نتایج جستجو برای: vincamine

تعداد نتایج: 46  

2016
Yun-Yun Ma Lin Sun Xiu-Juan Chen Na Wang Peng-Fei Yi Min Song Bo Zhang Yu-Zhong Wang Qiu-Hua Liang

Vascular calcification is an active process of osteoblastic differentiation of vascular smooth muscle cells; however, its definite mechanism remains unknown. Vinpocetine, a derivative of the alkaloid vincamine, has been demonstrated to inhibit the high glucose-induced proliferation of vascular smooth muscle cells; however, it remains unknown whether vinpocetine can affect the osteoblastic diffe...

Journal: :Pharmaceutical biology 2011
Berrin Ozçelik Murat Kartal Ilkay Orhan

OBJECTIVE Some natural products consisting of the alkaloids yohimbine and vincamine (indole-type), scopolamine and atropine (tropane-type), colchicine (tropolone-type), allantoin (imidazolidine-type), trigonelline (pyridine-type) as well as octopamine, synephrine, and capsaicin (exocyclic amine-type); the flavonoid derivatives quercetin, apigenin, genistein, naringin, silymarin, and silibinin; ...

Journal: :CNS neuroscience & therapeutics 2009
Csaba Nyakas Klára Felszeghy Róbert Szabó Jan N Keijser Paul G M Luiten Zsolt Szombathelyi Károly Tihanyi

Vinpocetine (ethyl-apovincaminate, Cavinton), a synthetic derivative of the Vinca minor alkaloid vincamine, has been used now for decades for prevention and treatment of cerebrovascular diseases predisposing to development of dementia. Both vinpocetine and its main metabolite cis-apovincaminic acid (cAVA) exert a neuroprotective type of action. Bilateral N-methyl-D-aspartate (NMDA)-induced neur...

2015
Vamshi K. Manda Bharathi Avula Olivia R. Dale Amar G. Chittiboyina Ikhlas A. Khan Larry A. Walker Shabana I. Khan

Background: Vinpocetine, a semi-synthetic derivative of vincamine, is a popular dietary supplement used for the treatment of several central nervous system related disorders. Despite its wide use, no pharmacokinetic drug interaction studies are reported in the literature. Due to increasing use of dietary supplements in combination with conventional drugs, the risk of adverse effects is on the r...

Journal: :Molecular pharmacology 1997
J Jakubík L Bacáková E E El-Fakahany S Tucek

It is well known that allosteric modulators of muscarinic acetylcholine receptors can both diminish and increase the affinity of receptors for their antagonists. We investigated whether the allosteric modulators can also increase the affinity of receptors for their agonists. Twelve agonists and five allosteric modulators were tested in experiments on membranes of CHO cells that had been stably ...

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