C-Nucleosides Derived from Simple Aromatic Hydrocarbons - Wikidata - awgldk - TriplyDB

C-Nucleosides Derived from Simple Aromatic Hydrocarbons

C-Nucleosides Derived from Simple Aromatic Hydrocarbons

http://www.wikidata.org/entity/Q33750525

about

Minor Groove Interactions between Polymerase and DNA: More Essential to Replication than Watson-Crick Hydrogen Bonds?Structure and Base Pairing Properties of a Replicable Nonpolar Isostere for Deoxyadenosine Selective and Stable DNA Base Pairing without Hydrogen Bonds.Varied Molecular Interactions at the Active Sites of Several DNA Polymerases: Nonpolar Nucleoside Isosteres as Probes.Genetically encoded multispectral labeling of proteins with polyfluorophores on a DNA backbone Measurement and theory of hydrogen bonding contribution to isosteric DNA base pairs.Oligodeoxyfluorosides: Strong Sequence Dependence of Fluorescence Emission Novel Nucleoside Analogues with Fluorophores Replacing the DNA Base Synthesis of 1-(2-deoxy-beta-D-ribofuranosyl)-2,4-difluoro-5-substituted-benzene thymidine mimics, some related alpha-anomers, and their evaluation as antiviral and anticancer agents.Pharmacokinetics and metabolism of the novel synthetic C-nucleoside, 1-(2-deoxy-beta-D-ribofuranosyl)-2,4-difluoro-5-iodobenzene: a potential mimic of 5-iodo-2'-deoxyuridine.Development of a universal nucleobase and modified nucleobases for expanding the genetic code.

P2860

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P2860

C-Nucleosides Derived from Simple Aromatic Hydrocarbons

http://www.wikidata.org/entity/Q33750525

description

1997 nî lūn-bûn

@nan

1997 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

1997 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

1997年の論文

@ja

1997年論文

@yue

1997年論文

@zh-hant

1997年論文

@zh-hk

1997年論文

@zh-mo

1997年論文

@zh-tw

1997年论文

@wuu

name

C-Nucleosides Derived from Simple Aromatic Hydrocarbons

@ast

C-Nucleosides Derived from Simple Aromatic Hydrocarbons

@en

type

label

C-Nucleosides Derived from Simple Aromatic Hydrocarbons

@ast

C-Nucleosides Derived from Simple Aromatic Hydrocarbons

@en

prefLabel

C-Nucleosides Derived from Simple Aromatic Hydrocarbons

@ast

C-Nucleosides Derived from Simple Aromatic Hydrocarbons

@en

P1433

Q33750525-7A9A4F5B-8D3F-41B2-9EE8-76409E11E092

P1476

Q33750525-320605DA-4D26-4E56-83E0-FB8D510C072B

P2093

Q33750525-4B8F8DF6-D84D-4091-9478-D2E7FE5ACD61

Q33750525-A5419547-4D4B-4406-8175-D4C8B3CCEC9D

Q33750525-F3132027-2A76-438D-92DF-12F641707F2E

P2860

Q33750525-084BB062-4870-4893-9086-BB925E4757E3

Q33750525-24813C56-996F-4B34-96DC-8DD28F492E12

Q33750525-28254ABF-DEF6-49C8-AE47-DEDE40570106

Q33750525-28D4A73B-7A0A-471E-AFD0-4A8D84EC8A45

Q33750525-305186A9-D224-4093-AFEE-49557592739E

Q33750525-6E8210DB-88B3-414B-815B-92DCF9768194

Q33750525-72BBC190-E52D-4024-8FBC-095CCDE9D276

Q33750525-7999B687-9154-4F9F-92AE-D291B8F92C34

Q33750525-848D733C-0151-4784-B75D-4762A505E2B5

Q33750525-89E12CF9-4004-45E7-9030-C32311A04D97

P304

Q33750525-A3E9CD10-A8F5-411E-A7D5-B5B7B6F3B911

P31

Q33750525-36EE7850-E9DB-427A-B6B8-8C99DC46EF36

P356

Q33750525-6FA6DD7E-355C-4D05-A32D-F10592B2CF88

P478

Q33750525-7FBCC513-091F-403F-B852-DFFB3847EF43

P577

Q33750525-F111D375-A867-49E0-8FFF-8F753F7BC785

P5875

Q33750525-FA6E2FE6-A948-4B45-A92D-AA311FFCBE34

P698

Q33750525-006B87AE-B32A-4EAD-9015-AA95D83E413B

P932

Q33750525-A24D24CF-7A55-4945-97D2-52F8764A66E9

P356

P1433

P1476

C-Nucleosides Derived from Simple Aromatic Hydrocarbons

@en

P2093

Eric T Kool

http://www.w3.org/2001/XMLSchema#string

Narayan C Chaudhuri

http://www.w3.org/2001/XMLSchema#string

Rex X-F Ren

http://www.w3.org/2001/XMLSchema#string

P2860

Solution structure of a bovine immunodeficiency virus Tat-TAR peptide-RNA complex

Influence of loop residues on the relative stabilities of DNA hairpin structures

Naphthalene, Phenanthrene, and Pyrene as DNA Base Analogues: Synthesis, Structure, and Fluorescence in DNA.

Hydrophobic, Non-Hydrogen-Bonding Bases and Base Pairs in DNA.

Formation of Stable DNA Loops by Incorporation of Nonpolar, Non-Hydrogen-Bonding Nucleoside Isosteres.

Experimental Measurement of Aromatic Stacking Affinities in the Context of Duplex DNA

Non-hydrogen bonding 'terminator' nucleosides increase the 3'-end homogeneity of enzymatic RNA and DNA synthesis.

Synthesis and biophysical studies of short oligodeoxynucleotides with novel modifications: a possible approach to the problem of mixed base oligodeoxynucleotide synthesis.

Synthesis of naturally occurring C-nucleosides, their analogs, and functionalized C-glycosyl precursors.

Aromatic Nonpolar Nucleosides as Hydrophobic Isosteres of Pyrimidine and Purine Nucleosides.

P304

341-347

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1055/S-1997-788

http://www.w3.org/2001/XMLSchema#string

P478

4

http://www.w3.org/2001/XMLSchema#string

P577

1997-04-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

42542368

http://www.w3.org/2001/XMLSchema#string

P698

20336193

http://www.w3.org/2001/XMLSchema#string

P932

2844787

http://www.w3.org/2001/XMLSchema#string