ライフサイエンスコーパス: stilbene

1 es, 2 dihydrochalcones, 4 flavan-3-ols and 2 stilbenes).

2 estigation of health-related effects of this stilbene.

3 ene, whereas C(3)G3 and C(2)G3 gave only cis-stilbene.

4 absorption spectrum blue-shifted from trans-stilbene.

5 functionalization of all eight corners with stilbene.

6 hen samples are expected to contain only one stilbene.

7 ion lifetimes compared to solutions of trans-stilbene.

8 f the second C-N bond accounts for the trans-stilbene.

9 red elimination of NO and formation of trans-stilbene.

10 e, and a cationic donor-acceptor substituted stilbene.

11 n converted to a new analogue of the natural stilbene.

12 iginal NHC-stabilized 1-silaketene 4 and cis-stilbene.

13 ons, 7 phenolic acids, 6 flavan-3-ols, and 1 stilbene.

14 ew route to the stereoselective synthesis of stilbenes.

15 en developed in order to form functionalized stilbenes.

16 tributed to exciton coupling between the two stilbenes.

17 he dihedral angle between donor and acceptor stilbenes.

18 ariation in genotypes that do not accumulate stilbenes.

19 flavonols, flavan-3-ols, phenolic acids, and stilbenes.

20 at are formed from the end-to-end linking of stilbenes.

21 m ions are reported from sterically hindered stilbene 1,1'-bi(benzocyclobutenylidene) 1, its dimethox

22 Reactions of hindered stilbenes 1 and 5 with Br 2/CDCl 3 were examined via NMR

23 llustrate our method by showing that E stiff stilbene (1,1'-Delta-biindan) with up to 700 pN of force

24 (E)-4,4'-Bis[bis(4-methoxyphenyl)amino]stilbene, 1, (E,E)-1,4-bis[4-[bis(4-methoxyphenyl)amino]

25 on OH- gradient-driven 4,4'-diisothiocyanato-stilbene-2, 2'-disulfonic acid-sensitive 36Cl- uptake ut

26 and Ca(2+)-dependent, 4,4'-diisothiocyanato-stilbene-2,2'-disulfonic acid (DIDS)-sensitive and gluco

27 l cells; and (iii) the 4,4'-diisothiocyanato-stilbene-2,2'-disulfonic acid (DIDS)-sensitive and Na(+)

28 benclamide, but not by 4,4'-diisothiocyanato-stilbene-2,2'-disulfonic acid (DIDS).

29 ility of 4-acetamido-4'-((iodoacetyl) amino) stilbene-2,2'-disulfonic acid, disodium salt (IASD), to

30 that NCBE mediates the 4,4'-diisothiocyanato-stilbene-2,2'-disulfonic acid-sensitive, Na(+)-dependent

31 le is the 1:1 charge-transfer complex trans--stilbene-2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodime

32 4,4'-bis[4-[bis(4-methoxyphenyl)amino]styryl]stilbene, 3, and (E,E,E,E)-1,4-bis(4-[4-[bis(4-methoxyph

33 in, 3-deoxyschweinfurthin B-like p-nitro-bis-stilbene (3dSB-PNBS), which displays biological activity

34 in the acute infection mouse model, just one stilbene (6-fold) and two pyridine-containing acetylene

35 whether resveratrol (3,5,4'-trihydroxy-trans-stilbene), a phytoalexin found in red grapes and blueber

36 It is noteworthy that trans-stilbene, a close structural analog of DES that lacks hy

37 We investigated stilbenes, a group of phenolic compounds found in Norway

38 tion rate between stilbene donor (Sd(+)) and stilbene acceptor (Sa(-)) linkers separated by AT bridge

39 d analysis of the formation and decay of the stilbene acceptor singlet state and of the charge-separa

40 istinguished the behavior of genotypes, with stilbene accumulation as the major metabolic event, alth

41 This stilbene also potentiated the apoptotic effects of borte

42 ic zinc carboxylate vertices joined by trans-stilbene, analogous to the isoreticular MOF (IRMOF) seri

43 Piceatannol, a stilbene analogue to resveratrol with higher antioxidant

44 hesis of a series of 30 monohydroxylated (E)-stilbene analogues is described.

45 We find that isomerization of these stilbene analogues is little effected by the presence of

46 ficient synthesis of hydroxyl-functionalized stilbene and 2-arylbenzo[b]furan derivatives and report

47 d in vitro and in vivo: 3,4'-dihydroxy-trans-stilbene and 3,4'-dihydroxybibenzyl (lunularin).

48 harge-transfer excited complex of an anionic stilbene and a cationic, parallel pi-stacked tryptophan.

49 quinones, a furanochromone, an isoflavone, a stilbene and an iridoid).

50 were found to afford higher solubilities of stilbene and azobenzene.

51 re probed through geometric isomerization of stilbene and azobenzene.

52 (50) = 11.5 muM), or an equimolar mixture of stilbene and chalcone (IC(50) = 32.5 muM) were less pote

53 Of the 92 stilbene and dihydrostilbene analogues synthesized, near

54 on oxidation of E-4,4'-bis[di(p-anisyl)amino]stilbene and E,E-2,5-bis{4-[di(p-anisyl)amino]styryl}-3,

55 g the rate-limiting enzymes in Norway spruce stilbene and flavonoid biosynthesis were actively transc

56 roof of concept we determined gamma of trans-stilbene and found it to be in excellent agreement with

57 rile are k = 6.1 x 10(5) M(-1) s(-1) for cis-stilbene and k = 1.4 x 10(5) M(-1) s(-1) for diphenylmet

58 were tentatively characterised and included stilbenes and ellagitannins as major components, followe

59 cs revealed that E. polonica transforms both stilbenes and flavonoids to muconoid-type ring-cleavage

60 presence of anthocyanins, condensed tannins, stilbenes and phenolic acids, well known for their biolo

61 the Scots pine heartwood extractives (mainly stilbenes and resin acids) are synthesized in the cells

62 henolic acids, flavan-3-ols, flavonols and a stilbene) and anthocyanins.

63 dynamics experiments on trans-stilbene, cis-stilbene, and azobenzene, with excitation to high-lying

64 ]tolane, E-4,4'-bis[di(4-methoxyphenyl)amino]stilbene, and E,E-1,4-bis{4-[di(4-methoxyphenyl)amino]st

65 is no emission similar to that of free trans-stilbene, and the state decays nonradiatively to the gro

66 ids and apocarotenoids, including retinoids, stilbenes, and related compounds.

67 he (Z)- or (E)-isomers of azobenzene (AB) or stilbene are used.

68 Stilbenes are a family of bioactive compounds found in p

69 Stilbenes are a small family of phenylpropanoids produce

70 Stilbenes are also derived from lignin during kraft pulp

71 Stilbenes are diphenyl ethene compounds produced natural

72 Plant stilbenes are phytoalexins that accumulate in a small nu

73 However, only a few stilbenes are present in the human diet.

74 Flavonoids and stilbenes are secondary metabolites produced in plants t

75 at, of the Scots pine heartwood extractives, stilbenes are synthesized in situ in the transition zone

76 d should be applicable to many other natural stilbenes as well.

77 the fruit exhibits flavonoid derivatives and stilbenes, as trans-piceatannol and resveratrol, as main

78 improving the biosynthesis of resveratrol, a stilbene associated a range of health-promoting activiti

79 TSs), which catalyze the biosynthesis of the stilbene backbone, seem to have evolved from chalcone sy

80 e the development of a family of fluorogenic stilbene-based vinyl amides and vinyl sulfonamides that

81 eted MR contrast agent, Gd-DODAS, based on a stilbene binding moiety and demonstrate its ability to s

82 form of cross talk between the activation of stilbene biosynthesis and the accumulation of anthocyani

83 d MYB15 in the transcriptional regulation of stilbene biosynthesis in grapevine.

84 s, the transcriptional regulation underlying stilbene biosynthesis is unknown.

85 During C. polonica infection, stilbene biosynthesis was up-regulated, as evidenced by

86 ors (TFs) from grapevine, which regulate the stilbene biosynthetic pathway.

87 of the controlled encapsulation state of the stilbene by correlation of fluorescence and (1)H NMR dat

88 acetonitrile and oxidation reactions of cis-stilbene by the two oxo derivatives, and apparent dispro

89 on on the reactivity of anodically generated stilbene cation radicals.

90 nfection model and provide new insights into stilbene cellular detoxification.

91 a synthetic route to derivatives of styrene, stilbene, chalcone, cinnamic acid, various fused carbo-

92 Novel stilbene-chalcone (S-C) hybrids were synthesized via a s

93 t peptide amphiphile containing its branched stilbene chromophore covalently linked to the hydrophili

94 Exciton coupling between the stilbene chromophores has little effect on the absorptio

95 e to the number of base pairs separating the stilbene chromophores, as a consequence of the distance

96 and structural dynamics experiments on trans-stilbene, cis-stilbene, and azobenzene, with excitation

97 Therefore, almonds contain the stilbene class of polyphenols in addition to the previou

98 Stilbene cleavage oxygenases (SCOs) cleave the central d

99 Cis-stilbene combretastatin A-4 (CA-4) and a large group of

100 Piceatannol, a promising health-promoting stilbene component, was the major PC in the fruit with a

101 Recently a new derivative of stilbene compound, isorhapontigenin (ISO), was isolated

102 onents being 3,5-dihydroxy-4-isopropyl-trans-stilbene (compound 1) and its stilbene epoxide (compound

103 rs fast irreversible protonation under these stilbene concentration conditions.

104 t was used to obtain significantly increased stilbene concentration in grapes.

105 To evaluate stilbene concentration, an HPLC-DAD method was validated

106 Tempranillo increased up 200% the total stilbene concentration, Grenache 60% and Graciano 50%.

107 However, stilbene concentrations actually declined during infecti

108 of recent experimental results on control of stilbene conformation and fluorescence in capsules.

109 and the level of sulphur dioxide applied on stilbene content and antioxidant activity have been stud

110 The stilbene content of the must significantly increased wit

111 ffect of pulsed electric fields (PEF) on the stilbene content of three grape varieties.

112 on of the yeast elicitor also enhanced grape stilbene content.

113 hmark materials such as solution-grown trans-stilbene crystals.

114 The stilbene derivative (Z)-2-(2-bromophenyl)-3-{[4-(1-methy

115 Our studies with a stilbene derivative called TMS (2,3',4,5'-tetramethoxyst

116 we have systematically evaluated a series of stilbene derivatives as myelin imaging agents.

117 a2-Co(NO2)P2W17O61}(8-) as oxidant and trans-stilbene derivatives as substrates point toward a reacti

118 These studies suggested that these stilbene derivatives can be used as myelin-imaging probe

119 Compounds 3e and 4e are fluorinated stilbene derivatives displaying high binding affinities

120 igand-based binding assays showed that these stilbene derivatives exhibited relatively high myelin-bi

121 S showed a variety of phenolic compounds and stilbene derivatives in different parts of germinated pe

122 Several of the cis-stilbene derivatives were significantly inhibitory again

123 ults strongly suggest that these fluorinated stilbene derivatives, [18F]3e and [18F]4e, are suitable

124 The XFs, stilbene derivatives, are different from other reported,

125 HU-DNA interface that can be targeted using stilbene derivatives.

126 insect infection model, we also observed two stilbene-derived metabolites that were dependent on the

127 The diversification of access to cis-stilbene diamine-derived imidazolines provided by this p

128 ctive aza-Henry approach to nonsymmetric cis-stilbene diamines and cis-imidazolines.

129 otonation of the electrochemically generated stilbene dianion demonstrate that, notwithstanding signi

130 ature voltammetric detection of highly basic stilbene dianions electrochemically generated by the red

131 ification of a porous MOF, Zn(4)O(trans-4,4'-stilbene dicarboxylate)(3), with Br(2) results in diaste

132 Reaction of trans-4,4'-stilbene dicarboxylic acid and zinc nitrate in N,N-dimet

133 kers, 4'-diisothiocyano-2,2'-disulfonic acid stilbene (DIDS) or niflumic acid (NFA).

134 haracterized as a 5,5'-diisothiocyanato-2-2'-stilbene (DIDS)-sensitive transporter in several tissues

135 ribenzoic acid, and 4,4'-diisothiocyano-2,2'-stilbene-disulfonic acid) but decreased under hypertonic

136 lacking TMs 6 and 7 are capable of forming a stilbene disulphonate-sensitive (36)Cl-influx pathway, r

137 of 3dSB-PNBS and dimethoxyphenyl-p-nitro-bis-stilbene (DMP-PNBS), a control compound, we show that th

138 ce for the charge recombination rate between stilbene donor (Sd(+)) and stilbene acceptor (Sa(-)) lin

139 the purine or pyrimidine blocks of a diblock stilbene donor-acceptor capped hairpin with locked nucle

140 s are easily distinguished from those of the stilbene donor/acceptor radical ion chromophores.

141 nsport dynamics of DNA hairpins possessing a stilbene electron acceptor and donor along with a modifi

142 occupation during charge transport between a stilbene electron donor and acceptor.

143 ectroscopy of DNA conjugates possessing both stilbene electron donor and electron acceptor chromophor

144 complexes of DNA capped hairpins possessing stilbene electron-acceptor and -donor chromophores separ

145 ation, the contents in piceatannol and other stilbenes, ellagitannins, and flavonols decreased while

146 linked by various moieties such as alkenes (stilbenes), enones (chalcones), or ethers was selected f

147 rovide a structural view for stereoselective stilbene epoxidation and functionalization in an inverte

148 However, stilbene epoxidation biosynthesis and its biological rol

149 urements and the isomeric distributions of Z-stilbene epoxidation products demonstrate that the activ

150 from Photorhabdus luminescens that catalyzes stilbene epoxidation.

151 sopropyl-trans-stilbene (compound 1) and its stilbene epoxide (compound 2).

152 (in THF) identical to the spectrum of trans-stilbene, except for [o-MeStilSiO(1.5)](8), which exhibi

153 V-vis absorptions are not changed from trans-stilbene, except for the ortho derivative, which is blue

154 While in trans-stilbene, excitation at 6 eV induces a phenyl twisting m

155 s paper reports the use of a grapevine-shoot stilbene extract (Vineatrol(R)) as a preservative in red

156 d energy was the most effective on the total stilbene extraction.

157 beta-CD was the most effective in recovering stilbenes, flavonols, and flavan-3-ols from grape pomace

158 High-resolution images of the stilbene fluorescence provided by macroscopy were supple

159 show that the prolonged luminescence is not stilbene fluorescence.

160 ses (SCOs) cleave the central double bond of stilbenes, forming two phenolic aldehydes.

161 was identified as isorhapontigenin (ISOR), a stilbene found in traditional Asian medicinal plants.

162 Therefore, we characterised stilbenes from Nonpareil, Butte and Carmel almond (Prunu

163 ever, is markedly decreased as the number of stilbene functional groups is increased.

164 precursor, such as Pd((R,R)-Me-Duphos)(trans-stilbene), gave the tertiary phosphines PMe(Ar')(Ar) in

165 The corresponding trans-stilbenes had little or no activity as tubulin polymeriz

166 P2-19G2 that has been elicited against trans-stilbene has unprecedented ability to produce bright lum

167 al product resveratrol, a polyphenolic trans-stilbene, has numerous biological activities and is a kn

168 eratrol, the basic unit of all other complex stilbenes, has received widespread attention because of

169 rge separation in capped hairpins in which a stilbene hole acceptor and hole donor are separated by A

170 and the highest occupied state (pi state on stilbene), however, is markedly decreased as the number

171 Interestingly, the respective individual stilbene (IC(50) > 100 muM), chalcone (IC(50) = 11.5 muM

172 It is found that the geometry of trans-stilbene in the ground as well as in the first excited s

173 r than that of red grapes, a major source of stilbene in the human diet.

174 nd emission spectra of free and encapsulated stilbene in two different capsules were calculated using

175 0) values (vs Fc(0/+)) for substituted trans-stilbenes in acetonitrile and (N111)(N112)BH2-NTf2 do no

176 re suitable for the determination of several stilbenes in complex samples.

177 es in the presence of base to generate trans-stilbenes in good to excellent yields (up to 99%).

178 sion and in the accumulation of glycosylated stilbenes in planta.

179 ation, whereas a more localized synthesis of stilbenes in stomata guard cells and cell walls is induc

180 The anion radicals of stilbenes in the collisionless isolated phase were synth

181 f thermal isomerization of constrained stiff stilbene increase sharply as the restoring force decreas

182 ith pCMBS; (ii) reduced in the presence of a stilbene inhibitor; and (iii) stimulated at more positiv

183 The stilbene inhibitors induce gene expression changes in Mt

184 ollowed to isolate and identify this unknown stilbene is described in the present work.

185 cage, the ground state of encapsulated trans-stilbene is distorted, with the two phenyl groups twiste

186 ective reductive coupling of benzaldehyde to stilbene is driven by subsurface Ti interstitials on vac

187 A rather uniform synthesis of stilbenes is induced after UV-C irradiation, whereas a m

188 hotocyclization reaction of dissymmetric bis-stilbenes is reported.

189 Resveratrol (3,4',5-trihydroxy-trans-stilbene) is a phytoalexin found in grapes that has anti

190 Resveratrol (3,5,4'-trihydroxy-trans -stilbene) is a well-known polyphenolic compound of red w

191 Piceatannol, a natural stilbene, is an analog and a metabolite of resveratrol.

192 these polyphenolic compounds - polyketides, stilbenes, isoflavones and catechins.

193 eV induces a phenyl twisting motion, in cis-stilbene it leads to an ultrafast ring-closing to form 4

194 studies established their structures as new stilbene-l-proline conjugates, prolbenes A (compound 3)

195 ondingly, NOV1 cleaves a wide range of other stilbene-like compounds with a 4'-OH group, offering pot

196 In both cases, the rigidity of the stilbene linker increases upon coordination to the inorg

197 d spectroscopic measurements reveal that the stilbene linkers in the dense structure 1 exhibit a smal

198 coordination environments connected by trans-stilbene links.

199 tramolecular [2+2] photocyclization of a bis-stilbene macrocycle was studied.

200 dulation of genes related to phenylpropanoid/stilbene metabolism highlighted the distinct metabolomic

201 gies mirror the relative polarization of the stilbene moieties and can be quantitatively correlated w

202 ne core was identified as replacement of the stilbene moiety.

203 freezing-in of orientational disorder of the stilbene molecule.

204 eries of highly luminescent oxadiazole-based stilbene molecules (OXD4, OXD8, OXD10, and OXD12) exhibi

205 erization reaction to take place between two stilbene molecules in the solid state.

206 ctive metabolite of the family of prenylated stilbenes named schweinfurthins, is only located in thes

207 ation of four simple phenylpropanoids, eight stilbenes, nine flavonoids, six related arithmetic param

208 Neither stilbene nor naphthalene are reduced by 1, but 1 reduces

209 The epoxidation of cis-stilbene occurred in the cavity of 14(out)-Mn(III)-1 and

210 ce imaging was developed to localize in situ stilbenes on the same stressed grapevine leaves.

211 on of 1a afforded predominantly either trans-stilbene or diphenyl glyoxime depending on solvent, temp

212 ts of selectivity, for two substrates: trans-stilbene oxide (t-SO) and trans-diphenylpropene oxide (t

213 trans-Stilbene oxide (TSO) induces drug metabolizing enzymes i

214 larly to the assay that used radioactive cis-stilbene oxide but with a greater discrimination between

215 The rearrangement of cis-stilbene oxide catalyzed by Al(2)O(3) was studied in the

216 a family of 1,2-diamines derived from trans-stilbene oxide that prevent HCV infection at nontoxic, l

217 activity against both epibromohydrin and cis-stilbene oxide, but with a relatively narrow range of su

218 Phenolic acids, flavanols, flavonols and stilbenes (PAFFS) were isolated from whole grapes, juice

219 enzothieno[3,2-b][1]benzothiophenes, via the stilbene pathway, is described.

220 periment and show that fluorescence of trans-stilbene persists in the large cage while it is quenched

221 an anthracene to generate the triptycene, a stilbene photocyclization to construct the helicene, and

222 dies revealed that CDs were able to increase stilbene photostability at 4 degrees C.

223 Stilbene phytoalexins, namely resveratrol, pterostilbene

224 nteraction of the silicon center(s) with the stilbene pi* orbital in both the corner and half cages.

225 proposed to result from interactions of the stilbene pi* orbitals with a LUMO centered within the ca

226 Stilbene polyphenols are present in some fruits and nuts

227 thases (CHSs) several times independently in stilbene-producing plants.

228 A series of symmetrical E-stilbene prolinamides that originated from the library-s

229 A series of cis- and trans-stilbenes related to combretastatin A-4 (1a), with a var

230 However, the content of stilbene represented by trans resveratrol-3-glucoside wa

231 for the first time provide evidence that the stilbene resveratrol targets PTP1B to inhibit PDGFR mito

232 -glucoside and quercetin 3-glucoside and the stilbenes resveratrol, piceatannol, astringin and isorha

233 ging, the goal of this study was to increase stilbenes (resveratrol (RV), pterostilbene (PT) and pino

234 rape and wine are the main dietary source of stilbenes, resveratrol and piceid being the most common

235 The total synthesis of the natural stilbene (+)-schweinfurthin G (8) has been accomplished

236 c DNA hairpins possessing donor and acceptor stilbenes separated by one to seven A:T base pairs.

237 9 compounds, 71 conformations), then for the stilbene series (18 compounds, 59 conformations), and fi

238 Although the models for the chalcone and stilbene series appeared slightly different when represe

239 ntinuation of our exploration to improve the stilbene series, the 3,5,6,8-tetrasubstituted quinoline

240 form capped hairpin structures in which one stilbene serves as a hairpin linker and the other as a h

241 Direct irradiation of trans-stilbene showed that C(5)G3 and C(4)G3 dendrimers afford

242 onomer, is essential for transduction of the stilbene signal into p53-dependent apoptosis of breast c

243 shifted by approximately 20 nm, as found for stilbene-siloxane macrocycles, suggesting some interacti

244 emission spectra characteristic of monomeric stilbenes, similar to the dicarboxylic acid in dilute so

245 , we show how a molecular force probe, stiff stilbene, simplifies force spectroscopy of localized rea

246 '-disulfonate) as a label for the disulfonic stilbene site and FM (fluorescein-5-maleimide) as a labe

247 Stilbene solubility was improved by the formation of inc

248 This work showed that stable stilbene solutions can be achieved using hydroxypropyl-C

249 to consistent and complementary data on the stilbene spatial distribution for the two stresses addre

250 The capping stilbene stabilizes the hairpin structures by ca. 2 kcal

251 A set of stilbene-substituted octasilicates [p-RStil(x)Ph(8-x)SiO

252 antimicrobial activities compared with their stilbene substrates, suggesting a metabolite attenuation

253 rticipation in defense mechanisms in plants, stilbenes, such as resveratrol, display important pharma

254 The stereospecific formation of trans-stilbene suggests a mechanism of decomposition in which

255 ion of phenylalanine ammonia-lyase (PAL) and stilbene synthase (STS) genes, followed by a rapid accum

256 A ligase (At4CL1) and Vitis vinifera (grape) stilbene synthase (VvSTS) to increase resveratrol levels

257 s evidenced by elevated transcript levels of stilbene synthase genes.

258 ENESIS-RELATED1, PATHOGENESIS-RELATED10, and stilbene synthase in PM-infected V. vinifera, suggesting

259 Although stilbene synthases (STSs), the key enzymes responsible f

260 Stilbene synthases (STSs), which catalyze the biosynthes

261 Among them, we identified genes of stilbene synthases, PR-10 proteins, and several transcri

262 t a conceptually different approach toward E-stilbene syntheses by photoinduced direct C-H arylation

263 emically generated by the reduction of trans-stilbene (t-Stb) and its derivatives (4-methoxy-, 2-meth

264 is achieved when the concentration of trans-stilbene, [t-Stb], appreciably exceeds the concentration

265 Pawhuskin A is a prenylated stilbene that functions as an antagonist of the kappa op

266 (NO2)P2W17O61}(8-) and one molecule of trans-stilbene that is sufficiently stable at room temperature

267 erein, we report on boronic acid-substituted stilbenes that limit TTR amyloidosis in vitro.

268 ssion strongly increased the accumulation of stilbenes that play a role in plant defense and human he

269 s was screened to identify substituted trans-stilbenes that were more active than resveratrol.

270 The substituted trans-stilbenes that were potent inhibitors of the activation

271 ecipitons (1,2-biphenylethenes; analogous to stilbenes) that are activated by a covalently attached o

272 Unlike exciton coupling between the stilbenes, there is no apparent dependence of the charge

273 he in-solution oxidative photocyclization of stilbenes to phenanthrenes is a well-known and synthetic

274 C. polonica converted stilbenes to ring-opened, deglycosylated, and dimeric pr

275 The content of the stilbenes trans-resveratrol and piceid as well as the an

276 d and calculated for planar ring-fluorinated stilbenes, trans-2,3,5,6,2',3',5',6'-octofluorostilbene

277 FPP) < (TMPyP) < (TPP) in reactions with cis-stilbene, triphenylamine, and triphenylphosphine.

278 ereo- and regioselectivity in solution-state stilbene-type photocycloadditions.

279 has 3-D symmetry, it appears that all of the stilbene units interact in the excited state, consistent

280 lts in diastereoselective bromination of the stilbene units.

281 preparation of nonsymmetrically substituted stilbenes using a one-pot two-step double Heck strategy.

282 added) and experimental (reduction of trans-stilbene) voltammograms to assess the capabilities of pa

283 A new, previously undescribed-in-grapes stilbene was found after UVC treatment.

284 At 25 degrees C in chloroform, while trans-stilbene was still the major product, some diphenyl glyo

285 Stilbenes were isolated from ethanolic almond extracts b

286 ymerization, the dimethylamino and bromo cis-stilbenes were the most potent of the new derivatives, t

287 f flavonols, anthocyanins, flavan-3-ols, and stilbenes, were detected.

288 e phenanthrene formation, in addition to cis-stilbene, whereas C(3)G3 and C(2)G3 gave only cis-stilbe

289 Resveratrol is a stilbene, which is one of a group of polyphenols in many

290 on a flexible and emissive linker molecule, stilbene, which retains its luminescence within these so

291 ates are always the pi and pi* states on the stilbene, which show very weak shifts with increasing de

292 ncentration of phenolic compounds, including stilbenes, whilst treatments with kresoxim-methyl, fluqu

293 Benzaldehyde reductively couples to stilbene with 100% selectivity and conversions of up to

294 l symmetry, indenoindene, a carbon-bridged E-stilbene with a centrosymmetry, shows elongated pi-conju

295 nteraction between oxyresveratrol (a type of stilbene with high biological activity) and modified cyc

296 t discovery of high amount of piceatannol, a stilbene with potent biological activities, highlight th

297 An interest in the schweinfurthins, natural stilbenes with significant antiproliferative activity, h

298 Photorhabdus species produce a family of stilbenes, with two major components being 3,5-dihydroxy

299 nd confirmed the expected orientation of the stilbene within the TTR binding sites.

300 esveratrol and a series of substituted trans-stilbenes without hydroxy groups were compared with resv