Name of Faculty: Shivakant Shukla Designation: A.P ... · action • Ionization, Solubility,...

Preview:

Citation preview

LNCT GROUP OF COLLEGES

Name of Faculty: Shivakant Shukla

Designation: A.P.

Department:LNCP

Subject:Medicinal Chemistry(BP-402T)

Unit:I

Topic:Introduction of Medicinal

Chemistry

Unit 1

Introduction, History and

development of Medicinal chemistry

Prof.Shivakant Shukla

LNCP, Bhopal (M.P)

Content

INTRODUCTION TO MEDICINAL CHEMISTRY • History and development of medicinal chemistry Physicochemical properties in relation to biological action

• Ionization, Solubility, Partition Coefficient, Hydrogen bonding, Protein binding, Chelation,

• Bioisosterism, Optical and Geometrical isomerism. Drug metabolism • Drug metabolism principles- Phase I and Phase II. • Factors affecting drug metabolism including stereo

chemical aspects.

CHEMISTRY

What is Chemistry? • Chemistry is known

as the central of science.

• It is a branch of physical science that studies the composition, structure, properties and changes of matter.

• MATTER = Solid / Liquid/ Gas.

PHYSICAL CHEMISTRY

• the branch of chemistry concerned with the application of the techniques and theories of physics to the study of chemical systems.

• Branches : chemical Kinetics, Electrochemistry, spectroscopy, photochemistry.

BRANCHES OF CHEMISTRY

INORGANIC CHEMISTRY

• deals with the synthesis and behaviour of inorganic and organometallic compounds

• Branches :Bioinorganic, Cluster, Material & Nuclear Chemistry

ORGANIC CHEMISTRY

• study of the structure, properties, and reactions of organic compounds and organic materials, i.e., matter in its various forms that contain carbon atoms.

• Branches : Biochemistry, biophysical, Biorganic, P’ceutical, Medicinal

WHAT IS MEDICINAL CHEMISTRY

• It is a discipline or intersection of chemistry

especially synthetic organic chemistry & pharmacology.

OR

• Medicinal chemistry involves discovery, development, identification & interpretation of Mode of action of biologically active compounds at molecular level.

Medicinal chemistry covers three Critical steps:

1. Discovery step • Involving choice of therapeutic target (receptor, enzyme & target group, cellular or in vivo model). • & identification or discovery and production of new active substances interacting with selected targets. Such compounds called LEAD COMPOUND.

2. An optimization step • Which deals with improvement of lead compound? • The optimization process takes primarily into account the increase in potency, selectivity and toxicity

3. Development stage • Whose purpose is continuation of improvement of pharmacokinetic properties

Primary objective of medicinal chemistry

Generally, we can identify the following stages in drug discovery, design and development

Drug discovery-finding a lead • Choose a disease. • Choose a drug target. • Identify a bioassay. • Find a lead compound. • Isolate and purify the lead

compound if necessary. • Determine the structure of the

lead compound if necessary. Drug design • Identify structure-activity

relationships (SARs) • Identify the pharmacophore.

• Improve target interactions (pharmacodynamics).

• Improve pharmacokinetic properties,

Drug development • Patent the drug. • Carry out preclinical trials (drug

metabolism, toxicology, formulation and stability test, pharmacology studies, etc).

• Design a manufacturing process (chemical and process development).

• Carry out clinical trials. • Register and market the drug. • Make money.

Finally medicinal chemistry ….

• Medicinal chemistry includes synthetic & computational aspects of the study of existing drugs and agents in development in

relation to their bioactivities i.e., understandings a SARs (Structure Activity Relationships).

OR

• It is a tailoring

of drug

How drugs can be discovered

Techniques involved in

• Random screening.

• Molecular manipulation.

e.g., hydrogenation of the parent thiazide diuretic chlorothiazide has increased the sodium losing, and decreased the potassium losing potential of the resultant compounds, thereby raising their potency and lessening side effects

• Molecular designing. In its simplest form, this may involve the synthesis of a naturally occurring substance, a hormone, a vitamin, or a precursor of a neurotransmitter, e.g.,levodopa for Parkinsonism

Metabolites of drugs. Sometimes active metabolites of drugs are found to possess therapeutic advantages over the parent compound, e.g., paracetamol is a metabolite of phenacetin and is effective as an analgesic, but does not cause renal damage.

• Serendipity. HAPPY OBSERVATION BY CHANCE e.g., penicillin as an antibacterial agent.

Origins of Medicinal Chemistry

Recommended