Time-resolved fluorescence studies of tomaymycin bonding to synthetic DNAs

about

Time-resolved fluorescence studies of tomaymycin bonding to synthetic DNAs

Item

http://www.wikidata.org/entity/Q38359507

description

1996 nî lūn-bûn

@nan

1996年の論文

@ja

1996年学术文章

@wuu

1996年学术文章

@zh-cn

1996年学术文章

@zh-hans

1996年学术文章

@zh-my

1996年学术文章

@zh-sg

1996年學術文章

@yue

1996年學術文章

@zh

1996年學術文章

@zh-hant

name

Time-resolved fluorescence studies of tomaymycin bonding to synthetic DNAs

@en

type

Item

label

Time-resolved fluorescence studies of tomaymycin bonding to synthetic DNAs

@en

prefLabel

Time-resolved fluorescence studies of tomaymycin bonding to synthetic DNAs

@en

P1476

Time-resolved fluorescence studies of tomaymycin bonding to synthetic DNAs

@en

P2093

K Maskos

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

M D Barkley

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

Q Chen

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

W J Walczak

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

P2860

Crystal structure of a covalent DNA-drug adduct: anthramycin bound to C-C-A-A-C-G-T-T-G-G and a molecular explanation of specificity

Characterization of the minor groove environment in a drug-DNA complex: bisbenzimide bound to the poly[d(AT)].poly[d(AT)]duplex.

Acidic domains around nucleic acids.

One- and two-dimensional 1H NMR, fluorescence, and molecular modeling studies on the tomaymycin-d(ATGCAT)2 adduct. Evidence for two covalent adducts with opposite orientations and stereochemistries at the covalent linkage site.

Conformations of complexes between pyrrolo[1,4]benzodiazepines and DNA segments.

Pyrrolo(1,4)benzodiazepine antitumor antibiotics. In vitro interaction of anthramycin, sibiromycin and tomaymycin with DNA using specifically radiolabelled molecules.

Characterization of a unique tomaymycin-d(CICGAATTCICG)2 adduct containing two drug molecules per duplex by NMR, fluorescence, and molecular modeling studies.

Pyrrol[1,4]benzodiazepine antibiotics. Proposed structures and characteristics of the in vitro deoxyribonucleic acid adducts of anthramycin, tomaymycin, sibiromycin, and neothramycins A and B.

Steady-state fluorescence and molecular-modeling studies of tomaymycin-DNA adducts.

Analysis of local helix geometry in three B-DNA decamers and eight dodecamers.

P304

1923-1932

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

P31

scholarly article

P356

10.1016/S0006-3495(96)79756-4

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

P407

English

P433

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

P478

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

P577

1996-04-01T00:00:00Z

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

P698

8785351

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

P932

1225161

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