Hemi-phorboxazole a: structure confirmation, analogue design and biological evaluation. - Wikidata - awgldk - TriplyDB

Hemi-phorboxazole a: structure confirmation, analogue design and biological evaluation.

Hemi-phorboxazole a: structure confirmation, analogue design and biological evaluation.

http://www.wikidata.org/entity/Q37345697

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Microscale methodology for structure elucidation of natural products.Phorboxazole Synthetic Studies: Design, Synthesis and Biological Evaluation of Phorboxazole A and Hemi-Phorboxazole A Related Analogues Structural requirements for the antiproliferative activity of pre-mRNA splicing inhibitor FR901464.INTEGRATED APPROACHES TO THE CONFIGURATIONAL ASSIGNMENT OF MARINE NATURAL PRODUCTS Synthesis of the phorboxazoles-potent, architecturally novel marine natural products.Natural product analogues: towards a blueprint for analogue-focused synthesis.Structure elucidation at the nanomole scale. 3. Phorbasides G-I from Phorbas sp.

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Hemi-phorboxazole a: structure confirmation, analogue design and biological evaluation.

http://www.wikidata.org/entity/Q37345697

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on August 2009

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Hemi-phorboxazole a: structure confirmation, analogue design and biological evaluation.

@en

Hemi-phorboxazole a: structure confirmation, analogue design and biological evaluation.

@nl

type

label

Hemi-phorboxazole a: structure confirmation, analogue design and biological evaluation.

@en

Hemi-phorboxazole a: structure confirmation, analogue design and biological evaluation.

@nl

prefLabel

Hemi-phorboxazole a: structure confirmation, analogue design and biological evaluation.

@en

Hemi-phorboxazole a: structure confirmation, analogue design and biological evaluation.

@nl

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Organic Letters

P1476

Hemi-phorboxazole a: structure confirmation, analogue design and biological evaluation.

@en

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Amos B Smith

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

Anne-Marie L Hogan

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

Doralyn S Dalisay

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

Tadeusz F Molinski

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

Zhuqing Liu

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

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The practical synthesis of a novel and highly potent analogue of bryostatin.

Use of an aqueous soluble tetrazolium/formazan assay for cell growth assays in culture.

Phorbasides A-E, cytotoxic chlorocyclopropane macrolide glycosides from the marine sponge Phorbas sp. CD determination of C-methyl sugar configurations.

Synthesis and biological evaluation of phorboxazole congeners leading to the discovery and preparative-scale synthesis of (+)-chlorophorboxazole a possessing picomolar human solid tumor cell growth inhibitory activity.

Design and synthesis of a potent phorboxazole C(11-15) acetal analogue.

(+)-Phorboxazole A synthetic studies. Identification of a series of highly cytotoxic C(45-46) analogues.

NMR quantitation of natural products at the nanomole scale.

Enantioselective total synthesis of borrelidin.

A tetrachloro polyketide hexahydro-1H-isoindolone, muironolide A, from the marine sponge Phorbas sp. natural products at the nanomole scale.

Chlorocyclopropane macrolides from the marine sponge Phorbas sp. assignment of the configurations of phorbasides A and B by quantitative CD.

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3766-3769

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scholarly article

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10.1021/OL9014317

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16

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11

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2009-08-01T00:00:00Z

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26700851

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19637861

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2743491

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