User talk:Udayaraja
Drug design From Wikipedia, the free encyclopedia Jump to: navigation, search
This article needs additional citations for verification.
Please help improve this article by adding reliable references. Unsourced material may be challenged and removed. (October 2007)
Drug design is the approach of finding drugs by design, based on their biological targets. Typically a drug target is a key molecule involved in a particular metabolic or signalling pathway that is specific to a disease condition or pathology, or to the infectivity or survival of a microbial pathogen.
Some approaches attempt to stop the functioning of the pathway in the diseased state by causing a key molecule to stop functioning. Drugs may be designed that bind to the active region and inhibit this key molecule. However these drugs would also have to be designed in such a way as not to affect any other important molecules that may be similar in appearance to the key molecules. Sequence homologies are often used to identify such risks.
Other approaches may be to enhance the normal pathway by promoting specific molecules in the normal pathways that may have been affected in the diseased state.
The structure of the drug molecule that can specifically interact with the biomolecules can be modeled using computational tools. These tools can allow a drug molecule to be constructed within the biomolecule using knowledge of its structure and the nature of its active site. Construction of the drug molecule can be made inside out or outside in depending on whether the core or the R-groups are chosen first. However many of these approaches are plagued by the practical problems of chemical synthesis.
Newer approaches have also suggested the use of drug molecules that are large and proteinaceous in nature rather than as small molecules. There have also been suggestions to make these using mRNA. Gene silencing may also have therapeutical applications.
Contents [hide] 1 Rational drug design 2 Computer-assisted drug design 3 Examples of designed drugs 4 See also 5 References 6 External links
[edit] Rational drug design Unlike the historical method of drug discovery, by trial-and-error testing of chemical substances on cultured cells or animals, and matching the apparent effects to treatments, rational drug design begins with a knowledge of specific chemical responses in the body or target organism, and tailoring combinations of these to fit a treatment profile. Due to the complexity of the drug design process two terms of interest are still serendipity and bounded rationality. Those challenges are caused by the large chemical space describing potential new drugs without side-effects.
A particular example of rational drug design involves the use of three-dimensional information about biomolecules obtained from such techniques as x-ray crystallography and NMR spectroscopy. This approach to drug discovery is sometimes referred to as structure-based drug design. The first unequivocal example of the application of structure-based drug design leading to an approved drug is the carbonic anhydrase inhibitor dorzolamide which was approved in 1995. [1][2]
Another important case study in rational drug design is imatinib, a tyrosine kinase inhibitor designed specifically for the bcr-abl fusion protein that is characteristic for Philadelphia chromosome-positive leukemias (chronic myelogenous leukemia and occasionally acute lymphocytic leukemia). Imatinib is substantially different from previous drugs for cancer, as most agents of chemotherapy simply target rapidly dividing cells, not differentiating between cancer cells and other tissues.
The activity of a drug at its binding site is one part of the design. Another to take into account is the molecule's druglikeness, which summarizes the necessary physical properties for effective absorption. One way of estimating druglikeness is Lipinski's Rule of Five.
[edit] Computer-assisted drug design
Computer-assisted drug design uses computational chemistry to discover, enhance, or study drugs and related biologically active molecules. Methods used can include simple molecular modeling, using molecular mechanics, molecular dynamics, semi-empirical quantum chemistry methods, ab initio quantum chemistry methods and density functional theory. The purpose is to reduce the number of targets for a good drug that have to be subjected to expensive and time-consuming synthesis and trialling.
[edit] Examples of designed drugs
Cimetidine, the prototypical H2-receptor antagonist from which the later members of the class were developed
dorzolamide, a carbonic anhydrase inhibitor used to treat glaucoma
Many of the atypical antipsychotics
Selective COX-2 inhibitor NSAIDs
SSRIs (selective serotonin reuptake inhibitors), a class of antidepressants
Zanamivir, an antiviral drug
Enfuvirtide, a peptide HIV entry inhibitor
Probenecid
nonbenzodiazepines like Zolpidem and Zopiclone
[edit] See also Drug development Drug discovery Designer drug Enzyme inhibitors Bioinformatics Cheminformatics Biomedical informatics Pharmaceutical company Polyanhydrides Medicinal chemistry#Training in medicinal chemistry Software for molecular modeling
[edit] References ^ Greer J, Erickson JW, Baldwin JJ, Varney MD (1994). "Application of the three-dimensional structures of protein target molecules in structure-based drug design". J Med Chem 37 (8): 1035–1054. doi:10.1021/jm00034a001. PMID 8164249. ^ Gubernator K, Böhm HJ (1998). Structure-Based Ligand Design, Methods and Principles in Medicinal Chemistry. Weinheim: Wiley-VCH.
[edit] External links Computer-assisted drug design software free demos Ascalaph software
[hide]v • d • eTopics in Medicinal Chemistry
ADME · Bioavailability · Chemogenomics · Drug design · Drug discovery · Enzyme inhibitor · Mechanism of action · New chemical entity · Pharmacodynamics · Pharmacokinetics · Pharmacology · Pharmacophore · Quantitative structure-activity relationship
Retrieved from "http://en.wikipedia.org/wiki/Drug_design"
Categories: Pharmacology | Experimental design | Clinical research | Medicinal chemistry | Drug discovery
Hidden category: Articles needing additional references from October 2007
ViewsArticle Discussion Edit this page History Watch Personal toolsUdayaraja My talk My preferences My watchlist My contributions Log out Navigation
Main page
Contents
Featured content
Current events
Random article
Search
Interaction
About Wikipedia Community portal Recent changes Contact Wikipedia Donate to Wikipedia Help Toolbox What links here Related changes Upload file Special pages Printable version Permanent link Cite this page Languages Español Français
This page was last modified on 11 August 2008, at 13:31. All text is available under the terms of the GNU Free Documentation License. (See Copyrights for details.) Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc., a U.S. registered 501(c)(3) tax-deductible nonprofit charity. Privacy policy About Wikipedia Disclaimers
Start a discussion with Udayaraja
Talk pages are where people discuss how to make content on Wikipedia the best that it can be. Start a new discussion to connect and collaborate with Udayaraja. What you say here will be public for others to see.
