About: Tubelactomicin A, a novel 16-membered lactone antibiotic, from Nocardia sp. II. Structure elucidation

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About: Tubelactomicin A, a novel 16-membered lactone antibiotic, from Nocardia sp. II. Structure elucidation Goto Sponge NotDistinct Permalink

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scientific article published on 01 October 2000

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в жовтні 2000 (uk) article scientifique publié en 2000 (fr) im Oktober 2000 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'ochobre de 2000 (ast) scientific article published on 01 October 2000 (en)
publication date	wds:Q73334414-8E4372AA-9860-4FD0-B8E3-2E67E1DF90CB
publication date	2000-10-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q73334414-F72CC6E1-9CF8-48B1-8282-42CD5F8F8F42
cites work	Tubelactomicin A, a novel 16-membered lactone antibiotic, from Nocardia sp. I. Taxonomy, production, isolation and biological properties.
access restriction status	wds:Q73334414-184729E0-147B-48FE-A0B2-1D350B60BF2E
access restriction status	open access
author name string	wds:Q73334414-58E78487-3990-4D75-A8C2-DFDE8F098141 wds:Q73334414-7490F93C-3388-4B1C-B78D-3E8FB63C79AB wds:Q73334414-E6841690-B14F-4F8D-BD1B-392277809915 wds:Q73334414-FC41FA97-ADFF-4A95-AC51-4649AFDE1CA0
author name string	H Nakamura T Takeuchi M Igarashi H Naganawa
rdfs:label	Tubelactomicin A, a novel 16-membered lactone antibiotic, from Nocardia sp. II. Structure elucidation (en) Tubelactomicin A, a novel 16-membered lactone antibiotic, from Nocardia sp. II. Structure elucidation (nl)
skos:prefLabel	Tubelactomicin A, a novel 16-membered lactone antibiotic, from Nocardia sp. II. Structure elucidation (en) Tubelactomicin A, a novel 16-membered lactone antibiotic, from Nocardia sp. II. Structure elucidation (nl)
name	Tubelactomicin A, a novel 16-membered lactone antibiotic, from Nocardia sp. II. Structure elucidation (en) Tubelactomicin A, a novel 16-membered lactone antibiotic, from Nocardia sp. II. Structure elucidation (nl)
title	wds:Q73334414-CD5475B1-F5B6-4537-A317-B7F97CA5992A
title	Tubelactomicin A, a novel 16-membered lactone antibiotic, from Nocardia sp. II. Structure elucidation (en)
page(s)	wds:Q73334414-7D9D2355-13D2-48FD-B5B0-A9CEBA9D54FB
page(s)	1102-1107
instance of	wds:Q73334414-710ADD0E-0E27-4F40-BBDC-B1F52C4D956F
instance of	scholarly article
main subject	wds:Q73334414-41BE3DB9-E5CA-4068-9216-DC0260C964BB wds:Q73334414-8C739C4B-D2CC-4290-8207-B5C236CA28FD wds:Q73334414-EDAD4395-E666-43C8-A14B-A09B26194EA6
main subject	Nocardia (1S,2E,4E,6S,7R,8E,13R,16R,17S,20S,21R,22S)-7,21-dihydroxy-6,13,16,20,24-pentamethyl-15-oxo-14-oxatricyclo[14.8.0.017,22]tetracosa-2,4,8,23-tetraene-8-carboxylic acid tubelactomicin A
PubMed ID	wds:Q73334414-64B3CDE6-E15E-4A40-BB68-76B93AA87E94
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11132954
PubMed ID	11132954
published in	wds:Q73334414-EA310EB5-C51C-4339-A7C5-047593DF418C
full work available at URL	wds:Q73334414-2A51E431-1362-4DC8-AF6F-6EF64D66850E
published in	The Journal of Antibiotics
full work available at URL	https://www.jstage.jst.go.jp/article/antibiotics1968/53/10/53_10_1102/_pdf
issue	wds:Q73334414-68258B60-58B7-497C-A33A-E92FE5353460
volume	wds:Q73334414-2012BBD8-AB55-43D3-A8E2-AD2C23089674
issue	10
volume	53
DOI	wds:Q73334414-BB481985-7B29-46ED-A168-5BA77FDF385D
DOI	http://dx.doi.org/10.7164/ANTIBIOTICS.53.1102
DOI	10.7164/ANTIBIOTICS.53.1102
online access status	wds:Q73334414-A80AE020-A195-4EFC-A0FC-3D1BDDC33564
online access status	open access
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73334414
is cites work of	A genome sequence-based approach to taxonomy of the genus Nocardia. Recent advances in natural product synthesis by using intramolecular Diels-Alder reactions. Functional diversity of Nocardia in metabolism Enzymatic catalysis of the Diels-Alder reaction in the biosynthesis of natural products Tubelactomicin A, a novel 16-membered lactone antibiotic, from Nocardia sp. I. Taxonomy, production, isolation and biological properties. Total synthesis of (+)-tubelactomicin A. 2. Synthesis of the upper-half segment and completion of the total synthesis New natural products to meet the antibiotic crisis: a personal journey Total syntheses of polyketide-derived bioactive natural products Hydroxyl-Assisted Carbonylation of Alkenyltin Derivatives: Development and Application to a Formal Synthesis of Tubelactomicin A Total synthesis of (+)-tubelactomicin A. 1. Stereoselective synthesis of the lower-half segment by an intramolecular Diels-Alder approach Total syntheses of natural tubelactomicins B, D, and E: establishment of their stereochemistries
is cites work of	wds:Q81759096-FCE5CF81-226A-42C2-9757-9CDAC9BE292C wds:Q48634003-7C3F26F8-A738-48E0-8294-E06DBAD87283 wds:Q92965508-4BB23B19-696C-4DB9-B4F5-B7135EA8C736 wds:Q87625801-5F43211B-F4FA-4216-95DC-2BBE4657CD63 wds:Q36561774-66C372DB-5118-41F2-AECA-38095453FE2F wds:Q34322921-053D0FCE-3E1E-4B35-B13A-DBFED353A10B wds:Q38131846-4B7DADD0-5B2C-4FE7-AD73-E7E11419A8D5 wds:Q80600257-CC338735-31D9-402E-A1F6-5C096F3B01BD wds:Q36340546-0A31582F-9132-4F8F-98C7-0B8AB67EE4D0 wds:Q48743376-D07519FE-2C8E-4DD8-B6C5-92A2565B0F47 wds:Q81759093-E01F079E-F2E2-4978-97B4-D23E835F2923
is pr:P248 of	wdref:78825b0ae6852c224aad973f9044bd54052611d0

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