نتایج جستجو برای: acridone
تعداد نتایج: 167 فیلتر نتایج به سال:
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection that causes COVID-19 disease is still a major public health concern around the world. main protease encoded by SARS-CoV-2 promising target for therapeutic development since it plays crucial role in virus’s life cycle. Repurposing known bioactive molecules an effective strategy to fast-track delivery of hits and leads dru...
BACKGROUND Tuberculosis (TB) is still a global health problem mainly due to development of resistance and co-infection with the Human immune Virus (HIV). Treatment of multi and extensively drug resistant TB requires use of second line drugs which are less efficacious, expensive and very toxic. This has necessitated a need to search for new treatment regimens especially from medicinal plants. Za...
A new quinolone alkaloid, megistolactone (1) was isolated from the bark of Sarcomelicope megistophylla. Its structure has been elucidated on the basis of MS and NMR data. From a biogenetic point of view, this compound should be considered as an oxidation product of 1,2,3,4-tetra-O-subsituted acridone alkaloids, which are also present in the bark.
The structures of two new dimeric acridone alkaloids, glycobismine-D (1) and -E (2), having a novel linkage as binary acridones, three monomeric acridones, glycocitrine-IV (3), -V (4), and -VI (5), and three quinolone alkaloids, glycocitlone-A (6), -B (7), and -C (8) from Glycosmis citrifolia (Willd.) Lindl. (Rutaceae) have been elucidated by spectrometric studies.
Several acridone alkaloids have been isolated from roots of Ruta graveolens (for summary see [1, 2]). One of the main alkaloids is rutacridone (1) which seems to be a precursor of several derivatives with hydroxyl or chlorine functions at the isopropyl moiety. As an intermediate an 18,19-epoxide of rutacridone could be postulated [1, 3] that has not yet been identified. Screening for antimicrob...
BACKGROUND In the present study, a series of N-substituted acridone derivatives was synthesized and evaluated against two haemorrhagic fever viruses (HFV). METHODS Compounds were tested against Junin virus (JUNV), an arenavirus agent of Argentine haemorrhagic fever, and dengue virus (DENV), a flavivirus agent of the most prevalent arthropod-borne viral disease in humans. RESULTS Among teste...
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