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Chiral Drugs: An Overview
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The first section introduces the general concept of chirality and its impact on the drug discovery and development. This part includes history of chiral drug development, key technologies for preparation of chiral drugs, and industrial applications of chiral technologies"--Provided by publisher.
Read more Show all links. Allow this favorite library to be seen by others Keep this favorite library private. Find a copy in the library Finding libraries that hold this item Hoboken, N. Presenting an overview of chiral drugs and their impact on the pharmaceutical industry, Chiral Drugs: Chemistry and Biological Action provides an integrated perspective of chiral drugs from concept, synthesis, and pharmaceutical properties. Reviews Editorial reviews. Publisher Synopsis "The book can be recommended to all those who are interested in this important and fast-growing field of research at the interface of chemistry, pharmacy, and medicine.
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Add a review and share your thoughts with other readers. Similar Items Related Subjects: 10 Chiral drugs. Drug development.
Structure-activity relationships Biochemistry Drug Discovery -- methods. Pharmaceutical Preparations -- chemistry. WordPress Shortcode. Rudra madhab , Student at Govt.
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Chiral Drugs: An Overview
No Downloads. Views Total views. Actions Shares. Embeds 0 No embeds. No notes for slide. Chiral drug 1. Bag Mr, M. Patra Dr. Singh Miss. Snehil Padhan Mr. ISOMERISM Isomers by definition are the molecules of identical atomic compositions molecular formulas , but with different bonding arrangements of atoms or orientation of their atoms in space.
The phenomenon is known as Isomerism. Simple example of constitutional isomerism is given examples of catechol, resorcinol, and hydroquinone all of these compounds having the same atomic composition C6H , but different bonding arrangements of atoms. These are thus distinct chemical entities with different chemical and physical properties. Optical isomers 2. Geometrical isomers 7. The object and mirror image pair of molecules has the same constituents and structural formula. Optical activity With chiral compounds, the plane of the polarized light is rotated through an angle.
A compound that rotates polarized light is said to be optically active With achiral compounds, the light that passes through the compound remains unchanged. A compound that does not change the plane of polarized light is said to be optically inactive
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