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1. An inactive or much less active form of drug which transformed to active drug in the body is a. Coated drug b. Specialized dosage form c. Prodrug d. Reservoir 2. Sodium pump is an example of a. G-protein receptors b. Ion channels c. Gene Transcription linked receptor  d. Enzyme-linked tyrosine kinase 3. As the length of a non-polar chain of aliphatic alcohol increases, its solubility in water    a. Increases b. Decreases c. No effect 4. More common force of attraction for drugs a. Covalent b. Electrostatic c. Hydrogen bonding d. Ionic 5. In organs and tissues that are well-perfuse, drug distribution is a. Faster b. Slower c. Negligible d. The same

1. An inactive or much less active form of drug which transformed to active drug in the body is a. Coated drug b. Specialized dosage form c. Prodrug d. Reservoir 2. Sodium pump is an example of a. G-protein receptors b. Ion channels c. Gene Transcription linked receptor  d. Enzyme-linked tyrosine kinase 3. As the length of a non-polar chain of aliphatic alcohol increases, its solubility in water    a. Increases b. Decreases c. No effect 4. More common force of attraction for drugs a. Covalent b. Electrostatic c. Hydrogen bonding d. Ionic 5. In organs and tissues that are well-perfuse, drug distribution is a. Faster b. Slower c. Negligible d. The same

World of Chemistry, 3rd edition
World of Chemistry, 3rd edition
3rd Edition
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Chapter21: Biochemistry
Section: Chapter Questions
Problem 63A
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1. An inactive or much less active form of drug which transformed to active drug in the body is

a. Coated drug

b. Specialized dosage form

c. Prodrug

d. Reservoir

2. Sodium pump is an example of

a. G-protein receptors

b. Ion channels

c. Gene Transcription linked receptor 

d. Enzyme-linked tyrosine kinase

3. As the length of a non-polar chain of aliphatic alcohol increases, its solubility in water 
 
a. Increases

b. Decreases

c. No effect

4. More common force of attraction for drugs

a. Covalent

b. Electrostatic

c. Hydrogen bonding

d. Ionic

5. In organs and tissues that are well-perfuse, drug distribution is

a. Faster

b. Slower

c. Negligible

d. The same


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