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The data presented in Chart 1 also suggests that the pharmacophore fit improves with each subsequent generation; the first generated compounds with at least 13 pharmacophore matches first appear in the fifth generation medicine 95a pill buy genuine aggrenox caps on line. Percentage of compounds that contain known adenosine ligand scaffolds (“Scaffolds”) medicine 8 letters buy aggrenox caps online pills, and the percentage of compounds with at least 11 medicine man movie aggrenox caps 200 mg cheap, 12, or 13 pharmacophore feature hits (“Hits11”/”Hits12”/”Hits13”) per generation (number of generations on X-axis). The generated molecules from all generations were collected and merged into one set (discarding duplicates), resulting in a set of 3. The resulting set of 242 hits was examined for novelty by matching the structures against a set of common adenosine receptor scaffolds and ring systems. These candidates were grouped by scaffold and ranked according to pharmacophore score, as provided in Figure S3 of Supporting Information, to aid further manual inspection. As mentioned above, different structures not known to be adenosine receptor ligands were generated and clustered into different groups (i. We observed that all these scaffolds contained substituents of different nature, at different positions on the scaffold. To investigate the qualities of the multi-objective evolutionary design method, we began with the preparation of six scaffolds (Figure 3), the selection of which was based on ease of synthesis according to a panel of in-house medicinal chemists. Moreover, we were interested in the influence of the suggested substituents; therefore, we began with simple substitution (methyl groups) if any on these six scaffolds. Chemical structures of selected scaffolds generated using the multi- objective evolutionary design method: [1,2,4]Triazolo[4,3-a]quinazolin-5-one (1), 4-Aza-5[H]-phenanthridin-6-one (2), 2-Methylpyrimido[1,2-a]benzimidazol- 4(10H)-one (3), 3,5,6,7-Tetrahydro-4H-cyclopenta[4,5]thieno[2,3-d]pyrimidin- 4-one (4), 5,6,7,8-Tetrahydro[1]benzothieno[2,3-d]pyrimidin-4(3H)-one (5). The 6:6:5 fused heteroaromatic system [1,2,4]triazolo[4,3-a]quinazolin-5-one (1) was 20 synthesized as previously reported, by the cyclization of 2-hydrazinoquinazolin-4- 21 one in formic acid. Compound 2 was synthesized using a slightly modified reported 185 Chapter 6 22 method, starting from the synthesis of the 2-(N,N- 23 diisopropylcarboxamido)phenylboronic acid, which was then used in a Suzuki- Miyaura cross-coupling reaction with 2-amino-3-bromopyridine under microwave conditions. Subsequently, cyclization of 2-(2-aminopyridin-3-yl)-N,N- diisopropylbenzamide using lithium diisopropylamide yielded the desired compound 2. The 6:5:6 fused heteroaromatic system 2-methylpyrimido[1,2-a]benzimidazol-4(10H)- one (3) was obtained by heating a mixture of 2-aminobenzimidazole and ethyl acetoacetate in the presence of phosphoryl chloride and phosphoric acid. Cyclization of 2-amino-5,6-dihydro-4H- cyclopenta[b]thiophene-3-carbonitrile and 2-amino-4,5,6,7-tetrahydro-1- benzothiophene-3-carbonitrile in formic acid at 110 °C yielded compounds 4 and 5, respectively Compound 6 was synthesized starting from the commercially available 3,4-dimethylphenylisocyanate, which was reacted with hydrazine hydrate to obtain the corresponding semicarbazide, and was subsequently condensed with cyclohexanecarboxaldehyde to afford the corresponding semicarbazone. Finally, alkaline potassium ferricyanide oxidation of this semicarbazone yielded the desired compound 6. Schemes showing the synthesis path and reaction conditions are in the Supporting Information (Schemes S1-S5). Initially, all compounds were screened at a single concentration of 10 µM on all four receptor subtypes. For compounds that inhibited radioligand binding for more than 30% at one or more receptor subtypes the K values were subsequentlyi determined (Table 1). Compound 3 appeared active on all four adenosine receptor subtypes, also in the micromolar range. We were happy with the 33% ‘hit rate’, but concluded at the same time that the evolution of chemistry towards A1 receptor selectivity was only partially successful. Inspection of the generated molecules that contained this 10H-pyrimido-[1,2-a]- benzimidazol-4-one scaffold, revealed that the insertion of a simple alkyl chain at the 187 Chapter 6 3 R position of the scaffold lead to high-scoring molecules. Therefore, we replaced the methyl group on scaffold 3 by different alkyl groups (Figure 4) and investigated the influence thereof on adenosine receptor affinity. A series of compounds were synthesized (3a-3k) by reacting the corresponding 2-aminobenzimidazole with the appropriate β-keto-ester under microwave conditions (see Supporting Information). For those derivatives that gave more than 50% displacement at 1 µM concentration, whole displacement curves were recorded to determine the K value ofi each compound. A linear propyl group at the R position (3b) also improved the Ki value compared to compound 3, but less so than the iso-propyl substituent. These findings prompted us to synthesize the cyclohexyl derivative 3c, which provides an 3 even bulkier substituent at the R position, yet not aromatic. As listed in Table 2, 3 inserting a phenyl ring at the R position lead to compound 3d with highest affinity on the A1 receptor, with a K value of 0. Interestingly, introducing methyl groups on both 188 Multi-Objective Evolutionary Ligand Design 1 2 R and R positions decreased interaction with the adenosine receptors (Table 2).

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The presence of such impurities may be carried out by performing prescribed specific tests in various official compendia in order to ascertain their presence within the stipulated limits symptoms after miscarriage aggrenox caps 200 mg without prescription. Obviously the amount of any single impurity present in an official substance is usually small medicine interactions buy aggrenox caps 200mg amex, and therefore medicine song 2015 discount aggrenox caps 200mg with mastercard, the normal visible-reaction-response to any test for that impurity is also quite small. Hence, it is necessary and important to design the individual test in such a manner so as to avoid possible errors in the hands of various analysts. It may be achieved by taking into consideration the following three cardinal factors, namely : (a) Specificity of the Tests : A test employed as a limit test should imply some sort of selective reaction with the trace impurity. It has been observed that a less specific test which limits a number of possible impurities rather instantly has a positive edge over the highly specific tests. Exmaple : Contamination of Pb2+ and other heavy metal impurities in Alum is precipitated by thioacetamide as their respective sulphides at pH 3. The sensitivity is governed by a number of variable factors having a common objective to yield reproducible results, for instance : (i) Gravimetric Analysis : The precipitation is guided by the concentration of the solute and of the precipitating reagent, reaction time, reaction temperature and the nature and amount of other substance(s) present in solution. A number of such tests shall be discussed here briefly with specific examples wherever possible and necessary : 1. Limits of Insoluble Matter The limits of insoluble matter present in pharmaceutical substances and stated in various official com- pendia are given below : S. Boric Acid Alcohol insoluble substances Absence of metallic borates and insoluble impurities 2. Chloramine Alcohol-insoluble matter : Sodium chloride impurity : Shake 1 g for 30 mts. The residue washed with 5 m1 of ethanol (96% v/v) and dried at 100 to 105°C and weighed. Filter, wash the residue on the filter with hot alcohol (90% v/v) until the washings cease to be coloured violet. In the same vein, tests for clarity of solution offer another means of limiting insoluble parent drug sub- stances in their correspondingly more highly water-soluble derivatives. Limits of Soluble Matter In order to detect the presence of some very specific impurities normally present in the official substances the limits of soluble impurities have been laid down in different pharmacopoeias. Water-soluble medium) filter through paper, previously washed with a mixture of 10 barium salts are highly ml dil. Magnesium : Prepare the sample solution by adding 10 ml Magnesium : of a 1% w/v soln. Limits of Moisture, Volatile Matter and Residual Solvents A good number of pharmaceutical substances usually absorb moisture on storage thereby causing deterioration. Such an anomaly can be safely restricted and limited by imposing an essential requirement for the loss in weight (Loss on Drying) when the pharmaceutical chemical is subjected to drying under specified conditions. The quantum of heat that may be applied to the substance varies widely as per the following norms : (a) Nature of the substance (b) Decomposition characterisics of the substance. Various official compendia recommended different temperatures and duration of drying either at atmos- pheric or reduced pressure (vacuum). Pharmaceutical Substance Drying Conditions Drying Time Prescribed Limit (°C) (Hrs. Pharmaceutical Substance Drying Conditions Drying Time Prescribed Limit (°C) (Hrs) (%) Inorganic Salt Hydrates : l. The chromatographic procedure may be carried out by employing : (a) A stainless-steel column (1 m × 2 mm) packed with porous polymer beads e. From the chromatograms obtained and taking into account any water detectable in solution (1), calculate the percentage w/w of water taking 0. Limits of Non-Volatile Matter Pharmaceutical chemicals belonging to the domain of inorganic as well as organic substances containing readily volatile matter for which the various official compendia prescribe limits of non-volatile matter. It is pertinent to mention here that the Pharmacopoeia usually makes a clear distinction between substances that are readily volatile and substances that are volatile upon strong ignition, for instance : (a) Readily Volatile : e. Limits of Residue on Ignition In fact, the limits of residue on ignition are basically applicable to the following two categories of pharmaceutical substances, namely : (a) Those which are completely volatile when ignited e. Limits of Loss on Ignition Official compendia include the limits of ‘loss on ignition’ which is generally applied to relatively stable pharmaceutical substances that are likely to contain thermolabile impurities.

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