Search results for "Pyrimidone"

showing 3 items of 3 documents

Preparation and Structures of Isoindolone- or Pyrimidone-Condensed Heterocycles Containing a Hydroxy Group on a Cyclohexane or Norbornane Moiety

2009

With DL-valinol, 3-amino-1-propanol and o-aminothiophenol, aroyl(bi/tri)cyclic lactones 1 and 2 were cy- clized to isoindole- 4-6, 8, 9, pyrimidinone- 10 or thiazepine- 7 condensed heterocycles. The ketal lactone 3 furnished the benzthiazoloisoindole 9 and mixtures of epimeric hydroxyphthalazinoquinazolinones 11 and 12. The structures were es- tablished by means of 1 H and 13 C NMR spectroscopy and in some cases by X-ray crystallography.

chemistry.chemical_classificationCyclohexaneOrganic ChemistryCarbon-13 NMRBiochemistryMedicinal chemistrychemistry.chemical_compoundchemistryThiazepineMoietyPyrimidoneNorbornaneIsoindoleLactoneLetters in Organic Chemistry
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Ein Bindungsstellenmodell für H2-Antagonisten vom 4-Pyrimidinon-Typ

1985

In einer Reihe von 17 Histamin-H2-antagonistisch wirksamen 5-substituierten 4-Pyrimidinonen wird durch Berechnung von Wechselwirkungsenergien ein Modell fur die Rezeptorbindungsstelle des Substituenten am C-5 des Pyrimidinons vorgeschlagen. Als Bindungsstelle fungiert die Aminosaure Arginin. A Binding Site Model for H2-Receptor Antagonists of the 4-Pyrimidone Type Based on calculations of the energies of interaction for a series of seventeen 5-substituted 4-pyrimidones with H2-antagonistic activity, a receptor binding site model for substituents at C-5 of the pyrimidone ring is proposed. The binding site is modeled using the amino acid arginine.

chemistry.chemical_classificationchemistry.chemical_compoundchemistryArginineStereochemistryDrug DiscoveryPharmaceutical SciencePyrimidoneBinding siteReceptor binding siteAmino acidArchiv der Pharmazie
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H2-antihistaminics. 20. Structure-activity relationships in H2-receptor antagonists containing a 4-pyrimidone moiety.

1984

In a series of 5,6-substituted 4- pyrimidones 1 a-v the H2-antihistaminic activity was determined (guinea-pig atrium) and lipophilicity data are given in form of Rmo -values. The influence of different substituents at position 5 or 6 of a pyrimidone moiety has been studied. Quantitative structure-activity analyses showed the importance of lipophilicity for drug activity. Additionally other physicochemical substituent-properties may play a major role.

PharmacologyStereochemistryImmunologyPharmacology toxicologyGuinea PigsHeartPyrimidinonesToxicologyLipidschemistry.chemical_compoundStructure-Activity RelationshipDrug activitychemistryHistamine H2 receptorHistamine H2 AntagonistsSolubilityLipophilicityMoietyAnimalsPharmacology (medical)PyrimidoneAgents and actions
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