Search results for "minoca"

showing 10 items of 26 documents

Kinetics of the intestinal uptake of zinc acexamate in normal and zinc-depleted rats.

1990

Abstract The uptake of zinc as acexamic acid salt in the small intestine of the anaesthetized rat was shown to be a two-phase process in normal animals. The first phase is rapid mucosal binding which satisfies the Freundlich isotherm equation and which involves about 30 per cent of the initially perfused zinc. The second phase was characterized as an apparent absorption step which obeys Michaelis-Menten and first-order combined kinetics, with the following parameters: Vm = 6.51 mg h−1; Km = 2.96 mg; ka = 0.306 h−1. In largely non-saturated conditions, an apparent global rate constant of about 2.50 h−1 was calculated. No significant interference due to endogenous zinc excretion into the smal…

Absorption (pharmacology)MaleKineticsPharmaceutical Sciencechemistry.chemical_elementZincExcretionReaction rate constantPharmacokineticsIntestine SmallmedicineAnimalsFreundlich equationIntestinal MucosaPharmacologyAminocaproatesSpectrophotometry AtomicRats Inbred StrainsSmall intestineRatsPerfusionZincmedicine.anatomical_structureBiochemistrychemistryIntestinal AbsorptionAminocaproic AcidBiophysicsThe Journal of pharmacy and pharmacology
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Low-loading asymmetric organocatalysis

2011

Asymmetric organocatalysis is now recognized as the third pillar of asymmetric synthesis. Recent years have witnessed increasing interest towards the use of highly active and stereoselective organocatalysts. This critical review documents the advances in the development of chiral organocatalysts which are systematically used in ≤3 mol% loading in all the sub-areas of the field, namely aminocatalysis, Brønsted acids and bases, Lewis acids and bases, hydrogen bond-mediated catalysis, phase transfer and N-heterocyclic carbene catalyses (194 references).

AminocatalysisMolecular StructureOrganic chemicalsBronsted BaseEnantioselective synthesisPillarSettore CHIM/06 - Chimica OrganicaGeneral ChemistryCatalysisBronsted acidCatalysisoragnocatalysichemistry.chemical_compoundchemistryphase-transfer catalysiOrganocatalysisOrganic chemistryLewis acids and basesOrganic ChemicalsBrønsted–Lowry acid–base theoryCarbeneChem. Soc. Rev.
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Synthesis of monodisperse oligomers of ɛ-aminocaproic acid up to a degree of polymerization of 25 by the Merrifield method (1)

1967

Chain-growth polymerizationPolymerizationChemistryDispersityPolymer chemistryGeneral EngineeringCationic polymerizationmedicineReversible addition−fragmentation chain-transfer polymerizationDegree of polymerizationAminocaproic acidIonic polymerizationmedicine.drugJournal of Polymer Science Part B: Polymer Letters
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C,N-chelated diaminocarbene platinum(II) complexes derived from 3,4-diaryl-1H-pyrrol-2,5-diimines and cis-dichlorobis(isonitrile)platinum(II): Synthe…

2020

The reaction of 3,4-diaryl-1H-pyrrol-2,5-diimines with cis-dichlorobis(isonitrile)platinum(II) affords the C,N-chelated diaminocarbene platinum(II) complexes, which have been fully characterized including molecular spectroscopy, single crystal X-ray diffraction and DFT calculations. The obtained platinum(II) complexes are effective catalysts for the hydrosilylation of alkynes and alkenes. Thus, the reaction of phenylacetylene with triethoxysilane leads to the formation of α- and β-(E)-vinylsilanes, generating TON's in the range of 103 to 104 and TOF's in the range of 102 to 103 h−1. Also, the cross-linked silicones, possessing the luminescence properties, were obtained by the hydrosilylatio…

LuminescenceHydrosilylationchemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistryCatalysisCatalysisInorganic Chemistrychemistry.chemical_compoundAnti-cancer activityPolymer chemistryluminescenceMaterials ChemistryChelationPhysical and Theoretical Chemistrydiaminocarbene platinum(II) complexescatalysis010405 organic chemistryOrganic Chemistryhydrosilylation0104 chemical scienceschemistryPhenylacetyleneDiaminocarbene platinum(II) complexesHydrosilylationTriethoxysilaneanti-cancer activityLuminescencePlatinumSingle crystalJournal of Organometallic Chemistry
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Effects of zinc acexamate on blood flow and prostanoid levels in the gastric mucosa of the rat

1989

The effects of the new antiulcer compound zinc acexamate on blood flow and prostanoid levels in the gastric mucosa have been studied. Zinc acexamate (30 and 300 mg/kg) dose-dependently prevents the reduction induced by the perfusion of noradrenaline (3.5 micrograms/kg.min, 30 min) in gastric mucosal blood flow, as measured by 3H-aniline clearance. Zinc acexamate pretreatment also increases the levels of prostaglandin E2 in the gastric mucosa of the rat, both under control conditions and after infusion with noradrenaline. The levels of thromboxane A2 and prostacyclin were not modified by zinc acexamate. These results confirm the importance of microcirculation in pathogenesis and the idea tha…

Malemedicine.medical_specialtyMetabolic Clearance RateClinical BiochemistryProstacyclinBiologyMicrocirculationNorepinephrinechemistry.chemical_compoundThromboxane A2Internal medicinemedicineGastric mucosaAnimalsProstaglandin E2Chromatography High Pressure LiquidAminocaproatesStomachProstanoidRats Inbred StrainsCell BiologyAnti-Ulcer AgentsRatsEndocrinologymedicine.anatomical_structurechemistryGastric MucosaRegional Blood FlowAminocaproic AcidProstaglandinsPerfusionmedicine.drugProstaglandins, Leukotrienes and Essential Fatty Acids
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Acute inferior myocardial infarction due to a large thrombus in the Left coronary sinus of valsalva.

2021

Background Masses in the ascending aorta are an uncommon source of coronary embolism: thrombi located on atherosclerotic aortic plaques are the most frequent cause. A floating thrombus, without evidence of ascending aortic pathology has rarely been reported Method We report a case of an unusual aortic route thromboembolism leading ST segment elevation Myocardial Infarction (STEMI). The patient was referred to the Hub Hospital to undergo urgent coronarography. The examination excluded atherosclerotic coronary arteries disease but an unusual persistence of contrast dye was found at the level of non-coronary sinus. The trans-esophageal echocardiography showed a mobile pedunculated echogenic ma…

Malemedicine.medical_specialtybusiness.industryAcute Inferior Myocardial InfarctionThrombosisGeneral MedicineInferior Wall Myocardial InfarctionSinus of ValsalvaCoronary embolismmedicine.diseaseInternal medicinemedicineCardiologyHumansThrombusMyocardial Infarction with Non Obstructive Coronary Artery (MINOCA) Aortic routeThrombectomy Coronary EmbolismCardiology and Cardiovascular MedicinebusinessCoronary sinusAgedCoronary artery disease
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High-Dose ϵ-Aminocaproic Acid Versus Aprotinin: Antifibrinolytic Efficacy in First-Time Coronary Operations

1998

The antifibrinolytic efficacy of a high-dose regimen of epsilon-aminocaproic acid (epsilon-ACA) was compared with aprotinin in first-time coronary operations.In a prospective, double-blinded, randomized study, 20 patients received high-dose epsilon-ACA (10 g both as a loading and cardiopulmonary bypass priming dose, 2.5 g/h until 4 hours after protamine), and another 20 patients received aprotinin (2 x 10(6) KIU [280 mg] for loading and priming, 0.5 x 10(6) KIU/h [70 mg/h]). Ten untreated patients served as controls.Both agents reduced postoperative levels of thrombin/antithrombin III complexes, D-dimers, fibrin degradation products, free plasma hemoglobin (epsilon-ACA versus aprotinin, p =…

Pulmonary and Respiratory MedicineAntifibrinolyticmedicine.drug_classHematocritHemostaticsFibrinlaw.inventionBlood Transfusion AutologousAprotininThrombinDouble-Blind MethodlawMyocardial RevascularizationmedicineCardiopulmonary bypassHumansBlood TransfusionAprotininProspective StudiesBlood CoagulationCardiopulmonary Bypassbiologymedicine.diagnostic_testbusiness.industryFibrinolysisAntithrombinAntifibrinolytic AgentsHematocritAnesthesiaAminocaproic Acidbiology.proteinSurgeryAminocaproic acidCardiology and Cardiovascular Medicinebusinessmedicine.drugThe Annals of Thoracic Surgery
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CCDC 141173: Experimental Crystal Structure Determination

2001

Related Article: Young Lag Cho, D.M.Rudkevich, A.Shivanyuk, K.Rissanen, J.Rebek Junior|2000|Chem.-Eur.J.|6|3788|doi:10.1002/1521-3765(20001016)6:20<3788::AID-CHEM3788>3.0.CO;2-Y

Space GroupCrystallographyCrystal SystemCrystal Structure25262728-tetrakis((N-n-Octylcarbamoyl)methoxy)-5111723-tetrakis(N-(p-tolyl)aminocarbamoyl)calix(4)arene methanol solvateCell ParametersExperimental 3D Coordinates
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CCDC 749023: Experimental Crystal Structure Determination

2010

Related Article: D.Siebler, C.Forster, K.Heinze|2010|Eur.J.Inorg.Chem.||523|doi:10.1002/ejic.200901051

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters1-(2-(5-(Dimethylamino)naphthalenesulfonylamino)propylcarbonylamino)-1'-(1-(naphthylmethylaminocarbonyl)ethylaminocarbonyl)ferrocene dichloromethane solvateExperimental 3D Coordinates
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CCDC 749024: Experimental Crystal Structure Determination

2010

Related Article: D.Siebler, C.Forster, K.Heinze|2010|Eur.J.Inorg.Chem.||523|doi:10.1002/ejic.200901051

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters1-(2-(5-(Dimethylamino)naphthalenesulfonylamino)propylcarbonylamino)-1'-(1-(naphthylmethylaminocarbonyl)ethylaminocarbonyl)ferroceneExperimental 3D Coordinates
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