About: Dihydropyrimidine calcium channel blockers. 2. 3-substituted-4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridines

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About: Dihydropyrimidine calcium channel blockers. 2. 3-substituted-4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridines Goto Sponge NotDistinct Permalink

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scientific article published on 01 September 1990

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у вересні 1990 (uk) article scientifique publié en 1990 (fr) im September 1990 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en setiembre de 1990 (ast) scientific article published on 01 September 1990 (en)
publication date	wds:Q68898212-6E508DB7-F1D3-473F-9AE2-02C65C592C5A
publication date	1990-09-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q68898212-E2AA8938-A26A-4A8A-903C-A9985D6F14DB
language of work or name	English
author name string	wds:Q68898212-10A69139-471B-491A-8B52-35AD61CAFE8F wds:Q68898212-21EC46B8-A1B2-4A6E-B658-EE6BA52EB22E wds:Q68898212-3A8E557D-7123-4127-96A8-FA2D177BC5AB wds:Q68898212-676E75E8-A7EF-46D9-9258-58920644C16F wds:Q68898212-6EA84159-3415-48EB-BA4B-D8F5D9BB313C wds:Q68898212-7CA8BBF0-61C9-4963-9F73-FAFFDBE4C9F7 wds:Q68898212-82F15D76-1369-4B20-A97F-53B4FA4BC6C6 wds:Q68898212-9A1955AA-8EAE-4375-A760-026A1822C264 wds:Q68898212-C9A3AE09-D7D4-4507-BE16-CF8099A93E23 wds:Q68898212-F120C560-3ED4-48F0-8D88-857844B0C5C0
author name string	J Schwartz S Moreland M F Malley B N Swanson D M Floyd G C Rovnyak J Z Gougoutas K M Smillie K S Atwal S D Kimball
rdfs:label	Dihydropyrimidine calcium channel blockers. 2. 3-substituted-4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridines (en) Dihydropyrimidine calcium channel blockers. 2. 3-substituted-4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridines (nl)
skos:prefLabel	Dihydropyrimidine calcium channel blockers. 2. 3-substituted-4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridines (en) Dihydropyrimidine calcium channel blockers. 2. 3-substituted-4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridines (nl)
name	Dihydropyrimidine calcium channel blockers. 2. 3-substituted-4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridines (en) Dihydropyrimidine calcium channel blockers. 2. 3-substituted-4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridines (nl)
title	wds:Q68898212-4C07C77A-EDE1-4B98-A96D-BA8CC9CF85FE
title	Dihydropyrimidine calcium channel blockers. 2. 3-substituted-4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridines (en)
page(s)	wds:Q68898212-C0BB69ED-1499-437F-85E0-0A0D09219116
page(s)	2629-2635
instance of	wds:Q68898212-CE891C6F-F679-4F9A-9342-D5D7A396AF22
instance of	scholarly article
PubMed ID	wds:Q68898212-7DAE19BC-6D28-40D5-8B54-AA9AFBBA06F7
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/2391701
PubMed ID	2391701
published in	wds:Q68898212-1576CDB7-4CCF-4EDB-9B8B-D4A142752C4A
published in	Journal of Medicinal Chemistry
issue	wds:Q68898212-6B9A1657-F80A-460D-BBB1-F23D1DF8D9DE
volume	wds:Q68898212-10594D02-E386-439A-8831-C2AB17D3AC72
issue	9
volume	33
DOI	wds:Q68898212-289957B6-2321-4E51-9523-7C4678A1F7FB
DOI	http://dx.doi.org/10.1021/JM00171A044
DOI	10.1021/JM00171A044
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q68898212
is cites work of	Biologically active dihydropyrimidones of the Biginelli-type--a literature survey 100 years of the biginelli dihydropyrimidine synthesis (2E)-3-(6-Meth-oxy-naphthalen-2-yl)-1-[4-(methyl-sulfan-yl)phen-yl]prop-2-en-1-one Highly versatile solid phase synthesis of biofunctional 4-aryl-3,4-dihydropyrimidines using resin-bound isothiourea building blocks and multidirectional resin cleavage The unexpected influence of aryl substituents in N-aryl-3-oxobutanamides on the behavior of their multicomponent reactions with 5-amino-3-methylisoxazole and salicylaldehyde p-TOLUENESULFONIC ACID-CATALYZED EFFICIENT SYNTHESIS OF DIHYDROPYRIMIDINES: IMPROVED HIGH YIELDING PROTOCOL FOR THE BIGINELLI REACTION Synthesis and in vitro calcium antagonist activity of 4-aryl-7,7-dimethyl/1,7,7-trimethyl-1,2,3,4,5,6,7,8-octahydroquinazoline-2,5-dione derivatives 5-Acetyl-4-(4-chloro-phen-yl)-6-methyl-3,4-dihydro-pyrimidine-2(1H)-thione Ultrasound promoted ZrCl(4) catalyzed rapid synthesis of substituted 1,2,3,4-tetrahydropyrimidine-2-ones in solvent or dry media. Ammonium Trifluoroacetate-Mediated Synthesis of 3,4-dihydropyrimidin-2(1H)-ones Recent progress in asymmetric Biginelli reaction. Dihydropyrimidinone positive modulation of delta-subunit-containing gamma-aminobutyric acid type A receptors, including an epilepsy-linked mutant variant Chiral separation of pharmacologically active dihydropyrimidinones with carboxymethyl-beta-cyclodextrin Ethyl 2-(2-acetoxy-benzyl-idene)-7-methyl-3-oxo-5-phenyl-2,3-dihydro-5H-1,3-thia-zolo[3,2-a]pyrimidine-6-carboxyl-ate Copper(II) sulfamate: an efficient catalyst for the one-pot synthesis of 3,4-dihydropyrimidine-2(1H)-ones and thiones. A mini-review on Biginelli adducts with notable pharmacological properties 5-Acetyl-4-(2-chloro-phen-yl)-6-methyl-3,4-dihydro-pyrimidine-2(1H)-thione. A Green, Expeditious, One-Pot Synthesis of 3, 4-Dihydropyrimidin-2(1H)-ones Using a Mixture of Phosphorus Pentoxide-Methanesulfonic Acid at Ambient Temperature Ultrasound-assisted synthesis of novel 4-(2-phenyl-1,2,3-triazol-4-yl)-3,4-dihydropyrimidin-(1H)-(thio)ones catalyzed by Sm(ClO(4))(3). An efficient synthesis of 3,4-Dihydropyrimidin-2(1H)-ones and thiones catalyzed by a novel Brønsted acidic ionic liquid under solvent-free conditions. A one-pot three-component synthesis of 4,6-diarylpyrimidin-2(1H)-ones (DAPMs) using atomized sodium in THF under sonic condition Synthesis, in vitro Anticancer and Antimicrobial Evaluation of Novel Substituted Dihydropyrimidines. FeCl₃∙6H₂O/TMSBr-Catalyzed Rapid Synthesis of Dihydropyrimidinones and Dihydropyrimidinethiones under Microwave Irradiation. Towards the synthesis of C-glycosylated dihydropyrimidine libraries via the three-component Biginelli reaction. A novel approach to artificial nucleosides
is cites work of	wds:Q36087819-85097DD5-713B-47EC-8F7D-1C3BDF3760AE wds:Q35030964-619FDAB3-20F2-4F24-9EB8-7EF21BEE3734 wds:Q37156888-D0208D1B-9DF1-48EF-8313-08917B42092B wds:Q37262520-7A8C392C-DBF5-483D-96F7-9B4D9ED0562A wds:Q74598010-12F43B37-5950-4D4C-BCF1-E32E0BD275D2 wds:Q34319139-1A52758D-5FC9-4D80-856B-0EB4661E0B61 wds:Q51025318-1F61807A-5C43-4307-AA86-7A90FEE17FDC wds:Q34261554-B56FBC33-3742-4C6D-87D7-DFAD166A57F5 wds:Q43081402-505C0FA8-4F56-46C4-BD3D-41F36BD9C804 wds:Q46118965-9119F757-E463-4339-87D7-7A4AD58195C8 wds:Q87137732-90235B74-8DE6-4699-94F7-6B1641FD7AC9 wds:Q28142674-EB7532C6-2849-4BEF-8013-05D6B840B511 wds:Q44321138-B69B390F-0965-4F1C-9BF2-8ADD4948CD61 wds:Q26800023-D3306CEE-85E7-47D0-98DA-9AF1ED40EF96 wds:Q38950357-A874E130-6572-4C1F-891F-28000DBE7DC7 wds:Q38099250-39A43EAA-5C0E-4C29-AB19-5F8FCB4993E0 wds:Q48095189-01AAE16F-57A2-4772-A36F-55A4C163077D wds:Q34272891-3D2BFCF9-D556-4321-83FF-E703488030A0 wds:Q34180577-4F4C1758-88D2-479B-AD79-1490878898F9 wds:Q56838896-6494EB66-AB47-4657-90A3-C65A6B30293A

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