The marinopyrroles, antibiotics of an unprecedented structure class from a marine Streptomyces sp. - Wikidata - awgldk - TriplyDB

The marinopyrroles, antibiotics of an unprecedented structure class from a marine Streptomyces sp.

The marinopyrroles, antibiotics of an unprecedented structure class from a marine Streptomyces sp.

http://www.wikidata.org/entity/Q33648791

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Targeting Cell Survival Proteins for Cancer Cell Death Activity of the streptogramin antibiotic etamycin against methicillin-resistant Staphylococcus aureus Total synthesis of the ammosamides.Production of induced secondary metabolites by a co-culture of sponge-associated actinomycetes, Actinokineospora sp. EG49 and Nocardiopsis sp. RV163.Structures, reactivities, and antibiotic properties of the marinopyrroles A-F Fijiolides A and B, inhibitors of TNF-alpha-induced NFkappaB activation, from a marine-derived sediment bacterium of the genus Nocardiopsis Maritoclax induces apoptosis in acute myeloid leukemia cells with elevated Mcl-1 expression Marinopyrrole derivatives with sulfide spacers as selective disruptors of Mcl-1 binding to pro-apoptotic protein Bim.Anthracimycin activity against contemporary methicillin-resistant Staphylococcus aureus.Novel anti-infective compounds from marine bacteria.Genetic insights into pyralomicin biosynthesis in Nonomuraea spiralis IMC A-0156.Unusual flavoenzyme catalysis in marine bacteria.Total synthesis and biological evaluation of marinopyrrole A and analogues.Pharmacological properties of the marine natural product marinopyrrole A against methicillin-resistant Staphylococcus aureus.Bioprospecting from marine sediments of New Brunswick, Canada: exploring the relationship between total bacterial diversity and actinobacteria diversity Discovery of marinopyrrole A (maritoclax) as a selective Mcl-1 antagonist that overcomes ABT-737 resistance by binding to and targeting Mcl-1 for proteasomal degradation Marinopyrrole derivatives as potential antibiotic agents against methicillin-resistant Staphylococcus aureus (I)Chlorizidine, a cytotoxic 5H-pyrrolo[2,1-a]isoindol-5-one-containing alkaloid from a marine Streptomyces sp.Marinopyrrole derivatives as potential antibiotic agents against methicillin-resistant Staphylococcus aureus (II).Chasing the treasures of the sea - bacterial marine natural products.Bioactive compounds from marine bacteria and fungi.The chemistry of isoindole natural products.Antineoplastic agents. 570. Isolation and structure elucidation of bacillistatins 1 and 2 from a marine Bacillus silvestris.Cytotoxic and Antimicrobial Napyradiomycins from Two Marine-Derived, MAR 4 Streptomyces Strains.Cyclic marinopyrrole derivatives as disruptors of Mcl-1 and Bcl-x(L) binding to Bim.Antibacterials from the sea.Screening strategies for discovery of antibacterial natural products.Marine bacteria: potential sources for compounds to overcome antibiotic resistance.Impact of copper-catalyzed cross-coupling reactions in natural product synthesis: the emergence of new retrosynthetic paradigms.Secondary metabolites from marine-derived microorganisms.The biocatalytic repertoire of natural biaryl formation.A twist of nature--the significance of atropisomers in biological systems.Marinopyrroles: Unique Drug Discoveries Based on Marine Natural Products.Evaluating Nitrogen-Containing Biosynthetic Products Produced by Saltwater Culturing of Several California Littoral Zone Gram-Negative Bacteria.Isolation of a small molecule with anti-MRSA activity from a mangrove symbiont Streptomyces sp. PVRK-1 and its biomedical studies in Zebrafish embryos Isolation and characterization of potential antibiotic producing actinomycetes from water and sediments of Lake Tana, Ethiopia.Screening of antibacterial producing actinomycetes from sediments of the caspian sea.Production of a compound against methicillin resistant Staphylococcus aureus (MRSA) from Streptomyces rubrolavendulae ICN3 & its evaluation in zebrafish embryos Marinopyrrole A target elucidation by acyl dye transfer.Anti-cancer drug discovery and development: Bcl-2 family small molecule inhibitors.

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P2860

The marinopyrroles, antibiotics of an unprecedented structure class from a marine Streptomyces sp.

http://www.wikidata.org/entity/Q33648791

description

2008 nî lūn-bûn

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2008 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2008 թվականի հունվարին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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name

The marinopyrroles, antibiotic ...... from a marine Streptomyces sp.

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The marinopyrroles, antibiotic ...... from a marine Streptomyces sp.

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type

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The marinopyrroles, antibiotic ...... from a marine Streptomyces sp.

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The marinopyrroles, antibiotic ...... from a marine Streptomyces sp.

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The marinopyrroles, antibiotic ...... from a marine Streptomyces sp.

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The marinopyrroles, antibiotic ...... from a marine Streptomyces sp.

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Organic Letters

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The marinopyrroles, antibiotic ...... from a marine Streptomyces sp.

@en

P2093

Alejandra Prieto-Davo

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

Chambers C Hughes

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Paul R Jensen

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William Fenical

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P2860

Statistical approaches for estimating actinobacterial diversity in marine sediments

Antibacterial natural products in medicinal chemistry--exodus or revival?

Natural products as sources of new drugs over the last 25 years

Salinosporamide A: a highly cytotoxic proteasome inhibitor from a novel microbial source, a marine bacterium of the new genus salinospora.

Structure and synthesis of the natural heptachloro-1'-methyl-1,2'-bipyrrole (Q1).

Developing a new resource for drug discovery: marine actinomycete bacteria.

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629-631

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scholarly article

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10.1021/OL702952N

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4

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18205372

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(-)-marinopyrrole A

(-)-marinopyrrole B

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2820876

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