1,N2-ethenoguanine and N2,3-ethenoguanine. Synthesis and comparison of the electronic spectral properties of these linear and angular triheterocycles related to the Y bases.
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Base-Modified Nucleosides: Etheno DerivativesStructure of the 1, N 2 -Etheno-2′-deoxyguanosine Lesion in the 3′-G(εdG)T-5′ Sequence Opposite a One-Base DeletionBasis of Miscoding of the DNA Adduct N2,3-Ethenoguanine by Human Y-family DNA PolymerasesReplication ofN2,3-Ethenoguanine by DNA PolymerasesEthenoguanines undergo glycosylation by nucleoside 2'-deoxyribosyltransferases at non-natural sitesReactions of 9-substituted guanines with bromomalondialdehyde in aqueous solution predominantly yield glyoxal-derived adducts.Magnesium ion-dependent triple-helix structure formed by homopurine-homopyrimidine sequences in supercoiled plasmid DNA.Synthesis of fluorescent nucleotide analogues: 5'-mono-, di-, and triphosphates of linear-benzoguanosine, linear-benzoinosine, and linear-benzoxanthosineFluorometric determination of adenosine nucleotide derivatives as measures of the microfouling, detrital, and sedimentary microbial biomass and physiological status.Translesion synthesis across 1,N2-ethenoguanine by human DNA polymerases.Cationic metal-specific structures adopted by the poly(dG) region and the direct repeats in the chicken adult beta A globin gene promoter.Transcriptional errors and ambiguity resulting from the presence of 1,N6-ethenoadenosine or 3,N4-ethenocytidine in polyribonucleotides.Detection of triple-helix related structures adopted by poly(dG)-poly(dC) sequences in supercoiled plasmid DNAStructural and Kinetic Analysis of Miscoding Opposite the DNA Adduct 1,N6-Ethenodeoxyadenosine by Human Translesion DNA Polymerase η.Release of N2,3-ethenoguanine from chloroacetaldehyde-treated DNA by Escherichia coli 3-methyladenine DNA glycosylase II.All four known cyclic adducts formed in DNA by the vinyl chloride metabolite chloroacetaldehyde are released by a human DNA glycosylaseAcremolin from Acremonium strictum is N(2),3-etheno-2'-isopropyl-1-methylguanine, not a 1H-azirine. Synthesis and structural revision.DNA adduct bypass polymerization by Sulfolobus solfataricus DNA polymerase Dpo4: analysis and crystal structures of multiple base pair substitution and frameshift products with the adduct 1,N2-ethenoguanine.New observations concerning the chloroacetaldehyde reaction with some tRNA constituents. Stable intermediates, kinetics and selectivity of the reaction.Fluorescent N2,N3-epsilon-adenine nucleoside and nucleotide probes: synthesis, spectroscopic properties, and biochemical evaluation.The reactions of thiouridines and thiouracils with chloroacetaldehyde; mechanistic considerationsTranscriptionally driven cruciform formation in vivo.Mechanisms of formation of DNA adducts from ethylene dihalides, vinyl halides, and arylamines.1,N2-Etheno-2'-deoxyguanosine adopts the syn conformation about the glycosyl bond when mismatched with deoxyadenosine.Oxidation and glycolytic cleavage of etheno and propano DNA base adducts.Structure of the 1,N2-etheno-2'-deoxyguanosine adduct in duplex DNA at pH 8.6.Structure of the 1,N2-ethenodeoxyguanosine adduct opposite cytosine in duplex DNA: Hoogsteen base pairing at pH 5.2.Induction of 1,N(2)-etheno-2'-deoxyguanosine in DNA exposed to beta-carotene oxidation products.New nucleoside analogs from 2-amino-9-(beta-D-ribofuranosyl)purine.
P2860
Q26747253-BDC1C0DC-4743-4FC5-9D24-0B240B80E27CQ27660111-58238A5E-619D-4151-BE41-2A372D530715Q27671647-9266C1FF-3747-4771-A3C5-9D87088BBCD7Q27678403-91F70DA7-1F6F-4D77-BFC6-ABFF00E01447Q28542779-650D6049-2D6E-49D8-BB9D-2B1FCEDCFEDFQ30940305-C5E98748-F6B4-47ED-A746-351EC79BC16AQ33576869-182CC8E4-36DB-4EE1-B80A-34A4E841BB49Q33971912-5FD17940-057F-4311-B8A5-5AA05514F1E9Q34044705-24E8C9AD-22D0-4ED4-80FA-A5B476FC99F7Q35087809-503410B2-C2F9-4B31-AB56-A8B9359E9DD0Q35232356-51D68830-6472-4D2D-A254-61F4A8E54C2CQ35700193-9B8436FB-08FD-4339-8235-2CC3E7BD2073Q35775473-994D78D6-2F52-4E61-B917-9DC39FD71531Q37065732-008581D6-EA79-4337-B6ED-567E9F2AA815Q37233432-A7440668-51E9-497D-83CD-ABA0563C6D9EQ37558531-8C8B2BC5-C6CB-4850-9ED4-617DD7E50328Q38313828-C2E9C10F-B9ED-41B7-840C-048844266F7FQ38324744-CD9CF67A-0181-41A5-94B8-0E57F44D7023Q39189418-7FC5BDB5-2E84-4DE2-BE72-166863989282Q40251007-8FA54F34-5498-4B2D-88FE-DB6C008AAE9AQ40499050-3533643E-6CF4-42DF-ACE0-984CD66AB197Q40535603-EB08E7A0-DA8B-44EB-9BF8-90D832CD6167Q40700909-0F7EA761-E053-474D-B844-0951C179FE2EQ41770062-40A94E15-0D62-45E6-8F13-97D47190A400Q41877393-E2D1FA68-6616-4744-8E7A-263B77EFDEF2Q42745425-71724576-FA1E-41E8-AF76-F51A4D35DD8EQ43176105-8FAF5851-F345-4A8F-B13A-B5312C6A376CQ44779075-9A2830AC-AEFD-4B56-A263-19F9B093C5ADQ44790885-F7B639B5-742C-42AA-9B16-C6BCA7E9D53D
P2860
1,N2-ethenoguanine and N2,3-ethenoguanine. Synthesis and comparison of the electronic spectral properties of these linear and angular triheterocycles related to the Y bases.
description
1977 nî lūn-bûn
@nan
1977年の論文
@ja
1977年論文
@yue
1977年論文
@zh-hant
1977年論文
@zh-hk
1977年論文
@zh-mo
1977年論文
@zh-tw
1977年论文
@wuu
1977年论文
@zh
1977年论文
@zh-cn
name
1,N2-ethenoguanine and N2,3-et ...... cycles related to the Y bases.
@en
1,N2-ethenoguanine and N2,3-et ...... cycles related to the Y bases.
@nl
type
label
1,N2-ethenoguanine and N2,3-et ...... cycles related to the Y bases.
@en
1,N2-ethenoguanine and N2,3-et ...... cycles related to the Y bases.
@nl
prefLabel
1,N2-ethenoguanine and N2,3-et ...... cycles related to the Y bases.
@en
1,N2-ethenoguanine and N2,3-et ...... cycles related to the Y bases.
@nl
P2093
P356
P1476
1,N2-ethenoguanine and N2,3-et ...... cycles related to the Y bases.
@en
P2093
Frihart CR
Leonard NJ
Sattsangi PD
P304
P356
10.1021/JO00440A020
P407
P577
1977-09-01T00:00:00Z