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The selectivity of a drug such as a PDE-5 inhibitor provides data on how selective a compound is with regard to the enzyme in question (here PDE-5), on which the ef cacy is desired compared to other enzymes (PDE 1 4 and 6 11), and on which an ef cacy has to be regarded undesirable Therefore the selectivity of a PDE inhibitor is assessed by comparing its potency (IC50) to inhibit a PDE in question (here PDE 1 4 and 6 11), and its potency to inhibit the PDE desired (here PDE-5) Selectivity Ratio: IC50 for a PDE in question IC50 for PDE-5 The selectivity ratio is used for all three PDE-5 inhibitors to show how selective they are for PDE-5, as compared to anyone of the other ten PDEs The higher this selectivity ratio is for PDE-5 compared to the PDE investigated, the more speci c the PDE-5 inhibitor can be considered In the clinical use all three PDE-5 inhibitors show, at the highest doses, a suf ciently high safety margin to all the other PDEs, except for sildena l which shows only a 11-fold higher selectivity ratio for PDE-5, and for vardena l which shows a 25-fold higher selectivity pro le for PDE-5 as compared to PDE-6 an enzyme exclusively located in the retina that is responsible for our color and brightness discrimination abilities In terms of PDE-11, an enzyme just recently isolated in several tissues (Table 71), without knowing in detail its physiologic function, the selectivity ratio of tadala l turned out to be only ve-fold higher for PDE-5

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Unambiguous identi cation of assets and obligations at the inception of the partnership is important for at least two reasons: (1) Partnership creditors have no claim against the assets of

Bogen, Advantages and Disadvantages of Partnership Maurice Moonitz and Louis H Jordan, Accounting An Analysis of Its Problems, 2 vols, rev ed (Holt, Rinehart and Winston, New York, 1963)

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The term pharmacodynamics covers all actions of a drug on the different body organs, and in turn on their functions (for example blood pressure, heart rate, vision) The pharmacodynamic interactions of any drug are in uenced by the number of receptors available in the target organ and the af nity of the compound for the receptors in question So for example it was just recently reported that vardena l has, with 85%, a clearly higher proportion of high-af nity components to the PDE-5 catalytic site than sildena l (with 50%) and tadala l (with 60%) [61] Given the fact that the high af nity components of a PDE-5 inhibitor show a considerably

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individual partners until the partnership assets have been exhausted (special cases are discussed in Parts III and VI of the UPA) (2) Unless speci cally provided for in the partnership agreement, partnership assets may be used only for partnership purposes; partners personal assets are, of course, subject to no such limitations

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The pharmacokinetic pro le of a drug comprises all the different steps between its entry into the body and its elimination In this regard of special interest is the speed of absorption, which is best de ned by

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Spire.PDF allows us to compress PDF document in the following two ways: Compressing content; Compressing image. Compressing content. In Spire.PDF, we ...

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