GO - Targets identified from studying the effects of drugs and toxins Flashcards

1
Q

Put these steps for the drug discovery process in order:

  1. Lead optimisation
  2. Marketing authorisation
  3. Target identification
  4. Formulation development
  5. Lead generation
  6. Pharmaceutical and Toxicity profiling
  7. Target validation
A

3, 7, 5, 1, 6, 4, 2

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2
Q

For a drug molecule to exert a pharmacological effect, an interaction between the ___ and the _____ must occur.

A

drug molecule

target molecule

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3
Q

This interaction between the drug molecule and target molecule requires:

A

1 - functional groups on both target molecule and drug molecule
2 - appropriate orientation in space of the drug functional groups relative to the target molecule functionality.
3. and can be explained in terms of bonding and reactivity between the two molecules.

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4
Q

State the bond types and order them from strongest to weakest.

A
Covalent
Ionic
Ion-dipole
Hydrogen
Hydrophobic
VWF
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5
Q

What is a pharmacophore

A

The combination of parameters essential for activity

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6
Q

Pharmacophoric descriptors are used to define a pharmacophores, including:

A

ionic, H-bonding, hydrophobic and eletrostatic interaction sites, define by atoms, ring centers and virtual points

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7
Q

The pharmacophore can be considered:

  • the largest common denominator shared by a set of. inactive molecules
  • the largest common denominator shared by a set of. active molecules
  • the largest common numerator shared by a set of. active molecules
  • the smallest common denominator shared by a set of. active molecules
A
  • the largest common denominator shared by a set of. active molecules
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8
Q

Structurally relevant (but different) molecules from natural resources frequently have similar ( but subtly different) ________, such as ________

A

biological activities

duration of action

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9
Q

Where did drugs come from in the past?

A

Food and toxins

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10
Q

What are two ways in which you can improve pharmacodynamic activity?

A
  1. Greater potency –> same effect with lower dose

2. Greater selectivity –> fewer s/es due to interaction with other targets

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11
Q

Most drugs have ‘side effects’. This is often the result of…

A

activity on other targets.

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12
Q

Opium alkaloids are obtained from the latex of….

A

Papaver somniferum

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13
Q

What properties are opium alkaloids known for?

A

sedating and analgesic.

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14
Q

Name a few opium alkaloids.

A
Noscapine
Thebaine
Papaverine
Morphine
Codiene
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15
Q

How is morphine administered

A

Subcutaneous injection

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16
Q

What activity does morphine show?

A
  • analgesic
  • antitussive
  • reduced gastric motility
  • respiratory depressant
17
Q

Morphine side effects

A
  • Constipation
  • Nausea and vomiting
  • Drowsiness
  • Respiratory depression
18
Q

What is an opiate antagonist?

A

Nalaxone

19
Q

Order the functional groups in order of polarity.

A

Amide > Acid > Alcohol > Ketone > Aldehyde > Amine > Ester > Ether > Alkene > Alkane

20
Q

What is the general term for opioid peptides

A

Endorphins

21
Q

Higher affinity for analgesic receptors =

A

greater potency

22
Q

Change susceptibility to metabolising enzymes =

A

change in duration of action

23
Q

Changing lipophilicity will

A

change penetration of CNS

24
Q

u-receptors are associated with all the main pharmacological effects of morphine:

A
  • analgesia
  • respiratory depression
  • emesis
  • tolerance
  • withdrawal symptoms
  • reduce gastric motility
25
Q

k- selective agonists produce….

they lack….

A

produce:

  • diuresis
  • sedation
  • analgesia
  • dysphoria

lack:

  • constipation
  • respiratory depression
  • addictive effects
26
Q

selective k- opioids with only peripheral action may be useful in relieving…..

A

inflammation and its associated pain

27
Q

d- selective agonists produce

A
  • analgesia

- convulsant activity

28
Q

Is Fentanyl or Morphine more potent? By how much? and because of what?

A

Fentanyl.
500 times more
greater lipophilicity