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Pyrrole-3-carboxylic acid | CAS:931-03-3
Pyrrole-3-carboxylic acid
  • 名称:3-吡咯羧酸; 吡咯-3-甲酸 | Pyrrole-3-carboxylic acid
  • CAS号:931-03-3
  • 别名:1H-Pyrrole-3-carboxylic acid
  • 分子式:C5H5NO2
  • 分子量:111.10
  • EINESC号:

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物理化学性质

熔点 209 ºC

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N2-hydroxyguanosine 5'-monophosphate is a time-dependent inhibitor of Escherichia coli guanosine monophosphate synthetase.M L Deras et al.Biochemistry, 38(1), 303-310 (1999-01-16) Identification of a subversive substrate of Trichomonas vaginalis purine nucleoside phosphorylase and the crystal structure of the enzyme-substrate complex.Yang Zang et al.The Journal of biological chemistry, 280(23), 22318-22325 (2005-04-09) Adenosine kinase from Schistosoma mansoni: structural basis for the differential incorporation of nucleoside analogues.Larissa Romanello et al.Acta crystallographica. Section D, Biological crystallography, 69(Pt 1), 126-136 (2013-01-01) Insights into phosphate cooperativity and influence of substrate modifications on binding and catalysis of hexameric purine nucleoside phosphorylases.Priscila O de Giuseppe et al.PloS one, 7(9), e44282-e44282 (2012-09-08) 2-Fluoroadenosine uptake by erythrocytes and endothelial cells studied by 19F-NMR.U K Decking et al.The American journal of physiology, 266(4 Pt 2), H1596-H1603 (1994-04-01) Synergistic inhibition of platelet aggregation by forskolin plus PGE1 or 2-fluoroadenosine: effects of 2',5'-dideoxyadenosine and 5'-methylthioadenosine.K C Agarwal et al.Biochemical pharmacology, 31(22), 3713-3716 (1982-11-15) Biodistribution and PET imaging of [(18)F]-fluoroadenosine derivatives.Mian M Alauddin et al.Nuclear medicine and biology, 34(3), 267-272 (2007-03-27) Expression of methylthioadenosine phosphorylase cDNA in p16-, MTAP- malignant cells: restoration of methylthioadenosine phosphorylase-dependent salvage pathways and alterations of sensitivity to inhibitors of purine de novo synthesis.Z H Chen et al.Molecular pharmacology, 52(5), 903-911 (1997-11-14) Fluorinated nucleic acid constituents: a carbon-13 nuclear magnetic resonance study of adenosine, cytidine, uridine, and their fluorinated analogues.J L Alderfer et al.Biochemistry, 21(11), 2738-2745 (1982-05-25) [The preparative method for 2-fluoroadenosine synthesis].V B Berzin et al.Bioorganicheskaia khimiia, 35(2), 210-214 (2009-06-20)
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