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Literature DB >> 5419046

Carbon-13 magnetic resonance. XVII. Pyrimidine and purine nucleosides.

A J Jones, D M Grant, M W Winkley, R K Robins.

Abstract

Entities: Chemical

Mesh：

Substances：

Year: 1970 PMID： 5419046 DOI： 10.1021/ja00716a042

Source DB: PubMed Journal: J Am Chem Soc ISSN： 0002-7863 Impact factor: 15.419

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8 in total

1. Steric and electrostatic effects at the C2 atom substituent influence replication and miscoding of the DNA deamination product deoxyxanthosine and analogs by DNA polymerases.

Authors: Huidong Zhang; Urban Bren; Ivan D Kozekov; Carmelo J Rizzo; Donald F Stec; F Peter Guengerich
Journal: J Mol Biol Date: 2009-07-14 Impact factor: 5.469

2. Guanosine 5'-diphosphate, 3'-diphosphate: assignment of structure by 13C nuclear magnetic resonance spectroscopy.

Authors: L Que; G R Willie; M Cashel; J W Bodley; G R Gray
Journal: Proc Natl Acad Sci U S A Date: 1973-09 Impact factor: 11.205

3. Nucleoside conformation is determined by the electronegativity of the sugar substituent.

Authors: W Guschlbauer; K Jankowski
Journal: Nucleic Acids Res Date: 1980-03-25 Impact factor: 16.971

4. Expression of mammalian glutathione S-transferase 5-5 in Salmonella typhimurium TA1535 leads to base-pair mutations upon exposure to dihalomethanes.

Authors: R Thier; J B Taylor; S E Pemble; W G Humphreys; M Persmark; B Ketterer; F P Guengerich
Journal: Proc Natl Acad Sci U S A Date: 1993-09-15 Impact factor: 11.205

5. Assignments in the carbon-13 nuclear magnetic resonance spectra of vitamin B12' coenzyme B12' and other corrinoids: application of partially-relaxed fourier transform spectroscopy.

Authors: D Doddrell; A Allerhand
Journal: Proc Natl Acad Sci U S A Date: 1971-05 Impact factor: 11.205

Carbon-13 magnetic resonance. XVII. Pyrimidine and purine nucleosides.

1. Steric and electrostatic effects at the C2 atom substituent influence replication and miscoding of the DNA deamination product deoxyxanthosine and analogs by DNA polymerases.

2. Guanosine 5'-diphosphate, 3'-diphosphate: assignment of structure by 13C nuclear magnetic resonance spectroscopy.

3. Nucleoside conformation is determined by the electronegativity of the sugar substituent.

4. Expression of mammalian glutathione S-transferase 5-5 in Salmonella typhimurium TA1535 leads to base-pair mutations upon exposure to dihalomethanes.

5. Assignments in the carbon-13 nuclear magnetic resonance spectra of vitamin B12' coenzyme B12' and other corrinoids: application of partially-relaxed fourier transform spectroscopy.

6. New manzamine alkaloids with activity against infectious and tropical parasitic diseases from an Indonesian sponge.

7. Hydrogen bonding of adenine derivatives to tyrosine side chain.

8. Pyramidamycins A-D and 3-hydroxyquinoline-2-carboxamide; cytotoxic benzamides from Streptomyces sp. DGC1.