About: Total Synthesis of 5-N-Acetylardeemin and Amauromine: Practical Routes to Potential MDR Reversal Agents

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

About: Total Synthesis of 5-N-Acetylardeemin and Amauromine: Practical Routes to Potential MDR Reversal Agents Goto Sponge NotDistinct Permalink

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

article

Attributes	Values
rdf:type	Item
description	article (en) ലേഖനം (ml) wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 1999 (uk) im Dezember 1999 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q56832922-F672B0B0-A8AD-4F51-856F-533431EBDD10
publication date	1999-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56832922-56EB3C62-3B2A-47E5-BFF3-6C92491E3913
language of work or name	English
cites work	wds:Q56832922-46D0E3F8-6749-40BB-9A40-B87510DAF8D4 wds:Q56832922-5DA53D6B-E3A1-42DA-BF70-624D89AFC8DA wds:Q56832922-B2E2AC34-3766-4574-AA36-03D9E0B17868 wds:Q56832922-C314DBDF-7736-45A1-9896-8FE57ACB1121
cites work	Amauromine, a new vasodilator Taxonomy, isolation and characterization. 5-N-Acetylardeemin, a novel heterocyclic compound which reverses multiple drug resistance in tumor cells. I. Taxonomy and fermentation of the producing organism and biological activity. 5-N-acetylardeemin, a novel heterocyclic compound which reverses multiple drug resistance in tumor cells. II. Isolation and elucidation of the structure of 5-N-acetylardeemin and two congeners Gypsetin, a new inhibitor of acyl-CoA:cholesterol acyltransferase produced by Nannizzia gypsea var. incurvata IFO 9228. I. Fermentation, isolation, physico-chemical properties and biological activity
author name string	wds:Q56832922-4395399B-445C-4018-823C-5FE1EBFA7EF1 wds:Q56832922-50BE0309-53C3-41E7-A3F1-F743AB184A23 wds:Q56832922-75D64F69-BB21-436A-8183-30BC9F203E90 wds:Q56832922-B1BD5728-8F67-4F42-90DD-5F9ADC4C2BAC wds:Q56832922-BE2B407B-D840-415F-B226-DF436EF3912C wds:Q56832922-F752F9BD-383A-44CC-A3A5-56D3E5F35E87
author name string	Stephen P. Marsden Danuta Zatorska William G. Bornmann Andrzej Zatorski Samuel J. Danishefsky Kristopher M. Depew
rdfs:label	Total Synthesis of 5-N-Acetylardeemin and Amauromine: Practical Routes to Potential MDR Reversal Agents (en) Total Synthesis of 5-N-Acetylardeemin and Amauromine: Practical Routes to Potential MDR Reversal Agents (nl)
skos:prefLabel	Total Synthesis of 5-N-Acetylardeemin and Amauromine: Practical Routes to Potential MDR Reversal Agents (en) Total Synthesis of 5-N-Acetylardeemin and Amauromine: Practical Routes to Potential MDR Reversal Agents (nl)
name	Total Synthesis of 5-N-Acetylardeemin and Amauromine: Practical Routes to Potential MDR Reversal Agents (en) Total Synthesis of 5-N-Acetylardeemin and Amauromine: Practical Routes to Potential MDR Reversal Agents (nl)
title	wds:Q56832922-D04416E8-5B58-474D-9A16-1DCA67F5F7CC
title	Total Synthesis of 5-N-Acetylardeemin and Amauromine: Practical Routes to Potential MDR Reversal Agents (en)
page(s)	wds:Q56832922-3F7A763C-31A8-48AC-8844-170203FEEBFD
page(s)	11953-11963
instance of	wds:Q56832922-5A34161C-F65C-434C-984E-13C59394E57D
instance of	scholarly article
published in	wds:Q56832922-7D175C8A-6009-46E8-9D81-6440D311B32C
published in	Journal of the American Chemical Society
issue	wds:Q56832922-93CE59B8-B511-4247-B0AD-17744FF3B896
volume	wds:Q56832922-F6A0DFEA-7214-47A2-9CC0-C3E3F9893108
issue	51
volume	121
DOI	wds:Q56832922-851DAA29-7A99-4991-9E12-9E2D76501E79
DOI	http://dx.doi.org/10.1021/JA991558D
DOI	10.1021/JA991558D
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56832922
is cites work of	Total synthesis of (+)-gliocladin C enabled by visible-light photoredox catalysis The medicinal chemistry of multidrug resistance (MDR) reversing drugs 3D-QSAR analysis of 2,4,5- and 2,3,4,5-substituted imidazoles as potent and nontoxic modulators of P-glycoprotein mediated MDR. Asymmetric conjugate addition of oxindoles to 2-chloroacrylonitrile: a highly effective organocatalytic strategy for simultaneous construction of 1,3-nonadjacent stereocenters leading to chiral pyrroloindolines Total synthesis of (-)-depyranoversicolamide B. Natural products as inspiration for the development of asymmetric catalysis Engaging unactivated alkyl, alkenyl and aryl iodides in visible-light-mediated free radical reactions. Enantioselective organocatalytic construction of pyrroloindolines by a cascade addition-cyclization strategy: synthesis of (-)-flustramine B. Structure, bioactivity and synthesis of natural products with hexahydropyrrolo[2,3-b]indole. Silver-promoted Friedel-Crafts reaction: concise total synthesis of (-)-ardeemin, (-)-acetylardeemin and (-)-formylardeemin Reversal of multidrug resistance in vitro and in vivo by 5-N-formylardeemin, a new ardeemin derivative Noncatalytic reaction of isonitriles and carboxylic acids en route to amide-type linkages Diastereoselective Oxidative C-N/C-O and C-N/C-N Bond Formation Tandems Initiated by Visible Light: Synthesis of Fused N-Arylindolines A rapid stereocontrolled synthesis of the 3a-hydroxy-pyrrolo[2,3-b]indole skeleton, a building block for 10b-hydroxy-pyrazino[1',2':1,5]pyrrolo[2,3-b]indole-1,4-diones Total synthesis of indotertine A and drimentines A, F, and G. Concise Total Synthesis of (+)-Bionectins A and C. Cobalt(II)/silver relay catalytic isocyanide insertion/cycloaddition cascades: a new access to pyrrolo[2,3-b]indoles. Synthesis and Anticancer Activity of Epipolythiodiketopiperazine Alkaloids Efficient total synthesis of novel bioactive microbial metabolites Total synthesis guided structure elucidation of (+)-psychotetramine Privileged scaffolds in synthesis: 2,5-piperazinediones as templates for the preparation of structurally diverse heterocycles. Concise Total Synthesis of (+)-Gliocladins B and C A Three-Step Entry to the Aspirochlorine Family of Antifungal Agents Asymmetric dearomatization of indoles through a Michael/Friedel-Crafts-type cascade to construct polycyclic spiroindolines. Complexity generation by chemical synthesis: a five-step synthesis of (-)-chaetominine from L-tryptophan and its biosynthetic implications. Recent developments in the chemistry of quinazolinone alkaloids Enantioselective total synthesis of (-)-flustramines A, B and (-)-flustramides A, B via domino olefination/isomerization/Claisen rearrangement sequence. Straightforward Access to Hexahydropyrrolo[2,3-b]indole Core by a Regioselective C3-Azo Coupling Reaction of Arenediazonium Compounds with Tryptamines Synthesis of Disubstituted Pyrazino-Oxazine Derivatives with Controlled Stereochemistry Total Synthesis of Dimeric HPI Alkaloids Synthesis of circumdatin F and sclerotigenin. Use of the 2-nitrobenzyl group for protection of a diketopiperazine amide; synthesis of ent -fumiquinazoline G Electrooxidation enables highly regioselective dearomative annulation of indole and benzofuran derivatives Organic chemistry: A radical step forward
is cites work of	wds:Q34680333-39CE1011-EF95-4C81-8B7A-5A907B6721F2 wds:Q38991900-C584BB16-82AB-4F9B-99BA-B10508FD414F wds:Q46347700-707A11E8-77AC-4F94-8079-6DD15B908D5D wds:Q46956947-CE24A7BF-0D60-48AE-9376-CF80B454CFDA wds:Q34517156-2F7DF97A-77AB-47C9-BC6D-D0FC1116FFD1 wds:Q36326591-21B30747-13CD-469A-A6F1-59CCE37D9267 wds:Q34181087-FA829B9E-5B1B-4E23-BAC6-41D9671BB9A2 wds:Q41207267-702A055C-0464-4AD8-9AFF-316DA786BE0B wds:Q41974936-42C39A1D-592B-4531-9DD7-F726F1BE916D wds:Q50277528-9ECAEDD3-8465-4ECD-80D0-BF8DB2978359 wds:Q61478682-ED9EDAB0-1157-40B4-B1FA-B4ECA149F63C wds:Q38567694-80ACE82A-A701-4667-BFE3-F5202CD629ED wds:Q37020407-D66824EA-8E81-4AA8-93D5-8A051CE61465 wds:Q39428507-5BF91D14-9E75-4D27-95B4-470A5F432D31 wds:Q51711930-395064EE-56C1-466D-82B4-5E06A956B0DD

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, 194 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software