B33706

应用筛选条件

关键词:'B33706'

显示 1-12 共 12 条结果关于 "B33706" 范围论文

Complete NMR data of methoxylated cis- and trans-stilbenes as well as 1,2-diphenylethanes.

Geunhyeong Jo et al.

Magnetic resonance in chemistry : MRC, 49(6), 374-377 (2011-04-01)

Resveratrol is a polyphenol isolated from many natural sources including grapes, mulberries, eucalyptus, spruce, lilies, and peanuts. The hydroxyl groups in polyphenols can be substituted with various functional groups, allowing production of multiple derivatives. NMR spectroscopy is used to identify

QSPR modeling of octanol/water partition coefficient for vitamins by optimal descriptors calculated with SMILES.

A A Toropov et al.

European journal of medicinal chemistry, 43(4), 714-740 (2007-07-17)

Simplified molecular input line entry system (SMILES) has been utilized in constructing quantitative structure-property relationships (QSPR) for octanol/water partition coefficient of vitamins and organic compounds of different classes by optimal descriptors. Statistical characteristics of the best model (vitamins) are the

o-Carborane as an electron-transfer mediator in electrocatalytic reduction.

Kohei Hosoi et al.

Chemical communications (Cambridge, England), 47(30), 8632-8634 (2011-07-02)

Electron transfer behavior of 1,2-diphenyl-o-carborane was investigated by cyclic voltammetry (CV). In the presence of 1,2-dibromo-1,2-diphenylethane, a significant catalytic current was observed. The macroscale electrocatalytic reduction of the dibromide using a catalytic amount (1 mol%) of the carborane mediator afforded

Design, synthesis, and biological evaluation of a new series of biphenyl/bibenzyl derivatives functioning as dual inhibitors of acetylcholinesterase and butyrylcholinesterase.

Wang D M, et al.

Molecules (Basel), 22(1), 172-172 (2017)

Some 1,2-diphenylethane derivatives as inhibitors of retinoic acid--metabolising enzymes.

V P Greer et al.

Journal of enzyme inhibition and medicinal chemistry, 18(5), 431-443 (2003-12-25)

In a search for novel inhibitors of RA-metabolising enzyme inhibitors as potential anti-cancer agents some 1,2-ethandiones, 2-hydroxyethanones and 1-ethylenedioxyethanones based on aryl-substituted 1,2-diphenylethane have been examined. Several of the compounds were weak inhibitors of the non-specific rat liver microsomal P450

Design, synthesis and molecular simulation studies of dihydrostilbene derivatives as potent tyrosinase inhibitors.

Argyro Vontzalidou et al.

Bioorganic & medicinal chemistry letters, 22(17), 5523-5526 (2012-07-28)

The synthesis, molecular modeling and biological evaluation of substituted deoxybenzoins and optimized dihydrostilbenes are reported. Preliminary structure-activity relationship data were elucidated and lead compounds suitable for further optimization were discovered. Dihydrostilbene 7 is a particularly potent inhibitor (IC(50)=8.44 μM, more

Potent microbial and tyrosinase inhibitors from stem bark of Bauhinia rufescens (Fabaceae).

Aminu Muhammad et al.

Natural product communications, 8(10), 1435-1437 (2013-12-21)

The stem bark extracts of Bauhinia rufescens Lam. (Fabaceae) yielded 6-methoxy-7-methyl-8-hydroxydibenz[b,f]oxepin, alpha-amyrin acetate, beta-sitosterol 3-O-beta-D-xylopyranoside, 4-(2'-Hydroxyphenethyl)-5-methoxy-2-methylphenol, menisdaurin and sequoyitol. Their structures were determined using spectroscopic methods and comparisons with the literature data. For the antimicrobial assay Gram-positive and Gram-negative bacterial

Tartaric acid-based amphiphilic macromolecules with ether linkages exhibit enhanced repression of oxidized low density lipoprotein uptake.

Dalia S Abdelhamid et al.

Biomaterials, 53, 32-39 (2015-04-22)

Cardiovascular disease initiates with the atherogenic cascade of scavenger receptor- (SR-) mediated oxidized low-density lipoprotein (oxLDL) uptake. Resulting foam cell formation leads to lipid-rich lesions within arteries. We designed amphiphilic macromolecules (AMs) to inhibit these processes by competitively blocking oxLDL

Towards a first-principles model of Fermi resonance in the alkyl CH stretch region: application to 1,2-diphenylethane and 2,2,2-paracyclophane.

Evan G Buchanan et al.

The Journal of chemical physics, 138(6), 064308-064308 (2013-02-22)

The spectroscopy of two flexible hydrocarbons, 1,2-diphenylethane (DPE) and 2,2,2-paracyclophane (TCP) is presented, and a predictive theoretical model for describing the alkyl CH stretch region of these hydrocarbons is developed. Ultraviolet hole-burning spectroscopy identified two isomers of DPE and a

Synthesis, biological evaluation, and docking studies of gigantol analogs as calmodulin inhibitors.

Adelfo Reyes-Ramírez et al.

European journal of medicinal chemistry, 46(7), 2699-2708 (2011-04-26)

Several analogs of gigantol (1) were synthesized to evaluate their effect on the complexes Ca(2+)-calmodulin (CaM) and Ca(2+)-CaM-CaM sensitive phosphodiesterase 1 (PDE1). The compounds belong to four structural groups including, 1,2-diphenylethanes (2-11), diphenylmethanes (13-15), 1,3-diphenylpropenones (16-18), and 1,3-diphenylpropanes (20-22). In

Flame?retardant and mechanical properties of high?density rigid polyurethane foams filled with decabrominated dipheny ethane and expandable graphite.

Ye L, et al.

Journal of Applied Polymer Science, 111(5), 2372-2380 (2009)

9,10-Dihydrophenanthrenes as phytoalexins of Orchidaceae. Biosynthetic studies in vitro and in vivo proving the route from L-phenylalanine to dihydro-m-coumaric acid, dihydrostilbene and dihydrophenanthrenes.

K H Fritzemeier et al.

European journal of biochemistry, 133(3), 545-550 (1983-07-01)

Hydroxy derivatives of 9,10-dihydrophenanthrenes, orchinol and hircinol, were isolated from bulbs of Orchidaceae which had been induced to accumulate phytoalexins. Incorporation of radioactive precursors, L-phenylalanine and various hydroxycinnamic acids, has been investigated by feeding experiments in vivo. m-Coumaric acid and

1/1