Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Nadia T. Al-Qurashi"'
Autor:
Thoraya A. Farghaly, Sami A. Al-Hussain, Magdi E. A. Zaki, Nadia T. Al-Qurashi, Salwa S. Alharbi, Zeinab A. Muhammad
Publikováno v:
Polycyclic Aromatic Compounds. :1-96
Autor:
Thoraya A. Farghaly, Ikhlass M. Abbas, Walid Hassan, Nadia T. Al-Qurashi, M. S. Lotfy, T. Ben Hadda
Publikováno v:
Russian Journal of Organic Chemistry. 56:1258-1271
The 1,3-dipolar cycloaddition of nitrile imines to 11-aryl-4-(arylmethylidene)-1,2,3,4,11,11a-hexahydrodibenzo[b,e][1,4]thiazepines possessing exocyclic C=C and endocyclic C=N bonds as dipolarophilic sites showed site selectivity, depending on the ty
Publikováno v:
Journal of Heterocyclic Chemistry. 57:611-620
Autor:
Abrar Bayazeed, Noof A. Alenazi, Amani M.R. Alsaedi, Mona H. Ibrahim, Nadia T. Al-Qurashi, Thoraya A. Farghaly
Publikováno v:
Journal of Molecular Structure. 1258:132653
Autor:
Thoraya A. Farghaly, Nadia T. Al-Qurashi, Sami A. Al-Hussain, Hanan Gaber Abdulwahab, Zeinab A. Muhammad, Magdi E. A. Zaki
Publikováno v:
Bioorganic chemistry. 105
Targeting VEGFR-2 signaling pathway is well-established as an important approach for the treatment of solid tumors, particularly renal cancer. Herein, novel indolyl-1,2,4-triazole hybrids were designed and synthesized as VEGFR-2 kinase inhibitors wit
Autor:
Huda K. Mahmoud, Hanan Gaber Abdulwahab, Nadia T. Al-Qurashi, Mohamed R. Shaaban, Thoraya A. Farghaly
Publikováno v:
European journal of medicinal chemistry. 208
Novel 2-indolinone thiazole hybrids were designed and synthesized as VEGFR-2 inhibitors based on sunitinib, an FDA-approved anticancer drug. The proposed structures of the prepared 2-indolinone thiazole hybrids were confirmed based on their spectral
Autor:
Amr S. Abouzied, Ismail Althagafi, Thoraya A. Farghaly, Mohammad Y. Alfaifi, Nadia T. Al-Qurashi, Mohamed R. Shaaban, Mohamed R. Abdel Aziz
Publikováno v:
Journal of Heterocyclic Chemistry. 56:391-399
Autor:
Huda K. Mahmoud, Thoraya A. Farghaly, Mohamed R. Shaaban, Mohamed M. Amin, Nadia T. Al-Qurashi
Publikováno v:
Mini-Reviews in Medicinal Chemistry. 18:1409-1421
Background Microwave assisted reactions offer a considerable advantages over conventional method reactions because the former results in substantial rate enhancement in a wide range of organic reactions. Objective we interested herein to prepare new
Publikováno v:
Journal of Heterocyclic Chemistry. 55:750-755
Publikováno v:
Journal of Molecular Structure. 1244:131263
In short reaction time with excellent yield, we designed and synthesized a series of indole linked azole ring at position-2 as thiazole and pyrazole moieties under microwaves irradiation. The structures and mechanistic pathways were discussed in this