Ofloxacin as a model hapten article in the analyst 1402. Ofloxacin, like other 4quinolones, is unusual among front line drugs available to treat bacterial infections since it affects bacterial dna synthesis, rather than cell wall or protein synthesis 2. A synthetic fluoroquinolone antibacterial agent, it inhibits the supercoiling activity of bacterial dna gyrase, halting dna replication. Ofloxacin 20 mgkg, norfloxacin 40 mgkg, pefloxacin mesylate dihydrate 40 mgkgand ciprofloxacin 50 mgkg were administered by gavage. What software is there available for quantitative structure activity relationship qsar pharmacological studies. Researchers tracked nearly 3,500 men and women ages 65 or older who took part in adult changes in thought act, a longterm study conducted by the university of washington and group health, a seattle health care system. Hence the combination of suitable metal and organic drug can result in a synergism of action, making it more effective against bacterial. Much can be inferred about the overall effects of various chemical modifications by better understanding how microbes become resistant to the action of fluoroquinolones.
I entered the data to arlequin and under genetic structure, the amova option is not active, is th. When taken by mouth or injection into a vein, these include pneumonia, cellulitis, urinary tract infections, prostatitis, plague, and certain types of infectious diarrhea. Program and abstracts of the 39th interscience conference on. Sildenafil structure activity relationship guaranteed quality without prescription. Ofloxacin binds to and inhibits bacterial topoisomerase ii dna gyrase and topoisomerase iv, enzymes involved in dna replication and repair, resulting in cell death in sensitive bacterial species. If the target structure is known, computational chemistry and molecular modelling software packages can be useful in identifying binding site interactions. New quantitative structureactivity relationships at n1 for the quinolone antibacterials.
If the target structure is known, computational chemistry and molecular modelling software packages can be useful in. Specifically, we focused on modification of the basic structure of ofloxacin by. The current knowledge of structureactivity relationships has been gained through the past development of a large number of compounds within the quinolone class. Masazumi imamuras 3 research works with 109 citations and 56 reads, including. The input is the chemical structure of the compound, and the software algorithms use quantitative structure activity relationships qsars. Sildenafil structure activity relationship fastshipping. Synthesis and structure activity relationships of 12fluorocyclopropyl3. Ofloxacin is an antibiotic drug used to treat bacterial infections.
Interestingly, ofloxacin has a tricyclic ring structure with a ch3 attached to the. The target molecules of quinolones and fluoroquinolones are bacterial gyrase and. As an optical active compound, ofloxacin has a pair of enantiomers. Copperii complexes with n,odonor ligands and ofloxacin. Hi, what sar structure activity relationship software would you recommend. Based on available data, an increased risk of teratogenic effects has not been observed following ofloxacin use during pregnancy padberg 2014. Ofloxacin is an antibiotic useful for the treatment of a number of bacterial infections. Ofloxacin is a fluoroquinolone antibacterial antibiotic. In our previous studies 5, 19, quantitative structure activity relationship qsar method was used for. The epitopes of the ofloxacin isomers were predicted using the hologram quantitative structure activity relationship hqsar and comparative molecular field analysis comfa approaches. Elucidating biotransformation pathways of ofloxacin in. Qsar in silico tools quantitative structureactivity. Structure activity relationships sar explore the relationship between a molecules biological activity and the three dimensional structure of the molecule.
Structures were drawn by chemdraw office 2008 software. Sar tools like cdd vault can detect correlations and build models used to evaluate new chemical structures to predict their biological activity. After the discovery of the fluoroquinolone norfloxacin, structureactivity relationships sar analysis of the fluoroquinolonic nucleus led to the development of new derivatives with. The results consistently show that the epitope of the chiral hapten should be primarily composed of the oxazine ring and the piperazinyl ring and mabs recognize. It has a role as a dna synthesis inhibitor, an antiinfective agent and an antibacterial drug. A new synthesis of 7hpyrido1,2,3de1,4benzoxazine derivatives including an antibacterial agent, ofloxacin. Disease recommendations osteomyelitis gramnegative bacterial infections ciprofloxacin bacterial diarrheal diseases ciprofloxacin used most commonly.
Inhibition of dna gyrase by levofloxacin and related. Unlike other fluoroquinolones, ofloxacin structure contains an oxazine ring linking the nitrogen at position 1 and carbon at position 8 of the quinolone nucleus. Sigmaaldrich offers abstracts and fulltext articles by hongtao mu, baoling wang, zhenlin xu, yuanming sun, xinan huang, yudong shen, sergei a eremin, anatoly v zherdev, boris b dzantiev, hongtao lei. This concept therefore points to the link between the chemical structures and biological and the biological. There is a relationship between molecular structures and their biological activity, and this principle is referred to as structure activity relationship sar. Synthesis and antibacterial activities of optically active. The demetra software tool can be used for toxicity prediction of molecules of pesticides and related compounds. Structure activity relationship data outlined the importance of the carboxyl group in the iosk structure, the etherification of which leads to the loss of the inhibitory activity, and the nmethyl group in compound iospefl, which is also essential for the activity.
Coverage against streptococcus pneumoniae is inadequate, making the use of ciprofloxacin inappropriate in patients with community. The structure activity relationship with the modifications of different positions of the ofl nucleus has been modified from anderson et al. Activity relationship of cocaine antagonists satendra singh department of medicinal chemistry and pharmaceutics, college of pharmacy, university of oklahoma health sciences center, oklahoma city, oklahoma 73190 received may 28, 1999 contents i. Ofloxacin is an oxazinoquinolone carrying carboxy, fluoro, methyl and 4methylpiperazino substituents. For interpretation of the references to color in this figure legend. In the terms of compounds 5 and 6 structure activity relationship, the antibacterial activity. Ofloxacin ophthalmic solution ofloxacin ophthalmic. Structure activity relationship sar is an approach designed to find relationships between chemical structure or structuralrelated properties and biological activity or target property of studied compounds. Structureactivity relationships sar explore the relationship between a molecules biological activity and the three dimensional structure of the molecule. Ofloxacin is metabolized in liver at the piperazinyl moiety following oral doses.
Its commonly used as an eye drop to treat conjunctivitis pink eye and corneal ulcers the tablet form of ofloxacin is. Ofloxacin floxin side effects, dosage, interactions. As an impressive alternative, quantitative structure activity relationship qsar analysis can be used to estimate the toxicity of ops identified during o 3 treatment of ppcps. Structureactivity relationships of the fluoroquinolones. Serum concentrations of ofloxacin may be lower during pregnancy than in nonpregnant patients giamarellou 1989. Media in category ofloxacin the following 10 files are in this category, out of 10 total. Fluoroquinolonesciprofloxacin exhibits good activity against pseudomonas aeruginosa and strong gram. Threedimensional quantitative structureactivity relationship 3d qsar and. Alomar, in profiles of drug substances, excipients and related methodology, 2009. The data obtained should be considered during the design of novel drugs based. Then this step will be followed by ofloxacin and therefore without greater change in the. An excellent summary of structureactivity relationships by tillotson 7 was. The toxicity estimation software tool test was developed to allow users to easily estimate the toxicity of chemicals using quantitative structure activity relationships qsars methodologies.
As the name suggests, this tool is dedicated to qsar modeling of small datasets. Fluorine atom at position c6 and various substitutions on the basic quinolone structure yielded fluoroquinolones, namely norfloxacin, ciprofloxacin, levofloxacin, moxifloxacin and numerous other agents. Some examples include ofloxacin, ciprofloxacin, perfloxacin, levofloxacin. It employs doublecrossvalidation approach modified and a set of optimum model selection techniques for performing the smalldataset qsar modelling.
The enzyme, identified as alcohol dehydrogenase synonym. S1c, f, which have differences in their biological activity. Ofloxacin crosses the placenta and produces measurable concentrations in the amniotic fluid. Quinolones are potent antimicrobial agents with a basic chemical structure of bicyclic ring. Rapidly and almost completely absorbed from gi tract. The mean serum ofloxacin concentration ranged from 0. Synthesis and structureactivity relationships of novel arylfluoroquinolone antibacterial agents. The electron attractive substituents on ring a enforce the activity no2brcf3cl ring b is necessary for activity the electron attractive substituents with small volume on benzene ring of c5 will enforce the activity the hydrolysis of amide and imine 10. Structure activity relationship sar is a method used in the detection of the chemical and biological activity relationship of compounds. Probing the stereoselective interaction of ofloxacin. Diffusion of oral ofloxacin hoe 280 into human prostatic tissue. Quinolone molecular structureactivity relationships. While we now have a considerable variety of clinically useful agents, it seems clear that improvements in antimicrobial activity are still possible. Ofloxacin has been used as successful antibiotic against various infection like chronic bronchitis, pneumonia, skin and skin structure infections, cervical gonorrhea, urinary tract infections etc.
Toxicity estimation software tool test safer chemicals. I would like to know what software is available to assist me in doing these studies. Other uses, along with other medications, include treating multidrug resistant tuberculosis. Chapter i quantitative structureactivity relationship in.
Chemistry, design, and structure activity relationship of. Chemical structure and pharmacokinetics of novel quinolone. Structure activity relationships of the fluoroquinolones. Structure activity relationship sar analysis software programs, such as oncologic and multicase mcase, work by analyzing the chemical structure of a compound of unknown toxicity and predicting its likelihood to be a carcinogen based on comparisons to the structures of compounds with known toxicity and programmed chemical and. Growth medium, inoculum size and serum had little influence on the activity of ofloxacin, but reduction of ph or the. Stereospecific recognition and quantitative structure. As such it is the concept of linking chemical structure to a chemical property e. Biology stack exchange is a question and answer site for biology researchers, academics, and students.
Ofloxacin pharmacokinetics absorption bioavailability. New quantitative structure activity relationships at n1 for the quinolone antibacterials. Structure activity relationship of sympathomimetic agent. This fused ring results in low metabolism of the drug in vivo. Qsars are mathematical models used to predict measures of toxicity from the physical characteristics of the structure of chemicals known as molecular descriptors. Sterimol is a program that calculates a set of five parameters. Insilico structure activity relationship and molecular docking study of. An excellent summary of structure activity relationships by tillotson was published in 1996, but considerable new information has been learned since that time. Stereospecific recognition and quantitative structureactivity relationship between antibodies and enantiomers.
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