Attributes | Values |
---|
rdf:type
| |
description
| - wetenschappelijk artikel (nl)
- articolo scientifico (pubblicato il 1996) (it)
- наукова стаття, опублікована в січні 1996 (uk)
- im Januar 1996 veröffentlichter wissenschaftlicher Artikel (de)
- artículu científicu espublizáu en xineru de 1996 (ast)
- artikull shkencor i botuar më 01 janar 1996 (sq)
- scientific article published on 01 January 1996 (en)
|
publication date
| |
publication date
| |
cites work
| |
cites work
| |
access restriction status
| |
access restriction status
| |
author name string
| |
author name string
| - H Irschik
- H Reichenbach
- K Gerth
- P Washausen
- G Hofle
|
rdfs:label
| - The jerangolids: A family of new antifungal compounds from Sorangium cellulosum (Myxobacteria). Production, physico-chemical and biological properties of jerangolid A (en)
- The jerangolids: A family of new antifungal compounds from Sorangium cellulosum (Myxobacteria). Production, physico-chemical and biological properties of jerangolid A (nl)
- The jerangolids: A family of new antifungal compounds from Sorangium cellulosum (Myxobacteria). Production, physico-chemical and biological properties of jerangolid A (sq)
|
skos:prefLabel
| - The jerangolids: A family of new antifungal compounds from Sorangium cellulosum (Myxobacteria). Production, physico-chemical and biological properties of jerangolid A (en)
- The jerangolids: A family of new antifungal compounds from Sorangium cellulosum (Myxobacteria). Production, physico-chemical and biological properties of jerangolid A (nl)
- The jerangolids: A family of new antifungal compounds from Sorangium cellulosum (Myxobacteria). Production, physico-chemical and biological properties of jerangolid A (sq)
|
name
| - The jerangolids: A family of new antifungal compounds from Sorangium cellulosum (Myxobacteria). Production, physico-chemical and biological properties of jerangolid A (en)
- The jerangolids: A family of new antifungal compounds from Sorangium cellulosum (Myxobacteria). Production, physico-chemical and biological properties of jerangolid A (nl)
- The jerangolids: A family of new antifungal compounds from Sorangium cellulosum (Myxobacteria). Production, physico-chemical and biological properties of jerangolid A (sq)
|
title
| |
title
| - The jerangolids: A family of new antifungal compounds from Sorangium cellulosum (Myxobacteria). Production, physico-chemical and biological properties of jerangolid A (en)
|
page(s)
| |
page(s)
| |
instance of
| |
instance of
| |
main subject
| |
main subject
| |
PubMed ID
| |
PubMed ID
| |
PubMed ID
| |
published in
| |
full work available at URL
| |
published in
| |
full work available at URL
| |
issue
| |
volume
| |
issue
| |
volume
| |
DOI
| |
DOI
| |
DOI
| - 10.7164/ANTIBIOTICS.49.71
|
online access status
| |
online access status
| |
is about
of | |
is cites work
of | - Total synthesis of (+)-ambruticin
- Characterization of product capture resin during microbial cultivations.
- KR025, a new cytotoxic compound from Myxococcus fulvus
- Myxobacterial secondary metabolites: bioactivities and modes-of-action.
- Myxobacteria: proficient producers of novel natural products with various biological activities--past and future biotechnological aspects with the focus on the genus Sorangium
- Analysis of the ambruticin and jerangolid gene clusters of Sorangium cellulosum reveals unusual mechanisms of polyketide biosynthesis.
- Polyunsaturated fatty acid biosynthesis in myxobacteria: different PUFA synthases and their product diversity
- The chemistry and biology of epothilones--the wheel keeps turning.
- Natural product synthesis using multicomponent reaction strategies
- The chemistry of gliding bacteria
- Chlorotonil A, ein Macrolid mit einzigartigergem-Dichlor-1,3-dionfunktion ausSorangium cellulosum, So ce1525
- Chlorotonil A, a macrolide with a unique gem-dichloro-1,3-dione functionality from Sorangium cellulosum, So ce1525
- Characterization of the biosynthetic gene cluster for the antifungal polyketide soraphen A from Sorangium cellulosum So ce26.
- Combined effects of the siderophore monosulfactam BAL30072 and carbapenems on multidrug-resistant Gram-negative bacilli.
- Chemoselective reductive cross-coupling of 1,5-diene-3-ols with alkynes: a facile entry to stereodefined skipped trienes
- Insights into the Distinct Mechanisms of Action of Taxane and Non-Taxane Microtubule Stabilizers from Cryo-EM Structures
- A novel functional assay for fungal histidine kinases group III reveals the role of HAMP domains for fungicide sensitivity
- Herboxidiene biosynthesis, production, and structural modifications: prospect for hybrids with related polyketide
- Comprehensive in Vitro Analysis of Acyltransferase Domain Exchanges in Modular Polyketide Synthases and Its Application for Short-Chain Ketone Production.
- Convergent and stereospecific synthesis of complex skipped polyenes and polyunsaturated fatty acids
- Palladium-catalyzed 1,4-difunctionalization of butadiene to form skipped polyenes
- Ligand-Controlled Regiodivergent and Enantioselective Copper-Catalyzed Hydroallylation of Alkynes.
- Total Synthesis of Jerangolid D
- The enterprise of synthesis: from concept to practice
- The antifungal polyketide ambruticin targets the HOG pathway
- On the mechanism of action of the myxobacterial fungicide ambruticin
- Total synthesis of jerangolid A.
- Intermolecular methoxycarbonylation of terminal alkynes catalyzed by palladium(II) bis(oxazoline) complexes
- Rieske non-heme iron-dependent oxygenases catalyse diverse reactions in natural product biosynthesis
- Urban park soil microbiomes are a rich reservoir of natural product biosynthetic diversity
- Iridium-catalyzed asymmetric hydrogenation of α-substituted α,β-unsaturated acyclic ketones: enantioselective total synthesis of (-)-mesembrine
- Antibiotics from Gram-negative bacteria: a comprehensive overview and selected biosynthetic highlights.
- Comparative Genomics Reveal the Animal-Associated Features of the <i>Acanthopleuribacteraceae</i> Bacteria, and Description of <i>Sulfidibacter corallicola</i> gen. nov., sp., nov
- Myxobacterial natural product assembly lines: fascinating examples of curious biochemistry.
- Use of in situ solid-phase adsorption in microbial natural product fermentation development
- Acyclic 1,4-Stereocontrol via the Allylic Diazene Rearrangement: Development, Applications, and the Essential Role of Kinetic E Stereoselectivity in Tosylhydrazone Formation.
|