Chapter 12: Q21CP (page 397)
List the factors that influence a drug’s bioavailability.
Short Answer
The rate and extent of the bioavailability of a drug molecule to the target molecule depend on pharmaceutical factors and pharmacological factors.
Chapter 12: Q21CP (page 397)
List the factors that influence a drug’s bioavailability.
The rate and extent of the bioavailability of a drug molecule to the target molecule depend on pharmaceutical factors and pharmacological factors.
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Get started for freeIn a bisubstrate reaction, a small amount of the first product P is isotopically labeled and added to the enzyme and the first substrate A. No B or Q is present. Will become isotopically labeled if the reaction follows a Ping Pong mechanism?
Is it necessary for measurements of reaction velocity to be expressed in units of concentration per time (M s⁻¹, for example) to calculate an enzyme's KM?
The KM for the reaction chymotrypsin with N-acetylvaline ethyl ester is , and the for the reaction of chymotrypsin with N-acetyltyrosine ethyl ester is . (a) Which substrate has the higher apparent affinity for the enzyme? (b) Which substrate is likely to give a higher value for ?
At what concentration of (expressed as a multiple of ) will ?
Determine the type of inhibition of an enzymatic reaction from the following data collected in the presence and absence of the inhibitor.
[S] (mM) | vₒ (mM min⁻¹) | vₒ with I present (mM min⁻¹) |
1 | 1.3 | 0.8 |
2 | 2.0 | 1.2 |
4 | 2.8 | 1.7 |
8 | 3.6 | 2.2 |
12 | 4.0 | 2.4 |
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