About: Enantioseparation of dihydropyridine derivatives by means of neutral and negatively charged beta-cyclodextrin derivatives using capillary electrophoresis

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About: Enantioseparation of dihydropyridine derivatives by means of neutral and negatively charged beta-cyclodextrin derivatives using capillary electrophoresis Goto Sponge NotDistinct Permalink

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scientific article published on 01 November 2000

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в листопаді 2000 (uk) im November 2000 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en payares de 2000 (ast) scientific article published on 01 November 2000 (en)
publication date	wds:Q73678347-771B6774-276B-450B-9D74-AC4C8686B360
publication date	2000-11-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q73678347-0924C45B-7B1F-4BD0-B702-CF3BD96317D1 wds:Q73678347-102061A0-1A8A-4C43-8FD1-ED12621C1671 wds:Q73678347-182E2CA0-B667-4D00-877A-8B7260BF5DCF wds:Q73678347-2596EDB8-3FD9-47E4-8A85-40FF1036D3A3 wds:Q73678347-491E74B7-D035-48C2-A053-6CDE0DA938F4 wds:Q73678347-755F973D-3355-4350-89B6-FF9C39CBCA50 wds:Q73678347-80FEBF51-4FC0-4E56-B93D-5202DF74C582 wds:Q73678347-81326690-53A2-46BC-94B8-23CA806F7BB9 wds:Q73678347-85BCC4D0-49E0-4091-929C-670B8D1BC7AE wds:Q73678347-919AABD8-FA94-49D5-945E-CE15A13B15E2 wds:Q73678347-FCF77CB3-759D-498F-A3F3-878A6FED9119
cites work	Identification of chiral drug isomers by capillary electrophoresis Resolution of newly synthesized racemic dihydropyridines with different chiral selectors by means of capillary electrophoresis Use of negatively charged sulfobutyl ether-β-cyclodextrin for enantiomeric separation by capillary electrophoresis Chiral resolution of cationic drugs of forensic interest by capillary electrophoresis with mixtures of neutral and anionic cyclodextrins The optical isomers of the 1,4-dihydropyridine BAY K 8644 show opposite effects on Ca channels Structural basis of drug binding to L Ca2+ channels Use of cyclodextrins in capillary zone electrophoresis When a truck becomes a motorcycle: the impact of sample load on a chiral capillary electrophoresis separation using mixtures of neutral and sulfated cyclodextrins Enantiomer separation of dihydropyridine calcium antagonists with cyclodextrins as chiral selectors: structural correlation Stereoselective pharmacokinetics of dihydropyridine calcium antagonists Control of enantiomer migration order in capillary electrophoresis separations using sulfobutyl ether beta-cyclodextrin
author name string	wds:Q73678347-D813A792-9B78-40C4-B097-34E6C5B33B49
author name string	Christians T
rdfs:label	Enantioseparation of dihydropyridine derivatives by means of neutral and negatively charged beta-cyclodextrin derivatives using capillary electrophoresis (en) Enantioseparation of dihydropyridine derivatives by means of neutral and negatively charged beta-cyclodextrin derivatives using capillary electrophoresis (nl)
skos:prefLabel	Enantioseparation of dihydropyridine derivatives by means of neutral and negatively charged beta-cyclodextrin derivatives using capillary electrophoresis (en) Enantioseparation of dihydropyridine derivatives by means of neutral and negatively charged beta-cyclodextrin derivatives using capillary electrophoresis (nl)
name	Enantioseparation of dihydropyridine derivatives by means of neutral and negatively charged beta-cyclodextrin derivatives using capillary electrophoresis (en) Enantioseparation of dihydropyridine derivatives by means of neutral and negatively charged beta-cyclodextrin derivatives using capillary electrophoresis (nl)
author	wds:Q73678347-EF9F3923-7027-4398-B960-E165ABFC3C34
author	Ulrike Holzgrabe
title	wds:Q73678347-990332C3-C9D5-4612-A54A-C33617D767ED
title	Enantioseparation of dihydropyridine derivatives by means of neutral and negatively charged beta-cyclodextrin derivatives using capillary electrophoresis (en)
page(s)	wds:Q73678347-B13FD530-3925-461B-869F-A36C4877000D
page(s)	3609-3617
instance of	wds:Q73678347-551B5BB6-FEAD-4CA6-AA51-491E47F89E70
instance of	scholarly article
PubMed ID	wds:Q73678347-03A532B1-F804-4F8A-B4BB-F937BAB62912
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11271478
PubMed ID	11271478
published in	wds:Q73678347-BCA31384-8C58-4A28-B571-ACAED41DEF11
published in	Electrophoresis
issue	wds:Q73678347-F41DD014-2000-41EA-AE4C-9DE67B4AD786
volume	wds:Q73678347-953B3EC8-AA2B-42E5-8419-724F3277369E
issue	17
volume	21
DOI	wds:Q73678347-BB07585E-C23B-4507-8581-9D02B1C60DAB
DOI	http://dx.doi.org/10.1002/1522-2683(200011)21:17%3C3609::AID-ELPS3609%3E3.0.CO;2-0
DOI	10.1002/1522-2683(200011)21:17<3609::AID-ELPS3609>3.0.CO;2-0
describes a project that uses	wds:Q73678347-8E27EF92-CA82-4A7C-98FF-AD7A22E6679E
describes a project that uses	capillary electrophoresis
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73678347
is cites work of	New single-isomer chiral selector for capillary electrophoresis: the highly water-soluble heptakis(2-N,N-dimethylcarbamoyl)-beta-cyclodextrin Evaluation of the impurity profile of amino acids by means of CE. Capillary electrophoresis method for the determination of isradipine enantiomers: stability studies and pharmaceutical formulation analysis A selective HPLC method for determination of lercanidipine in tablets The role of cyclodextrins in chiral capillary electrophoresis Development of a stability-indicating CE assay for the determination of amlodipine enantiomers in commercial tablets. Evidences of cyclodextrin-mediated enantioselective photodegradation of rac-nicardipine by capillary electrophoresis Spectrophotometric determination of labetalol and lercanidipine in pure form and in pharmaceutical preparations using ferric-1,10-phenanthroline Enantioseparation of chiral thiobarbiturates using cyclodextrin-modified capillary electrophoresis Nimodipine: analytical profile Direct Enantiomeric Resolution of Seventeen Racemic 1,4-Dihydropyridine-Based Hexahydroquinoline Derivatives by HPLC.
is cites work of	wds:Q30646154-4D2EC7D0-84D7-4763-8E6B-A18F28C6EDE8 wds:Q44298121-5613A904-1EB0-4FEE-8D3B-5207401CECD8 wds:Q36735584-ED0E650E-BF2F-420F-9CC0-60E42200C2AD wds:Q43758315-952F60CB-2000-4184-824D-0F3209E72540 wds:Q37141832-18EDCE9B-E4BD-44DC-82F1-65A853537DF1 wds:Q85066025-82CC7677-5998-4A98-8BB8-0425E243B7FF wds:Q42719463-729992E2-AB01-4694-BD02-E50A707C1467 wds:Q43766213-843A1574-BB72-459D-84ED-8F72A8A20F60 wds:Q43758311-C67143BC-6801-451E-BE57-67C4016D8170 wds:Q46263522-6AAA4545-ADF3-417C-BDA3-1B1F56D283D0 wds:Q64962051-5669ACC4-57FF-4613-B26D-DB64531692F5

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