Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Hoda Atapour-Mashhad"'
1
Akademický článek
Preparation and characterization of novel nanostructured lipid carriers (NLC) and solid lipid nanoparticles (SLN) containing coenzyme Q10 as potent antioxidants and antityrosinase agents
Autor: Hoda Atapour-Mashhad, Zahra Tayarani-Najaran, Shiva Golmohammadzadeh
Publikováno v: Heliyon, Vol 10, Iss 11, Pp e31429- (2024)
We developed novel and optimal Q10-NLC/SLN formulations as antioxidant and anti-tyrosinase agents. The formulations were analyzed for particle size, morphology, entrapment efficiency (EE %), and long-term stability. The in vitro drug release and in v
Externí odkaz: https://doaj.org/article/024dd35fca054c789a919087ff6f8292
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2
Synthesis and evaluation of cytotoxicity of 6-amino-4-aryl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitriles
Autor: Ali Shiri, Mehdi Bakavoli, Abdolhossien Massoudi, Hoda Atapour-Mashhad, Mohammad Soukhtanloo
Publikováno v: Russian Journal of Bioorganic Chemistry. 42:316-322
Several derivatives of 6-amino-4-aryl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitriles were synthesized via Biginelli type reaction and tested for their anti-proliferative activity on human breast cancer (MCF-7) and human colon carcinoma (HT29)
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c0a4003812d6d2e854c61bcb0ef4346
https://doi.org/10.1134/s1068162016020047
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3
Synthesis and Antiproliferative Evaluation of New Pyrimido[1,6-a]Thieno[2,3-d]Pyrimidine Derivatives
Autor: Ali Shiri, Hoda Atapour-Mashhad, Mohammad Soukhtanloo, Mehdi Bakavoli, Abdolhossien Massoudi, Seyed Mohamadreza Parizadeh
Publikováno v: Journal of Heterocyclic Chemistry. 54:366-374
A facile one-pot synthesis of new pyrimido[1,6-a]thieno[2,3-d]pyrimidin-4-ones , is reported via base-catalyzed reaction of 2-amino-3-cyanothiophenes , with 2,4-dichloro-5-bromo-6-methylpyrimidine . Subsequent treatment of the products with several a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8e2da7edc8e2d859a3ddc9478f0641ea
https://doi.org/10.1002/jhet.2592
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4
Pyrimidooxadiazine and triazolopyrimidooxadiazine derivatives: Synthesis and cytotoxic evaluation in human cancer cell lines
Autor: Mehdi Bakavoli, Ali Shiri, Zahra Tayarani-Najaran, Hoda Atapour-Mashhad, Seyed Hadi Mousavi, Marzieh Akbarzadeh
Publikováno v: Scopus-Elsevier
In vitro antiproliferative activities of some pyrimido[4,5-e][1,3,4]oxadiazine and [1,2,4]triazolo[4',3':1,2]pyrimido[4,5-e][1,3,4]oxadiazine derivatives were examined in human malignant cancer cell lines. All synthesized compounds inhibited the grow
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62b05ee05612697ada67a801a55df007
https://doi.org/10.1134/s1068162015020077
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5
Synthesis of new derivatives of 3-aryl-1,5-dimethyl-1H-[1,2,4]triazolo[4′,3′:1,2]pyrimido[4,5-e][1,3,4]oxadiazines as potential antiproliferative agents
Autor: Zahra Tayarani-Najaran, Mehdi Bakavoli, Ali Shiri, Mohammad Rahimizadeh, Hoda Atapour-Mashhad, Mohsen Nikpour, Marzieh Akbarzadeh, Seyed Hadi Mousavi
Publikováno v: Journal of Heterocyclic Chemistry. 48:183-187
Starting from pyrimido[4,5-e][1,3,4]oxadiazines (3a, 3b, 3c), a synthetic pathway to [1,2,4]triazolo[4′,3′:1,2]pyrimido[4,5-e][1,3,4]oxadiazines (5a, 5b, 5c, 5d, 5e, 5f, 5g, 5h, 5i) is described. The reaction of pyrimido[4,5-e][1,3,4]oxadiazines
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3825bde755900d330e7b2da07320c417
https://doi.org/10.1002/jhet.509
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6
Synthesis and Anticancer Evaluation of New Derivatives of 3-Phenyl-1,5-Dimethyl-1H-[1,2,4]Triazolo[4′,3′:1,2]Pyrimido[4,5-e][1,3,4]Oxadiazine
Autor: Zahra Tayarani-Najaran, Mohammad Rahimizadeh, Seyed Hadi Mousavi, Marzieh Akbarzadeh, Ali Shiri, Mehdi Bakavoli, Hoda Atapour-Mashhad
Publikováno v: Journal of Chemical Research. 34:403-406
The synthesis of new derivatives of 3-phenyl-1,5-dimethyl-1H-[1,2,4]triazolo[4′,3′:1,2]pyrimido[4,5-e][1,3,4]oxadiazines 5a–e and 7a–e is described through heterocyclisation of hydrazino derivative (3) with aromatic aldehydes or carbon disulf
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::94cac386370df26c13958981eaefdf14
https://doi.org/10.3184/030823410x520778
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7
Investigation into the reaction of 2-amino-4,5-dimethylthiophene-3-carboxamide with iso(and isothio)cyanates under microwave irradiation
Autor: Niloofar Tavakoli-Hoseini, Hoda Atapour-Mashhad, Mohammad Rahimizadeh, Abolghasem Davoodnia
Publikováno v: Heteroatom Chemistry. 20:346-349
The reaction of 2-amino-4,5-dimethyl- thiophene-3-carboxamide with iso(and isothio) cyanates for the synthesis of thieno[2,3-d]pyrimidines has been investigated. The reactions under microwave irradiation in the presence of N,N-dimethyl acetamide as s
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9411d0600e3b47b85c3869f9a4df2619
https://doi.org/10.1002/hc.20557
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9
ChemInform Abstract: Investigation into the Reaction of 2-Amino-4,5-dimethylthiophene-3-carboxamide with Iso(and Isothio)cyanates under Microwave Irradiation
Autor: Mohammad Rahimizadeh, Abolghasem Davoodnia, Hoda Atapour-Mashhad, Niloofar Tavakoli-Hoseini
Publikováno v: ChemInform. 41
The reaction of 2-amino-4,5-dimethyl- thiophene-3-carboxamide with iso(and isothio) cyanates for the synthesis of thieno[2,3-d]pyrimidines has been investigated. The reactions under microwave irradiation in the presence of N,N-dimethyl acetamide as s
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f17142acb9035aa1ce46e155c9d822ce
https://doi.org/10.1002/chin.201016152
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