Bibliografías temáticas / Geiparvarin / Artículos de revistas
Siga este enlace para ver otros tipos de publicaciones sobre el tema: Geiparvarin.

Artículos de revistas sobre el tema "Geiparvarin"

Autor: Grafiati
Publicado: 10 de marzo de 2023

Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros

Elija tipo de fuente:

Consulte los 40 mejores artículos de revistas para su investigación sobre el tema "Geiparvarin".

Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.

También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.

Explore artículos de revistas sobre una amplia variedad de disciplinas y organice su bibliografía correctamente.

1

Rampa, Angela, Piero Valenti, Paolo Da Re, Milvia Chicca, Simonetta Gasperini y Giuseppe Colombo. "Geiparvarin Regioisomers". Collection of Czechoslovak Chemical Communications 57, n.º 1 (1992): 153–58. http://dx.doi.org/10.1135/cccc19920153.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
2

RAMPA, A., P. VALENTI, P. DA RE, M. CHICCA, S. GASPERINI y G. COLOMBO. "ChemInform Abstract: Geiparvarin Regioisomers." ChemInform 23, n.º 19 (22 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199219330.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
3

Valenti, Piero, Maurizio Recanatini, Paolo Da Re, Wilma Galimbeni, Nilla Avanzi y Stefania Filippeschi. "Xanthone Analogue of Geiparvarin". Archiv der Pharmazie 318, n.º 10 (1985): 923–26. http://dx.doi.org/10.1002/ardp.19853181012.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
4

Kang, S. H. y C. Y. Hong. "Simple synthetic routes to geiparvarin". Tetrahedron Letters 28, n.º 6 (enero de 1987): 675–78. http://dx.doi.org/10.1016/s0040-4039(00)95810-6.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
5

Baraldi, P. G., A. Barco, S. Benetti, A. Casolari, S. Manfredini, G. P. Pollini y D. Simoni. "Isoxazoles-mediated synthesis of geiparvarin and dihydrogeiparvarin". Tetrahedron 44, n.º 4 (enero de 1988): 1267–72. http://dx.doi.org/10.1016/s0040-4020(01)85907-x.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
6

Baraldi, Pier Giovanni, M. Guarneri, S. Manfredini, D. Simoni, J. Balzarini y E. De Clercq. "Synthesis and cytostatic activity of geiparvarin analogs". Journal of Medicinal Chemistry 32, n.º 2 (febrero de 1989): 284–88. http://dx.doi.org/10.1021/jm00122a002.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
7

Calas, Patrick y Claire Amato. "A Novel Geiparvarin Analogue Possessing a Fluorinated Segment". Synthesis, n.º 17 (2003): 2709–12. http://dx.doi.org/10.1055/s-2003-42446.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
8

Bocca, Claudia, Ludovica Gabriel y Antonella Miglietta. "Cytoskeleton-interacting activity of geiparvarin, diethylstilbestrol and conjugates". Chemico-Biological Interactions 137, n.º 3 (septiembre de 2001): 285–305. http://dx.doi.org/10.1016/s0009-2797(01)00261-7.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
9

Chimichi, Stefano, Marco Boccalini, Alessia Salvador, Francesco Dall'Acqua, Giuseppe Basso y Giampietro Viola. "Synthesis and Biological Evaluation of New Geiparvarin Derivatives". ChemMedChem 4, n.º 5 (11 de mayo de 2009): 769–79. http://dx.doi.org/10.1002/cmdc.200900009.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
10

Manfredini, S., P. G. Baraldi, R. Bazzanini, M. Guarneri, D. Simoni, J. Balzarini y E. De Clercq. "Geiparvarin Analogs. 4.1. Synthesis and Cytostatic Activity of Geiparvarin Analogs Bearing a Carbamate Moiety or a Furocoumarin Fragment on the Alkenyl Side Chain". Journal of Medicinal Chemistry 37, n.º 15 (julio de 1994): 2401–5. http://dx.doi.org/10.1021/jm00041a019.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
11

Baraldi, Pier Giovanni, Achille Barco, Simonetta Benetti, Mario Guarneri, Stefano Manfredini, Gian Piero Pollini y Daniele Simoni. "A new nitrile oxide based synthesis of the antitumor agent geiparvarin". Tetrahedron Letters 26, n.º 43 (enero de 1985): 5319–22. http://dx.doi.org/10.1016/s0040-4039(00)95027-5.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
12

MANFREDINI, S., P. G. BARALDI, R. BAZZANINI, M. GUARNERI, D. SIMONI, J. BALZARINI y E. DE CLERCQ. "ChemInform Abstract: Geiparvarin Analogues. Part 4. Synthesis and Cytostatic Activity of Geiparvarin Analogues Bearing a Carbamate Moiety or a Furocoumarin Fragment on the Alkenyl Side Chain." ChemInform 25, n.º 51 (18 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199451156.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
13

Chen, Yeh-Long, Tai-Chi Wang, Cherng-Chyi Tzeng y Nein-Chen Chang. "Geiparvarin Analogues: Synthesis and Anticancer Evaluation ofα-Methylidene-γ-butyrolactone-Bearing Coumarins". Helvetica Chimica Acta 82, n.º 2 (10 de febrero de 1999): 191–97. http://dx.doi.org/10.1002/(sici)1522-2675(19990210)82:2<191::aid-hlca191>3.0.co;2-p.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
14

Viola, Giampietro, Daniela Vedaldi, Francesco dall'Acqua, Giuseppe Basso, Silvia Disarò, Monica Spinelli, Barbara Cosimelli, Marco Boccalini y Stefano Chimichi. "Synthesis, Cytotoxicity, and Apoptosis Induction in Human Tumor Cells by Geiparvarin Analogues". Chemistry & Biodiversity 1, n.º 9 (septiembre de 2004): 1265–80. http://dx.doi.org/10.1002/cbdv.200490089.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
15

Baraldi, Pier G., Stefano Manfredini, Daniele Simoni, Mojgan Aghazadeh Tabrizi, Jan Balzarini y Erik De Clercq. "Geiparvarin Analogs. 3. Synthesis and cytostatic activity of 3(2H)-furanone and 4,5-dihydro-3(2H)-furanone congeners of geiparvarin, containing a geraniol-like fragment in the side chain." Journal of Medicinal Chemistry 35, n.º 10 (mayo de 1992): 1877–82. http://dx.doi.org/10.1021/jm00088a025.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
16

Miglietta, Antonella, Claudia Bocca, Ludovica Gabriel, Angela Rampa, Alessandra Bisi y Piero Valenti. "Antimicrotubular and cytotoxic activity of geiparvarin analogues, alone and in combination with paclitaxel". Cell Biochemistry and Function 19, n.º 3 (2001): 181–89. http://dx.doi.org/10.1002/cbf.919.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
17

Jiang, Fuling, Guang-Jie Wang, Ping Huang, Shu Chen, He Xiao, Liang Zhang y Hua Zou. "Geiparvarin Inhibits OS Metastasis through Upregulation of ANGPTL4 Expression by Inhibiting miRNA-3912-3p Expression". Evidence-Based Complementary and Alternative Medicine 2022 (12 de abril de 2022): 1–8. http://dx.doi.org/10.1155/2022/4663684.

Texto completo
Resumen
Background. Geiparvarin (GN) is a natural compound with anticancer activity. However, the effect of GN on osteosarcoma (OS) and the anticancer mechanism of GN are still unclear. Methods. Cell viability was measured by MTT assay. Invasion and migration were measured by transwell assay. The miRNAs, genes, and signaling pathways affected by GN were confirmed by whole-genome sequencing and bioinformatics analysis. The expression level of mRNA and protein was measured by qRT-PCR and western blot. Animal experiment was performed for confirming the GN anticancer effect and side effect in vivo. Results. Our results show that GN significantly inhibits OS cell growth and metastasis in vitro. In vivo experiment also showed that GN dramatically suppressed OS lung metastasis and no side effects were found. GN treatment inhibited OS metastasis through upregulating the ANGPTL4 expression. In addition, GN inhibited the expression of miR-3912-3p, which targets ANGPTL4. Conclusion. Our data clearly indicate that GN is a candidate drug for OS treatment, and GN plays its role through miR-3912-3p/ANGPTL4 in OS.
Los estilos APA, Harvard, Vancouver, ISO, etc.
18

Chimichi, Stefano, Marco Boccalini, Barbara Cosimelli, Giampietro Viola, Daniela Vedaldi y Francesco Dall'Acqua. "New geiparvarin analogues from 7-(2-oxoethoxy)coumarins as efficient in vitro antitumoral agents". Tetrahedron Letters 43, n.º 42 (octubre de 2002): 7473–76. http://dx.doi.org/10.1016/s0040-4039(02)01798-7.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
19

Inoue, Y., K. Ohuchi, S. Imaizumi, H. Hagiwara y H. Uda. "New Syntheses of Geiparvarin and 2,5-Dimethyl-3(2H)-furanone Via Co2Mediated Bond Reorganization". Synthetic Communications 20, n.º 19 (noviembre de 1990): 3063–68. http://dx.doi.org/10.1080/00397919008051526.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
20

Zhang, Yikai, Zhiliang Lv, Hanyu Zhong, Dongping Geng, Mingfeng Zhang, Tao Zhang, Yongmei Li y Ke Li. "Convenient synthesis of novel geiparvarin analogs with potential anti-cancer activity via click chemistry". European Journal of Medicinal Chemistry 53 (julio de 2012): 356–63. http://dx.doi.org/10.1016/j.ejmech.2012.04.026.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
21

Zhang, Yikai, Zhiliang Lv, Hanyu Zhong, Dongping Geng, Mingfeng Zhang, Tao Zhang, Yongmei Li y Ke Li. "ChemInform Abstract: Convenient Synthesis of Novel Geiparvarin Analogues with Potential Anticancer Activity via Click Chemistry." ChemInform 43, n.º 43 (27 de septiembre de 2012): no. http://dx.doi.org/10.1002/chin.201243142.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
22

Chen, Yeh-Long, Tai-Chi Wang, Cherng-Chyi Tzeng y Nein-Chen Chang. "ChemInform Abstract: Geiparvarin Analogues: Synthesis and Anticancer Evaluation of α-Methylidene-γ-butyrolactone-Bearing Coumarins." ChemInform 30, n.º 43 (13 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199943253.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
23

Chimichi, Stefano, Marco Boccalini, Giancarlo Cravotto y Ornelio Rosati. "A new convenient route to enantiopure 2-coumarinyloxypropanals: application to the synthesis of optically active geiparvarin analogues". Tetrahedron Letters 47, n.º 14 (abril de 2006): 2405–8. http://dx.doi.org/10.1016/j.tetlet.2006.01.151.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
24

INOUE, Y., K. OHUCHI, S. IMAIZUMI, H. HAGIWARA y H. UDA. "ChemInform Abstract: New Syntheses of Geiparvarin and 2,5-Dimethyl-3(2H)-furanone via CO2- Mediated Bond Reorganization." ChemInform 22, n.º 15 (23 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199115180.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
25

Villemin, Didier, Paul-Alain Jaffrès y Messaoud Hachémi. "An abnormal reaction of esters of 3-hydroxy-3-methylbutan-2-one. A rapid synthesis of bullatenone and geiparvarin". Tetrahedron Letters 38, n.º 4 (enero de 1997): 537–38. http://dx.doi.org/10.1016/s0040-4039(96)02365-9.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
26

VILLEMIN, D., P. A. JAFFRES y M. HACHEMI. "ChemInform Abstract: An Abnormal Reaction of Esters of 3-Hydroxy-3-methylbutan-2-one. A Rapid Synthesis of Bullatenone and Geiparvarin." ChemInform 28, n.º 17 (4 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199717231.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
27

Tsuge, Otohiko, Shuji Kanemasa y Hiroyuki Suga. "An Entry to 5-(1-Alkenyl)-3(2H)-furanones through Cycloaddition of Phosphorus-Functionalized Nitrile Oxide to Acetylene Alcohols. An Effective Synthesis of Geiparvarin". Chemistry Letters 16, n.º 2 (5 de febrero de 1987): 323–26. http://dx.doi.org/10.1246/cl.1987.323.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
28

BARALDI, P. G., A. BIGONI, M. GUARNERI, S. MANFREDINI, G. P. POLLINI y D. SIMINI. "ChemInform Abstract: Application of (3 + 2)Nitrile Oxide Cycloaddition Chemistry to the Construction of Retinoid Skeleton and to a New Formal Synthesis of (.+- .)-Ascofuranone and Geiparvarin." ChemInform 25, n.º 16 (19 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199416157.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
29

Simoni, Daniele, Stefano Manfredini, Mojgan Aghazadeh Tabrizi, Rita Bazzanini, Pier G. Baraldi, Jan Balzarini y Erik De Clercq. "Geiparvarin analogs. 2. Synthesis and cytostatic activity of 5-(4-arylbutadienyl)-3(2H)-furanones and of N-substituted 3-(4-oxo-2-furanyl)-2-buten-2-yl carbamates". Journal of Medicinal Chemistry 34, n.º 11 (noviembre de 1991): 3172–76. http://dx.doi.org/10.1021/jm00115a004.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
30

Aghazade Tabrizi, M., P. G. Baraldi, M. Guarneri, S. Manfredini, G. P. Pollini y D. Simoni. "A [3+2] nitrile oxide intermolecular cycloaddition approach to 4,5-dihydro-3(2H)-furanone and 3(2H)-furanone ring systems: application to the formal synthesis of (±)-ascofuranone and geiparvarin." Tetrahedron Letters 32, n.º 5 (enero de 1991): 683–86. http://dx.doi.org/10.1016/s0040-4039(00)74859-3.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
31

TABRIZI, M. A., P. G. BARALDI, M. GUARNERI, S. MANFREDINI, G. P. POLLINI y D. SIMONI. "ChemInform Abstract: A (3 + 2)Nitrile Oxide Intermolecular Cycloaddition Approach to 4,5- Dihydro-3(2H)-furanone and 3(2H)-Furanone Ring Systems: Application to the Formal Synthesis of (.+-.)-Ascofuranone and Geiparvarin." ChemInform 22, n.º 50 (22 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199150136.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
32

Carotti, Angelo, Antonio Carrieri, Stefano Chimichi, Marco Boccalini, Barbara Cosimelli, Carmela Gnerre, Andrea Carotti, Pierre-Alain Carrupt y Bernard Testa. "Natural and synthetic geiparvarins are strong and selective MAO-B inhibitors. synthesis and SAR studies". Bioorganic & Medicinal Chemistry Letters 12, n.º 24 (diciembre de 2002): 3551–55. http://dx.doi.org/10.1016/s0960-894x(02)00798-9.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
33

VALENTI, P., M. RECANATINI, P. DA RE, W. GALIMBENI, N. AVANZI y S. FILIPPESCHI. "ChemInform Abstract: Xanthone Analogue of Geiparvarin." Chemischer Informationsdienst 17, n.º 11 (18 de marzo de 1986). http://dx.doi.org/10.1002/chin.198611224.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
34

KANG, S. H. y C. Y. HONG. "ChemInform Abstract: Simple Synthetic Routes to Geiparvarin." ChemInform 18, n.º 36 (8 de septiembre de 1987). http://dx.doi.org/10.1002/chin.198736185.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
35

Amato, Claire y Patrick Calas. "A Novel Geiparvarin Analogue Possessing a Fluorinated Segment." ChemInform 35, n.º 16 (20 de abril de 2004). http://dx.doi.org/10.1002/chin.200416185.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
36

Wang, Bin, Shu Chen, Hua Zou, Jia Du, Zhiming Zhang y Ping Huang. "Geiparvarin inhibits the progression of osteosarcoma by down-regulating COX2 expression". Current Cancer Drug Targets 23 (8 de diciembre de 2022). http://dx.doi.org/10.2174/1568009623666221208113432.

Texto completo
Resumen
Background: Geiparvarin (GN) is a natural compound isolated from the leaves of Geijera parviflora and exhibits anticancer activity. Nevertheless, little is known about its anticancer mechanism and anti-osteosarcoma (OS) effects. Aim: This study explored whether GN effectively inhibits the growth and metastasis of osteosarcoma (OS) through a series of in vitro and in vivo experiments. Methods: Cell proliferation was measured by colony formation and MTT assays, and cell invasion was detected by Transwell assay. Flow cytometry and caspase-3 activity assays were carried out to examine cell apoptosis, and western blot analysis was performed to assess protein expression. In the animal experiments, the changes in relevant indexes were determined by immunohistochemistry and tumor vessel imaging. Results: Animal experiments showed that GN treatment significantly inhibited the growth and lung metastasis of OS, accompanied by increased apoptosis. In addition, GN treatment notably diminished COX2 expression and angiogenesis in OS. Moreover, COX2 overexpression nullified GN-induced decline in angiogenesis, growth, and lung metastasis and increased apoptosis in OS. Of note, the body weight of mice was enhanced after GN treatment, and the pathological examination manifested that GN treatment did not cause any damage to major organs. Conclusion: Our data indicated that GN might depress the growth, metastasis, and angiogenesis of OS by decreasing COX2 expression, suggesting GN is a favorable candidate drug for OS treatment without side effects. Hence, it can be concluded that geiparvarin inhibits OS progression by reducing COX2 expression.
Los estilos APA, Harvard, Vancouver, ISO, etc.
37

BARALDI, P. G., A. BARCO, S. BENETTI, A. CASOLARI, S. MANFREDINI, G. P. POLLINI y D. SIMONI. "ChemInform Abstract: Isoxazole-Mediated Synthesis of Geiparvarin and Dihydrogeiparvarin." ChemInform 19, n.º 25 (21 de junio de 1988). http://dx.doi.org/10.1002/chin.198825360.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
38

BARALDI, P. G., M. GUARNERI, S. MANFREDINI, D. SIMONI, J. BALZARINI y E. DE CLERCQ. "ChemInform Abstract: Synthesis and Cytostatic Activity of Geiparvarin Analogues." ChemInform 20, n.º 29 (18 de julio de 1989). http://dx.doi.org/10.1002/chin.198929147.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
39

BARALDI, P. G., A. BARCO, S. BENETTI, M. GUARNERI, S. MANFREDINI, G. P. POLLINI y D. SIMONI. "ChemInform Abstract: A New Nitrile Oxide Based Synthesis of the Antitumor Agent Geiparvarin." Chemischer Informationsdienst 17, n.º 8 (25 de febrero de 1986). http://dx.doi.org/10.1002/chin.198608182.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
40

TSUGE, O., S. KANEMASA y H. SUGA. "ChemInform Abstract: An Entry to 5-(1-Alkenyl)-3(2H)-furanones Through Cycloaddition of Phosphorus-Functionalized Nitrile Oxide to Acetylene Alcohols. An Effective Synthesis of Geiparvarin." ChemInform 18, n.º 42 (20 de octubre de 1987). http://dx.doi.org/10.1002/chin.198742173.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
Ofrecemos descuentos en todos los planes premium para autores cuyas obras están incluidas en selecciones literarias temáticas. ¡Contáctenos para obtener un código promocional único!

Pasar a la bibliografía