In drug development, enzyme inhibition studies play a very important role since drugs are often used to target specific enzymes, as illustrated in the example of lovastatin. An important consideration when assessing drug potential is the drug's affinity for the selected target. (The higher the affinity, the better the candidate.) The K₁ is often used in studies to measure the affinity of drug candidates toward their target. Based on your understanding of K₁, which drug would be the BEST candidate for further development? Drug C: K₁= 9.1 x 107 M Drug E: K₁=3.5 × 10³ mm Drug D: K₁=5.5 × 10³ μM Drug B: K₁=2.5 x 10 mm Drug A: K₁=4.5 × 10³ mm
In drug development, enzyme inhibition studies play a very important role since drugs are often used to target specific enzymes, as illustrated in the example of lovastatin. An important consideration when assessing drug potential is the drug's affinity for the selected target. (The higher the affinity, the better the candidate.) The K₁ is often used in studies to measure the affinity of drug candidates toward their target. Based on your understanding of K₁, which drug would be the BEST candidate for further development? Drug C: K₁= 9.1 x 107 M Drug E: K₁=3.5 × 10³ mm Drug D: K₁=5.5 × 10³ μM Drug B: K₁=2.5 x 10 mm Drug A: K₁=4.5 × 10³ mm
Biochemistry
9th Edition
ISBN:9781319114671
Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Chapter1: Biochemistry: An Evolving Science
Section: Chapter Questions
Problem 1P
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Transcribed Image Text:In drug development, enzyme inhibition studies play a very important role since drugs are often
used to target specific enzymes, as illustrated in the example of lovastatin. An important
consideration when assessing drug potential is the drug's affinity for the selected target. (The
higher the affinity, the better the candidate.) The K₁ is often used in studies to measure the affinity
of drug candidates toward their target. Based on your understanding of K₁, which drug would be
the BEST candidate for further development?
Drug C: K₁= 9.1 x 107 M
Drug E: K₁ = 3.5 × 10³ mm
Drug D: K₁=5.5 × 10³ μM
Drug B: K₁=2.5 × 10 mm
Drug A: K₁=4.5 x 10 mm
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