups for Optimizing Photocatalytic Water Splitting. Acta Physico-Chimica Sinica, 2024, 40(12): 2405005-. doi: 10.3866/PKU.WHXB202405005

    17. [17]

      Jin Tong Shuyan Yu . Crystal Engineering for Supramolecular Chirality. University Chemistry, 2024, 39(3): 86-93. doi: 10.3866/PKU.DXHX202308113

    18. [18]

      Yonghui ZHOURujun HUANGDongchao YAOAiwei ZHANGYuhang SUNZhujun CHENBaisong ZHUYouxuan ZHENG . Synthesis and photoelectric properties of fluorescence materials with electron donor-acceptor structures based on quinoxaline and pyridinopyrazine, carbazole, and diphenylamine derivatives. Chinese Journal of Inorganic Chemistry, 2024, 40(4): 701-712. doi: 10.11862/CJIC.20230373

    19. [19]

      Renxiao Liang Zhe Zhong Zhangling Jin Lijuan Shi Yixia Jia . A Palladium/Chiral Phosphoric Acid Relay Catalysis for the One-Pot Three-Step Synthesis of Chiral Tetrahydroquinoline. University Chemistry, 2024, 39(5): 209-217. doi: 10.3866/PKU.DXHX202311024

    20. [20]

      Wenlong LIXinyu JIAJie LINGMengdan MAAnning ZHOU . Photothermal catalytic CO2 hydrogenation over a Mg-doped In2O3-x catalyst. Chinese Journal of Inorganic Chemistry, 2024, 40(5): 919-929. doi: 10.11862/CJIC.20230421

Metrics
  • PDF Downloads(392)
  • Abstract views(418)
  • HTML views(7)

通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索
Address:Zhongguancun North First Street 2,100190 Beijing, PR China Tel: +86-010-82449177-888
Powered By info@rhhz.net

/

DownLoad:  Full-Size Img  PowerPoint
Return