Lead Compounds Flashcards

1
Q

What is the progression of a drug?

A

Target Identification
Lead identification
SAR (structure activity relationship), Design and synthesis.
Formulation delivery
Toxicology
Clinical Trials
Patients

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2
Q

What does formulation delivery involve?

A

Checking its bioavailability –> pill more ideal than IV.
Potent direct to target so it doesn’t harm rest of body.

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3
Q

What is toxicology?

A

What metabolism does to the drug. Animal testing to human testing.

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4
Q

How can targets be identified?

A

Molecular biology techniques.
Identification of drug targets.
High throughout screening
Human genome project

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5
Q

What is the process of target identification?

A

Start with single target. (usually enzymes).
Enzyme or protein-protein interaction or receptor.
Target must be validated. (Long pharmacology process if stop does it repair disease state).
Develop a method for identifying molecules that bind/inhibit/activate.
Develop a high-throughput screen (can we screen a lot of compounds).

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6
Q

How do you validate a target?

A

Knockouts - usually mice in which the gene is deleted.
SiRNA
CRISPR/Cas - a type of molecular knockout.
Antisense - RNA targeted oligonucleotide - target RNA to stop proteins being created.
Small molecules - Which stop proteins from doing its action.

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7
Q

What is a lead compound?

A

A molecule with the desired biological activity. EG enzyme inhibition, receptor binding (antagonist and agonist), receptor maybe a protein/nucleic acid.
Prototype for eventual drug- study and develop analogues will lead to final marketable drugs.

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8
Q

What is a lead compound not?

A

It isn’t necessarily a “druggable” compound.
It may not be very active.
It may not be bioavailable.
It may generate lots of side effects.

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9
Q

Where can lead compounds come from?

A
  • Natural products (eg plants & fungus).
  • Medical folklore - ethnobotany (traditional eg use of mushrooms).
  • **Screening synthetic libraries **(pharmaceutical companies have libraries they go through to see if any good compounds).
  • Existing drugs (drugs exist with ideal affect).
  • Combinational synthesis (not popular - put reagents in big pot to see what comes out).
  • Natural substrate (eg find enzyme with similar affect you want and create drug)
  • Computer Aided design (Popular - model it)
  • Serendipity (luck)
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10
Q

What is an example of natural products?

A

Doxorubicin - antitumor anthracycline. Used in the clinic but limited by cardiac side effects.
—> Mitoxantrone - Synthetic anthraquinone. Used in the clinic but limited by toxic side effects but not cardiac.
—-> AQ4N - Synthetic anthraquinone. Prodrug. Currently in phase II clinical trial - avoids toxic and cardiac side effects.

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11
Q

What is an example of ethnobotany?

A

Snowdrop (plant).
1950s - Pharmacologist noted locals rubbed on forehead.
‘52 - isolated galanthamine.
Treatment for poliomyelitis. Now is Alzheimers disease.

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12
Q

What are some examples of natural products (biological drugs)?

A
  • Insulin
  • Interferon
  • Monoclonal antibodies. (Trastuzumab (Herceptin))
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13
Q

What are some examples of synthetic libraries?

A

May be patented for a different reason unrelated to what you need a lead compound for.
Eg Viagra (originally heart drug).

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14
Q

What is an example of existing drugs?

A

Thalidomide - originally drug for morning sickness, still used for leprosy treatment in some countries.
Analogues of it are being used to develop as anti-angiogenic agents in cancer chemotherapy.

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15
Q

What are analogues

A

In chemistry, analogs or analogues are compounds in which one/more individual atoms have been replaced, either with a different atom, or with a diff functional group. Also it can refer to a substance which is similar in structure to another substance.

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16
Q

What examples of natural ligands for lead compounds?

A

5-Hydroxytryptamine binds to 5-HT receptors in brain. Sumatriptan is a 5HT antagonist used in the treatment of migraine.

17
Q

What is fragment based chemistry?

A

Take small fragments and see where they fit. High or micromolar ideally –> link together.

18
Q

How do you check fragment based chemistry?

A

Utilise NMR spectroscopy or crystallography.
Can use ligands of low affinity (mM to microM).
Can screen at high concs.
Hit rates high - fragments lack complexity.
Molecular weights low (up to 250Da).
Manipulation increases Mw but still low.

19
Q

What can an ester bond be?

A

H-acceptor

20
Q

What can aromatic rings be?

A

pi pi stacking.

21
Q

What can Ketone do?

A

H-bond acceptor

22
Q

What can alkyls be?

A

Hydrophobic interactions