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Biochemical Pharmacology

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A phrase to hide the fact that we are sneaking a subject of medical interest ... Example: Atropine (Atropa belladonna) Acetylcholine ... – PowerPoint PPT presentation

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Title: Biochemical Pharmacology


1
Biochemical Pharmacology
  • What is it?
  • A fancy way of saying pharmacology
  • A phrase to hide the fact that we are sneaking a
    subject of medical interest into the UW
    biochemistry curriculum
  • An indication that we are not going to discuss
    prescriptions for your grandmothers aching knee
  • What is it not?
  • A claim that we do understand the mechanism of
    action of each practically useful drug in
    biochemical terms
  • A claim that enzyme mechanisms and receptor
    structures, or even cell biology are sufficient
    to understand drug action in the human body

2
What are drugs?
Or, more precisely, do they have anything in
common at all? 1. The smallest drug
3
2. A large drug molecule
4
3. More typical sizes of drug molecules
5
Target molecules of drug action The angiotensin
pathway
6
Drug targets in the angiotensin pathway
N-Asp-Arg-Val-Tyr-Ile-His-Pro-Phe-His-Leu-Val-Ile
-His-Asn- ?
Renin
Angiotensin I
Asp-Arg-Val-Tyr-Ile-His-Pro-Phe-His-Leu
  • Renin Enzyme inhibitors prevent the production
    of angiotensin I

Example Remikiren
7
Drug targets in the angiotensin pathway
Angiotensin I
Asp-Arg-Val-Tyr-Ile-His-Pro-Phe-His-Leu
Converting enzyme
Angiotensin II
Asp-Arg-Val-Tyr-Ile-His-Pro-Phe
  • Converting enzyme Enzyme inhibitors prevent the
    production of angiotensin II, the active
    mediator.

Example Enalapril
8
Drug targets in the angiotensin pathway
Angiotensin II
Saralasin
vascular smooth muscle cell
Receptor
response (increased blood pressure)
Asp-Arg-Val-Tyr-Ile-His-Pro-Phe
Angiotensin II
Sar-Arg-Val-Tyr-Val-His-Pro-Ala
Saralasin
(Sarcosine N-methylglycine)
9
Drugs and physiological mediators (1)
Angiotensin II
vascular smooth muscle cell
Receptor
response (increased blood pressure)
Angiotensin II
Asp-Arg-Val-Tyr-Ile-His-Pro-Phe
Saralasin
Sar-Arg-Val-Tyr-Val-His-Pro-Ala
(Sarcosine N-methylglycine)
10
Non-peptide inhibitors of peptide receptors
11
Drugs and physiological mediators
Histamine
stomach mucosal epithelial cell
Receptor
response HCl secretion
ulcer
Histamine
Cimetidine
12
Histamine receptor subtypes
Histamine
Allergic reaction
H1 receptor
H2 receptor
Ulcer
Cimetidine
Cyclizine
13
Drug discovery and development strategies
  • Rational design. Example HIV protease inhibitor
    (saquinavir)

14
Drug discovery and development strategies
  • Rational design. Example HIV protease inhibitor
    (saquinavir)
  • Analyze biological function The protease is
    essential for viral multiplication
  • Obtain crystal structure of enzyme, tailor
    inhibitors to fit into active site
  • Test and modify, take to clinical testing and
    application

15
Drug discovery and development strategies
  • Brute force Example Prontosil rubrum, the
    first sulfonamide antimicrobial agent
  • Systematically test every new (or old) compound
    for drug activity no matter which purpose it
    was designed for
  • If you stumble upon something, figure out how it
    works

Prontosil rubrum
Sulfanilamide, the active metabolite
p-Aminobenzoic acid, a precursor of folic acid in
bacteria
16
Drug discovery and development strategies
  • Traditional medicine. Example Atropine (Atropa
    belladonna)
  • Isolate the active components from
    therapeutically useful and / or toxic plants
  • Elucidate structure, mode of action
  • Create novel derivatives with improved properties

Acetylcholine
17
Drug discovery and development strategies
  • Mere chance. Example Penicillin (Penicillium
    notatum)
  • Forget to properly cover your petri dish
  • Find a mold that kills bacteria (Sir Alexander
    Fleming, 1928)
  • Wait until somebody purifies the active
    ingredient and makes it available for clinical
    use (Florey and Chain, 1942)

18
Commercial drug development
In vitro studies
Isolate / synthesize a lead compound (a
candidate drug) vary and optimize
Animal testing
Test efficacy, toxicity, selectivity,
pharmacokinetics
Clinical testing
Test efficacy, toxicity, selectivity,
pharmacokinetics Phase 1 Limited series of
healthy volunteers Phase 2 Actual patients with
the corresponding disease Phase 3 Double-blind
studies against placebo or reference treatment
Approval
Review by the authorities be ready to expend
bribes at this stage
Marketing
Patents expire in 15-20 years (varies with
country) after that, generic drugs tend to take
out market share
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