نتایج جستجو برای: colo 205

تعداد نتایج: 12324  

Journal: :Molecules 2013
Pi-Yu Chen Jen-Der Wu Kai-Yih Tang Chieh-Chou Yu Yueh-Hsiung Kuo Wen-Bin Zhong Ching-Kuo Lee

A new enynyl-benzenoid, antrocamphin O (1,4,7-dimethoxy-5-methyl-6-(3'-methylbut-3-en-1-ynyl)benzo[d][1,3]dioxide), and the known benzenoids antrocamphin A and 7-dimethoxy-5-methyl-1,3-benzodioxole, were isolated from the fruiting bodies of Antrodia camphorata (Taiwanofungus camphoratus). The structure of antrocamphin O was unambiguously assigned by the analysis of spectral data (including 1D a...

Journal: :Chemical & pharmaceutical bulletin 2003
Tian-Shung Wu Dau-Min Lin Li-Shian Shi Amooru Gangaiah Damu Ping-Chung Kuo Yao-Hau Kuo

From the stems of Rubia wallichiana DECNE, thirty-four structurally related compounds were isolated and identified. Three of them, namely rubiawallin-A (1), -B (2), and -C (3), constitute the first report of their occurrence from the natural source. Their structures were determined by comprehensive analyses of their 1D and 2D NMR, and electron impact (EI) mass spectral data. Furthermore, an in ...

Journal: :Bioorganic & medicinal chemistry letters 2012
Ravindra M Kumbhare Umesh B Kosurkar M Janaki Ramaiah Tulshiram L Dadmal S N C V L Pushpavalli Manika Pal-Bhadra

A new series of isoxazoles and triazoles linked 2-phenyl benzothiazole were synthesized and evaluated for their anticancer activity. These compounds have been tested for their cytotoxicity three cancer cell lines. Among the compounds tested, compound 5d showed good cytotoxicity against Colo-205 and A549 cells in comparison to standard control PMX 610(1). Further compound 5d has been tested for ...

Journal: :Molecules 2010
Taeyoung Choi Eunsook Ma

A series of racemic indole C5-O-substituted seco-cyclopropylindole (seco-CI) compounds 1-5 were prepared by coupling in the presence of EDCI of 1-(tert-butyloxycarbonyl)-3-(chloromethyl)indoline (seg-A) with 5-hydroxy-, 5-O-methylsulfonyl, 5-O-aminosulfonyl, 5-O-(N,N-dimethylaminosulfonyl)- and 5-O-benzyl-1H-indole-2-carboxylic acid as seg-B. Compounds 1-5 were tested for cytotoxic activity aga...

Journal: :Biomolecules 2021

A series of thiosemicarbazone-coumarin hybrids (HL1-HL3 and H2L4) has been synthesised in 12 steps used for the preparation mono- dinuclear copper(II) complexes, namely Cu(HL1)Cl2 (1), Cu(HL2)Cl2 (2), Cu(HL3)Cl2 (3) Cu2(H2L4)Cl4 (4), isolated hydrated or solvated forms. Both organic their dicopper(II) complexes were comprehensively characterised by analytical spectroscopic techniques, i.e., ele...

Journal: :Biomaterials 2013
Shou-Cheng Wu Kun-Liang Lin Tzu-Pin Wang Shey-Cherng Tzou Gyan Singh Ming-Hung Chen Tian-Lu Cheng Chiao-Yun Chen Gin-Chung Liu Te-Wei Lee Shao-Hwa Hu Yun-Ming Wang

The coupling of specific antibodies to imaging agents often improves imaging specificity. However, free amine groups designed for the coupling can cause nonspecific binding of the imaging agents. We report here development of a nanocarrier, MnMEIO-silane-NH2-mPEG nanoparticles (NPs), consisting of a manganese-doped iron oxide nanoparticle core (MnMEIO), a copolymer shell of silane and amine-fun...

Journal: :Journal of leukocyte biology 1999
A D Watts N H Hunt M C Madigan G Chaudhri

Tumor necrosis factor alpha (TNF-alpha) is initially synthesized as a type II integral membrane protein (transmembrane TNF-alpha) after macrophage activation. In this study we have investigated some aspects of the regulation of expression and biological activity of transmembrane TNF-alpha by both soluble TNF-alpha receptors (sTNF-alphaR) and inhibitors of TNF-alpha processing. We show, using th...

Journal: :Molecular cancer therapeutics 2007
Barry R Davies Armelle Logie Jennifer S McKay Paul Martin Samantha Steele Richard Jenkins Mark Cockerill Sue Cartlidge Paul D Smith

Constitutive activation of the extracellular signal-regulated kinase 1/2 (ERK1/2) mitogen-activated protein kinase (MAPK) signaling pathway in human cancers is often associated with mutational activation of BRAF or RAS. MAPK/ERK kinase 1/2 kinases lie downstream of RAS and BRAF and are the only acknowledged activators of ERK1/2, making them attractive targets for therapeutic intervention. AZD62...

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