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1181por Zhou, Guang-Feng, Xie, Cong-Qiang, Xue, Jian-Xia, Wang, Jing-Bo, Yang, Yu-Zhuo, Zheng, Chang-Bo, Luo, Rong-Hua, Yang, Ren-Hua, Chen, Wen, Yang, Liu-Meng, Wang, Yue-Ping, Zhang, Hong-Bin, He, Yan-Ping, Zheng, Yong-TangEnlace del recurso
Publicado 2022
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1182“…Computational tools in investigating of spectral heterocyclic compounds ranges based on pyrimidine‑2‑thiones, take some importance in identifying their molecular and electronic behavior. …”
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1183“…Three-dimensional quantitative structure-activity relationship (3D-QSAR) analyses, based on a series of forty-seven thieno-pyrimidine derivatives, were performed to identify the key structural features for the inhibitory biological activities. …”
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1184“…[Image: see text] Synthesis of a new series of 20 compounds bearing the thieno[2,3-d]pyrimidine-4-one scaffold was achieved. The inhibitory activity of these compounds was performed over 60 cell lines of human tumor at single and five dose concentrations. …”
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1185“…In this paper, the binding modes and inhibitory mechanisms of four 7H-pyrrolo[2,3-d]pyrimidine competitive inhibitors of PAK4 were investigated at the molecular level, mainly using molecular dynamics simulations and binding free energy calculations. …”
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1186por Bayanati, Maryam, Khoramjouy, Mona, Faizi, Mehrdad, Movahed, Mahsa Azami, Mahboubi-Rabbani, Mohammad, Zarghi, Afshin“…The present study was aimed at the synthesis and evaluation of a new series of benzo[4,5]imidazo[1,2-a]pyrimidine having a methylsulfonyl group as COX-2 (cyclooxygenase-2) inhibitor pharmacophore. …”
Publicado 2023
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1187por Poggialini, Federica, Vagaggini, Chiara, Brai, Annalaura, Pasqualini, Claudia, Crespan, Emmanuele, Maga, Giovanni, Perini, Cecilia, Cabella, Noemi, Botta, Lorenzo, Musumeci, Francesca, Frosini, Maria, Schenone, Silvia, Dreassi, Elena“…The therapeutic use of tyrosine kinase inhibitors (TKIs) represents one of the successful strategies for the treatment of glioblastoma (GBM). Pyrazolo[3,4-d]pyrimidines have already been reported as promising small molecules active as c-Src/Abl dual inhibitors. …”
Publicado 2023
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1188
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1189por Monti, Ludovica, Liu, Lawrence J., Varricchio, Carmine, Lucero, Bobby, Alle, Thibault, Yang, Wenqian, Bem-Shalom, Ido, Gilson, Michael, Brunden, Kurt R., Brancale, Andrea, Caffrey, Conor R., Ballatore, CarloEnlace del recurso
Publicado 2023
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1190“…Previous single-cell RNA-sequencing (scRNA-seq) suggested that the pyrimidine-base analog (5′-iodo-2′-deoxyuridine, IdU) could generally amplify noise without substantially altering mean-expression levels but scRNA-seq technical drawbacks potentially obscured the penetrance of IdU-induced transcriptional noise amplification. …”
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1191por Al-Muntaser, Samia M., Al-Karmalawy, Ahmed A., El-Naggar, Abeer M., Ali, Ali Khalil, Abd El-Sattar, Nour E. A., Abbass, Eslam M.“…Therefore, twenty-two novel 4-thiophenyl-pyrazole, pyridine, and pyrimidine derivatives were designed and examined as dual EGFR/VEGFR-2 inhibitors. …”
Publicado 2023
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1192“…A sulfonated poly-4-vinyl pyridinium (PVPy-IL-B-SO(3)H) containing an acidic pyridinium/HSO(3)(−) ionic liquid moiety was prepared and used as a catalyst for the three-component reaction of malononitrile with 1-alkylindoline-2,3-diones and 1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione or methyl 5-hydroxy-1H-pyrazole-3-carboxylate, leading to methyl 6′-amino-5′-cyano-2-oxo-2′H-spiro[indoline-3,4′-pyrano[2,3-c]pyrazole]-3′-carboxylates or -3,4′-pyrano[2,3-d]pyrimidine]-6′-carbonitrile derivatives under ultrasonic irradiation conditions. …”
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1193por Antolinc, Kris, Brodnik, Helena, Grošelj, Uroš, Štefane, Bogdan, Petek, Nejc, Svete, JurijEnlace del recurso
Publicado 2023
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1194por Chen, Shaojun, He, Xinmiao, Qin, Ziliang, Li, Gang, Wang, Wentao, Nai, Zida, Tian, Yaguang, Liu, Di, Jiang, Xinpeng“…Moreover, we identified PyrR-regulating pyrimidine biosynthesis, which further improved its internalization and colocalization with macrophages. …”
Publicado 2023
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1195por Martín-Montes, Álvaro, Jimenez-Falcao, Sandra, Gómez-Ruiz, Santiago, Marín, Clotilde, Mendez-Arriaga, José M.“…Four 7-oxo-5-phenyl-1,2,4-triazolo[1,5-a]pyrimidine (HftpO) first-row transition complexes (Cu, Co, Ni, Zn) have been studied for the first time in vitro against five different species of Leishmania spp. …”
Publicado 2023
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1196“…Some novel annulated pyrido[2,3-d]pyrimidines 6 and 7 were synthesized stereoselectively by intramolecular hetero Diels–Alder reactions involving 1-oxa-1,3-butadienes.…”
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1197“…In the crystal structure of the title compound, C(23)H(21)N(3)O(2)S, all ring atoms of the imidazo[1,2-a]benzothieno[3,2-d]pyrimidine system are essentially coplanar and the phenyl ring is twisted with respect to it [dihedral angle = 72.60 (9)°]. …”
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1198
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1199Ethyl 4-(4-hydroxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate monohydratepor Das, Ushati, Chheda, Shardul B., Pednekar, Suhas R., Karambelkar, Narendra P, Guru Row, T. N.“…Between dimers, single N—H⋯O hydrogen bonds are formed between the other N—H group of each pyrimidine ring and the hydroxyl groups. The water molecules accept O—H⋯O hydrogen bonds from the hydroxyl groups and donate hydrogen bonds to the ester groups.…”
Publicado 2008
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1200“…The asymmetric unit of the title complex, [Cu(2)(CN)(2)(C(20)H(16)N(6)S(2))](n), contains one Cu(I) cation, one cyanide ligand and half of a centrosymmetric 1,2-bis[4-(3-pyridyl)pyrimidin-2-ylsulfanyl]ethane (bppe) ligand. The Cu(I) atom displays a trigonal coordination geometry, being surrounded by one C atom from one cyanide anion and two N atoms from one cyanide and one bppe ligand. …”
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