Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Marjan, Azimzadeh Arani"'
Autor:
Mohammad Shafiei, Kamal Alimohammadi, Mohammad Eghtedari, Fatemeh Safari, Marjan Azimzadeh Arani, Alireza Foroumadi, Yaghoub Sarrafi
Publikováno v:
Polycyclic Aromatic Compounds. 42:4359-4373
Quinoline-based structures possess various types of biological activities and recently have attracted attention as an antitumor scaffold via different known anti-cancer mechanisms. In this study, a...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e7e3fba9c9f4a228deaf3d9649ad93c
https://doi.org/10.1080/10406638.2021.1892778
https://doi.org/10.1080/10406638.2021.1892778
Autor:
Seyed Esmail, Sadat-Ebrahimi, Maryam, Mirmohammadi, Zahra, Mojallal Tabatabaei, Marjan, Azimzadeh Arani, Sogol, Jafari-Ashtiani, Mahsa, Hashemian, Parham, Foroumadi, Azadeh, Yahya-Meymandi, Setareh, Moghimi, Mohammad Hassan, Moshafi, Peiman, Norouzi, Susan, Kabudanian Ardestani, Alireza, Foroumadi
Publikováno v:
Iranian Journal of Pharmaceutical Research : IJPR
In this study, a series of novel compounds based on 5-(5-nitrothiophene-2-yl)-1,3,4-thiadiazole possessing (het) aryl thio pendant at C-2 position of thiadiazole ring is developed and evaluated as antileishmanial agents using MTT colorimetric assay.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2251bedbd4624b859efa66ac32e5e076
https://pubmed.ncbi.nlm.nih.gov/32184848
https://pubmed.ncbi.nlm.nih.gov/32184848
Autor:
Abbas Motamedi, Ali Mohebbi, Sarah M. Nasseri, Rainer Herges, Marjan Azimzadeh Arani, Hossein Reza Darabi, Rohoullah Firouzi, Christian Näther
Publikováno v:
Supramolecular Chemistry. 21:632-637
A new Z,Z-stilbenophane was synthesised and characterised. According to an X-ray structure analysis, the structure has a saddle shape, with the π-electrons of the double bonds and the oxygen atoms pointing towards the centre of a cavity. The ligand
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::767a96b6bee2a45ac6d21c72d448e77a
https://doi.org/10.1080/10610270802657650
https://doi.org/10.1080/10610270802657650
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 139:1185-1189
The existence of a short C–H ⋯ π (alkyl–alkyne) interaction in the structure of a strained and relatively rigid tolanophane is expected to hinder the rotation about the C–C sp3 single bond. Variable-temperature NMR experiments (performed in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e01ce4d6b84ae709fb5ba1f5ffecab7
https://doi.org/10.1007/s00706-008-0912-6
https://doi.org/10.1007/s00706-008-0912-6
Publikováno v:
Chemical Monthly / Monatshefte für Chemie; Oct2008, Vol. 139 Issue 10, p1185-1189, 5p