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681por Yang, Fei, Liu, Fang, Min, Yong, Shi, Liqiao, Liu, Manli, Wang, Kaimei, Ke, Shaoyong, Gong, Yan, Yang, Ziwen“…Two series of novel steroidal[17,16-d]pyrimidines derived from natural epiandrosterone and androsterone were designed and synthesized, and these compounds were screened for their potential anticancer activities. …”
Publicado 2023
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682por El-Kalyoubi, Samar, El-Sebaey, Samiha A., Rashad, A. M., AL-Ghulikah, Hanan A., Ghorab, Mostafa M., Elfeky, Sherin M.Enlace del recurso
Publicado 2023
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683por Kim, Na Young, Vishwanath, Divakar, Xi, Zhang, Nagaraja, Omantheswara, Swamynayaka, Ananda, Kumar Harish, Keshav, Basappa, Shreeja, Madegowda, Mahendra, Pandey, Vijay, Sethi, Gautam, Lobie, Peter E., Ahn, Kwang Seok, Basappa, Basappa“…Herein, a JNK-targeting compound has been developed that may be of utility in HER2-positive mammary carcinoma. The design of a pyrimidine-and coumarin-linked structure targeting JNK was explored and the lead structure PC-12 [4-(3-((2-((4-chlorobenzyl)thio) pyrimidin-4-yl)oxy)propoxy)-6-fluoro-2H-chromen-2-one (5d)] was observed to selectively inhibit the proliferation of HER2-positive BC cells. …”
Publicado 2023
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684por Alanazi, Ashwag S., Mirgany, Tebyan O., Alsaif, Nawaf A., Alsfouk, Aisha A., Alanazi, Mohammed M.“…The designed derivatives comprise isatin and pyrrolo[2,3-d]pyrimidine scaffolds in their structures with a hydrazine linking the two pharmacophores. …”
Publicado 2023
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685por Persaud, Avinash K., Bernier, Matthew C., Massey, Michael A., Agrawal, Shipra, Kaur, Tejinder, Nayak, Debasis, Xie, Zhiliang, Weadick, Brenna, Raj, Ruchika, Hill, Kasey, Abbott, Nicole, Joshi, Arnav, Anabtawi, Nadeen, Bryant, Claire, Somogyi, Arpad, Cruz-Monserrate, Zobeida, Amari, Foued, Coppola, Vincenzo, Sparreboom, Alex, Baker, Sharyn D., Unadkat, Jashvant D., Phelps, Mitch A., Govindarajan, RajgopalEnlace del recurso
Publicado 2023
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686por Xie, Chaochao, Xiao, Guiying, Guo, Qianling, Wu, Xiaoxue, Zi, Guofu, Ding, Wanjian, Hou, Guohua“…A highly enantioselective rhodium-catalyzed reductive dearomatization of 7-substituted pyrazolo[1,5-a]pyrimidines has been realized for the first time by two strategies to afford chiral 4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidines with excellent enantioselectivities of up to 98% ee. …”
Publicado 2023
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687“…The imbalance of tumor metabolic pathways is associated with tumor formation and proliferation. Pyrimidine metabolism (PyM) is a complex enzyme network that incorporates nucleoside salvage, de novo nucleotide synthesis, and catalytic pyrimidine degradation. …”
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688“…In the pursuit of developing more potent and effective targeted kinase inhibitors (TKIs), a series of new compounds, specifically halogenated ‘(E)-4-((7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)-N’-benzylidenebenzohydrazides’, were successfully synthesized in three steps with high yields. …”
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689
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690“…The transitions between pyrimidine and purine-rich regions of the genomes are rapid and are easily visible on a pyrimidine-purine walk graph. …”
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691por Hussey, H J, Todorov, P T, Field, W N, Inagaki, N, Tanaka, Y, Ishitsuka, H, Tisdale, M J“…The fluorinated pyrimidine nucleoside, 5′-deoxy-5-fluorouridine (5′-dFUrd) has been shown to effectively attenuate the progress of cachexia in the murine adenocarcinomas MAC16 and colon 26 as well as in the human uterine cervical carcinoma xenograft, Yumoto. …”
Publicado 2000
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692por Puffer, Barbara, Kreutz, Christoph, Rieder, Ulrike, Ebert, Marc-Olivier, Konrat, Robert, Micura, Ronald“…Here, we present a systematic investigation on the application of 5-fluoro pyrimidines to probe DNA and RNA secondary structures. …”
Publicado 2009
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693
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694por Frizzo, Clarissa P., Campos, Patrick T., Marzari, Mara R. B., Machado, Pablo, Martins, Marcos A. P.“…In the title compound, C(15)H(12)F(3)N(3), the pyrazolo[1,5-a]pyrimidine system ring is essentially planar with a maximum deviation from the mean plane of 0.014 (1) Å. …”
Publicado 2007
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695
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696por El-Ghamry, Hoda, Issa, Raafat, El-Baradie, Kamal, Isagai, Keiko, Masaoka, Shigeyuki, Sakai, Ken“…The title molecule, C(17)H(13)N(5)O(4)S, has a trans configuration with respect to the diazenyl (azo) group. The pyrimidine ring and the terminal benzene ring are inclined at angles of 89.38 (4) and 1.6 (6)°, respectively, with respect to the central benzene ring. …”
Publicado 2008
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697“…The two chelating 2-methyl-4-oxopyrido[1,2-a]pyrimidin-9-olate ligands and the coordinated water molecule form the Zn coordination. …”
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698
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699“…The dihedral angles between the pyrazole and pyrimidine rings are 1.28 (17) and 1.56 (17)° in the two molecules. …”
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700por Jasinski, Jerry P., Butcher, Ray J., Hakim Al-Arique, Q. N. M., Yathirajan, H. S., Narayana, B.“…The chloroethyl side chain is in a synclinal conformation, nearly orthogonal to the pyrimidine ring, with a dihedral angle between the chloroethyl side chain and the pyrimidine ring of 88.5 (1)°. …”
Publicado 2009
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