Zobrazeno 1 - 10
of 268
pro vyhledávání: '"V. Gasparotto"'
Publikováno v:
Animal, Vol 12, Iss 2, Pp 434-444 (2018)
Little is known about cheese-making efficiency at the individual cow level, so our objective was to study the effects of herd productivity, individual herd within productivity class and breed of cow within herd by producing, then analyzing, 508 model
Externí odkaz:
https://doaj.org/article/77c4b9bc6bdd485baf29f08f7f6d6e07
Autor:
E. Z. Godinho, H. V. Gasparotto
Publikováno v:
Revista SODEBRAS. 17:49-55
Publikováno v:
Animal, Vol 12, Iss 2, Pp 434-444 (2018)
Little is known about cheese-making efficiency at the individual cow level, so our objective was to study the effects of herd productivity, individual herd within productivity class and breed of cow within herd by producing, then analyzing, 508 model
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0046814fa655767cef1c33bb57c7a12b
http://hdl.handle.net/11577/3266407
http://hdl.handle.net/11577/3266407
Autor:
Piskor, Tomislav1,2 (AUTHOR) tomislav.piskor@quantumsimulations.de, Pinski, Peter1 (AUTHOR), Mast, Thilo1 (AUTHOR), Rybkin, Vladimir1 (AUTHOR) tomislav.piskor@quantumsimulations.de
Publikováno v:
International Journal of Molecular Sciences. Aug2024, Vol. 25 Issue 15, p8530. 12p.
3-Substituted 7-Phenyl-Pyrroloquinolinones Show Potent Cytotoxic Activity in Human Cancer Cell Lines
Publikováno v:
Journal of Medicinal Chemistry. 50:5509-5513
A novel series of 3-alkyl-substituted 7-phenyl-3H-pyrrolo[3,2-f]quinolin-9-ones (7-PPyQs) was synthesized with the aim to optimize the cytotoxic activity of recently identified PPyQs, promising inhibitors of tubulin polymerization. All compounds inhi
Autor:
Gianfranco Chiarelotto, Ignazio Castagliuolo, Giorgio Palu, Lisa Dalla Via, Luisa Barzon, Vincenzo Pezzi, Maria Grazia Ferlin, V. Gasparotto
Publikováno v:
Journal of Medicinal Chemistry. 48:3417-3427
In our search for potential new anticancer drugs, we designed and synthesized a series of tricyclic compounds containing the antimitotic 2-phenylazaflavone chromophore fused to a pyrrole ring in a pyrroloquinoline structure. Compounds 8, 18, 19, 22,
Autor:
Rui, Jiayu1 (AUTHOR) ruijiayu1@163.com, Cheng, Siru1 (AUTHOR), Ren, He1 (AUTHOR), Cui, Sheng1 (AUTHOR), Huang, Jian1 (AUTHOR) jhuang@njtech.edu.cn
Publikováno v:
Polymers (20734360). Jun2024, Vol. 16 Issue 11, p1497. 12p.
Publikováno v:
ChemInform. 39
The newly synthesized 1-[4-(3H-pyrrolo[3,2-f]quinolin-9-ylamino)-phenyl]-ethanone hydrochloride showed high antiproliferative activity by mixed mechanisms of action. The compound acts by forming an intercalative complex with DNA and inhibiting DNA to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60ce2d9a94d2ac6b64f3441c728d6b40
http://hdl.handle.net/11577/2472070
http://hdl.handle.net/11577/2472070
Autor:
Vincenzo Pezzi, Maria Grazia Ferlin, Giampietro Viola, Ignazio Castagliuolo, Paola Brun, Daniela Montanaro, Giorgio Palu, V. Gasparotto, Gianfranco Chiarelotto
Publikováno v:
Journal of medicinal chemistry. 49(6)
The newly synthesized 7-phenyl-3H-pyrrolo[3,2-f]quinolinones 16-26 and previously 27 and 28 were assayed for their in vitro antiproliferative activity on tumor cell lines, and the lead compound 16 in vivo on a singenic hepatocellular carcinoma in Bal