Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Mohsen M Kamel"'
Publikováno v:
Journal of Heterocyclic Chemistry. 57:69-80
Autor:
Mohsen M. Kamel, Rasha S. Gouhar
Publikováno v:
Journal of Heterocyclic Chemistry. 55:2082-2089
Autor:
Magdalena Milczarek, Ahmad F. Eweas, Joanna Wietrzyk, Abdel-mohsen M. Soliman, Mohsen M. Kamel
Publikováno v:
Egyptian Journal of Chemistry. 61:330-340
Some new and known substituted 1,2,3,4-tetrahydroacridines incorporated at their position nine with various sulfa drug or thiosemicarbazide moieties were synthesized. Biologically, these compounds were investigated for their antiproliferative activit
Publikováno v:
American journal of perinatology. 37(5)
Objective This study aimed to evaluate soluble cluster of differentiation 14 subtype (sCD14-ST), also named presepsin, as an early marker for the diagnosis of culture-proven early-onset sepsis (EOS) in neonates and to assess its relation to disease s
Autor:
Rasha S. Gouhar, Mohsen M. Kamel, Wael S. I. Abou-Elmagd, Dina H. El-Ghonamy, Magdy I. El-Zahar
Publikováno v:
Research on Chemical Intermediates. 43:1301-1327
Because of the well-known chemotherapeutic activity of pyrimidoquinolines, a new series of the title compounds were synthesized and biologically screened for their antimicrobial and anti-oxidant activities. The intermediate compound, 2-amino-1-cycloh
Publikováno v:
QJM: An International Journal of Medicine. 111
Publikováno v:
Acta poloniae pharmaceutica. 74(1)
A number of 2,3-disubstituted-1-cyclohexyl 4-(3,4-dimethoxyphenyl-1,4,5,6,7,8)-hexahydroquinolines and 5-(3,4-dimethoxyphenyl-10-cyclohexyl-3,4,5,6,7,8,9,10-octahydro)-3H-pyrimido[4,5-b]quinolines were synthesized and evaluated for antimicrobial acti
Autor:
Manal M. Anwar, Yasmin M. Syam, Samia A. Elseginy, Mohsen M Kamel, Somaia S. Abd El-Karim, Tamer Nasr, Hanan F. Ali
Publikováno v:
Mini reviews in medicinal chemistry. 19(3)
Objective: Inhibition of dipeptidyl peptidase IV (DPP-4) is currently one of the most valuable and potential chemotherapeutic regimes for the medication of Type 2 Diabetes Mellitus (T2DM). Method: Based on linagliptin, this study discusses the design
Publikováno v:
Research on Chemical Intermediates. 39:3417-3426
Praziquantel, 2-(cyclohexylcarbonyl)-1,2,3,6,7,11b-hexahydro-4H-pyrazino[2,1-a]isoquinolin-4-one, was used as the parent starting material to synthesize a new series of praziquantel-3-arylidene derivatives 1a–c and praziquantel–Mannich bases 2a
Publikováno v:
European Journal of Medicinal Chemistry. 45:2117-2131
Three series of Spiro [(2H,3H) quinazoline-2,1′-cyclohexan]-4(1H)-one derivatives have been synthesized. Some of the novel quinazolinone derivatives IIe, VIIIc, XIc, XIIb, XIIc, XVIb showed considerable potent anti-inflammatory and analgesic activi