About: Diketopiperazines from marine organisms.

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About: Diketopiperazines from marine organisms. Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

scientific article published on December 2010

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 2010 (ast) наукова стаття, опублікована в грудні 2010 (uk) مقالة علمية نشرت في ديسمبر 2010 (ar) scientific article published on December 2010 (en)
publication date	wds:Q37821421-7EB24EB1-DE3E-4131-BA8E-02BB14F0A02D
publication date	2010-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37821421-DD091ECF-F476-4AEE-9E3C-92502075B7B4
language of work or name	English
cites work	wds:Q37821421-08FFF24B-BE49-4ECE-B892-999850CDE581 wds:Q37821421-106A0EEA-6088-4153-93E6-3ABAAA8E1D47 wds:Q37821421-39956AC1-42B2-48F9-8104-0EDD241C38D1 wds:Q37821421-530E027E-24D5-4D43-9AFE-1832F65694F7 wds:Q37821421-8D8CAAC0-3F90-4024-BC89-0E4F5A4DC7A2 wds:Q37821421-CCB1629B-D57E-4EA9-8E72-2EC89F42061A wds:Q37821421-E3611EAA-24F5-49C9-A8F6-B86AC3E2FE2D wds:Q37821421-E70DEFFE-00E1-4698-8992-0CD0C8AF463E wds:Q37821421-E7AD163C-5689-4DB6-86EC-9F8278E54A2F wds:Q37821421-F74B23A9-4FDF-452C-840B-43CA45503966 wds:Q37821421-FEED9968-0A70-4B49-A987-36123A56E86C
cites work	A novel chitinase inhibitor from a marine bacterium, Pseudomonas sp Notoamides A–D: Prenylated Indole Alkaloids Isolated from a Marine-Derived Fungus,Aspergillus sp Inhibition of c-fos proto-oncogene induction by Sch 52900 and Sch 52901, novel diketopiperazine produced by Gliocladium sp. Tryprostatins A and B, novel mammalian cell cycle inhibitors produced by Aspergillus fumigatus Leptosins O-S, Cytotoxic Metabolites of a Strain of Leptosphaeria Sp. Isolated from a Marine Alga Gliocladins A - C and Glioperazine ; Cytotoxic Dioxo- or Trioxopiperazine Metabolites from a Gliocladium Sp. Separated from a Sea Hare Cyclo(L-leucyl-L-prolyl) produced by Achromobacter xylosoxidans inhibits aflatoxin production by Aspergillus parasiticus Golmaenone, a new diketopiperazine alkaloid from the marine-derived fungus Aspergillus sp. New dioxopiperazine metabolites from a Fusarium species separated from a marine alga. Marine bacteria, VIII. Maremycin A and B, new diketopiperazines from a marineStreptomyces sp. Chemistry of the cytotoxic principles of the ma rine fungus Lignincola laevis
author name string	wds:Q37821421-353F6B97-F758-412E-9018-4B1C4FEBF149 wds:Q37821421-66FAC6A6-5017-4BA6-AA2C-A12865777B3A wds:Q37821421-68D4F5C0-342E-4479-98F2-8762F73384A3
author name string	Xuefeng Zhou Tunhai Xu Riming Huang
rdfs:label	Diketopiperazines from marine organisms. (en) Diketopiperazines from marine organisms. (nl) Diketopiperazines from marine organisms. (ast)
skos:prefLabel	Diketopiperazines from marine organisms. (en) Diketopiperazines from marine organisms. (nl) Diketopiperazines from marine organisms. (ast)
name	Diketopiperazines from marine organisms. (en) Diketopiperazines from marine organisms. (nl) Diketopiperazines from marine organisms. (ast)
author	wds:Q37821421-DD759B57-8F0E-4B54-A4D6-14EE60479CCF wds:Q37821421-E37FAA56-9149-4278-8E78-16BE8D086FA1
author	Yonghong Liu Xianwen Yang
title	wds:Q37821421-32830951-6A62-4511-BA0E-5FCF4EDE36B5
title	Diketopiperazines from marine organisms (en)
page(s)	wds:Q37821421-EC565240-F435-4A10-8E77-A0745B133B9A
page(s)	2809-2829
instance of	wds:Q37821421-908D50F9-B505-4EDB-8C64-25FD51C1D70D wds:Q37821421-a2a771e7-a40b-47a5-b955-3c14357f3eab
instance of	review article scholarly article
main subject	wds:Q37821421-D4540DC4-19D5-4DF0-A2B6-BCF966CE4123
main subject	marine organism
PubMed ID	wds:Q37821421-B0CA4174-90F6-4F79-B3DF-9B76D9C2E8EB
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/21161995
PubMed ID	21161995
published in	wds:Q37821421-60C50ED2-858F-43C7-9E3B-566ACF18710A
published in	Chemistry and Biodiversity
issue	wds:Q37821421-68858199-3BC1-4F4A-BF7D-4937CA325703
volume	wds:Q37821421-3F7074F9-1B7A-46C3-B349-D3F9E964038F
issue	12
volume	7
DOI	wds:Q37821421-BF20CE2B-1991-431A-B4DF-FC22762FA9E4
DOI	http://dx.doi.org/10.1002/CBDV.200900211
DOI	10.1002/CBDV.200900211
ResearchGate publication ID	wds:Q37821421-7DB13DC5-40BC-4938-A5E8-3FDAE3A3CE84
ResearchGate publication ID	49686996
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37821421
is cites work of	Inhibitory Effects of Diketopiperazines from Marine-Derived Streptomyces puniceus on the Isocitrate Lyase of Candida albicans The nonribosomal synthesis of diketopiperazines in tRNA-dependent cyclodipeptide synthase pathways. Diketopiperazines produced by the halophilic archaeon, Haloterrigena hispanica, activate AHL bioreporters. Exo-metabolome of Pseudovibrio sp. FO-BEG1 analyzed by ultra-high resolution mass spectrometry and the effect of phosphate limitation Direction of aminoacylated transfer RNAs into antibiotic synthesis and peptidoglycan-mediated antibiotic resistance Tentative biosynthetic pathways of some microbial diketopiperazines Quinoxaline-, dopamine-, and amino acid-derived metabolites from the edible insect Protaetia brevitarsis seulensis Quorum-sensing inhibitory compounds from extremophilic microorganisms isolated from a hypersaline cyanobacterial mat. Total synthesis of epicoccin G. Synthesis and biological evaluation of epidithio-, epitetrathio-, and bis-(methylthio)diketopiperazines: synthetic methodology, enantioselective total synthesis of epicoccin G, 8,8'-epi-ent-rostratin B, gliotoxin, gliotoxin G, emethallicin E, and ha Isolation and structural determination of the antifouling diketopiperazines from marine-derived Streptomyces praecox 291-11. Isolation, Purification, and Characterization of Five Active Diketopiperazine Derivatives from Endophytic Streptomyces SUK 25 with Antimicrobial and Cytotoxic Activities Concise Total Synthesis of (+)-Bionectins A and C.

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