2. Which is a false statement regarding non-competitive enzyme inhibitor? (a) It binds to an allosteric site of the enzyme (b) It does not compete with the natural substrate for binding to the active site of the enzy (c) Its binding to the enzyme can induce a conformational change of the enzyme (d) It can be used in combination therapies with a competitive inhibitor (e) It usually is a mimic of the natural enzyme substrate 3. What is the purpose of structure-activity-relationship (SAR) studies? (a) To identify the drug target (b) To improve the pharmacokinetic properties of the drug (c) To determine which atoms or functional groups are important to the activity of a drug (d) To simplify the synthesis of the drug

Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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2. Which is a false statement regarding non-competitive enzyme inhibitor?
(a) It binds to an allosteric site of the enzyme
(b) It does not compete with the natural substrate for binding to the active site of the enzy
(c) Its binding to the enzyme can induce a conformational change of the enzyme
(d) It can be used in combination therapies with a competitive inhibitor
(e) It usually is a mimic of the natural enzyme substrate
3. What is the purpose of structure-activity-relationship (SAR) studies?
(a) To identify the drug target
(b) To improve the pharmacokinetic properties of the drug
(c) To determine which atoms or functional groups are important to the activity of a drug
(d) To simplify the synthesis of the drug
(e) To optimise activity of the drug
Transcribed Image Text:2. Which is a false statement regarding non-competitive enzyme inhibitor? (a) It binds to an allosteric site of the enzyme (b) It does not compete with the natural substrate for binding to the active site of the enzy (c) Its binding to the enzyme can induce a conformational change of the enzyme (d) It can be used in combination therapies with a competitive inhibitor (e) It usually is a mimic of the natural enzyme substrate 3. What is the purpose of structure-activity-relationship (SAR) studies? (a) To identify the drug target (b) To improve the pharmacokinetic properties of the drug (c) To determine which atoms or functional groups are important to the activity of a drug (d) To simplify the synthesis of the drug (e) To optimise activity of the drug
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