
Pyrrole-3-carboxylic acid | CAS:931-03-3
Pyrrole-3-carboxylic acid
- Name:Pyrrole-3-carboxylic acid
- CAS:931-03-3
- Synonyms:1H-Pyrrole-3-carboxylic acid
- Molecular Formula:C5H5NO2
- Molecular Weight:111.10
- EINESC:
Description
Properties
Melting point | 209 ºC |
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Safety
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SDS
Source | SDS/MSDS Samples |
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Alfa-Aesar | View & Download |
Sigma-Aldrich | View & Download |
TCI | View & Download |
Synthetic Route
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More
Articles
Peer-Reviewed Papers
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)
Remarks
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