About: Michael-type addition of illudin S, a toxic substance from Lampteromyces japonicus, with cysteine and cysteine-containing peptides in vitro

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Michael-type addition of illudin S, a toxic substance from Lampteromyces japonicus, with cysteine and cysteine-containing peptides in vitro 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 01 February 1996

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в лютому 1996 (uk) article scientifique publié en 1996 (fr) im Februar 1996 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en febreru de 1996 (ast) artikull shkencor i botuar më 01 shkurt 1996 (sq) scientific article published on 01 February 1996 (en)
publication date	wds:Q71982065-29FBFF9E-00F7-49E6-AC83-AD8DD070BC9B
publication date	1996-02-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q71982065-0B6A476E-5028-4490-BBE2-5E1AF533485B
language of work or name	English
cites work	wds:Q71982065-0566871F-C136-42AD-8DE0-DA5037C8672D wds:Q71982065-0677A980-908C-487C-AB31-DF8ABA2C7396 wds:Q71982065-25CC8856-8EC9-46C3-8802-B26E38243369 wds:Q71982065-34BF686F-A739-4A99-AAB6-178B239C32B7 wds:Q71982065-6B9B1A4E-CF3D-4484-B607-3E2E0DA2B051 wds:Q71982065-6CB13CB7-654D-48AC-8F5A-75C76B2C01AB wds:Q71982065-6DEFEE1B-6CA0-4E2F-A52D-1479B44B6FD9 wds:Q71982065-6FD87AAA-3952-415E-84D5-90B0C23D3331 wds:Q71982065-8991C95F-F37C-49B3-B993-11B2BF64D6FB wds:Q71982065-F9F2FD98-93E7-41AB-B9F0-0A3EBDC2ECDB
cites work	Enzymes catalysing conjugations of glutathione with alpha-beta-unsaturated carbonyl compounds Illudin s (lampterol) On the mechanism of toxicity of illudins: the role of glutathione Metabolism of illudin S, a toxic principle of Lampteromyces japonicus, by rat liver. I. Isolation and identification of cyclopropane ring-cleavage metabolites Metabolism by rat liver cytosol of illudin S, a toxic substance of Lampteromyces japonicus. II. Characterization of illudin S-metabolizing enzyme FUNGAL METABOLITES. THE STRUCTURES OF THE NOVEL SESQUITERPENOIDS ILLUDIN-S AND -M Isolation of Lampterol, an Antitumour Substance from Lampteromyces japonicus STRUCTURE AND REACTIONS OF ILLUDIN-S (LAMPTEROL) STEREOCHEMISTRY OF ILLUDIN-S (LAMPTEROL) Distribution of enzymes that catalyse reactions of glutathione with alpha beta-unsaturated compounds
access restriction status	wds:Q71982065-7FB9FC00-D41D-43E2-B46E-6B1B8724CF41
access restriction status	open access
author name string	wds:Q71982065-3B1D9685-B610-4CBA-9864-B213C504CAF7 wds:Q71982065-9159651A-FA3D-4FB1-B557-7EF8CEA8C262 wds:Q71982065-AF4526C6-972A-4691-9635-23627C87DF0A wds:Q71982065-C59E80E7-0308-4538-A87D-09A4C0E5AD5A
author name string	K Tanaka T Inoue Y Tezuka T Kikuchi
rdfs:label	Michael-type addition of illudin S, a toxic substance from Lampteromyces japonicus, with cysteine and cysteine-containing peptides in vitro (en) Michael-type addition of illudin S, a toxic substance from Lampteromyces japonicus, with cysteine and cysteine-containing peptides in vitro (nl) Michael-type addition of illudin S, a toxic substance from Lampteromyces japonicus, with cysteine and cysteine-containing peptides in vitro (sq)
skos:prefLabel	Michael-type addition of illudin S, a toxic substance from Lampteromyces japonicus, with cysteine and cysteine-containing peptides in vitro (en) Michael-type addition of illudin S, a toxic substance from Lampteromyces japonicus, with cysteine and cysteine-containing peptides in vitro (nl) Michael-type addition of illudin S, a toxic substance from Lampteromyces japonicus, with cysteine and cysteine-containing peptides in vitro (sq)
name	Michael-type addition of illudin S, a toxic substance from Lampteromyces japonicus, with cysteine and cysteine-containing peptides in vitro (en) Michael-type addition of illudin S, a toxic substance from Lampteromyces japonicus, with cysteine and cysteine-containing peptides in vitro (nl) Michael-type addition of illudin S, a toxic substance from Lampteromyces japonicus, with cysteine and cysteine-containing peptides in vitro (sq)
title	wds:Q71982065-B637FA68-A137-4BFB-AC12-D2F7552103B2
title	Michael-type addition of illudin S, a toxic substance from Lampteromyces japonicus, with cysteine and cysteine-containing peptides in vitro (en)
page(s)	wds:Q71982065-FED9D4CA-0946-4D2D-A68F-9B9C5FA63E57
page(s)	273-279
instance of	wds:Q71982065-E6B2A63C-1A6C-46C8-AEC4-650AB5D3FE17
instance of	scholarly article
main subject	wds:Q71982065-04F63718-D0D7-470F-895E-75DF56D379CF wds:Q71982065-0B2DAA01-7339-4910-BDB1-94F77A69759D wds:Q71982065-3B0A1A30-240D-4ADC-A90E-20D26EF75E8F wds:Q71982065-CE3F2D12-6363-4FFA-89AD-F01DAEB8F407
main subject	Lampteromyces japonicus Omphalotus guepiniiformis Omphalotus guepiniformis illudin S
PubMed ID	wds:Q71982065-B4B3E358-786E-4962-959D-E2AF4DF4A5A4
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/8998835
PubMed ID	8998835
published in	wds:Q71982065-430D0E88-2AE4-42D6-9BD3-E2576C23F3C4
full work available at URL	wds:Q71982065-4BE8FD09-F554-49BE-A47F-B0BCD65F0015
published in	Chemical & Pharmaceutical Bulletin
full work available at URL	https://www.jstage.jst.go.jp/article/cpb1958/44/2/44_2_273/_pdf
issue	wds:Q71982065-6DF5EEE0-9396-4D84-B7C3-7F476CA5E793
volume	wds:Q71982065-B8FC2659-9F2C-4651-A166-9CAFD0FE7EE0
issue	2
volume	44
DOI	wds:Q71982065-7218FD79-E5E2-49F7-AFCE-FDECF0D33EB9
DOI	http://dx.doi.org/10.1248/CPB.44.273
DOI	10.1248/CPB.44.273
online access status	wds:Q71982065-E4BAC2E5-974F-410A-9BDE-8304CA2E6BF9
online access status	open access
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q71982065
is cites work of	Anticancer active illudins: recent developments of a potent alkylating compound class Mass spectrometry Profiling patterns of glutathione reductase inhibition by the natural product illudin S and its acylfulvene analogues Identification of illudins in Omphalotus nidiformis and Omphalotus olivascens var. indigo by column liquid chromatography-atmospheric pressure chemical ionization tandem mass spectrometry Chemistry and biology of acylfulvenes: sesquiterpene-derived antitumor agents. Quantification of acylfulvene- and illudin S-DNA adducts in cells with variable bioactivation capacities. Covalent Modifiers: A Chemical Perspective on the Reactivity of α,β-Unsaturated Carbonyls with Thiols via Hetero-Michael Addition Reactions Total synthesis of the sesquiterpene (+/-)-illudin C via an intramolecular nitrile oxide cycloaddition Susceptibility of the antioxidant selenoenyzmes thioredoxin reductase and glutathione peroxidase to alkylation-mediated inhibition by anticancer acylfulvenes Sulfotransferase-independent genotoxicity of illudin S and its acylfulvene derivatives in bacterial and mammalian cells. Mechanistic insight into 3-methylmercaptopropionate metabolism and kinetical regulation of demethylation pathway in marine dimethylsulfoniopropionate-catabolizing bacteria Constituents of the Fruiting Body of Poisonous Mushroom Omphalotus japonicus
is cites work of	wds:Q33737904-B498FDC1-9A42-4909-86B2-15E13850C3F7 wds:Q33420355-14737F31-95B9-44CF-9E2E-E036CABC4919 wds:Q77191443-F132A5E8-76A3-4458-9283-66D1948C7124 wds:Q35535940-7D830F01-FAFE-4101-AACA-16B138548A99 wds:Q29248430-E3CC55D2-7A0C-4104-9DFE-EC74CDFC792B wds:Q37381349-5CD62841-8940-4DD9-9801-710EEE52AC0F

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 180 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2025 OpenLink Software