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  • 1
    ISSN: 1432-1041
    Keywords: Idrapril ; ACE-inhibition ; Hypertension ; essential ; active renin ; angiotensin II ; blood pressure ; pharmacodynamics ; pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Abstract Idrapril is the prototype of a new class of ACE inhibitors, characterised by the presence of a hydroxdmic group. Six untreated in-patients with essential hypertension were given single oral doses of the calcium salt of idrapril, idrapril calcium (200 mg) and placebo according to a double blind, randomised experimental design. Supine and upright blood pressure, heart rate, plasma idrapril serum ACE, active renin and angiotensin II were measured at timed intervals for 24 hours after dosing. Plasma idrapril reached a peak after 2 hours (3.01 μ·ml−1), and by 12 hours the compound had al most disappeared (67 ng·ml−1). Derived t1/2 was 1.4–2.2 h. ACE activity was suppressed [from 77.9 to 3.3 after 2 hours and 11.8 after 12 hours nmol−1·min−1·ml] and angiotensin II production inhibited [from 8.8 to 3.1 (after 1 hour) and 7.5 (after 12 hours) pg·ml−1] for up to 12 h, while active renin rose up to 24 h [from 12.3 to 20.1 (after 8 hours) and 17.5 (after 24 hours) pg·ml−1]. Compared to placebo, idrapril calcium significantly lowered both supine blood pressure starting at 4 hours (idrapril calcium 140/93 mmHg; placebo 157/101 mmHg) up to 24 hours (idrapril calcium 142/91 mmHg; placebo: 155/97 mmHg), and upright blood pressure starting at 3 hours (idrapril calcium 135/95 mmHg; placebo 147/100 mmHg) up to 24 hours (idrapril calcium 132/92 mmHg; placebo 145/100 mmHg). Idrapril calcium appears to be an effective ACE inhibitor in essential hypertension, with a hypotensive action for up to 24 h.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Clinica Chimica Acta 66 (1976), S. 331-343 
    ISSN: 0009-8981
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 1209-1232 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The terpolymerization of ethylene, propylene, and methylcyclopentadienyl-5-endonorborn-2-enylmethane (III) by means of different vanadium-based coordination catalysts was investigated. The structure of III and its isomeric composition was studied by using vapor-phase chromatography, mass spectrometry, and NMR, infrared, and ultraviolet spectroscopy. The catalyst system V Acac3-Et2AlCl was used under different conditions, and the influence of several variables regulating the terpolymerization process were related to the properties of the resulting terpolymers (EPTM). The insertion of III into EPTM chains takes place randomly and does not influence the random distribution of comonomers. The selective opening of the norbornene double bond of III has been demonstrated by use of 2,3-dihydro-III as model compound. Tritiated III gave a radiochemical titer of unsaturation in excellent agreement with the value deduced from ultraviolet measurements. The influence of Lewis bases added to VAcac3-Et2AlCl catalyst is discussed.
    Additional Material: 19 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 9 (1971), S. 1575-1598 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A detailed investigation of the terpolymerization reaction of ethylene and propylene with 1-isopropylidene-dicyclopentadiene (II) was carried out by empolying vanadiumbased anionic coordinate catalysts [preferentially V(Acac)3—AlEt2Cl]. The influence of some polymerization parameters, i.e., concentration of II, of the catalyst; polymerization time, etc., were particularly examined. The catalysts were found to be active in C2H4—II copolymerization also, but neither C3H6—II copolymer nor II homopolymer were obtained. By using the 5,6-dihydro derivative of II as comonomer, it was found through ultraviolet, infrared, and NMR analyses that the incorporation of II in polyethylene or ethylene-propylene chains took place randomly and by selective opening of the norbornene double bond. The quantitative determination of the unsaturation present in C2H4—C3H6—II terpolymer was studied by means of absorption of iodine halides and through a spectroscopic ultraviolet method. Reference was made to terpolymer samples containing 14C-labeled II. The content of II was generally less than 35 wt-% both in copolymer and in terpolymer prepared. The relatively high reactivity of II is discussed in terms of norbornene ring strain and compared with the reactivity of 1-isopropylidene-3a,4,7,7a-tetrahydroindene (I) previously reported.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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