酶抑制剂 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "酶抑制剂" in Chinese language version.

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20nih.gov

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19doi.org

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3web.archive.org

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3archive.org

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1elsevier.com

610^th place

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1ntu.edu.tw

2,798^th place

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1oregonstate.edu

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1jstor.org

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archive.org

Price N, Hames B, Rickwood D. Proteins LabFax. BIOS Scientific Publishers. 1996. ISBN 978-0-12-564710-6.
Loo JA, DeJohn DE, Du P, Stevenson TI, Ogorzalek Loo RR. Application of mass spectrometry for target identification and characterization. Medicinal Research Reviews. July 1999, 19 (4): 307–19. PMID 10398927. doi:10.1002/(SICI)1098-1128(199907)19:4<307::AID-MED4>3.0.CO;2-2.
Duke SO. Overview of herbicide mechanisms of action. Environmental Health Perspectives. July 1990, 87: 263–71. JSTOR 3431034. PMC 1567841 . PMID 1980104. doi:10.2307/3431034.

doi.org

Srinivasan B, Tonddast-Navaei S, Roy A, Zhou H, Skolnick J. Chemical space of Escherichia coli dihydrofolate reductase inhibitors: New approaches for discovering novel drugs for old bugs. Medicinal Research Reviews. September 2018. PMID 30192413. doi:10.1002/med.21538.
Srinivasan B, Tonddast-Navaei S, Skolnick J. Ligand binding studies, preliminary structure-activity relationship and detailed mechanistic characterization of 1-phenyl-6,6-dimethyl-1,3,5-triazine-2,4-diamine derivatives as inhibitors of Escherichia coli dihydrofolate reductase. European Journal of Medicinal Chemistry. October 2015, 103: 600–14 [2019-02-18]. PMC 4610388 . PMID 26414808. doi:10.1016/j.ejmech.2015.08.021. （原始内容存档于2020-10-01）.
Srinivasan B, Skolnick J. Insights into the slow-onset tight-binding inhibition of Escherichia coli dihydrofolate reductase: detailed mechanistic characterization of pyrrolo [3,2-f] quinazoline-1,3-diamine and its derivatives as novel tight-binding inhibitors. The FEBS Journal. May 2015, 282 (10): 1922–38. PMC 4445455 . PMID 25703118. doi:10.1111/febs.13244.
Srinivasan B, Rodrigues JV, Tonddast-Navaei S, Shakhnovich E, Skolnick J. Rational Design of Novel Allosteric Dihydrofolate Reductase Inhibitors Showing Antibacterial Effects on Drug-Resistant Escherichia coli Escape Variants. ACS Chemical Biology. July 2017, 12 (7): 1848–1857. PMC 5819740 . PMID 28525268. doi:10.1021/acschembio.7b00175 （英语）.
Srinivasan B, Rodrigues JV, Tonddast-Navaei S, Shakhnovich E, Skolnick J. Correction to Rational Design of Novel Allosteric Dihydrofolate Reductase Inhibitors Showing Antibacterial Effects on Drug-Resistant Escherichia coli Escape Variants. ACS Chemical Biology. May 2018, 13 (5): 1407. PMID 29688000. doi:10.1021/acschembio.7b00759.
Leatherbarrow, RJ. Using linear and non-linear regression to fit biochemical data. Trends in Biochemical Sciences. 1990, 15 (12): 455–8. PMID 2077683. doi:10.1016/0968-0004(90)90295-M （英语）.
Tseng, SJ; Hsu, JP. A comparison of the parameter estimating procedures for the Michaelis-Menten model. Journal of Theoretical Biology. 1990, 145 (4): 457–64. PMID 2246896. doi:10.1016/S0022-5193(05)80481-3.
Adam GC, Cravatt BF, Sorensen EJ. Profiling the specific reactivity of the proteome with non-directed activity-based probes. Chemistry & Biology. January 2001, 8 (1): 81–95. PMID 11182321. doi:10.1016/S1074-5521(00)90060-7.
Maurer T, Fung HL. Comparison of methods for analyzing kinetic data from mechanism-based enzyme inactivation: application to nitric oxide synthase. AAPS PharmSci. 2000, 2 (1): 68–77. PMC 2751003 . PMID 11741224. doi:10.1208/ps020108.
Loo JA, DeJohn DE, Du P, Stevenson TI, Ogorzalek Loo RR. Application of mass spectrometry for target identification and characterization. Medicinal Research Reviews. July 1999, 19 (4): 307–19. PMID 10398927. doi:10.1002/(SICI)1098-1128(199907)19:4<307::AID-MED4>3.0.CO;2-2.
Koppitz M, Eis K; Eis. Automated medicinal chemistry. Drug Discov. Today. 2006, 11 (11–12): 561–8. PMID 16713909. doi:10.1016/j.drudis.2006.04.005.
Scapin G. Structural biology and drug discovery. Curr. Pharm. Des. 2006, 12 (17): 2087–97. PMID 16796557. doi:10.2174/138161206777585201.
Gohlke H, Klebe G; Klebe. Approaches to the description and prediction of the binding affinity of small-molecule ligands to macromolecular receptors. Angew. Chem. Int. Ed. Engl. August 2002, 41 (15): 2644–76. PMID 12203463. doi:10.1002/1521-3773(20020802)41:15<2644::AID-ANIE2644>3.0.CO;2-O.
Maggi M, Filippi S, Ledda F, Magini A, Forti G. Erectile dysfunction: from biochemical pharmacology to advances in medical therapy. European Journal of Endocrinology. August 2000, 143 (2): 143–54. PMID 10913932. doi:10.1530/eje.0.1430143.
McGuire JJ. Anticancer antifolates: current status and future directions. Current Pharmaceutical Design. 2003, 9 (31): 2593–613. PMID 14529544. doi:10.2174/1381612033453712.
Katz AH, Caufield CE. Structure-based design approaches to cell wall biosynthesis inhibitors. Current Pharmaceutical Design. 2003, 9 (11): 857–66. PMID 12678870. doi:10.2174/1381612033455305.
Okar DA, Lange AJ. Fructose-2,6-bisphosphate and control of carbohydrate metabolism in eukaryotes. BioFactors. 1999, 10 (1): 1–14. PMID 10475585. doi:10.1002/biof.5520100101.
Tan S, Evans R, Singh B. Herbicidal inhibitors of amino acid biosynthesis and herbicide-tolerant crops. Amino Acids. March 2006, 30 (2): 195–204. PMID 16547651. doi:10.1007/s00726-005-0254-1.
Duke SO. Overview of herbicide mechanisms of action. Environmental Health Perspectives. July 1990, 87: 263–71. JSTOR 3431034. PMC 1567841 . PMID 1980104. doi:10.2307/3431034.

elsevier.com

linkinghub.elsevier.com

Srinivasan B, Tonddast-Navaei S, Skolnick J. Ligand binding studies, preliminary structure-activity relationship and detailed mechanistic characterization of 1-phenyl-6,6-dimethyl-1,3,5-triazine-2,4-diamine derivatives as inhibitors of Escherichia coli dihydrofolate reductase. European Journal of Medicinal Chemistry. October 2015, 103: 600–14 [2019-02-18]. PMC 4610388 . PMID 26414808. doi:10.1016/j.ejmech.2015.08.021. （原始内容存档于2020-10-01）.

jstor.org

Duke SO. Overview of herbicide mechanisms of action. Environmental Health Perspectives. July 1990, 87: 263–71. JSTOR 3431034. PMC 1567841 . PMID 1980104. doi:10.2307/3431034.

nih.gov

ncbi.nlm.nih.gov

Srinivasan B, Tonddast-Navaei S, Roy A, Zhou H, Skolnick J. Chemical space of Escherichia coli dihydrofolate reductase inhibitors: New approaches for discovering novel drugs for old bugs. Medicinal Research Reviews. September 2018. PMID 30192413. doi:10.1002/med.21538.
Srinivasan B, Tonddast-Navaei S, Skolnick J. Ligand binding studies, preliminary structure-activity relationship and detailed mechanistic characterization of 1-phenyl-6,6-dimethyl-1,3,5-triazine-2,4-diamine derivatives as inhibitors of Escherichia coli dihydrofolate reductase. European Journal of Medicinal Chemistry. October 2015, 103: 600–14 [2019-02-18]. PMC 4610388 . PMID 26414808. doi:10.1016/j.ejmech.2015.08.021. （原始内容存档于2020-10-01）.
Srinivasan B, Skolnick J. Insights into the slow-onset tight-binding inhibition of Escherichia coli dihydrofolate reductase: detailed mechanistic characterization of pyrrolo [3,2-f] quinazoline-1,3-diamine and its derivatives as novel tight-binding inhibitors. The FEBS Journal. May 2015, 282 (10): 1922–38. PMC 4445455 . PMID 25703118. doi:10.1111/febs.13244.
Srinivasan B, Rodrigues JV, Tonddast-Navaei S, Shakhnovich E, Skolnick J. Rational Design of Novel Allosteric Dihydrofolate Reductase Inhibitors Showing Antibacterial Effects on Drug-Resistant Escherichia coli Escape Variants. ACS Chemical Biology. July 2017, 12 (7): 1848–1857. PMC 5819740 . PMID 28525268. doi:10.1021/acschembio.7b00175 （英语）.
Srinivasan B, Rodrigues JV, Tonddast-Navaei S, Shakhnovich E, Skolnick J. Correction to Rational Design of Novel Allosteric Dihydrofolate Reductase Inhibitors Showing Antibacterial Effects on Drug-Resistant Escherichia coli Escape Variants. ACS Chemical Biology. May 2018, 13 (5): 1407. PMID 29688000. doi:10.1021/acschembio.7b00759.
Holdgate, GA. Making cool drugs hot: isothermal titration calorimetry as a tool to study binding energetics. BioTechniques. 2001, 31 (1): 164–6, 168, 170 passim. PMID 11464510 （英语）.
Leatherbarrow, RJ. Using linear and non-linear regression to fit biochemical data. Trends in Biochemical Sciences. 1990, 15 (12): 455–8. PMID 2077683. doi:10.1016/0968-0004(90)90295-M （英语）.
Tseng, SJ; Hsu, JP. A comparison of the parameter estimating procedures for the Michaelis-Menten model. Journal of Theoretical Biology. 1990, 145 (4): 457–64. PMID 2246896. doi:10.1016/S0022-5193(05)80481-3.
Adam GC, Cravatt BF, Sorensen EJ. Profiling the specific reactivity of the proteome with non-directed activity-based probes. Chemistry & Biology. January 2001, 8 (1): 81–95. PMID 11182321. doi:10.1016/S1074-5521(00)90060-7.
Maurer T, Fung HL. Comparison of methods for analyzing kinetic data from mechanism-based enzyme inactivation: application to nitric oxide synthase. AAPS PharmSci. 2000, 2 (1): 68–77. PMC 2751003 . PMID 11741224. doi:10.1208/ps020108.
Loo JA, DeJohn DE, Du P, Stevenson TI, Ogorzalek Loo RR. Application of mass spectrometry for target identification and characterization. Medicinal Research Reviews. July 1999, 19 (4): 307–19. PMID 10398927. doi:10.1002/(SICI)1098-1128(199907)19:4<307::AID-MED4>3.0.CO;2-2.
Koppitz M, Eis K; Eis. Automated medicinal chemistry. Drug Discov. Today. 2006, 11 (11–12): 561–8. PMID 16713909. doi:10.1016/j.drudis.2006.04.005.
Scapin G. Structural biology and drug discovery. Curr. Pharm. Des. 2006, 12 (17): 2087–97. PMID 16796557. doi:10.2174/138161206777585201.
Gohlke H, Klebe G; Klebe. Approaches to the description and prediction of the binding affinity of small-molecule ligands to macromolecular receptors. Angew. Chem. Int. Ed. Engl. August 2002, 41 (15): 2644–76. PMID 12203463. doi:10.1002/1521-3773(20020802)41:15<2644::AID-ANIE2644>3.0.CO;2-O.
Maggi M, Filippi S, Ledda F, Magini A, Forti G. Erectile dysfunction: from biochemical pharmacology to advances in medical therapy. European Journal of Endocrinology. August 2000, 143 (2): 143–54. PMID 10913932. doi:10.1530/eje.0.1430143.
McGuire JJ. Anticancer antifolates: current status and future directions. Current Pharmaceutical Design. 2003, 9 (31): 2593–613. PMID 14529544. doi:10.2174/1381612033453712.
Katz AH, Caufield CE. Structure-based design approaches to cell wall biosynthesis inhibitors. Current Pharmaceutical Design. 2003, 9 (11): 857–66. PMID 12678870. doi:10.2174/1381612033455305.
Okar DA, Lange AJ. Fructose-2,6-bisphosphate and control of carbohydrate metabolism in eukaryotes. BioFactors. 1999, 10 (1): 1–14. PMID 10475585. doi:10.1002/biof.5520100101.
Tan S, Evans R, Singh B. Herbicidal inhibitors of amino acid biosynthesis and herbicide-tolerant crops. Amino Acids. March 2006, 30 (2): 195–204. PMID 16547651. doi:10.1007/s00726-005-0254-1.
Duke SO. Overview of herbicide mechanisms of action. Environmental Health Perspectives. July 1990, 87: 263–71. JSTOR 3431034. PMC 1567841 . PMID 1980104. doi:10.2307/3431034.

ntu.edu.tw

juang.bst.ntu.edu.tw

Enzyme 3,4. [2018-08-27]. （原始内容存档于2021-04-13）.

oregonstate.edu

BB 450 Oregon State University. [2018-08-27]. （原始内容存档于2020-10-01）（英语）.

web.archive.org

Srinivasan B, Tonddast-Navaei S, Skolnick J. Ligand binding studies, preliminary structure-activity relationship and detailed mechanistic characterization of 1-phenyl-6,6-dimethyl-1,3,5-triazine-2,4-diamine derivatives as inhibitors of Escherichia coli dihydrofolate reductase. European Journal of Medicinal Chemistry. October 2015, 103: 600–14 [2019-02-18]. PMC 4610388 . PMID 26414808. doi:10.1016/j.ejmech.2015.08.021. （原始内容存档于2020-10-01）.
Enzyme 3,4. [2018-08-27]. （原始内容存档于2021-04-13）.
BB 450 Oregon State University. [2018-08-27]. （原始内容存档于2020-10-01）（英语）.