Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Cintia Duró"'
Autor:
Cintia Duró, Tamás Jernei, Krisztina J. Szekeres, Győző G. Láng, Rita Oláh-Szabó, Szilvia Bősze, Ildikó Szabó, Ferenc Hudecz, Antal Csámpai
Publikováno v:
Molecules, Vol 27, Iss 19, p 6758 (2022)
Utilizing McMurry reactions of 4,4′-dihydroxybenzophenone with appropriate carbonyl compounds, a series of 4-Hydroxytamoxifen analogues were synthesized. Their cytotoxic activity was evaluated in vitro on four human malignant cell lines (MCF-7, MDA
Externí odkaz:
https://doaj.org/article/49a4e742db584e8c8b6af2cd7a625652
Autor:
Márton Kalabay, Zsófia Szász, Orsolya Láng, Eszter Lajkó, Éva Pállinger, Cintia Duró, Tamás Jernei, Antal Csámpai, Angéla Takács, László Kőhidai
Publikováno v:
Pharmaceuticals, Vol 15, Iss 3, p 314 (2022)
Tamoxifen is a long-known anti-tumor drug, which is the gold standard therapy in estrogen receptor (ER) positive breast cancer patients. According to previous studies, the conjugation of the original tamoxifen molecule with different functional group
Externí odkaz:
https://doaj.org/article/d056e206006744b4a549989a7e47e9a0
Autor:
Tamás Jernei, Cintia Duró, Antonio Dembo, Eszter Lajkó, Angéla Takács, László Kőhidai, Gitta Schlosser, Antal Csámpai
Publikováno v:
Molecules, Vol 24, Iss 22, p 4077 (2019)
By means of copper(I)-and ruthenium(II)-catalyzed click reactions of quinine- and quinidine-derived alkynes with azide-substituted chalcones a systematic series of novel cinchona-chalcone hybrid compounds, containing 1,4-disubstituted- and 1,5-disubs
Externí odkaz:
https://doaj.org/article/b30599c6f0bf4b2293c3a81e6232cfa6
Autor:
József Murányi, Cintia Duró, Bianka Gurbi, István Móra, Attila Varga, Krisztina Németh, József Simon, Miklós Csala, Antal Csámpai
Publikováno v:
International Journal of Molecular Sciences
Volume 24
Issue 4
Pages: 3456
Volume 24
Issue 4
Pages: 3456
In a search for novel therapeutic options for head and neck squamous cell carcinomas (HNSCCs) generally treated with limited therapeutic success, we synthesized a series of novel erlotinib–chalcone molecular hybrids with 1,2,3-triazole and alkyne l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cdbf6b8289ac544e81c863c1a3542ae
Autor:
László Kőhidai, Cintia Duró, Gitta Schlosser, Angéla Takács, Antonio Dembo, Eszter Lajkó, Tamás Jernei, Antal Csámpai
Publikováno v:
Molecules
Volume 24
Issue 22
Molecules, Vol 24, Iss 22, p 4077 (2019)
Volume 24
Issue 22
Molecules, Vol 24, Iss 22, p 4077 (2019)
By means of copper(I)-and ruthenium(II)-catalyzed click reactions of quinine- and quinidine-derived alkynes with azide-substituted chalcones a systematic series of novel cinchona-chalcone hybrid compounds, containing 1,4-disubstituted- and 1,5-disubs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80280169f47ea7f0d36151fabd902853
https://pubmed.ncbi.nlm.nih.gov/31718009
https://pubmed.ncbi.nlm.nih.gov/31718009