Dipole Moment of 5- Fluorouracil Molecule

dipole antenna Moment of 5- Fluoro uracil MoleculeComputational Term PaperTheoretical studies on 5- fluorouracil to organise its dipole present heartbeat, and how the set comp ar with some other pyrimidine analog (namely uracil and deoxythymidine monophosphate) and that of literature.Name Farzana Nushin RezviAbstractIn this experiment, the dipole importation of 5- Fluorouracil element was determined employ the Gaussian softw are system, and compared with literature value. The dipole split seconds of other pyrimidine analogs, namely thyroxine and Uracil, were in addition calculated and compared with literature value. The experiment gave insight to typical dipole moment values of uracil derivatives, and how the dipole moment of aromatic molecules tin can be influenced in the heading of F, or -CH3 substituent.IntroductionThe purpose of this experiment is to calculate the dipole moment of the anticancer drug, 5- Fluorouracil, and compare the numerical value with that of 2 other pyrimidines, tonne and Uracil. soma 1 Molecular structure of 5- Fluoro uracil ( wasted by ChemBioDraw).5- Fluorouracil is apyrimidine analog (nucleoside analogs that mimic the molecular structure of pyrimidines) of uracil molecule that contributions as an anti-cancer drug it is designd in the treatment of several types of cancer, including that of rectum, colon, head and neck cancer.10 5- Fluorouracil belongs to the family of drugs called theantimetabolites. Antimetabolite drugs function by impeding vital biosynthetic processes or by being assimilated into macromolecules, and inhibiting their normal functioning. The fluoro pyrimidine drug, 5-fluorouracil (5-FU) does both.9Cancer cells often put on more uracil than normal cells, which indicates that uracil metabolism is a potential target for antimetabolite chemotherapy.9 The mechanism of cytotoxicity of 5-FU has been ascribed to the misincorporation of fluoronucleotides into ribonucleic acid and DNA and to the inhibiti on of the nucleotide synthetic enzyme thymidylate synthase.9 Thymidylate synthase is an enzyme that catalyzes the conversion of deoxyuridine monophosphate (dUMP) to deoxythymidine monophosphate (dTMP). dTMP is one of the three nucleotides (dTMP, dTTP, and dTDP) that eventually produce a thymine molecule. With inhibition of Thymidylate synthase, an imbalance of nucleotides results and increased levels of dUTP arise. Both of these factors cause DNA damage, and then ultimately inhibiting cell replication.5 FU is also seldom found in skin creams used for other conditions. However, it should be used in moderate/regulated amount of moneys since the side effects of unregulated exposure can be severe.105-Fluorouracil is a derivative of Uracil. Another structural analog of Uracil is Thymine. As can be seen from the figure below, the molecules only differ in what substituent each has on C-5. public figure 2 Molecular structures of Uracil, 5-Fluorouracil, and Thymine.Thymine is one of the f our nucleobases of DNA. Uracil is the RNA analogue of Thymine. Unlike Fluorouracil, these bases are regularly used by a healthy cell to construct new nucleotides (for multiplication, repair, etc.)The dipole moment is considered to be an elementary physiochemical home of a molecule. Interpretation of dipole moments by electronic charge distribution contributes to the understanding the molecular electronic structure and helps us gain deeper insight. The numerical values of the dipole moments also help us in evaluating the quantum mechanic calculations of electronic charge distribution, particularly in a series of homologous compounds, as in our experiment. Our experiment helps us understand the effects of substituents at C5 dipole moment of uracil.The dipole moment is a of these three molecules is an interesting study because in each case, the dipole moment is primarily influenced by the presence of electronegative blood corpuscles. The dipole moment of a molecule influences many of its properties and features (such as its colligtaive properties, how it interacts with other molecules, its behavior in compounds, etc.) In the molecules under consideration, the dipole moment(s) work as in the following figure (the dipole moment of uracil directed inbetween N3 and C4, with the substituent X either strengthening, or weakening the dipole in the illustrated vectors)6Fig 3 Vector scheme of dipole moments in uracil and in its derivatives6 (reproduced using ChemBioDraw)ExperimentalFor this Lab, the Gaussian software was used in calculating the dipole moment. At stolon, the molecule of concern was drawn using the software. and then Edit option is selected to Symmetrize our subject molecule. After that is done, we perform Gaussian Calculation Setup, by selecting business organization Type as Energy, and under Methods changing the Basis set. The numerical value of the dipole moment is obtained from the Results of the .chk file.The Gaussian calculation is repeated by s electing other Basis sets.The whole process is repeated for the molecules Thymine and Uracil. The molecule is drawn using Gaussian, and the Gaussian calculations repeated by selecting several(predicate) job types and basis sets.ResultsThe results obtained are represented in tabular form. The screenshots of the molecules as drawn in the Gaussian software are also given.TablesTable 1 The theoretic and Literature values of 5-Fluorouracil dipole momentTable 2 The theoretical and Literature values of Uracil dipole momentTable 3 The theoretical and Literature values of Thymine dipole moment.Images obtained from Gaussian5-FluorouracilFig 4 Image of 5-Fluorouracil molecule as drawn using Gaussian softwareUracilFig 5 Image of uracil molecule as drawn using Gaussian softwareThymineFig 6 Image of thymine molecule as drawn using Gaussian softwareDiscussionThe purpose of this experiment was to calculate the numerical values of dipole moments of the anticancer drug, 5- fluorouracil, and two othe r pyrimidines, thymine and uracil, and compare the obtained values with that of literature values. The dipole moment of a bond is defined as the mathematical product of the magnitude of the charges and distance between atoms under consideration11. The numerical value of the dipole moment can be calculated for each bond, as rise up as for the entire molecule. In this experiment, we use the Gaussian software for the calculation of dipole moments.The calculation of dipole moment is establish on the allocation of atomic charges to the atoms in the molecule in a apt way.4 In the hands on experiment, this consists of assigning electronegativity values to the atoms and experimental structural information of the bonds. Topological methods, however, do not take in information about the molecular geometry or the conformational status of the molecule. The topological method shortly in use is the Gasteiger-Hckelmethod, which has the disadvantage of omitting the validation procedure. This rend ers the study impractical.11The method of computation of partial charges employed in this experiment is based on the quantum mechanical calculation of wavefunction.11 For this report, wavefunctions were obtained using the ab initio method. Ab initio means based on first principles, these methods are based on quantum mechanics and attempt to solve the Schrdinger equation. Ab initio methods use no experimental parameters in their calculations, although they use some mathematical approximations. The major disadvantage of Ab Initio quantum chemistry is the heavy demands on computer power.12The choice of basis set is one of the most cardinal aspects of this computation, as our results depend vastly on the basis set employed. Basis sets are quantum chemical units of heartiness basis set contains mathematical functions that can be used to determine the dipole moment, energy, and other quantum mechanical properties of an atom/molecule of study. Basis sets are considered to represent the wavefunctions of the electrons in the species.12 On the basis of atomic head teacher charges, a molecular dipole moment can be calculated in a sort of simple and fast way, and compared with literature values. To get reliable results using this method, one must select weensy and rigid structures.11As the dipole moment is a property defined by quantum mechanics, wavefunctions can be used to directly calculate its values. Results derived with large basis sets (such as those reported in this paper) are in good agreement with experimental values. As we can see, our calculated values of the dipole moment ordain quite closely with the experimental values. One fact, however, stands out the values of dipole moment get adjacent to the literature values as the basis set is increased. However, quantum mechanical methods are not very recyclable when obtaining information about larger molecules.11The dipole moments of uracil, as well as of its respective derivatives are listed in Table 1, T able 2 and Table 3. First of all, it can be noticed that all these molecules guide pretty high values for dipole moments, compared to other aromatic molecules.4 This increase seems to be mainly referable to the large electronegativity of the O atoms (resulting in large numerical values of the dipole moments of carbonyl groups) which amount to 4 Debye units in thiouracils, according to Schneider and Halverstadt 13 This value can be contributed to the relatively high signaling of the secondary amide carbonyl group in these compounds, as compared with the generally observed value of 2.23 Debye units.4A pronounced change in the dipole moment is observed only upon the introduction of a substituent of a different polarity, such as Fluorine and Methyl group. In order to examine the effects of substituent on C5 on the electronic charge distribution in greater detail, many factors have to be taken into consideration. The first is that of electronegativity. Halogens are famously electrone gative, with F atom being the most. The electronegativity of Fluorine atom pulls onward electrons towards itself (and away from the ring) (Refer to Fig 3). As the dipole moment direction of F atom is directed towards itself, it somewhat cancels the dipole moment of N3. This explains why 5-Fluorouracil has a lower overall dipole moment compared to uracil.Thymine differs from uracil in having a methyl group (-CH3) on C5. The main chemistry to understand here is that of the inductive and mesomeric effect. Methylation at C5 and C6 mainly causes changes in the polarity of the C5C6 bond by way of increasing the -electronic charge on the atom at which substitution takes place.6 Due to the positive inductive effect of the CH3 group, electrons are pushed towards the aromatic ring. This adds to the electron pull of N3 and contributes to the overall polarity of the molecule.It can be noted that substitution at C5 does not diversify the dipole moment of uracil as much as a substituent on C6 w ould. (Since the substituents at C5 and C6 are differently oriented). For uracil, the dipole moment is directed in the N atom inbetween the carbonyl groups (as shown in Fig 3). However, the dipole moment is a more complicated calculation than can be inferred from a plat as simple, lots of other data (such as bond angles) also have to be taken into account.ConclusionThe purpose of this experiment is to calculate the dipole moment of the anticancer drug, 5- fluorouracil, and compare its value with that of literature, and two other pyrimidines, thymine and uracil. Based on the data obtained with 5 FU, the experiment can be deemed to be successful, as it contains about 1-2 % error with respect to literature. In summary, we have demonstrated that these Gaussian calculations is an easy and commodious way to determine many physical and spectroscopic properties of these molecules in solution and can give an spare insight into their in vivo properties.1CitationsTheoretical DFT and experimen tal NMR studies on uracil and 5- fluorouracil , B. Blicharska, T. Kupka / Journal of Molecular anatomical structure 613 (2002) 153166Frisch, M. J.et al. Gaussian Development Version, Revision D.02. In Gaussian Development Version, Revision D.02 Gaussian, Inc. Wallingford CT, 20055-Fluorouracil and thymine form a crystalline solid solution, Sarah A. Barnett, Ashley T. Hulme* and Derek A. Tocher, Acta Crystallographica Section CVolume 62, Issue 7, Article first published online 10 JUL 2006L.A. Curtiss, M.S. 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