About: Apicularens A and B, new cytostatic macrolides from Chondromyces species (myxobacteria): production, physico-chemical and biological properties

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About: Apicularens A and B, new cytostatic macrolides from Chondromyces species (myxobacteria): production, physico-chemical and biological properties Goto Sponge NotDistinct Permalink

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scientific article published on 01 December 1998

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 1998 (uk) article scientifique publié en 1998 (fr) im Dezember 1998 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'avientu de 1998 (ast) scientific article published on 01 December 1998 (en)
publication date	wds:Q74523174-BB340A41-117D-4F5D-949B-33A74AF83BF8
publication date	1998-01-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q74523174-0AA5DBAB-87C9-4CB7-924D-1EBEE2388E42 wds:Q74523174-14B27C18-99EA-4E93-944E-A2AC04E6CF79 wds:Q74523174-337ACB9D-3A6C-44ED-B1E5-AA3720905E62 wds:Q74523174-49BE9074-F9F8-43F5-9D79-1136AF2AA925 wds:Q74523174-DD921A07-428E-42A4-82A7-66FFF17DBAC0
cites work	Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays Chondramides A approximately D, new antifungal and cytostatic depsipeptides from Chondromyces crocatus (myxobacteria). Production, physico-chemical and biological properties. Saframycin Mx1, a new natural saframycin isolated from a myxobacterium Crocacin, a new electron transport inhibitor from Chondromyces crocatus (myxobacteria). Production, isolation, physico-chemical and biological properties The chondramides: cytostatic agents from myxobacteria acting on the actin cytoskeleton
access restriction status	wds:Q74523174-FD2EE8DB-37D5-4FBE-9B4B-91F42586CBB5
access restriction status	open access
author name string	wds:Q74523174-10BB57CE-4F91-4A73-8A0D-005583707D39 wds:Q74523174-4B3998D2-3507-4F43-A68E-213F0BBE8297 wds:Q74523174-7BEFA490-B2BC-40D1-B8D9-5F8586ECF71C wds:Q74523174-C848FB3F-0E4E-4FBF-A7E1-ACCAF895F35E wds:Q74523174-D36F5CFF-8F7E-4353-B61D-8EAF4E107C7B
author name string	R Jansen G Höfle H Reichenbach B Kunze F Sasse
rdfs:label	Apicularens A and B, new cytostatic macrolides from Chondromyces species (myxobacteria): production, physico-chemical and biological properties (en) Apicularens A and B, new cytostatic macrolides from Chondromyces species (myxobacteria): production, physico-chemical and biological properties (nl)
skos:prefLabel	Apicularens A and B, new cytostatic macrolides from Chondromyces species (myxobacteria): production, physico-chemical and biological properties (en) Apicularens A and B, new cytostatic macrolides from Chondromyces species (myxobacteria): production, physico-chemical and biological properties (nl)
name	Apicularens A and B, new cytostatic macrolides from Chondromyces species (myxobacteria): production, physico-chemical and biological properties (en) Apicularens A and B, new cytostatic macrolides from Chondromyces species (myxobacteria): production, physico-chemical and biological properties (nl)
title	wds:Q74523174-328CA30A-336A-46DD-AB0A-D533DEB2E7B0
title	Apicularens A and B, new cytostatic macrolides from Chondromyces species (myxobacteria): production, physico-chemical and biological properties (en)
page(s)	wds:Q74523174-979ECE4D-E3B7-404F-AAA3-16BF25B01714
page(s)	1075-1080
instance of	wds:Q74523174-2433C073-8A50-4113-89C9-AC31624A9F4A
instance of	scholarly article
main subject	wds:Q74523174-30992D2C-69D1-49F2-8434-C5D10EBAFD71 wds:Q74523174-4CF2F121-B08F-44B6-BE24-72409AF63B14 wds:Q74523174-89C40047-7A98-40CC-AAAB-5AB303CF3722 wds:Q74523174-98DB9C0F-7C84-4B26-9EF3-467D005AF778 wds:Q74523174-E4B5BFB2-FE1C-4C72-9CC3-2D65179B3FC9 wds:Q74523174-ED717E7E-D9CD-4F01-9A72-D5FFEBEA9440
main subject	Chondromyces Chondromyces robustus (2Z,4Z)-N-[(E)-3-[(1S,11S,13R,15S)-15-[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-hydroxy-9-oxo-10,17-dioxatricyclo[11.3.1.03,8]heptadeca-3(8),4,6-trien-11-yl]prop-1-enyl]hepta-2,4-dienamide (2Z,4Z)-N-[(E)-3-[(1S,11S,13R,15R)-15-[(2R,3S,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-hydroxy-9-oxo-10,17-dioxatricyclo[11.3.1.03,8]heptadeca-3(8),4,6-trien-11-yl]prop-1-enyl]hepta-2,4-dienamide Apicularen B apicularen A
PubMed ID	wds:Q74523174-AEFB5C49-D38B-44B1-AE87-0834B1E991C6
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10048565
PubMed ID	10048565
published in	wds:Q74523174-5FB283F6-60BC-4403-9B10-C5BAE5BC489F
full work available at URL	wds:Q74523174-D301D6B6-68F7-4704-827A-CB0DF48F9AB2
published in	The Journal of Antibiotics
full work available at URL	https://www.jstage.jst.go.jp/article/antibiotics1968/51/12/51_12_1075/_pdf
issue	wds:Q74523174-ECE0C242-D6BD-455D-BE20-5E04AB80E72C
volume	wds:Q74523174-9A3BDE06-701C-44A0-A1CF-C20785EE47E9
issue	12
volume	51
DOI	wds:Q74523174-ACF029C4-09B2-423D-892D-F7F5B0B631A4
DOI	http://dx.doi.org/10.7164/ANTIBIOTICS.51.1075
DOI	10.7164/ANTIBIOTICS.51.1075
online access status	wds:Q74523174-7D22B98F-6341-4A6F-96B9-0175B2F34EF9
online access status	open access
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q74523174
is cites work of	Metabolites from symbiotic bacteria De novo formal synthesis of (-)-apicularen A via an iterative asymmetric hydration sequence Characterization of the microbial community and polyketide biosynthetic potential in the palmerolide-producing tunicate Synoicum adareanum Formal total synthesis of oximidine II via a Suzuki-type cross-coupling macrocyclization employing potassium organotrifluoroborates Online analysis of xestodecalactones A-C, novel bioactive metabolites from the fungus Penicillium cf. montanense and their subsequent isolation from the sponge Xestospongia exigua Discovery of complex mixtures of novel long-chain quorum sensing signals in free-living and host-associated marine alphaproteobacteria 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 Novel natural parabens produced by a Microbulbifer bacterium in its calcareous sponge host Leuconia nivea Total synthesis of (-)-apicularen A. Chemistry and Biology of Salicylihalamide A and Related Compounds The chemistry of gliding bacteria V-ATPase inhibitors and implication in cancer treatment. Antibiotics from myxobacteria Isolation, biology and chemistry of the disorazoles: new anti-cancer macrodiolides Inhibitors of V-ATPases: old and new players Synthesis of enamides related to the salicylate antitumor macrolides using copper-mediated vinylic substitution Copper-Catalyzed Coupling of Amides and Carbamates with Vinyl Halides CuI/N,N-dimethylglycine-catalyzed coupling of vinyl halides with amides or carbamates Nitric oxide production by the vacuolar-type (H+)-ATPase inhibitors bafilomycin A1 and concanamycin A and its possible role in apoptosis in RAW 264.7 cells Utilizing the power of microbial genetics to bridge the gap between the promise and the application of marine natural products Myxobacteria, producers of novel bioactive substances De novo synthesis of natural products via the asymmetric hydration of polyenes The role of 1,3-dithianes in natural product synthesis Total synthesis of (+)-crocacin D. Total synthesis of (+)-crocacin C. The binding site of the V-ATPase inhibitor apicularen is in the vicinity of those for bafilomycin and archazolid. Archazolid and apicularen: novel specific V-ATPase inhibitors

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