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321“…In the title compound, C(11)H(9)ClN(4)O(2), the dihedral angle between the aromatic rings is 79.67 (8)°. π–π stacking between centrosymmetrically related pairs of pyrimidine rings occurs along [100] [centroid–centroid separations = 3.4572 (8) and 3.5433 (7) Å].…”
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322por Aznan, Aina Mardia Akhmad, Abdullah, Zanariah, Ng, Seik Weng, Tiekink, Edward R. T.Enlace del recurso
Publicado 2011
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323“…Their main difference is the torsion angles, ranging from 1.6 (5) to 5.9 (5)°, between the methyl group and the pyrimidine plane. A pair of intermolecular N—H⋯N hydrogen bonds link molecules A and C into a twisted dimer with a dihedral angle of 32.9 (1)° between the two pyrimidine rings, creating an R (2) (2)(8) motif. …”
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324“…In the title compound, C(13)H(10)BrN(3)O(3), the pyrimidine and benzene rings are twisted with an interplanar angle of 58.4 (1)°. …”
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325por Kandeel, Manal M., Mohamed, Lamia W., Abd El Hamid, Mohammed K., Negmeldin, Ahmed T.“…A new series of pyrazolo[3,4-d]pyrimidines has been synthesized. The new compounds were tested for their antitumor activity on 60 different cell lines, and some of the compounds were found to have potent antitumor activity. …”
Publicado 2012
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326por Velázquez-Olvera, Stephania, Salgado-Zamora, Héctor, Velázquez-Ponce, Manuel, Campos-Aldrete, Elena, Reyes-Arellano, Alicia, Pérez-González, Cuauhtémoc“…BACKGROUND: Imidazo[1,2-a]pyridines and pyrimidines are important organic fluorophores which have been investigated as biomarkers and photochemical sensors. …”
Publicado 2012
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327“…The dihedral angle between the phenyl and pyrimidine ring is 16.49 (6)°. An intramolecular N—H⋯N hydrogen bond stabilizes the molecular conformation. …”
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328por Bassoude, Ibtissam, Berteina-Raboin, Sabine, Essassi, El Mokhtar, Guillaumet, Gérald, El Ammari, Lahcen“…The fused pyrazole and pyrimidine rings in the title compound, C(13)H(10)ClN(3), are almost coplanar, their planes being inclined to one another by 0.8 (2)°. …”
Publicado 2013
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329“…In the crystal of the title compound, C(6)H(9)N(3)·C(6)H(8)O(2), the 2-amino-4,6-dimethylpyrimidine and sorbic acid molecules are linked through N—H⋯O and O—H⋯N hydrogen bonds, which generate a cyclic bimolecular heterosynthon with an R (2) (2)(8) graph-set motif. …”
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330por Zhao, Hang, Guo, Xiurong, He, Shiliang, Zeng, Xin, Zhou, Xinglong, Zhang, Chaoliang, Hu, Jing, Wu, Xiaohua, Xing, Zhihua, Chu, Liangyin, He, Yang, Chen, Qianming“…Here we study the mechanism of the formation of a complex flower-shaped supramolecular structure of pyrimido[4,5-d]pyrimidine nucleosides by dynamic light scattering, scanning electron microscopy, differential scanning calorimetry, nuclear magnetic resonance and X-ray analysis. …”
Publicado 2014
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331por Sviripa, Vitaliy M., Zhang, Wen, Balia, Andrii G., Tsodikov, Oleg V., Nickell, Justin R., Gizard, Florence, Yu, Tianxin, Lee, Eun Y., Dwoskin, Linda P., Liu, Chunming, Watt, David S.Enlace del recurso
Publicado 2014
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332“…Under the auspices of the Pilot Scale Library Program of the NIH Roadmap Initiative, we produced and report herein a diverse library of 181 purine, pyrimidine, and 1,2,4-triazole-N-acetamide analogues which were prepared in a parallel high throughput solution-phase reaction format. …”
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333por Kuppast, Bhimanna, Spyridaki, Katerina, Lynch, Christophina, Hu, Yueshan, Liapakis, George, Davies, Gareth E., Fahmy, Hesham“…Based on pharmacophore of the CRF1 receptor antagonists, a new series of thiazolo[4,5-d] pyrimidines were synthesized as Corticotropin-releasing factor (CRF) receptor modulators and the prepared compounds carry groups shown to produce optimum binding affinity to CRF receptors. …”
Publicado 2015
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334Structural basis of pyrimidine-pyrimidone (6–4) photoproduct recognition by UV-DDB in the nucleosomepor Osakabe, Akihisa, Tachiwana, Hiroaki, Kagawa, Wataru, Horikoshi, Naoki, Matsumoto, Syota, Hasegawa, Mayu, Matsumoto, Naoyuki, Toga, Tatsuya, Yamamoto, Junpei, Hanaoka, Fumio, Thomä, Nicolas H., Sugasawa, Kaoru, Iwai, Shigenori, Kurumizaka, Hitoshi“…We present the first atomic-resolution pictures of the detrimental DNA cross-links of neighboring pyrimidine bases within the nucleosome, and provide the mechanistic framework for lesion recognition by UV-DDB in chromatin.…”
Publicado 2015
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335por Rabinovich, Shiran, Adler, Lital, Yizhak, Keren, Sarver, Alona, Silberman, Alon, Agron, Shani, Stettner, Noa, Sun, Qin, Brandis, Alexander, Helbling, Daniel, Korman, Stanley, Itzkovitz, Shalev, Dimmock, David, Ulitsky, Igor, Nagamani, Sandesh CS, Ruppin, Eytan, Erez, AyeletEnlace del recurso
Publicado 2015
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336por Henley, Robert Y., Vazquez-Pagan, Ana G., Johnson, Michael, Kanavarioti, Anastassia, Wanunu, Meni“…Herein we show that covalent modification of one or both of the pyrimidine bases by an osmium bipyridine complex leads to measureable differences in the blockade amplitudes of DNA molecules. …”
Publicado 2015
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337“…Overall, we find that Hoogsteen-position pyrimidines support triple helix stability and function and that thermodynamic stability, based on EMSA results, is necessary but not sufficient for stabilization activity of the MALAT1 triple helix in cells. …”
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338por Park, Dong Ik, Dournes, Carine, Sillaber, Inge, Uhr, Manfred, Asara, John M., Gassen, Nils C., Rein, Theo, Ising, Marcus, Webhofer, Christian, Filiou, Michaela D., Müller, Marianne B., Turck, Christoph W.“…The integrated -omics data indicate purine and pyrimidine metabolism pathway activity differences between PLF and PSF mice. …”
Publicado 2016
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339por Leija, Christopher, Rijo-Ferreira, Filipa, Kinch, Lisa N., Grishin, Nick V., Nischan, Nicole, Kohler, Jennifer J., Hu, Zeping, Phillips, Margaret A.“…The human pathogenic parasite Trypanosoma brucei possess both de novo and salvage routes for the biosynthesis of pyrimidine nucleotides. Consequently, they do not require salvageable pyrimidines for growth. …”
Publicado 2016
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340“…Given the unique properties of the OCF(3) group and the ubiquity of pyridine and pyrimidine in biologically active molecules and functional materials, trifluoromethoxylated pyridines and pyrimidines could serve as valuable building blocks for the discovery and development of new drugs, agrochemicals, and materials.…”
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