نتایج جستجو برای: chromane

تعداد نتایج: 58  

2008
C. INAGAKI

An alkaline saponification method containing pyrogallol is usually applied for the determination of tocopherols. Although there are some metabolites of ƒ¿-tocopherol in tissues, it is not yet clear whether they are true metabolites or degradation products from the alkaline saponi fication. Since it was shown that ƒ¿-tocopheryl spirodimer, a metabolite of ƒ¿-tocopherol, was degraded mainly to a ...

Journal: :Fitoterapia 2010
Patel Mohanakumara Nambiar Sreejayan Vaidayanathan Priti Bheemanahally Thimmappa Ramesha Gudasalamani Ravikanth Kotiganahalli Narayanagowda Ganeshaiah Ramesh Vasudeva John Mohan Thankayyan Retnabai Santhoshkumar Prabhu Dutt Mishra Viswakarma Ram Ramanan Uma Shaanker

Rohitukine, a chromane alkaloid, is a precursor of flavopiridol, a promising anti-cancer compound. Currently in Phase III clinical trials, flavopiridol is a potent inhibitor of several cyclin-dependent kinases (CDKs). Rohitukine was first reported from Amoora rohituka (0.083% dry weight) followed by that in Dysoxylum binectariferum (0.9% dry weight), both belonging to the family Meliaceae. Here...

Journal: :Molecules 2018
Jarosław Popłoński Eliza Turlej Sandra Sordon Tomasz Tronina Agnieszka Bartmańska Joanna Wietrzyk Ewa Huszcza

Synthesis of minor prenylflavonoids found in hops and their non-natural derivatives were performed. The antiproliferative activity of the obtained compounds against some human cancer cell lines was investigated. Using xanthohumol isolated from spent hops as a lead compound, a series of minor hop prenylflavonoids and synthetic derivatives were obtained by isomerization, cyclisation, oxidative-cy...

Journal: :iranian journal of chemistry and chemical engineering (ijcce) 2010
babak heidary alizadeh mohsen vosooghi mehdi khoobi azita javidnia fatemeh panah,

chromanone derivatives demonstrate remarkable cytotoxity against a varieties of cancer cell lines. novel 9-[hydroxy(substitutedphenyl)methyl]-2,2-dimethyl-2,3,8,9- tetrahydro-4h,10h-pyrano[2,3-f]chromene-4,10-diones as glyasperin analogues were synthesized in four steps from known 4-chromone 1. the key step was the preparation of chromane dione 5a by regioselective intramolecular cyclization re...

Journal: :Acta Crystallographica Section E Structure Reports Online 2011

2015
Roumaissa Belguedj Sofiane Bouacida Hocine Merazig Aissa Chibani Abdelmalek Bouraiou

In the title mol-ecule, C15H12O3, the C atoms bearing the hy-droxy group and the phenyl ring are disordered over two sets of sites with refined occupancies of 0.573 (7) and 0.427 (7). There is also disorder of the phenyl ring but the hy-droxy group was refined as ordered. The dihedral angles between the benzene ring of the chromane ring system and the phenyl ring are 89.7 (2)° for the major com...

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