Download Chemistry for Pharmacy Students: General, Organic and by Satyajit Sarker, Lutfun Nahar PDF

By Satyajit Sarker, Lutfun Nahar

"This publication has succeeded in masking the elemental chemistry necessities required by way of the pharmaceutical technology scholar… the undergraduate reader, be they chemist, biologist or pharmacist will locate this an enticing and beneficial read." –Journal of Chemical Biology, may perhaps 2009Chemistry for Pharmacy scholars is a student-friendly advent to the foremost components of chemistry required via all pharmacy and pharmaceutical technology scholars. The booklet offers a complete assessment of a number of the components of common, organic items chemistry (in relation to drug molecules).Clearly dependent to augment scholar realizing, the booklet is split into six transparent sections. The e-book opens with an summary of basic features of chemistry and their value to fashionable existence, with specific emphasis on medicinal functions. The textual content then strikes directly to a dialogue of the innovations of atomic constitution and bonding and the basics of stereochemistry and their value to pharmacy- when it comes to drug motion and toxicity. a variety of features of aliphatic, fragrant and heterocyclic chemistry and their pharmaceutical value are then lined with ultimate chapters natural reactions and their purposes to drug discovery and improvement and average items chemistry.accessible advent to the major parts of chemistry required for all pharmacy measure coursesstudent-friendly and written at a degree appropriate for non-chemistry studentsincludes studying targets in the beginning of every chapterfocuses at the actual houses and activities of drug molecules

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Extra resources for Chemistry for Pharmacy Students: General, Organic and Natural Product Chemistry 2007

Sample text

The valence electrons that are not being shared are the nonbonding electrons or lone pair electrons, and they are shown in the Lewis structure by dots around the symbol of the atom. A species that has an unpaired electron are called radicals. Usually they are very reactive, and are believed to play significant roles in aging, cancer and many other ailments. In neutral organic compounds, C forms four bonds, N forms three bonds (and a lone pair), O forms two bonds (and two lone pairs) and H forms one bond.

Here the H atoms on C2 –C3 and C5 –C6 are eclipsed, which results in an increased torsional strain. Also, the H atoms on C1 and C4 are close enough to produce steric strain. e. e. around the ring equator) positions. Six hydrogen atoms are in the axial positions and six others in the equatorial positions. Each carbon atom in the cyclohexane chair conformation has an axial hydrogen and an equatorial hydrogen atom, and each side of the ring has three axial and three equatorial hydrogen atoms. aH eH He Ha He Ha He He He aH Ha Ha Chair conformation of cyclohexane Six axial (a) and six equatorial (e) hydrogen atoms aH eH He Ha H He a H e aH Ha Ha He He Chair conformation of cyclohexane Diaxial interaction When all 12 substituents are hydrogen atoms, there is no steric strain.

6 Significance of chemical bonding in drug–receptor interactions Most drugs interact with receptor sites localized in macromolecules that have protein-like properties and specific three-dimensional shapes. A receptor is the specific chemical constituents of the cell with which a drug interacts to produce its pharmacological effects. One may consider that every protein that acts as the molecular target for a certain drug should be called a receptor. However, this term mainly incorporates those proteins that play an important role in the intercellular communication via chemical messengers.

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