Zobrazeno 1 - 10
of 122
pro vyhledávání: '"Edward, Turos"'
Publikováno v:
Frontiers in Pharmacology, Vol 10 (2019)
Nanoparticle-based antibiotic constructs have become a popular area of investigation in the biomedical sciences. Much of this work has pertained to human diseases, largely in the cancer therapy arena. However, considerable research has also been devo
Externí odkaz:
https://doaj.org/article/9ced1d0860284799a1de41aa122d3d11
Autor:
Maryam Alborz, Roya Pournejati, Javad Ameri Rad, Aliasghar Jarrahpour, Hamid Reza Karbalaei‐Heidari, Jean Michel Brunel, Edward Turos
Publikováno v:
ChemistrySelect
ChemistrySelect, 2022, 7 (29), ⟨10.1002/slct.202202306⟩
ChemistrySelect, 2022, 7 (29), ⟨10.1002/slct.202202306⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7de06fa2dbb3271da84eb7b7fc30f540
https://doi.org/10.1002/slct.202202306
https://doi.org/10.1002/slct.202202306
Autor:
Roghayeh Heiran, Ahmad Gholami, Azza Troudi, Carole Digiorgio, Edward Turos, Jean Michel Brunel, Elham Riazimontazer, Aliasghar Jarrahpour
Publikováno v:
ChemistrySelect. 6:5313-5319
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e7642abaf6248e935a39f0707d0308d
https://doi.org/10.1002/slct.202101194
https://doi.org/10.1002/slct.202101194
Publikováno v:
International Journal of Molecular Sciences. 24:8659
Sulfur-containing molecules have a long history of bioactivity, especially as antibacterial agents in the fight against infectious pathogens. Organosulfur compounds from natural products have been used to treat infections throughout history. Many com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f209d589b8c4ae6490a939f66e6105f
https://doi.org/10.3390/ijms24108659
https://doi.org/10.3390/ijms24108659
Autor:
Elahe Haddadi, S. Masoud Nabavizadeh, Edward Turos, Banafsheh Rastegari, Aliasghar Jarrahpour, Mohammad Bashiri, Somaye Karimian
Publikováno v:
Medicinal Chemistry Research. 30:258-284
A [2+2]-cycloaddition of bis-isatin Schiff bases 5a–b and 7 with activated aryloxyacetic acid derivatives 8a–d afforded bis-spiroisatino β-lactams with aliphatic and aromatic spacers. The structures of the synthesized 2-oxindoles and spirooxindo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2f943a4d2ce47cc360b1a0c6b2685a1
https://doi.org/10.1007/s00044-020-02659-5
https://doi.org/10.1007/s00044-020-02659-5
Autor:
Ana-Belén García, Lindsey N. Shaw, Jessie L Allen, Edward Turos, Bridget G. Budny, María-Paz Cabal, Timothy E. Long
Publikováno v:
J Antibiot (Tokyo)
The expanded microbiological evaluation of a series of rifastures, novel spiropiperidyl rifamycin derivatives, against clinically relevant ESKAPE bacteria has identified several analogs with promising in vitro bioactivities against antibiotic-resista
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b7173eb68d8dc5e251faea3d12bcebb
https://doi.org/10.1038/s41429-020-0346-x
https://doi.org/10.1038/s41429-020-0346-x
Autor:
Javad Ameri Rad, Mohammad Ghanbari, Edward Turos, Aida Iraji, Sedigheh Kianpour, S. Masoud Nabavizadeh, Nassim Borazjani, Aliasghar Jarrahpour, Maryam Behzadi, Gyula Batta, Marzieh Dadkhah Aseman
Publikováno v:
Medicinal Chemistry Research. 29:1355-1375
This article reports the diastereoselective synthesis of some novel naphthalimido and bis-naphthalimido β-lactam derivatives and a preliminary evaluation of their anticancer properties. The reactions were completely diastereoselective, leading exclu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b55eadac7b714d2cb2a31f8cad8690e
https://doi.org/10.1007/s00044-020-02552-1
https://doi.org/10.1007/s00044-020-02552-1
Autor:
Aliasghar Jarrahpour, Mohammad Bashiri, Zahra Amirghofran, Banafsheh Rastegari, Saeed Malek-Hosseini, Zahra Zareshahrabadi, Mohammad Motamedifar, Edward Turos, Kamiar Zomorodian, Aida Iraji, Cambyz Irajie, Mahtab Haddadi
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 151:821-835
A novel collection of tripodal β-lactam derivatives with 1,3,5-triazine as the central core is presented for the first time. The diastereoselective synthesis of tris-β-lactams was achieved via a [2 + 2] cycloaddition reaction between s-triazine-bas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a92f9ed7576c02af7a0d2f9ab12bc2a
https://doi.org/10.1007/s00706-020-02592-8
https://doi.org/10.1007/s00706-020-02592-8
Publikováno v:
ChemistrySelect. 4:5950-5953
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88e8f8b45e1e736a95966236a1575b84
https://doi.org/10.1002/slct.201900385
https://doi.org/10.1002/slct.201900385
Autor:
Marzieh Dadkhah Aseman, Roya Pournejati, Hamid Reza Karbalaei-Heidari, Edward Turos, Masoud Nabavizadeh, Aliasghar Jarrahpour, Javad Ameri Rad
Publikováno v:
ChemistrySelect. 4:2741-2746
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c019cb5eec12e9504b520993775d0644
https://doi.org/10.1002/slct.201803785
https://doi.org/10.1002/slct.201803785