2,4-Dithiothymine as a potent UVA chemotherapeutic agent.
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Ultrafast Independent N-H and N-C Bond Deformation Investigated with Resonant Inelastic X-Ray Scattering.A Static Picture of the Relaxation and Intersystem Crossing Mechanisms of Photoexcited 2-ThiouracilThe origin of efficient triplet state population in sulfur-substituted nucleobases.Distortion dependent intersystem crossing: A femtosecond time-resolved photoelectron spectroscopy study of benzene, toluene, and p-xylene.Oxidatively-generated damage to DNA and proteins mediated by photosensitized UVAHnRNP A1 Alters the Structure of a Conserved Enterovirus IRES Domain to Stimulate Viral Translation.Intersystem Crossing Pathways in the Noncanonical Nucleobase 2-Thiouracil: A Time-Dependent Picture.Visible-Light-Mediated Excited State Relaxation in Semi-Synthetic Genetic Alphabet: d5SICS and dNaM.Electronic relaxation pathways of the biologically relevant pterin chromophore.Decoding the Molecular Basis for the Population Mechanism of the Triplet Phototoxic Precursors in UVA Light-Activated Pyrimidine Anticancer Drugs.The excited-state decay mechanism of 2,4-dithiothymine in the gas phase, microsolvated surroundings, and aqueous solution.Can a Six-Letter Alphabet Increase the Likelihood of Photochemical Assault to the Genetic Code?Triplet state formation and quenching dynamics of 2-mercaptobenzothiazole in solution.Photorelaxation and Photorepair Processes in Nucleic and Amino Acid Derivatives.Optical absorption and magnetic circular dichroism spectra of thiouracils: a quantum mechanical study in solution.2-Thiouracil intersystem crossing photodynamics studied by wavelength-dependent photoelectron and transient absorption spectroscopies.Excited-State Dynamics of the Thiopurine Prodrug 6-Thioguanine: Can N9-Glycosylation Affect Its Phototoxic Activity?A theoretical study of the light-induced cross-linking reaction of 5-fluoro-4-thiouridine with thymine.The Triplet State of 6-thio-2'-deoxyguanosine: Intrinsic Properties and Reactivity Toward Molecular Oxygen.Photoelectron spectra of 2-thiouracil, 4-thiouracil, and 2,4-dithiouracil.Short-time dynamics of 2-thiouracil in the light absorbing S2(ππ(∗)) state.The involvement of triplet receiver states in the ultrafast excited state processes of small esters.
P2860
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P2860
2,4-Dithiothymine as a potent UVA chemotherapeutic agent.
description
2014 nî lūn-bûn
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2014年の論文
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2014年学术文章
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name
2,4-Dithiothymine as a potent UVA chemotherapeutic agent.
@en
2,4-Dithiothymine as a potent UVA chemotherapeutic agent.
@nl
type
label
2,4-Dithiothymine as a potent UVA chemotherapeutic agent.
@en
2,4-Dithiothymine as a potent UVA chemotherapeutic agent.
@nl
prefLabel
2,4-Dithiothymine as a potent UVA chemotherapeutic agent.
@en
2,4-Dithiothymine as a potent UVA chemotherapeutic agent.
@nl
P50
P356
P1476
2,4-Dithiothymine as a potent UVA chemotherapeutic agent
@en
P2093
Steffen Jockusch
P304
17930-17933
P356
10.1021/JA510611J
P407
P577
2014-12-17T00:00:00Z