About: Consensus superiority of the pharmacophore-based alignment, over maximum common substructure (MCS): 3D-QSAR studies on carbamates as acetylcholinesterase inhibitors

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

About: Consensus superiority of the pharmacophore-based alignment, over maximum common substructure (MCS): 3D-QSAR studies on carbamates as acetylcholinesterase inhibitors 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 June 2009

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 2009 (uk) artículu científicu espublizáu en xunu de 2009 (ast) scientific article published on 01 June 2009 (en)
publication date	wds:Q83830002-09DBF93C-C423-40D1-918C-C71FA0F288E0
publication date	2009-06-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q83830002-4D75D10B-4EE9-4F9C-8E1B-10FD68B075F4 wds:Q83830002-BEE8DD0A-7DC2-486D-84D6-072FACD8BC67
author name string	Anil K Saxena Shailendra S Chaudhaery
rdfs:label	Consensus superiority of the pharmacophore-based alignment, over maximum common substructure (MCS): 3D-QSAR studies on carbamates as acetylcholinesterase inhibitors (en) Consensus superiority of the pharmacophore-based alignment, over maximum common substructure (MCS): 3D-QSAR studies on carbamates as acetylcholinesterase inhibitors (nl)
skos:prefLabel	Consensus superiority of the pharmacophore-based alignment, over maximum common substructure (MCS): 3D-QSAR studies on carbamates as acetylcholinesterase inhibitors (en) Consensus superiority of the pharmacophore-based alignment, over maximum common substructure (MCS): 3D-QSAR studies on carbamates as acetylcholinesterase inhibitors (nl)
name	Consensus superiority of the pharmacophore-based alignment, over maximum common substructure (MCS): 3D-QSAR studies on carbamates as acetylcholinesterase inhibitors (en) Consensus superiority of the pharmacophore-based alignment, over maximum common substructure (MCS): 3D-QSAR studies on carbamates as acetylcholinesterase inhibitors (nl)
author	wds:Q83830002-C4A8E73A-AC54-4D80-84C9-169F8FF11153
author	Kuldeep K Roy
title	wds:Q83830002-365416C2-1B28-40A6-830E-FB10CD346142
title	Consensus superiority of the pharmacophore-based alignment, over maximum common substructure (MCS): 3D-QSAR studies on carbamates as acetylcholinesterase inhibitors (en)
page(s)	wds:Q83830002-D65B4E20-F759-4415-B09D-174405C2C96F
page(s)	1590-1601
instance of	wds:Q83830002-898DF986-BA6C-45E3-B541-E7FBE68365C2
instance of	scholarly article
main subject	wds:Q83830002-38CD9707-6D9A-4366-BF3C-C9D129B3E696
main subject	maximum common substructure
PubMed ID	wds:Q83830002-67891491-7BCB-4A74-8823-7AB110540D10
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/19441865
PubMed ID	19441865
DBLP publication ID	wds:Q83830002-B18D3A7A-DFE3-49C9-9D84-B208869707B5
DBLP publication ID	https://dblp.org/rec/journals/jcisd/ChaudhaeryRS09
DBLP publication ID	journals/jcisd/ChaudhaeryRS09
published in	wds:Q83830002-D2FD6E34-D93E-4F45-A535-77A4FF0EC254
published in	Journal of Chemical Information and Modeling
issue	wds:Q83830002-247AD060-55EB-41EB-BE97-0A5A5EB926FD
volume	wds:Q83830002-977BC582-DE09-4B0E-938D-28CDB80D9DD3
issue	6
volume	49
DOI	wds:Q83830002-0BF62DEB-4810-431E-B7B5-A706F06EBA3B
DOI	http://dx.doi.org/10.1021/CI900049E
DOI	10.1021/CI900049E
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q83830002
is cites work of	Molecular Docking Guided Comparative GFA, G/PLS, SVM and ANN Models of Structurally Diverse Dual Binding Site Acetylcholinesterase Inhibitors. Benefits of statistical molecular design, covariance analysis, and reference models in QSAR: a case study on acetylcholinesterase Comparative Molecular Field Analysis (CoMFA) and Comparative Molecular Similarity Indices Analysis (CoMSIA) studies on α(1A)-adrenergic receptor antagonists based on pharmacophore molecular alignment Identification of potentially potent Heme Oxygenase-1 inhibitors through 3D-QSAR coupled to scaffold hopping analysis. Discovery of High-Affinity Cannabinoid Receptors Ligands through a 3D-QSAR Ushered by Scaffold-Hopping Analysis Combining structure-based pharmacophore modeling, virtual screening, and in silico ADMET analysis to discover novel tetrahydro-quinoline based pyruvate kinase isozyme M2 activators with antitumor activity Discovery of novel focal adhesion kinase inhibitors using a hybrid protocol of virtual screening approach based on multicomplex-based pharmacophore and molecular docking Rationalizing lead optimization by consensus 2D- CoMFA CoMSIA GRIND (3D) QSAR guided fragment hopping in search of γ-secretase inhibitors Combined structure-based pharmacophore and 3D-QSAR studies on phenylalanine series compounds as TPH1 inhibitors Molecular docking studies of natural alkaloids as acetylcholinesterase (AChE1) inhibitors in Aedes aegypti Repurposing of FDA-Approved Drugs for Treating Iatrogenic Botulism: A Paired 3D-QSAR/Docking Approach†
is cites work of	wds:Q30620538-458424BB-C500-406E-A5ED-09AB4EB73E73 wds:Q84790487-0C4C9B2D-9CC1-4C82-B20C-5D9E385173F2 wds:Q28727996-F99EA3BE-347F-4CF2-9289-147296E7D158 wds:Q28709966-24488B50-FE94-4964-8A9D-721F34D3D443 wds:Q111349074-2D12C6DF-8059-4FEB-B8EC-4171A4F832DD wds:Q28655910-058920A0-63D8-44C5-9BC9-970F5DAEBE9D wds:Q58696615-703D43D7-8755-4956-90D8-16322ABA31E7 wds:Q91485205-A41E05BC-B2F4-4BC5-B395-9F824C827EF0 wds:Q39550895-17E78AEF-F055-446F-A10B-0A61769E3B3E wds:Q52564046-96A1656E-8A6C-4B93-9A98-F755E17C842C wds:Q38988090-6DFB6DBD-A061-4F55-8F18-2B576450EBDE

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