(Q43928215)

English

Covalent analogues of DNA base-pairs and triplets. Part 2: synthesis and cytostatic activity of bis(purin-6-yl)acetylenes,-diacetylenes and related compounds

scientific article published in April 2002

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scholarly article

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Europe PubMed Central

PubMed publication ID

28 November 2017

Covalent analogues of DNA base-pairs and triplets. Part 2: synthesis and cytostatic activity of bis(purin-6-yl)acetylenes,-diacetylenes and related compounds (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

author name string

Ivan Votruba

2

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Europe PubMed Central

PubMed publication ID

28 November 2017

language of work or name

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publication date

1 April 2002

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Europe PubMed Central

PubMed publication ID

28 November 2017

Bioorganic & Medicinal Chemistry Letters

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Europe PubMed Central

PubMed publication ID

28 November 2017

12

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Europe PubMed Central

PubMed publication ID

28 November 2017

7

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Europe PubMed Central

PubMed publication ID

28 November 2017

1055-1058

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

DNA Cross-Linking Agents as Antitumor Drugs

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Selective reaction to a flipping cytidine of the duplex DNA mediated by triple helix formation

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Covalently Cross-Linked Watson-Crick Base Pair Models

1 reference

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Synthesis of DNA Oligomers Possessing a Covalently Cross-Linked Watson-Crick Base Pair Model

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Solution structure of n-type DNA oligomers possessing a covalently cross-linked Watson-Crick base pair model

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Tautomerization dynamics of a model base pair in DNA.

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Controlled interaction between nucleic acid bases. Intramolecular stacking interactions between two adenine rings

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Isolation and identification of cross-links from formaldehyde-treated nucleic acids

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Simple models of nucleic acid interactions. 1. Base--base interactions in 1,2-Di)adenosin-N6-yl)ethane and 1,4-Di(adenosin-N6-yl)butane

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2′(3′)-O-L-Aminoacyl derivatives of “bridged” adenine ribonucleosides as substrates for ribosomal peptidyltransferase

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Synthesis of dicytidylyl-(3'-5')-1,2-di(adenosin-N6-yl)ethane and dicytidylyl-(3'-5')-1,4-di(adenosin-N6-yl)butane: covalently joined terminals of two transfer ribonucleic acids and their behavior toward snake venom phosphodiesterase

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Inhibition of ribosomal peptidyltransferase with 2'(3')-O-acetyl-2 inches(3 inches)-O-glycyl-1,2-di(adenosin-N6-yl)ethane and -1,4-di(adenosin-N6-yl)butane. Effect of alkyl chain length

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Analogs of 6-methyl-9.beta.-D-ribofuranosylpurine

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Adenosine receptor ligands-recent developments part I. Agonists

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Synthesis and cytostatic activity of substituted 6-phenylpurine bases and nucleosides: application of the Suzuki-Miyaura cross-coupling reactions of 6-chloropurine derivatives with phenylboronic acids

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Use of the Suzuki reaction for the synthesis of aryl-substituted heterocycles as corticotropin-releasing hormone (CRH) antagonists

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9-Benzylpurines with inhibitory activity against Mycobacterium tuberculosis

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Oxidative Coupling of Acetylenes. II1

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Identifiers

10.1016/S0960-894X(02)00077-X

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

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