Prepared By
Dr. Krishnaswamy. G
Faculty
DOS & R in Organic Chemistry
Tumkur University
Tumakuru
For
I M.Sc., I Semester
DOS & R in Organic Chemistry
Tumkur University
Tumakuru
MEDICINAL CHEMISTRY
MEDICINAL CHEMISTRY
Chemical compounds
which shows
Physiological /
biological /
therapeutic action
Medicine or Drug
Physiological /
biological /
therapeutic action of
any compounds
depends on structure
and its arrangements
‘Medicinal chemistry concerns the discovery, the development,
the identification and the interpretation of the mode of action of biologically
active compounds at the molecular level.
IUPAC Definition
New
Molecules
Biological
Characterization
Chemical
Characterization
Structure
property
relationship
Organic Chemistry
(Concerns Design &
Synthesis)
- Natural Products
- New synthetic approaches
Medicinal Chemistry
(Concerns Molecules)
- Identification
- Optimization
Pharmaceutical Chemistry
(Concerns Products)
- Analysis
-Bioavailability
-- Bioequivalence
- Physicochemical properties
-Conformation
-- Stereochemistry
- ADME
-Toxicity
- Molecular Modeling
- QSAR
Name The word Drug derived from Greek
“Pharmacon” means drug
The word Medicine derived from Latin
“Medicus” means healing
Definition Substances which can change the
physical and physiological state -
Drug
Substances that have definite form and
therapeutic use for treatment -
Medicine
Drug is a substance which cures the
disease but is habit forming, causes
addiction and has serious side
effects.
Medicine is a chemical substance which
cures the disease, has negligible toxicity
and does not cause any addiction
Amount Drug does not have any definite form
and dose.
Medicine has definite form and dose.
Relation with API Drug = API (Active Pharmaceutical
Ingredient)
Medicine = API ± Excipients
Potency Drugs are active potent compound. Medicines are administrative form of
drug.
Source Plants, animals, microorganisms,
synthetic, minerals
Drug and excipient.
Comparison All drugs are not medicines All medicines are drugs
Selectivity Non selective Selective
Example Paracetamol Napa (paracetamol) 500 mg tablet
Difference between Drug and Medicine
Disintegration of
dosage form.
Dissolution of
active substance
Absorption
Distribution
Metabolism
Excretion
Drug-receptor
interaction in
target tissue
Pharmaceutical Phase
Pharmacokinetic Phase
Pharmacodynamic Phase
Drug available
for absorption
Drug available
for action
Three Phases of Drug action
DOSE
Pharmacology Pharmacon logos
+
=
Drug To study
Study of Drug, Drugs effect on body and Body response for the Drug.
Pharmacology Pharmacokinetic Pharmacodynamics
+
=
The purpose of studying pharmcokinetics and
pharmacodynamics is to understand the drug action,
therapy, design, development and evaluation.
Pharmacokinetics is what the Body Does To The Drug
like how the drug is absorbed, Distributed,
Metabolized and Excreted by the body – Drug
Disposition.
Pharmacodynamics is what the Drug Does To The
Body which may be the therapeutic effect or the
adverse side effect – Drug Action.
Nomenclature of Drugs
Drugs have three or more names.
These names are the following:
a) Code number or code designation;
b) Chemical name;
c) Proprietary, trivial, brand or trade name;
d) Nonproprietary, generic, official, or common name; and
e) Synonym and other names.
The code number is usually formed with the initials of the laboratory or the
chemist or the research team that prepared or tested the drug the first time,
following by a number. It does not identify the chemical nature or structure
of the drug. Its use is discontinued as soon as an adequate name is chosen.
The chemical name is the only one that describes unambiguously the
chemical structure of a drug, identifying it fully and exactly. It is given
according to rules of nomenclature of chemical compounds. Since the
chemical name is sometimes very elaborate, it is not suitable for routine
usage.
a) Code number or code designation;
b) Chemical name;
The proprietary name is the individual name selected and used by
manufacturers. If a drug is manufactured by more than one company
c) Proprietary, trivial, brand or trade name;
The nonproprietary name refers to the common, established name by
which a drug is known as an isolated substance, irrespective of its
manufacturer. It is chosen by official agencies, such as the U.S. Adopted
Names (USAN) Council, the American Pharmaceutical Association, and
other.
d) Nonproprietary, generic, official, or common name;
Synonyms are names given by different manufacturers to the same drug or
old nonproprietary names. Some drugs may have several names.
e) Synonym and other names.
EXAMPLE: Paracetamol
Chemical Name: N-(4-hydroxyphenyl)acetamide
Non Proprietary Name:
British Approved Name (BAN): Paracetamol
United States Adopted Name (USAN): Acetaminophen
Proprietary Name:
Panadol, Calpol, Adol
Official Name:
Acetaminophen
Classification of Drugs
Drugs can be classified according to various criteria. Usually,
they are classified according to
a) Chemical Nature,
b) Source,
c) Target organ / Site of Action,
d) Mechanism of action and
e) Therapeutic use.
Classification based on Chemical Nature
Inorganic Drugs Organic Drugs
Metals and their salts
(FeSO4, MgSO4)
Non metals includes
sulphur
Alkaloids
(Atropine, Morphine)
Proteins
(Insulin, Oxytocin)
Esters, Amide, Alcohol
Classification based on Source
Plants (Morphine,
Atropine)
Animals (Insulin)
Microorganism
(Pencillin)
Mineral
(Sodium chloride)
Sulphoamides Amoxicillin, Ampicillin
Natural source Synthetic source Semi Synthetic source
Classification based on Target organ / Site of Action
Drug acting on CNS (Diazepam)
Drug acting on Respiratory System (Bromhexamine)
Drug acting on GIT (Omeprazole)
Drug acting on Urinary system (Magnesium
sulphate)
Drug acting on Reproductive System (Oxytocin)
Classification based on Mechanism of action
Inhibitor of Bacterial Cell wall synthesis (Pencillin)
Inhibitor of Bacterial protein synthesis (Tetracycline)
Calcium Channel Blocker (Nifedipine)
Classification based on Therapeutic use
Antimicrobials – Drugs which are used to cure diseases caused by microbes
or microorganisms such as bacteria, fungi, virus etc.
Anti-infectives
Antibacterials – Drugs which are used to cure diseases caused by bacteria.
Antifungals – Drugs which are used to cure diseases caused by fungi.
HO
NH2 H
N
O N
S
O
OH
O
Chemical structure of Amoxicillin
Chemical structure of Fluconazole
Antitubercular - Drug used to treat tuberculosis caused by Mycobacterium
tuberculosis.
N
H
N
O
NH2 Chemical structure of Isoniazid
Antivirals - Drug used to prevent and treat HIV/AIDS .
Chemical structure of Abacavir
Antibiotics – Chemical substance which in low concentration either kill or
inhibit the growth of microorganisms intervening in their metabolic process.
They are classified into two classes
(1) Bactericidal which is used to kill bacteria
(2) Bacteriostatic which is used to inhibit the growth of bacteria.
N
N
O
F
OH
O
HN
Chemical structure of Ciprofloxacin
Analgesics – Drugs which reduce pain without causing impairment of consciousness,
mental confusion of disorder of the nervous system.
These are classified into following two categories
Non-narcotic Analgesics: Aspirin and paracetamol are the most important examples
of non-addictive analgesics.
Narcotic Analgesics: Drugs which when administered in small doses relieve pain and
produce sleep are called narcotics. However, in large doses, they produce laziness,
coma and may ultimately cause death.
Central Nervous System Drugs
Antiseptics and Disinfectants
The chemical substances which prevent the growth of micro-organisms or may
even kill them when applied to living tissues like skin, are called Antiseptic.
Examples of Antiseptic:
Dettol: It is a mixture of chloroxylenol and terpineol in a suitable solvent. It is widely
used for cuts, wounds etc.
Iodine: It is used as a tincture of iodine(a 2-3% sol. of iodine in alcohol and water)
The chemical substances which are used to kill harmful micro-organisms but are
not safe to be applied to the living tissues are called Disinfectants.
Examples of Disinfectants:
1% solution of phenol is a disinfectant.
Example: A 0.2% solution of phenol is used as an antiseptic but 1% solution of
phenol is used as a disinfectants.
Antacids: Excess production of Hydrochloric acid in our stomach cause
irritation and pain. Sometimes in severe cases, ulcers can also be produced
in the stomach. Hence, ‘the substances which neutralize the excess acid
and raise the pH to an appropriate level in stomach are called Antacids’.
Examples: Sodium Bicarbonate, magnesium hydroxide etc.
Structure of drug Cimetidine
The secretion of pepsin and hydrochloric acid is stimulated by Histamine.
Therefore, the drug cimetidine was developed to stop the interaction of histamine
with the receptors that are present in the stomach wall. As a result, less
hydrochloric acid is released and the problem of hyperacidity can be solved.
Anti-cancer drugs also called antineoplastic drug, any drug that is effective in the
treatment of malignant, or cancerous, disease.
Cis platin (Cis-dichlorodiammineplatinum(II)) is alkylating agent binds to DNA and
leads to cancer cell death
Pt
NH3
NH3
Cl
Cl
Chemical structure of Cisplatin
N
H
NH
F
O
O
Chemical structure of 5-Fluorouracil
Antineoplastic agent used to treat various kinds of cancer namely colorectal,
breast, stomach, pancreatic and cervical.
OH
O
Chemical structure of Ibuprufen
Anti-inflammatory drugs also known as Nonsteroidal anti-
inflammatory drugs (NSAIDs) block the COX enzymes and reduce prostaglandins
throughout the body. As a consequence, ongoing inflammation, pain, and fever
are reduced.
Tranquilizers also known as antidepressant drugs used for the treatment of
stress, fatigue, mild and severe mental diseases.
Noradrenaline is one of the several neurotransmitters which play an important
role in mood change. If the level of noradrenaline in the body is low, then the
message transfer process becomes slow and the person suffers depression.
Chemical structure of Iproniazid
Diuretics also called water pills medication designed to increase the amount of
water and salt expelled from the body as urine.
The most common condition treated with diuretics is high blood pressure.
The drugs reduce the amount of fluid in your blood vessels, and this helps
lower your blood pressure.
Antimalarial drugs used to treat malaria caused by Plasmodium species.
Chemical structure of Chloroquine
Chemical structure of Furosemide
Drug can produce toxic / adverse effect in addition to
therapeutic / pharmacological effect.
No drug is free from side effects
With some drugs toxic effect may be minor while with certain
drugs there may be serious problems.
Toxicology: Branch of Science deals with the amount of an
agent that causes an adverse action in living system.
In order to get an idea about the safety of drugs therapeutic
index can be used.
THERAPEUTIC INDEX
THERAPEUTIC INDEX =
Dosage of a drug that cause a toxic / lethal effect
Dosage of a drug that causes therapeutic effect
THERAPEUTIC INDEX =
LD 50
ED 50
THERAPEUTIC INDEX =
TD 50
ED 50
Animals Humans
DOSE: Amount of drug administered
Median Lethal Dose(LD 50)
Dose which kills 50 % or half the population of animal
tested.
Median Toxic Dose(TD 50)
Dose which kills 50 % or half the population of humans
tested.
Dose which produce the desired response in 50 % or
half the population of animal / humans tested.
Median Effective Dose(ED 50)
Higher the therapeutic index = Safer is the drug
Therapeutic index (> 10) = Safe drug
Therapeutic index (4 – 10) = Relatively safe
Therapeutic index (2 – 4) = Toxic
Therapeutic index (< 2) = Highly Toxic
THERAPEUTIC INDEX
ED 50 LD / TD 50
%
Response
%
Death
50
100
50
100
THERAPEUTIC EFFECT
TOXIC EFFECT
Dose (mg/kg)
Drug Safety - THERAPEUTIC INDEX
Half Maximal Effective Concentration (EC 50)
The drug concentration producing 50% of a maximal
effect
Example: Administering a 1000 mg dose of acetaminophen
(ED50) orally will result in a plasma concentration of 15 mg/ml
(EC50), which produces effective pain relief in 50% of adult
patients.
Half Maximal Inhibitory Concentration (IC 50)
Drug needed to inhibit a given biological process or biological
component by 50%.
-log (IC 50)
pIC 50 =
(IC 50) values can be expressed in terms of pIC 50
An assay is a process of analyzing
a substance to determine its composition or quality
The biological or pharmacological potency of drug
1) Chemical assay – Chemical methods are employed for
estimation of the concentration.
Qualitative: Extraction, Distillation, Precipitation and other
physicochemical methods.
Quantitative: Volume or Weight
Types of assay
2) Bio assay – an analytical method to determine concentration
or potency of a substance by its effect on living cells or tissues.
Chemical assay
More Precise
Less time consuming
Active constituent and
structure fully established
Less sensitive
Bio assay
 Less Precise
More time consuming
Active constituent and
structure not known
More sensitive
Medicinal chemistry
Immuno assay – an analytical method which uses antibodies as
reagent to quantitate or detect specific analyte.
Antibody and antigen complexes used as means of measurable
results.
Metabolites Antimetabolites
Definition Any substances produced by
or taking part in a metabolic
reaction Metabolites
Any substances (medicine) that
compete with or inhibits the
normal metabolic process
often by acting analogue of an
essential metabolite –
Antimetabolites
Example Uracil 5-Fluorouracil
Structure
Role Thymidylate synthetase (TS)
enzyme for DNA synthesis
Inhibits Thymidylate synthetase
(TS) enzyme for DNA synthesis
↓ dTMP → ↓ DNA and ↓ protein synthesis
PHARMACOPHORE
“An ensemble of steric and electronic features that is necessary
to ensure the optimal supramolecular interaction with a
specific biological target and to trigger or block its biological
response”.
PHARMACOPHORE UNITS
In Drug Design the term pharmacophore refers to a set of
features that is common to a series of active molecules.
Hydrogen bond donors and acceptors, positively and
negatively charged group and hydrophobic region are typical
features. Such features are referred as pharmacophoric groups
Medicinal chemistry

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Medicinal chemistry

  • 1. Prepared By Dr. Krishnaswamy. G Faculty DOS & R in Organic Chemistry Tumkur University Tumakuru For I M.Sc., I Semester DOS & R in Organic Chemistry Tumkur University Tumakuru MEDICINAL CHEMISTRY
  • 2. MEDICINAL CHEMISTRY Chemical compounds which shows Physiological / biological / therapeutic action Medicine or Drug Physiological / biological / therapeutic action of any compounds depends on structure and its arrangements ‘Medicinal chemistry concerns the discovery, the development, the identification and the interpretation of the mode of action of biologically active compounds at the molecular level. IUPAC Definition
  • 3. New Molecules Biological Characterization Chemical Characterization Structure property relationship Organic Chemistry (Concerns Design & Synthesis) - Natural Products - New synthetic approaches Medicinal Chemistry (Concerns Molecules) - Identification - Optimization Pharmaceutical Chemistry (Concerns Products) - Analysis -Bioavailability -- Bioequivalence - Physicochemical properties -Conformation -- Stereochemistry - ADME -Toxicity - Molecular Modeling - QSAR
  • 4. Name The word Drug derived from Greek “Pharmacon” means drug The word Medicine derived from Latin “Medicus” means healing Definition Substances which can change the physical and physiological state - Drug Substances that have definite form and therapeutic use for treatment - Medicine Drug is a substance which cures the disease but is habit forming, causes addiction and has serious side effects. Medicine is a chemical substance which cures the disease, has negligible toxicity and does not cause any addiction Amount Drug does not have any definite form and dose. Medicine has definite form and dose. Relation with API Drug = API (Active Pharmaceutical Ingredient) Medicine = API ± Excipients Potency Drugs are active potent compound. Medicines are administrative form of drug. Source Plants, animals, microorganisms, synthetic, minerals Drug and excipient. Comparison All drugs are not medicines All medicines are drugs Selectivity Non selective Selective Example Paracetamol Napa (paracetamol) 500 mg tablet Difference between Drug and Medicine
  • 5. Disintegration of dosage form. Dissolution of active substance Absorption Distribution Metabolism Excretion Drug-receptor interaction in target tissue Pharmaceutical Phase Pharmacokinetic Phase Pharmacodynamic Phase Drug available for absorption Drug available for action Three Phases of Drug action DOSE
  • 6. Pharmacology Pharmacon logos + = Drug To study Study of Drug, Drugs effect on body and Body response for the Drug. Pharmacology Pharmacokinetic Pharmacodynamics + =
  • 7. The purpose of studying pharmcokinetics and pharmacodynamics is to understand the drug action, therapy, design, development and evaluation. Pharmacokinetics is what the Body Does To The Drug like how the drug is absorbed, Distributed, Metabolized and Excreted by the body – Drug Disposition. Pharmacodynamics is what the Drug Does To The Body which may be the therapeutic effect or the adverse side effect – Drug Action.
  • 8. Nomenclature of Drugs Drugs have three or more names. These names are the following: a) Code number or code designation; b) Chemical name; c) Proprietary, trivial, brand or trade name; d) Nonproprietary, generic, official, or common name; and e) Synonym and other names.
  • 9. The code number is usually formed with the initials of the laboratory or the chemist or the research team that prepared or tested the drug the first time, following by a number. It does not identify the chemical nature or structure of the drug. Its use is discontinued as soon as an adequate name is chosen. The chemical name is the only one that describes unambiguously the chemical structure of a drug, identifying it fully and exactly. It is given according to rules of nomenclature of chemical compounds. Since the chemical name is sometimes very elaborate, it is not suitable for routine usage. a) Code number or code designation; b) Chemical name;
  • 10. The proprietary name is the individual name selected and used by manufacturers. If a drug is manufactured by more than one company c) Proprietary, trivial, brand or trade name; The nonproprietary name refers to the common, established name by which a drug is known as an isolated substance, irrespective of its manufacturer. It is chosen by official agencies, such as the U.S. Adopted Names (USAN) Council, the American Pharmaceutical Association, and other. d) Nonproprietary, generic, official, or common name;
  • 11. Synonyms are names given by different manufacturers to the same drug or old nonproprietary names. Some drugs may have several names. e) Synonym and other names. EXAMPLE: Paracetamol Chemical Name: N-(4-hydroxyphenyl)acetamide Non Proprietary Name: British Approved Name (BAN): Paracetamol United States Adopted Name (USAN): Acetaminophen Proprietary Name: Panadol, Calpol, Adol Official Name: Acetaminophen
  • 12. Classification of Drugs Drugs can be classified according to various criteria. Usually, they are classified according to a) Chemical Nature, b) Source, c) Target organ / Site of Action, d) Mechanism of action and e) Therapeutic use.
  • 13. Classification based on Chemical Nature Inorganic Drugs Organic Drugs Metals and their salts (FeSO4, MgSO4) Non metals includes sulphur Alkaloids (Atropine, Morphine) Proteins (Insulin, Oxytocin) Esters, Amide, Alcohol
  • 14. Classification based on Source Plants (Morphine, Atropine) Animals (Insulin) Microorganism (Pencillin) Mineral (Sodium chloride) Sulphoamides Amoxicillin, Ampicillin Natural source Synthetic source Semi Synthetic source
  • 15. Classification based on Target organ / Site of Action Drug acting on CNS (Diazepam) Drug acting on Respiratory System (Bromhexamine) Drug acting on GIT (Omeprazole) Drug acting on Urinary system (Magnesium sulphate) Drug acting on Reproductive System (Oxytocin)
  • 16. Classification based on Mechanism of action Inhibitor of Bacterial Cell wall synthesis (Pencillin) Inhibitor of Bacterial protein synthesis (Tetracycline) Calcium Channel Blocker (Nifedipine)
  • 17. Classification based on Therapeutic use Antimicrobials – Drugs which are used to cure diseases caused by microbes or microorganisms such as bacteria, fungi, virus etc. Anti-infectives Antibacterials – Drugs which are used to cure diseases caused by bacteria. Antifungals – Drugs which are used to cure diseases caused by fungi. HO NH2 H N O N S O OH O Chemical structure of Amoxicillin Chemical structure of Fluconazole
  • 18. Antitubercular - Drug used to treat tuberculosis caused by Mycobacterium tuberculosis. N H N O NH2 Chemical structure of Isoniazid Antivirals - Drug used to prevent and treat HIV/AIDS . Chemical structure of Abacavir
  • 19. Antibiotics – Chemical substance which in low concentration either kill or inhibit the growth of microorganisms intervening in their metabolic process. They are classified into two classes (1) Bactericidal which is used to kill bacteria (2) Bacteriostatic which is used to inhibit the growth of bacteria. N N O F OH O HN Chemical structure of Ciprofloxacin
  • 20. Analgesics – Drugs which reduce pain without causing impairment of consciousness, mental confusion of disorder of the nervous system. These are classified into following two categories Non-narcotic Analgesics: Aspirin and paracetamol are the most important examples of non-addictive analgesics. Narcotic Analgesics: Drugs which when administered in small doses relieve pain and produce sleep are called narcotics. However, in large doses, they produce laziness, coma and may ultimately cause death. Central Nervous System Drugs
  • 21. Antiseptics and Disinfectants The chemical substances which prevent the growth of micro-organisms or may even kill them when applied to living tissues like skin, are called Antiseptic. Examples of Antiseptic: Dettol: It is a mixture of chloroxylenol and terpineol in a suitable solvent. It is widely used for cuts, wounds etc. Iodine: It is used as a tincture of iodine(a 2-3% sol. of iodine in alcohol and water)
  • 22. The chemical substances which are used to kill harmful micro-organisms but are not safe to be applied to the living tissues are called Disinfectants. Examples of Disinfectants: 1% solution of phenol is a disinfectant. Example: A 0.2% solution of phenol is used as an antiseptic but 1% solution of phenol is used as a disinfectants.
  • 23. Antacids: Excess production of Hydrochloric acid in our stomach cause irritation and pain. Sometimes in severe cases, ulcers can also be produced in the stomach. Hence, ‘the substances which neutralize the excess acid and raise the pH to an appropriate level in stomach are called Antacids’. Examples: Sodium Bicarbonate, magnesium hydroxide etc. Structure of drug Cimetidine The secretion of pepsin and hydrochloric acid is stimulated by Histamine. Therefore, the drug cimetidine was developed to stop the interaction of histamine with the receptors that are present in the stomach wall. As a result, less hydrochloric acid is released and the problem of hyperacidity can be solved.
  • 24. Anti-cancer drugs also called antineoplastic drug, any drug that is effective in the treatment of malignant, or cancerous, disease. Cis platin (Cis-dichlorodiammineplatinum(II)) is alkylating agent binds to DNA and leads to cancer cell death Pt NH3 NH3 Cl Cl Chemical structure of Cisplatin N H NH F O O Chemical structure of 5-Fluorouracil Antineoplastic agent used to treat various kinds of cancer namely colorectal, breast, stomach, pancreatic and cervical.
  • 25. OH O Chemical structure of Ibuprufen Anti-inflammatory drugs also known as Nonsteroidal anti- inflammatory drugs (NSAIDs) block the COX enzymes and reduce prostaglandins throughout the body. As a consequence, ongoing inflammation, pain, and fever are reduced. Tranquilizers also known as antidepressant drugs used for the treatment of stress, fatigue, mild and severe mental diseases. Noradrenaline is one of the several neurotransmitters which play an important role in mood change. If the level of noradrenaline in the body is low, then the message transfer process becomes slow and the person suffers depression. Chemical structure of Iproniazid
  • 26. Diuretics also called water pills medication designed to increase the amount of water and salt expelled from the body as urine. The most common condition treated with diuretics is high blood pressure. The drugs reduce the amount of fluid in your blood vessels, and this helps lower your blood pressure. Antimalarial drugs used to treat malaria caused by Plasmodium species. Chemical structure of Chloroquine Chemical structure of Furosemide
  • 27. Drug can produce toxic / adverse effect in addition to therapeutic / pharmacological effect. No drug is free from side effects With some drugs toxic effect may be minor while with certain drugs there may be serious problems. Toxicology: Branch of Science deals with the amount of an agent that causes an adverse action in living system. In order to get an idea about the safety of drugs therapeutic index can be used.
  • 28. THERAPEUTIC INDEX THERAPEUTIC INDEX = Dosage of a drug that cause a toxic / lethal effect Dosage of a drug that causes therapeutic effect THERAPEUTIC INDEX = LD 50 ED 50 THERAPEUTIC INDEX = TD 50 ED 50 Animals Humans DOSE: Amount of drug administered
  • 29. Median Lethal Dose(LD 50) Dose which kills 50 % or half the population of animal tested. Median Toxic Dose(TD 50) Dose which kills 50 % or half the population of humans tested. Dose which produce the desired response in 50 % or half the population of animal / humans tested. Median Effective Dose(ED 50)
  • 30. Higher the therapeutic index = Safer is the drug Therapeutic index (> 10) = Safe drug Therapeutic index (4 – 10) = Relatively safe Therapeutic index (2 – 4) = Toxic Therapeutic index (< 2) = Highly Toxic
  • 31. THERAPEUTIC INDEX ED 50 LD / TD 50 % Response % Death 50 100 50 100 THERAPEUTIC EFFECT TOXIC EFFECT Dose (mg/kg) Drug Safety - THERAPEUTIC INDEX
  • 32. Half Maximal Effective Concentration (EC 50) The drug concentration producing 50% of a maximal effect Example: Administering a 1000 mg dose of acetaminophen (ED50) orally will result in a plasma concentration of 15 mg/ml (EC50), which produces effective pain relief in 50% of adult patients.
  • 33. Half Maximal Inhibitory Concentration (IC 50) Drug needed to inhibit a given biological process or biological component by 50%. -log (IC 50) pIC 50 = (IC 50) values can be expressed in terms of pIC 50
  • 34. An assay is a process of analyzing a substance to determine its composition or quality The biological or pharmacological potency of drug 1) Chemical assay – Chemical methods are employed for estimation of the concentration. Qualitative: Extraction, Distillation, Precipitation and other physicochemical methods. Quantitative: Volume or Weight Types of assay
  • 35. 2) Bio assay – an analytical method to determine concentration or potency of a substance by its effect on living cells or tissues. Chemical assay More Precise Less time consuming Active constituent and structure fully established Less sensitive Bio assay  Less Precise More time consuming Active constituent and structure not known More sensitive
  • 37. Immuno assay – an analytical method which uses antibodies as reagent to quantitate or detect specific analyte. Antibody and antigen complexes used as means of measurable results.
  • 38. Metabolites Antimetabolites Definition Any substances produced by or taking part in a metabolic reaction Metabolites Any substances (medicine) that compete with or inhibits the normal metabolic process often by acting analogue of an essential metabolite – Antimetabolites Example Uracil 5-Fluorouracil Structure Role Thymidylate synthetase (TS) enzyme for DNA synthesis Inhibits Thymidylate synthetase (TS) enzyme for DNA synthesis
  • 39. ↓ dTMP → ↓ DNA and ↓ protein synthesis
  • 40. PHARMACOPHORE “An ensemble of steric and electronic features that is necessary to ensure the optimal supramolecular interaction with a specific biological target and to trigger or block its biological response”.
  • 42. In Drug Design the term pharmacophore refers to a set of features that is common to a series of active molecules. Hydrogen bond donors and acceptors, positively and negatively charged group and hydrophobic region are typical features. Such features are referred as pharmacophoric groups