What are drugs and where do they come from Flashcards

1
Q

What are the 4 broad classes of protein receptors?

A

G Protein Coupled Receptors (targeted by highest number of current small molecule drugs)

Ion channels (second most common receptors targeted)

Kinases

Nuclear receptors

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2
Q

What does the “pharmacodynamics” refer to?

A

What drug does to body

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3
Q

What does the word “pharmacokinetics” refer to?

A

What body does to drug

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4
Q

What kind of molecules are typically used in pharmacology?

A

Small molecules. (due to ease and they access the body readily via GI tract)

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5
Q

What are the pros and cons of using small molecule drugs?

A

Pros:
Easy to prepare by synthetic chemists. (easy to confirm purity and structures are straightforward)

Affordable to make

Easy to copy when patent expires.

Body is accessed easily via oral route.

Cons:

Multiple receptors can be activated leading to unwanted side effects

Drug-drug interactions are more common

Problems with toxicity

Metabolism in liver is often extensive

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6
Q

What are the pros and cons of using biologic drugs?

A

Pros:
Specific to 1 receptor and rarely subject to DDIs

Metabolism isn’t very extensive

Cons:
Expensive to make

Hard to get into the body

hard to copy when patent expires

Structures are complex so it’s hard to test purity

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7
Q

What are the types of names used in pharmacology?

A

Chemical name

Generic name

Brand name

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8
Q

What does the chemical name describe?

A

Chemical structure of the drug and is often complex and not suitable for daily use

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9
Q

What does the generic name describe?

A

Simplified drug names which have roots and endings that provide clues of which drugs they are.

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10
Q

What does brand name describe?

A

Invented by marketing division of drug companies

Intended to be marketable

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11
Q

How are new drugs discovered?

A

Bioprospecting

Disease-model screening

Me-too optimisation

Astute clinical observation

Rational drug design

Irrational high-throughput discovery

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12
Q

What is bioprospecting?

A

Systematic testing of naturally procured materials for pharmacological activity.

(Many species including sea sponges, microorganisms, and animal venoms are rich in bioactive substances)

25% of current medicines have a natural origin.

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13
Q

What is disease-model screening?

A

Using animal models of disease and then treating these models with drugs.

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14
Q

What is me-too optimization?

A

Structurally related molecules created by competing pharmaceutical companies to make a drug have better features over another.

A successful me-too drug will displace original molecule from the market

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15
Q

What is astute clinical observation?

A

When unexpected effects follow testing of new molecules in humans resulting in therapeutic benefits being discovered. (this is less common nowadays due to better technologies for testing pharmacology of new molecules)

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16
Q

What is rational drug design?

A

Very sophisticated understanding of a molecular drug target results in production of a drug that fits that target and either stimulates or inhibits it.

17
Q

What is irrational high-throughput discovery?

A

Using automated computer programs to generate large libraries of molecules and drugs and so theoretical molecules are tested against receptors until some drugs work.

Screening massive libraries in this way has held the pharmaceutical industry back due to the invested effort that went into this