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Opioid Analgesics

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Title: Opioid Analgesics


1
Opioid Analgesics
  • Mallika Doss
  • April 10, 2008

2
Overview
  • History
  • Morphine
  • SAR of Morphine
  • Drug Dissection of Morphine
  • Morphine Analogues
  • Opioid Receptors Receptor Binding
  • Agonists and Antagonists
  • Why you feel happy ?
  • Endogenous Opioid peptides
  • The Future

3
The History
  • First use in Mesopotamia
  • First recorded use in China
  • 632 AD Opium reaches Spain, Persia, and India
  • 17th century Tobacco comes to China
  • 1644 Chinese emperor bans tobacco
  • 19th century China closes its doors to the
    world
  • Deprived of tobacco, Chinese people start smoking
    opium!
  • Opium production in China couldnt keep up with
    demand. British East India company sees
    opportunity.
  • 1830s 1 million of opium smuggled into China
    via Port Canton.

4
The History
  • Chinese authorities burnt down the port British
    traders outraged.
  • 1839-42 Opium Wars Chinese were defeated and
    forced to lease trading port to Britain.
  • 19th century Opium dens common in Britain.
  • 1882 Addictive properties of opium discovered
    but largely ignored.
  • 1909 IOC set up to curb opium production
  • 1924 Opium production went underground

5
Morphine
  • Named after the Greek God, Morpheus (God of
    dreams)
  • Good for treating dull, constant pain rather than
    sharp, periodic pain
  • Side effects
  • Excitation
  • Euphoria
  • Nausea
  • Pupil constriction
  • Constipation
  • Tolerance and Dependence
  • Depression of breathing

Maximize
Minimize
6
Morphine - SAR
Phenolic OH ?
? Aromatic ring
Required
Required
? N-methyl group
Ether bridge ?
Required
Not Required
? Double bond at 7-8
6-alcohol ?
Not Required
Not Required
7
Morphine Drug Dissection
Loss of activity
E
Activity retained
D
B
C
Morphinans
Benzomorphans
4-phenylpiperidines
Methadone
8
Morphine Analogues - Codeine
  • How its related
  • Methyl ether of morphine
  • Activity
  • 20 that of morphine
  • Pro-drug of morphine
  • Metabolized by O-demethylation in the liver to
    make morphine

Codeine
9
Morphine Analogues - Codeine
  • Treats
  • Moderate pain
  • Coughs
  • diarrhea
  • Marketed as
  • Tylenol with Codeine
  • Hydrocodone
  • Vicodin (with Thebaine)

10
Morphine Analogues - Heroine
  • How its related
  • 3,6-diacetyl ester of morphine
  • Activity
  • 2x that of morphine
  • Polar groups are hidden, making it easy to cross
    BBB.
  • Treats
  • Pain in terminally ill patients
  • Side effects
  • Euphoria, addiction, tolerance
  • Marketed as
  • Heroin, dope

Heroine
11
Morphine Analogues - Heroine
  • 6-acetylmorphine
  • How its related
  • 6-acetyl of morphine
  • Activity
  • 4x that of morphine!
  • Polarity decreased, but phenol is ready to bind
    receptor
  • Side effects Very potent!!
  • Euphoria, addiction, etc.
  • Marketed as
  • NOTHING! Its banned from production in many
    countries

6-acetylmorphine
12
Morphine Analogues - Morphinans
  • How its related
  • Ether bridge removed
  • Activity
  • 5x that of morphine
  • Advantage
  • It can be taken orally
  • Lasts longer
  • Easier to synthesize
  • Side effects
  • High toxicity, comparable dependence
  • Marketed as
  • Levo-Dromoran

Levorphanol
13
Morphine Analogues - Benzomorphans
  • How its related
  • Rings C and D removed
  • Activity
  • 4x that of morphine
  • Advantages
  • No addictive properties
  • Does not depress breathing
  • Lasts longer
  • Side effects
  • Hallucinogenic
  • Marketed as
  • Prinadol, Norphen
  • Fortal, Talwin NX

Phenazocine
Pentazocine
14
Morphine Analogues 4-phenylpiperidines
  • Fentanyl
  • How its related
  • Rings B,C,D removed
  • Activity
  • 100x that of morphine
  • Advantages
  • Cross BBB efficiently
  • Really easy to make
  • Rapid onset, short duration
  • Can be administered any way (IV, oral,
    transdermal, buccal)

Fentanyl
15
Morphine Analogues 4-phenylpiperidines
  • Used for
  • Anesthesia
  • Chronic pain management
  • Side effects
  • Sudden respiratory depression
  • More addictive than heroin
  • Less euphoria, more sedation
  • Marketed as
  • Sufenta (used in ? surgery)
  • Carfentanil (used in vet practice)
  • Percopop, OxyContin, magic (heroin/cocaine)

16
Morphine Analogues - Methadone
  • How its related
  • Rings B,C,D,E opened
  • Activity
  • lt Morphine
  • Used to
  • Ween addicts off heroine or morphine
  • Advantages
  • Can be given orally
  • Less severe side effects
  • Marketed as
  • Dolophine, Amidone, Methadose

17
Morphine analogues - Naltrexone
  • How its related
  • Cyclopropylmethylene added to morphine
  • Activity
  • None?!
  • Morphine antagonists
  • Used to treat
  • Morphine overdose
  • Heroin addicts post-rehab
  • Advantages
  • No side effects
  • Marketed as
  • Revia, Depade, Vivitrol

Naltrexone
Nalorphine
18
Agonists and Antagonists
Equatorial Antagonist binding area
Axial Agonist binding area
19
SIDE NOTE
  • Other factors important to receptor binding
  • Stereochemistry
  • Enantiomers of many of the analogues were tested
    for analgesic activity. Overall, they didnt have
    any.
  • Rigidification
  • Used to maintain active formation and eliminate
    alternative conformations
  • Increases selectivity for receptors

20
Opioid Receptors
  • Receptor-binding motif
  • Phenol OH
  • Aromatic ring
  • Amine group

21
Opioid Receptors
Most strongly binds morphine
Receptor type Location Effects
µ Brain, spinal cord Analgesia, Respiratory depression, euphoria, addiction, ALL pain messages blocked
? Brain, spinal cord Analgesia, sedation, all non-thermal pain messages blocked
d Brain Analgesia, antidepression, dependence
Best bet for a safe analgesic
22
Receptor binding - µ
  • Opening of the K channel hyperpolarizes the
    membrane
  • Action potential not sent
  • Ca2 not released
  • Reduces neurotransmitter release

Morphine
µ
K
K
Hyper-polarized!
K
K
23
Receptor Binding - ?
  • Binding causes closing of Ca2 channels
  • Neurotransmitters not released
  • Pain message not sent

Morphine
?
Ca2
Ca2
Ca2
Ca2
24
Why you feel happy
25
Why you feel happy
  • Heroin modifies the action of dopamine in the
    brain.
  • Once crossing the blood-brain barrier, heroin is
    converted to morphine, which acts as an agonist.
  • This binding inhibits the release of GABA from
    the nerve terminal, reducing the inhibitory
    effect of GABA on dopaminergic neurones.
  • The increased activation of dopaminergic neurones
    and the release of dopamine into the synaptic
    cleft results in activation of the post-synaptic
    membrane.
  • Continued activation of the dopaminergic reward
    pathway leads to the feelings of euphoria and the
    high associated with heroin use.

26
Endogenous Opioid Peptides
  • Your bodys natural painkillers
  • Have a preference for the d-receptor
  • Alternative method of pain relief ? inhibit the
    peptidases that degrade them ? thiorphan (still
    new)
  • 3 types of EOPs
  • Enkephalins
  • Dynorphins
  • Endorphins

Met-enkephalin
27
The Future
  • Find an agonist that solely binds to the
    ?-receptor
  • Explore the µ-receptor subtypes further to see if
    any of them dont cause harmful side effects
  • Peripheral opiate receptors avoid BBB obstacle
  • Block postsynaptic receptors involved in the
    transmission of a pain signal
  • GABA
  • Agonists for the cannabinoid receptor

28
References
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