Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Dalia M. Ahmed"'
Autor:
Dina A. Refaay, Mohammed I. Abdel-Hamid, Amal A. Alyamani, Mamdouh Abdel Mougib, Dalia M. Ahmed, Amr Negm, Amr M. Mowafy, Amira A. Ibrahim, Rania M. Mahmoud
Publikováno v:
Plants, Vol 11, Iss 6, p 735 (2022)
Cyanobacteria comprise a good natural resource of a potential variety of neuro-chemicals, including acetylcholinesterase inhibitors essential for Alzheimer’s disease treatment. Accordingly, eight different cyanobacterial species were isolated, iden
Externí odkaz:
https://doaj.org/article/7b709724647f41d18dc1a0f224049769
Publikováno v:
Pharmaceuticals, Vol 15, Iss 2, p 197 (2022)
UDP-galactopyranose mutase (UGM) is an essential enzyme involved in the bacterial cell wall synthesis, and is not present in mammalian cells. Thus, UGM from Mycobacterium tuberculosis (Mtb) represents a novel and attractive drug target for developing
Externí odkaz:
https://doaj.org/article/ed15a3e25e424bc09d3063742b997473
Publikováno v:
Medicinal Chemistry Research. 31:894-904
Publikováno v:
Clinical Reviews & Cases. 4
Leishmania, a protozoan parasite, is the causative agent of leishmaniosis. It lives and multiplies within the harsh environment of macrophages. Infection of macrophages by the intracellular protozoan Leishman leads to downregulation of a number of ma
Publikováno v:
Mini-Reviews in Medicinal Chemistry. 21:118-131
Background: Thiazolopyrimidine analogues are versatile synthetic scaffold possessing wide spectrum of biological interests involving potential anticancer activity. Objective: To report the synthesis of novel bromothiazolopyrimidine derivatives and th
Publikováno v:
Clinical Reviews & Cases. 3
Introduction: In Sudan Hepatitis B virus, (HBV) infection is the most common cause of acute and chronic hepatitis, cirrhosis, and hepatocellular carcinoma (HCC) worldwide, interferon γ INF γ is significantly associated with chronic hepatitis B viru
Publikováno v:
European journal of medicinal chemistry. 122
Novel tetrazole-based diselenides and selenoquinones were synthesized via azido-Ugi and sequential nucleophilic substitution (SN) strategy. Molecular docking study into mammalian TrxR1 was used to predict the anticancer potential of the newly synthes
Publikováno v:
Open Chemistry, Vol 8, Iss 4, Pp 919-927 (2010)
The interaction of [Pd(DAP)(H2O)2]2+ (DAP = 1,3-diaminopropane) with some selected bio-relevant ligands, containing different functional groups, were investigated. The ligands used are dicarboxylic acids, amino acids, peptides and DNA constituents. S
Publikováno v:
Ain-Shams Journal of Anaesthesiology. 8:402
Background Local anesthetic adjuvants have been studied previously to prolong the duration of analgesia after peripheral nerve block and thus reduce postoperative adverse reactions associated with excessive systemic analgesic intake. The aim of this