نتایج جستجو برای: vinca minor

تعداد نتایج: 82449  

Journal: :Zeitschrift fur Naturforschung. Teil B, Chemie, Biochemie, Biophysik, Biologie und verwandte Gebiete 1968
I Ognyanov B Pyuskyulev I Kompis T Sticzay G Spiteller M Shamma R J Shine

On direct comparison by TLC and IR we established that the alkaloids A-5 and A-4, first isolated from Vinca herbacea W. K . 1 are identical to the oxindole alkaloid majdine (I), later isolated from Vinca major L. 2' 3 and with its isomer isomajdine (II), prepared by heating of (I) in acetic anhydride 2. Based upon some spectroscopic evidence it was claimed2, that majdine was a diastereomer of c...

Journal: :Plant physiology 2016
Dylan Levac Paulo Cázares Fang Yu Vincenzo De Luca

Members of the Apocynaceae plant family produce a large number of monoterpenoid indole alkaloids (MIAs) with different substitution patterns that are responsible for their various biological activities. A novel N-methyltransferase involved in the vindoline pathway in Catharanthus roseus showing distinct similarity to γ-tocopherol C-methyltransferases was used in a bioinformatic screen of transc...

Journal: :Molecules 2017
Qi Chen Xueyan Lu Xiaorui Guo Qingxi Guo Dewen Li

Catharanthus roseus (C. roseus) and Vinca minor (V. minor) are two common important medical plants belonging to the family Apocynaceae. In this study, we used non-targeted GC-MS and targeted LC-MS metabolomics to dissect the metabolic profile of two plants with comparable phenotypic and metabolic differences. A total of 58 significantly different metabolites were present in different quantities...

Journal: :Clinical journal of oncology nursing 2009
Lisa Hartkopf Smith

The most commonly reported reason for errors is that a syringe containing a vinca alkaloid is mistaken for a syringe containing an intrathecal medication. Very few medications, including chemotherapeutic agents, can be administered safely into the intrathecal space. Most intrathecal chemotherapy errors involve the accidental injection of vincristine; however, all of the vinca alkaloids (vinblas...

Journal: :Cancer research 2001
M Kavallaris A S Tait B J Walsh L He S B Horwitz M D Norris M Haber

Vinca alkaloids are used extensively in the treatment of childhood acute lymphoblastic leukemia (ALL) and despite their usefulness, drug resistance remains a serious clinical problem. Vinca alkaloids bind to the beta-tubulin subunit of the alpha/beta-tubulin heterodimer and inhibit polymerization of microtubules. Recent studies have implicated altered beta-tubulin isotype expression and mutatio...

Journal: :Journal of the neurological sciences 2005
Balázs Gulyás Christer Halldin Adám Vas Richard B Banati Evgeny Shchukin Sjoerd Finnema Jari Tarkainen Károly Tihanyi Géza Szilágyi Lars Farde

Vinpocetine, a synthetic derivative of the Vinca minor alkaloid vincamine, is a widely used drug in neurological practice. We tested the hypothesis that vinpocetine binds to peripheral benzodiazepine binding sites (PBBS) and is therefore a potential ligand of PBBS. Positron emission tomography (PET) measurements in two cynomolgous monkeys showed that pretreatment with vinpocetine markedly reduc...

Journal: :Cancer research 1977
R W Tucker R J Owellen S B Harris

In two hamster cell lines that differed 100-fold in their vinblastine sensitivity, dissolution of the mitotic spindle by vinblastine in living cells correlated with cytotoxicity from vinblastine expressed as suppression of colony formation. The effect on the spindle apparatus occurred in 30 sec or less and thus provides a rapid assay for determining the cytotoxic effects of the Vinca alkaloids,...

Journal: :Cancer letters 1994
P Morata J Jiménez-Mesa I Núñez de Castro F M Sánchez-Jiménez

Naturally occurring vinca alkaloids, vincristine and vinblastine, at micromolar concentrations enhanced the ornithine decarboxylase activity in a dose-response manner in primary cultures of Ehrlich ascites carcinoma cells. After 8 h of culture in the presence or absence of vinblastine, cycloheximide was added to the medium, a 4.5-fold increase in the half-life of the ornithine decarboxylase act...

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