About: Sterospecificity of hydrolytic enzymes in their reaction with optically active organophosphorus compounds. I. The reaction of cholinesterases and paraoxonase with S-alkyl P-nitrophenyl methylphosphonothiolates

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

About: Sterospecificity of hydrolytic enzymes in their reaction with optically active organophosphorus compounds. I. The reaction of cholinesterases and paraoxonase with S-alkyl P-nitrophenyl methylphosphonothiolates 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 December 1965

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 1965 (uk) im Dezember 1965 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 01 December 1965 (en) artículu científicu espublizáu n'avientu de 1965 (ast)
publication date	wds:Q68557903-7547E65F-DCE8-4012-AB77-6AE6D6630F77
publication date	1965-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q68557903-8C57CE00-F1C8-4C01-B823-A4A934FB2725
language of work or name	English
author name string	wds:Q68557903-1352E929-0F8A-40F9-AEA3-46CE33E43070 wds:Q68557903-91F236D7-5060-4FF6-B744-D4C69F4151BE
author name string	A J Oooms H L Boter
rdfs:label	Sterospecificity of hydrolytic enzymes in their reaction with optically active organophosphorus compounds. I. The reaction of cholinesterases and paraoxonase with S-alkyl P-nitrophenyl methylphosphonothiolates (en) Sterospecificity of hydrolytic enzymes in their reaction with optically active organophosphorus compounds. I. The reaction of cholinesterases and paraoxonase with S-alkyl P-nitrophenyl methylphosphonothiolates (nl)
skos:prefLabel	Sterospecificity of hydrolytic enzymes in their reaction with optically active organophosphorus compounds. I. The reaction of cholinesterases and paraoxonase with S-alkyl P-nitrophenyl methylphosphonothiolates (en) Sterospecificity of hydrolytic enzymes in their reaction with optically active organophosphorus compounds. I. The reaction of cholinesterases and paraoxonase with S-alkyl P-nitrophenyl methylphosphonothiolates (nl)
name	Sterospecificity of hydrolytic enzymes in their reaction with optically active organophosphorus compounds. I. The reaction of cholinesterases and paraoxonase with S-alkyl P-nitrophenyl methylphosphonothiolates (en) Sterospecificity of hydrolytic enzymes in their reaction with optically active organophosphorus compounds. I. The reaction of cholinesterases and paraoxonase with S-alkyl P-nitrophenyl methylphosphonothiolates (nl)
title	wds:Q68557903-564EC837-016C-46F0-9181-5B83F3008F05
title	Sterospecificity of hydrolytic enzymes in their reaction with optically active organophosphorus compounds. I. The reaction of cholinesterases and paraoxonase with S-alkyl P-nitrophenyl methylphosphonothiolates (en)
page(s)	wds:Q68557903-7F8B9699-5C50-4532-8BD3-D74D9311B058
page(s)	1839-1845
instance of	wds:Q68557903-76577AE4-69FF-45A2-A547-F9E56A2DCA66
instance of	scholarly article
PubMed ID	wds:Q68557903-C31983C6-CBC4-4584-9A4B-C368E6E0CFF9
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/4286530
PubMed ID	4286530
published in	wds:Q68557903-5AF0B3FC-1097-4911-AA34-092CAEF37C4F
published in	Biochemical Pharmacology
issue	wds:Q68557903-F48AFB02-7B20-489B-BAFE-3DC77CF9E167
volume	wds:Q68557903-B7CD51D2-F787-4DC8-8D0B-FFEFF692D845
issue	12
volume	14
DOI	wds:Q68557903-FFB6E629-7CE1-4ACB-8C3F-D2A8097E090B
DOI	http://dx.doi.org/10.1016/0006-2952(65)90274-1
DOI	10.1016/0006-2952(65)90274-1
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q68557903
is cites work of	Stereoselectivity and Affinity in Molecular Pharmacology Studies on the optically active isomers of O, O-diethyl malathion and O, O-diethyl malaoxon Stereochemistry, a basis for sophisticated nonsense in pharmacokinetics and clinical pharmacology The toxicological properties of impurities in malathion Cholinergic and anticholinergic drugs, do they act on common receptors? Relationships between the structure of organophosphorus compounds and their activity as acetylcholinesterase inhibitors The affinity and phosphorylation constants of the optical isomers of O,O-diethyl malaoxon and the geometric isomers of phosdrin with acetylcholinesterase Inhibition of acetylcholinesterase by the enantiomers of isopropyl S-2-trimethylammonioethyl methylphosphonothioate iodide. Affinity and phosphorylation constants The inhibition of cholinesterase by organophosphorus compounds in the presence of substrate Optically active organophosphoramides. O-2,4-dichlorophenyl O-methyl isopropylphosphoramidothioate and some related compounds Organophosphate inhibitors The stereospecificity of hydrolysis of methyl n-butyl p-nitrophenyl phosphate by serum phosphotriesterases (EC 3.1.1.2) and by acetylcholinesterases (EC 3.1.1.7)
is cites work of	wds:Q39133633-43582F8C-5ABD-43AA-B8BE-A2571B64E6E5 wds:Q39161235-6C13F609-D829-4692-AE5F-86A79E7BD06E wds:Q42237134-8A1E2FFE-59D8-432D-A3DD-E93C03D902A1 wds:Q71262068-BEFD7426-1B86-423D-8D70-736F4F09A1A7 wds:Q28321101-AF040FC8-3496-4830-9471-CE8EDA7637B6 wds:Q47838947-5D94F762-970A-42B1-98EF-6C50F7987760 wds:Q52503068-75F3D028-F7D6-4472-9FF1-CCB6C5C9F11F wds:Q70927532-FA3E0410-66EC-4F53-8322-D6BCEA8DCB73 wds:Q71774201-6728CF4F-CACC-433D-B468-42DBF86E8E15 wds:Q34054672-A849FFC3-A1E7-4D58-8A0D-219F2738993A wds:Q72371532-FB199B15-1DC9-4E8D-B271-CF40602C8DB9

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