ライフサイエンスコーパス: DMSO

1 DMSO also alters the mechanical properties of the erythr

2 DMSO causes a drastic decrease in the range of the steri

3 DMSO concentrations higher than 4% (v/v) destabilize the

4 DMSO was used for the first time to extract faecal metab

5 DMSO-d6/GL and DMSO-d6/GL-d8 binary mixture solvents see

6 DMSO-d6/GL must be preferred to DMSO-d6/GL-d8 for the st

7 DMSO-d6/GL-d8 is more appropriate for organic compounds

8 creased MTT activity compared to vehicle (1% DMSO) pretreatment.

9 At XDMSO >0.1, DMSO enters the lipid interface and restricts the lipid

10 for FG2 HSA nanoparticles (0.4 mg/kg), FG 2 DMSO/saline (0.4 and 8 mg/kg) and a reference compound,

11 AMG9810 (50 mg/kg) or vehicle (2% DMSO/5% Tween 80/10 ml/kg saline) was injected intraperi

12 ated ion pairs [K(+)-(DMSO)(n)-ClO(4) (-) + (DMSO)(m)-ClO(4) (-)] and the anions being unsolvated (in

13 of CYP142A1 toward unfolding even up to 40% DMSO.

14 d bis(p-nitrophenyl) phosphate (BNPP) in 80% DMSO solution at pH values in the range 8.5-12.0.

15 e corresponding alpha-ketoaldehydes by new a DMSO-NaBr-H2SO4 oxidation system in yields up to 90% wit

16 An unprecedented copper acetate-DMSO promoted methylthiolation of arenes and heteroarene

17 e perfusion, mice were randomly administered DMSO, Nec-1 (3.2 mg/kg/day) and Nec-1s (1.6 mg/kg/day) v

18 dimsyl anion, formed from a strong base and DMSO (solvent), is responsible for inducing the initiati

19 With 20 mol % of DABCO as catalyst and DMSO as the solvent high yields have been achieved for d

20 nt polarities (i.e., toluene, MeOH, DMF, and DMSO).

21 te, acetone, alcohol, acetonitrile, DMF, and DMSO, identify complex solvent systems, as well as disti

22 Furthermore, EtOH and DMSO can disrupt the main driving forces of these intera

23 DMSO-d6/GL and DMSO-d6/GL-d8 binary mixture solvents seem to be so far

24 s binary solvents, DMSO-d6/glycerol (GL) and DMSO-d6/glycerol-d8 (GL-d8), is reported for the first t

25 etone oxidation, employing catalytic HBr and DMSO, followed by imidazole condensation with aldehydes.

26 inexpensive and readily available iodine and DMSO with a short reaction time.

27 s of experiments with radical scavengers and DMSO-d6 and ESI-MS observations.

28 nylacetonitriles 1 with elemental sulfur and DMSO in the presence of a catalytic amount of DABCO, we

29 Interestingly, freshly synthesized and DMSO-solubilized 1 was inactive.

30 erties of the hydrazones in both toluene and DMSO were assessed offering insights into the kinetics a

31 used histone H3 fractions from untreated and DMSO-treated Murine ErythroLeukemia (MEL) cells.

32 ivation by potassium bifluoride in anhydrous DMSO.

33 ssue cultures with water and with an aqueous DMSO solution.

34 y competitive H2S and cyanide ion in aqueous DMSO media.

35 molecular iodine and sodium azide in aqueous DMSO providing a general access to geminal diazides.

36 ition-metal-free coupling reaction of aryne, DMSO, and activated alkyne for the synthesis of 2-[( o-m

37 m a single lead at nanomole-scale amounts as DMSO-d(6) stock solutions with a known structure and con

38 Compounds such as DMSO and hexamethylene bisacetamide (HMBA) have been use

39 observe that higher order glymes as well as DMSO improve the solubility of Mg salts, but only the lo

40 to a mechanistic understanding of biological DMSO production in surface seawater.

41 n unexpected increase in non-hydrogen-bonded DMSO near the eutectic point (ca. 35 mol %) which also c

42 [Fe(14)], Tp(-), hydrotris(pyrazolyl)borate; DMSO, dimethyl sulfoxide), which has a fluctuating valen

43 d 8 mg/kg) and a reference compound, BTZ043, DMSO/saline (0.4 and 8 mg/kg).

44 ce consisting of (i) potassium tert-butoxide/DMSO-catalyzed (E)-stereoselective C-H functionalization

45 alovirus promoter, was markedly increased by DMSO treatment.

46 monstrating that Talpha-1 changes induced by DMSO are fully reversible and that Talpha-1 peptides pre

47 renes, using molecular iodine as a catalyst, DMSO as a stoichiometric oxidant, and different nucleoph

48 unced, especially, in the presence of Chatos DMSO extract.

49 eral structure [4-R-pyH](+)trans-[Ru(III)Cl4(DMSO)(4-R-py)](-), where 4-R-py stands for a 4-substitut

50 nity toward carboxylates in very competitive DMSO/water mixtures.

51 In contrast, DMSO both protects against heme loss and increases the s

52 tion of T cells formulated in a conventional DMSO based cryoprotectant and processed in conventional

53 esence of a very strong H-bonding cosolvent (DMSO), which slowed the observed rates by up to 2 orders

54 cy range of 500-4000 cm(-1) for cyclohexane, DMSO, acetonitrile, methanol, water, benzene, and toluen

55 n after dissolution into either D2 O or [D6 ]DMSO.

56 O(S2)2picolinate] (Mo-pic) is stable in a d6-DMSO solution after heating at 100 degrees C, in air, re

57 SRS microscopy was used to image D2O, PG-d8/DMSO-d6, and the nail through the O-D, -CD2, and -CH2 bo

58 th groups of TAC/DOCA mice (cRbm20(DeltaRRM)-DMSO and cRbm20(DeltaRRM)-raloxifene).

59 TAC/DOCA cRbm20(DeltaRRM)-DMSO mice developed LV hypertrophy and a marked increase

60 oxide (DMSO)-injected mice (cRbm20(DeltaRRM)-DMSO) as the control.

61 which either no additive, dimethylsulfoxide (DMSO), or N-methylpyrrolidine-2-thione (NMPT) is added.

62 solvent, for example, in dimethylsulfoxide (DMSO), the two isomers interconvert to each other.

63 canines were divided into dimethylsulfoxide (DMSO) group and 10 mM, 15 mM, and 20 mM A-803467 groups.

64 r that is required by the dimethylsulfoxide (DMSO) reductase family of enzymes, which includes the ni

65 obial oxidation of DMS to dimethylsulfoxide (DMSO) represents a major sink of DMS in surface seawater

66 iven conversion of DMS to dimethylsulfoxide (DMSO).

67 sions compared to 50% in dimethylsulphoxide (DMSO).

68 Concentrations of DMSP, DMSO(2), and methanesulfonic acid (MSA) did not decrease

69 t with tetra-n-butylammonium fluoride in dry DMSO.

70 We therefore evaluated DMSO perfusion rates by X-ray computed tomography, ice c

71 In these experiments, DMSO:acetone (1:40 v/v) solution of 17AAG (500 nmol) was

72 For DMSO, a first-order dependence of decomposition rates on

73 ntrated solutions reduces the available free DMSO molecules that can react with Na and renders the TF

74 hylammonium lead halide films processed from DMSO-containing solution.

75 tion that reaction products that result from DMSO reacting with MA(+) in the precursor solution are r

76 on constant value of K = 4900 M(-1) in a H2O/DMSO (50:50 v/v) binary solvent mixture.

77 erto unexplored reagent combination PPh3.HBr-DMSO is exemplified with multiple highly diverse one-ste

78 al calculations were performed at the IEFPCM(DMSO)/B3LYP-D3/6-311+G(d,p) level of theory and compared

79 tor ensembles, Fe(II)(bpy)(2)(CN)(2)-[Pt(II)(DMSO)Cl(2)](2) (1) and Fe(II)(bpy)(2)(CN)(2)-[Au(I)Cl](2

80 In DMSO, a retroaldol reaction followed by fast intramolecu

81 In DMSO, the half-lives of nitrone 3 and 4-OOH adducts were

82 ctivation energy as high as 63 kJ mol(-1) in DMSO-d(6) solution (DFT prediction for a model compound

83 pG2 cells were exposed for 24 h to PCB 11 in DMSO or DMSO alone.

84 DB) showed turn-on response toward Mn(2+) in DMSO and acetonitrile, respectively.

85 s 2a-g and benzylidenemalonates 2h and 2i in DMSO were determined photometrically at 20 degrees C.

86 Dissolution of CP 3 in DMSO favors Co-S bond heterolysis, yielding the diamagne

87 ith 4(2-amino-1H-imidazol-5-yl)phenol (4) in DMSO.

88 ransport and kinetic requirements, KPF(6) in DMSO is identified as a promising electrolyte for K-O(2)

89 s (with gauche populations of 87% and 92% in DMSO-d(6), respectively), their anions, on the other han

90 onic acids promoted by copper(II) acetate in DMSO provides an attractive alternative to the earlier r

91 were performed using methanesulfonic acid in DMSO and followed by proton NMR.

92 3- and 4-substituted phenylboronic acids in DMSO is nonlinear, with a small negative slope for elect

93 cid recognizes zwitterions of amino acids in DMSO, and its UV absorption maximum undergoes a signific

94 tives having more tendency of aggregation in DMSO-water mixed solvent showed significant increase of

95 rt a quantitative solvent effect analysis in DMSO/water mixtures for (i) the hydrolysis reaction of d

96 d the assignment in 7 M urea (pH 2.3) and in DMSO.

97 ubppm levels (<1.0 ppm) in THF as well as in DMSO-H2O.

98 ns in 3 mM solutions of the azoporphyrins in DMSO was switched between 3.5 and 1.7 s.

99 and nitroarenes using tert-butoxide base in DMSO at room temperature.

100 the solvent, either complete single bond (in DMSO) or double bond (in cyclohexane) rotation can be in

101 tion of the corresponding HE with KO(t)Bu in DMSO at rt.

102 Although catalytic KO(t)Bu in DMSO is sufficient to allow imine generation, stoichiome

103 the presence of a nitrogen-base catalyst in DMSO.

104 the acidity (pK(a)) of organic compounds in DMSO, which was achieved with the aid of the equation K(

105 tants (K(a)) of several organic compounds in DMSO.

106 interactions at millimolar concentrations in DMSO.

107 assembled reactive ester block copolymers in DMSO.

108 According to (1)H and (13)C NMR data, in DMSO-d(6) solution, the 6-1H tautomer predominates, wher

109 allo-supramolecular scaffolds over 4 days in DMSO at 60 degrees C.

110 The plasma sample simply diluted in DMSO allowed the recovery of various amounts of sunitib,

111 , Leu-Tyr, Gly-Tyr, and Ala-Tyr dissolved in DMSO-d6/GL (8:2, v/v) and of an apolar mixture made of b

112 llal, (+)-limonene, and flavone dissolved in DMSO-d6/GL-d8 (5:5, v/v) by means of spin diffusion in h

113 of ethylenediaminetetraacetic acid (EDTA) in DMSO exerts superior control over wafer coverage and fil

114 enantioselective fluorescence enhancement in DMSO solution.

115 uent organoid generation by slow freezing in DMSO supplemented media.

116 issue and from bulk tissues slowly frozen in DMSO supplemented media.

117 same band gap was also measured for GTUB5 in DMSO.

118 s demonstrated using precipitation of LiF in DMSO as a driving force.

119 the base and t-Bu(3)PHBF(4) as the ligand in DMSO at 120 degrees C in a sealed tube delivers the 2-su

120 dipalmitoylphosphatidylcholine membranes in DMSO-water mixtures quantify the hydration- and solvatio

121 in we report the enhanced stability of Na in DMSO solutions containing concentrated sodium trifluorom

122 Treatment of 5 with 1.5 equiv of NaOMe in DMSO at 140 degrees C for 0.5 h gave 6 in good yields.

123 This step was studied by (1)H NMR in DMSO-d(6).

124 ulation reveal the Na(+) solvation number in DMSO and the formation of Na(DMSO)3 (TFSI)-like solvatio

125 No C-H deactivation was observed in DMSO after addition of Li(+) and Mg(2+).

126 e applied to other ET reactions performed in DMSO.

127 paringly soluble, based on permethylation in DMSO as the initial derivatization step.

128 n treating or dissolving acylated purines in DMSO as they are prone to isomerization.

129 oss-coupling reactions take place rapidly in DMSO in good yields and efficiently proceed in the prese

130 he rate and selectivity of LLB-A reaction in DMSO-D6 is explained with the controlled and online NMR

131 vents, where MK-2 was most easily reduced in DMSO, which may suggest a combination of solvent effect

132 ies of anions as tetrabutylammonium salts in DMSO and MeCN were studied by (1)H and (11)B NMR as well

133 rge data set of (13)C NMR chemical shifts in DMSO are presented with TMS as the calculated reference

134 NMR titration studies in DMSO revealed an anion affinity order of F(-) > AcO(-) >

135 versible addition of methanol to styrenes in DMSO -d(6) solvent.

136 GenX was unstable in DMSO, but stable and negative for toxicity when diluted

137 ydrodynamic radius decreases with increasing DMSO concentration up to 10 mol% DMSO.

138 Interestingly, DMSO platinum complexes show low cytotoxicity in the non

139 Only the reaction mechanism involving DMSO as a nucleophilic reactant is in harmony with the e

140 mation of solvent-separated ion pairs [K(+)-(DMSO)(n)-ClO(4) (-) + (DMSO)(m)-ClO(4) (-)] and the anio

141 partial anion solvation [predominantly K(+)-(DMSO)(n)-OTf(-)].

142 ted pyrazoles have been achieved using K2CO3-DMSO.

143 rbonyl compounds or amidines utilizing K2CO3/DMSO at ambient temperature that provides a straightforw

144 hree molecules of acetylene activated by KOH/DMSO and KOBu(t)/DMSO superbase systems.

145 ryl pyrazoles to (E)-styryl pyrazoles in KOH/DMSO system.

146 alkynes using a super basic solution of KOH/DMSO has been described.

147 ed out to elucidate the mechanism of the KOH/DMSO superbase catalyzed ketones nucleophilic addition t

148 he R5 or R4 position of the phenyl ring; L = DMSO and P(C6H4CF3-p)3) has been prepared.

149 solution of the reductant Cp2Co, Mn((N,O)L)(DMSO) undergoes a ligand-centered solid-state reduction

150 n(III) affords the chain compound Mn((N,O)L)(DMSO).

151 rming using 2 M EG + 1 M PG and 2 M EG + 1 M DMSO.

152 viability (72.6% +/- 10.5%) comprised 1.3 M DMSO, 0.1 M trehalose and 1.5% BSA; cell viability was s

153 Measured DMSO pKa values for a series of rigid tricyclic adamanta

154 -4b indicated that weaker donors (THF, MeCN, DMSO, MeOH, and even H2O) likewise promote this pathway,

155 y important anions in a highly polar medium (DMSO + 0.5% H2O).

156 ven in a highly competitive solvent mixture (DMSO-d(6) + H(2)O 95:5 v/v).

157 increasing DMSO concentration up to 10 mol% DMSO.

158 ead group and that, from 10 mol% to 20 mol%, DMSO acts to gradually collapse head groups down onto th

159 Moreover, DMSO works as a cryogenic protector avoiding solidificat

160 -) ligand, the corresponding [Ru(phbpy)(N-N)(DMSO-kappaS)](+)complexes are chiral.

161 five cyclometalated complexes Ru(phbpy)(N-N)(DMSO-kappaS)](PF(6)) ([1]PF(6)-[5]PF(6)) were synthesize

162 ation number in DMSO and the formation of Na(DMSO)3 (TFSI)-like solvation structure.

163 Raman spectra of NaTFSI/DMSO electrolytes and ab initio molecular dynamics simul

164 osized complex, [Fe(Tp)(CN)(3)](8)[Fe(H(2)O)(DMSO)](6) (abbreviated as [Fe(14)], Tp(-), hydrotris(pyr

165 The ZnCl(2)-H(2)O-DMSO electrolyte enables Zn anodes in Zn||Ti half-cell t

166 lvation of DMSO with Zn(2+) and strong H(2)O-DMSO interaction inhibit the decomposition of solvated H

167 e to a higher Gutmann donor number (29.8) of DMSO than that (18) of H(2)O.

168 This at least partly explains ability of DMSO to promote ccHBV infection in such cell lines.

169 simple protocol involving the activation of DMSO by chlorotrimethysilane is described for the chemos

170 ss from the adduct position, the addition of DMSO leads to the formation of an insertion complex capa

171 As expected, the addition of DMSO to water reduces G(s).

172 afforded by the addition of a low amount of DMSO in conjunction with the inherent temporal control e

173 follicles due to the high concentrations of DMSO used.

174 The toxic effect of DMSO and K(2)CrO(4) was dynamically monitored by measuri

175 rations below 10 mol%, the primary effect of DMSO is to decrease the solvated volume of the PC head g

176 an erythrocytes to investigate the effect of DMSO when added to the membrane-solvating environment.

177 Although the effects of DMSO on the membrane structure and the headgroup dehydra

178 In this study, the effects of DMSO on the structure and interactions of avidin and Myc

179 es with angstrom resolution as a function of DMSO concentration from 0 mol% to 20 mol%.

180 is desirable to understand the influence of DMSO concentration on the dissociation or unfolding beha

181 The majority of DMSO molecules solvating Na(+) in concentrated solutions

182 lar hydrogen bonds was ruled out by means of DMSO titration, DOSY experiments, and steric considerati

183 indicated the exceptional nucleophilicity of DMSO.

184 -1) s(-1), while the subsequent oxidation of DMSO to dimethyl sulfone (DMSO(2)) is much slower (0.4 M

185 ) were determined in absence and presence of DMSO.

186 tructural analysis detected typical signs of DMSO toxicity, such as mitochondria degeneration, altera

187 intermediate oxidized by a basic solution of DMSO or atmospheric oxygen led to the desired sp(3) C-H

188 The preferential solvation of DMSO with Zn(2+) and strong H(2)O-DMSO interaction inhib

189 cells, which agrees with the common usage of DMSO in dermal medicine.

190 authors of the original paper to the use of DMSO and to improper handling.

191 The widespread use of DMSO as a cosolvent, along with its unusual attributes,

192 Given the frequent use of DMSO in biochemical and biophysical assays, it is desira

193 t-order dependence of decomposition rates on DMSO concentration was established.

194 on of the latter using either K3[Fe(CN)6] or DMSO/conc.

195 A volume of 0.1 ml of A-803467 or DMSO was injected into the LSG.

196 measured photometrically in acetonitrile or DMSO solution at 20 degrees C.

197 o an environmentally relevant dose of BPA or DMSO control.

198 s were exposed for 24 h to PCB 11 in DMSO or DMSO alone.

199 on, and the same amount of SAHA injection or DMSO was followed at day 2.

200 diation at a wavelength of 365 nm of MeCN or DMSO solutions of 3-6 results, depending on the expositi

201 did not alter cell viability in untreated or DMSO-treated cells; however it did increase CG effect.

202 ter, we began treatment with ZINC40099027 or DMSO, staining the mucosa for phosphorylated FAK and Ki-

203 The capacity of peach DMSO extracts to inhibit Candida albicans growth was mor

204 thod for the deuteration of pseudoacids (pKa,DMSO = 14-19) with chloroform-d1.

205 ansfer catalyst [Ir(H)(2) (eta(2) -pyruvate)(DMSO)(IMes)].

206 mistry models were used to directly quantify DMSO/water hydrogen-bond populations in binary mixtures.

207 A's characteristic Raman signals to quantify DMSO, PG and FMD concentrations in the supernatants.

208 revealed no adverse effects of the residual DMSO after the solvent replacement.

209 The slow, DMSO frozen tissue yielded organoids with more accurate

210 In addition, the decomposition of solvated DMSO forms Zn(12)(SO(4))(3)Cl(3)(OH)(15).5H(2)O, ZnSO(3)

211 pound fluorescein, where the organic solvent DMSO is exchanged against an aqueous buffer.

212 nt (chloroform) and high-dielectric solvent (DMSO) to experimentally study the solvent-dependent conf

213 ion was performed in polar aprotic solvents (DMSO), the formation of their 5-CF3-substituted isomers

214 e of two new highly viscous binary solvents, DMSO-d6/glycerol (GL) and DMSO-d6/glycerol-d8 (GL-d8), i

215 Specifically, DMSO was found to effectively destabilize the hydration

216 idence for three distinct regimes: 1) strong DMSO-water interactions (<30 mol %), 2) ideal-solution-l

217 cies are dominant at 10 mol %, due to strong DMSO-water interactions.

218 etely abolished DMS oxidation and subsequent DMSO formation.

219 The sulfolane/water and sulfolane/DMSO-d(6) binary NMR solvents are reported for the indiv

220 y dissolved in sulfolane/water and sulfolane/DMSO-d(6) solvents blends by means of homonuclear select

221 quent oxidation of DMSO to dimethyl sulfone (DMSO(2)) is much slower (0.4 M(-1) s(-1)).

222 ally involves the use of dimethyl sulfoxide (DMSO) acting as an organic solvent for simultaneous samp

223 solution calorimetry in dimethyl sulfoxide (DMSO) and differential scanning calorimetry.

224 can tolerate up to 3.9% dimethyl sulfoxide (DMSO) and up to 10% serum, which shows its compatibility

225 concentrated LiNO(3) in dimethyl sulfoxide (DMSO) as an additive for a fluoroethylene-carbonate (FEC

226 higher concentrations of dimethyl sulfoxide (DMSO) as the temperature was reduced.

227 solution containing 10% dimethyl sulfoxide (DMSO) at 21 degrees C.

228 ds using only KO(t)Bu in dimethyl sulfoxide (DMSO) at rt.

229 nic acid (PFOS), or 0.4% dimethyl sulfoxide (DMSO) daily from 0-5 d post fertilization (dpf).

230 Dimethyl sulfoxide (DMSO) disrupts the hydrogen-bond networks in water.

231 Dimethyl sulfoxide (DMSO) has been broadly used in biology as a cosolvent, a

232 ells was attributable to dimethyl sulfoxide (DMSO) in culture medium, NTCP overexpression, and HBV ge

233 mprised of Ficoll 70 and dimethyl sulfoxide (DMSO) in presence or absence of fetal bovine serum (FBS)

234 mixing volatile additive dimethyl sulfoxide (DMSO) into aqueous PEDOT:PSS solutions followed by contr

235 us electrolyte by adding dimethyl sulfoxide (DMSO) into ZnCl(2)-H(2)O, in which DMSO replaces the H(2

236 Dimethyl sulfoxide (DMSO) is a common solvent and biological additive posses

237 Dimethyl sulfoxide (DMSO) is a promising solvent for this battery but its in

238 Dimethyl sulfoxide (DMSO) is widely used in a number of biological and biote

239 ) in a series of toluene/dimethyl sulfoxide (DMSO) mixtures and find that the experimental values sho

240 Compound 7 in dimethyl sulfoxide (DMSO) or ethanol solutions exists in the form of 7-1H an

241 the presence of KOBu(t)/dimethyl sulfoxide (DMSO) or NaOBu(t)/DMSO systems under exceptionally mild

242 Dimethyl sulfoxide (DMSO) or sulfide ligands have positive and negative role

243 ilms are obtained from a dimethyl sulfoxide (DMSO) solution via a transitional SnI2.3DMSO intermediat

244 and acetylene in the KOH/dimethyl sulfoxide (DMSO) superbase medium (here abbreviated as the KOA reac

245 ts: water, methanol, and dimethyl sulfoxide (DMSO) were investigated at varying concentrations for th

246 M) supplemented with 10% dimethyl sulfoxide (DMSO), 15% human serum albumin (HSA) and 0.1% hyaluronan

247 Dimethyl sulfoxide (DMSO), but not pyrenebutyrate (PB), ethanol, oleic acid,

248 , propylene glycol (PG), dimethyl sulfoxide (DMSO), glycerol (GLY), and methanol (METH; listed in ord

249 ntains a small amount of dimethyl sulfoxide (DMSO), the adduct is able to move to a solvent-exposed c

250 ts very fast with DMS to dimethyl sulfoxide (DMSO), with a second-order rate constant of 1.6 x 10(9)

251 methyl methacrylate) and dimethyl sulfoxide (DMSO)-compatible poly(2-hydroxyethyl methacrylate) gels

252 taRRM)-raloxifene), with dimethyl sulfoxide (DMSO)-injected mice (cRbm20(DeltaRRM)-DMSO) as the contr

253 onium persulfate (AP) or dimethyl sulfoxide (DMSO).

254 common organic solvent, dimethyl sulfoxide (DMSO).

255 the dominant pathway in dimethyl sulfoxide (DMSO).

256 O(4), HgSO(4) salts, and dimethyl sulfoxide (DMSO).

257 CPAs such as dimethyl-sulfoxide (DMSO), propylene glycol (PG), and formamide (FMD), routi

258 roxyl radical scavenger (dimethyl sulfoxide, DMSO), and different pH values.

259 on with a polycation in dimethyl sulphoxide (DMSO), the solution was applied underwater to various su

260 ene glycol (PG-d8), and dimethyl sulphoxide (DMSO-d6) were separately applied to the dorsal surface o

261 acetylene activated by KOH/DMSO and KOBu(t)/DMSO superbase systems.

262 enes, and guanidine catalyzed by the KOBu(t)/DMSO system leads to 2-aminopyrimidines in up to 80% yie

263 OBu(t)/dimethyl sulfoxide (DMSO) or NaOBu(t)/DMSO systems under exceptionally mild conditions (14 deg

264 via the addition of trifluoroethanol (TFE), DMSO, DMF and acetone, uniform fiber-like nanoparticles

265 late with the catalytic activity better than DMSO pKa values and appear to be a better measure of aci

266 lity, leading to the general assumption that DMSO-induced structural changes in cell membranes and th

267 We postulate that DMSO acts as an efficient cryoprotectant even at low con

268 ken in its entirety, these results show that DMSO is likely to have a differential effect on heteroge

269 Tandem MS/MS experiments showed that DMSO could modify the dissociation pathway of CYP142A1,

270 The DMSO removal performance could be significantly increase

271 olves hydrogen bonding between water and the DMSO aggregate species.

272 s amphipathic helix and that it enhances the DMSO cryopreservation of adherent cell lines.

273 eptional solubility of over 700 mg/mL in the DMSO formulation solvent.

274 Repeated screening of the DMSO aliquot of synthesized 1 revealed increasing APOBEC

275 ) was significantly smaller than that of the DMSO group (172.80 +/- 13.68%) (P < 0.05).

276 In addition, some of the DMSO platinum complexes effectively inhibit angiogenesis

277 -resistant A2780cisR cells, with most of the DMSO platinum complexes exhibiting IC50 values in the su

278 ssible without a significant decrease of the DMSO removal performance.

279 d to be smaller (121.60 +/- 10.40%) than the DMSO group, though the difference was not statistically

280 reated with 3 uM of SB505124, as compared to DMSO.

281 n HSA nanoparticles was enhanced compared to DMSO/phosphate buffered saline (PBS) or albumin/PBS solu

282 Purified Tmm oxidizes DMS to DMSO at a 1:1 ratio.

283 heterotrophic bacterium, can oxidize DMS to DMSO using trimethylamine monooxygenase (Tmm).

284 DMSO-d6/GL must be preferred to DMSO-d6/GL-d8 for the study of biological active compoun

285 onse of the two types of liposome systems to DMSO in terms of the bilayer thermotropic behavior, avai

286 ng products in high yields, up to 92%, using DMSO as a solvent with a broad substrate scope in an und

287 an oxidation reaction enabled just by using DMSO as the solvent as well as an oxidant.

288 Extraction using DMSO and acetone has shown to be appropriate for voltamm

289 ity through a chemical stimulus, by varying [DMSO]0/[Y(OTf)3]0 ratio from 0 to 30 during the polymeri

290 SAHA (25 mg/kg) (n = 30) or vehicle (DMSO) (n = 30) was delivered through intraperitoneal inj

291 etting were simultaneously actuated by water-DMSO solvent exchange.

292 extensively studied, the mechanism by which DMSO invokes its effect on lipid membranes and the direc

293 ulfoxide (DMSO) into ZnCl(2)-H(2)O, in which DMSO replaces the H(2)O in Zn(2+) solvation sheath due t

294 )(Ph)(CCHC){Au(IPr)}(2)(SOMe(2))]NTf(2) with DMSO.

295 Disrupting the capsule with DMSO, ultrasound, or mechanical shear stress resulted in

296 ed bone marrow leukemic burden compared with DMSO or Ara-C alone, thus prolonging mouse survival.

297 Compared with DMSO, concentration-dependent prolonged action potential

298 ome-wide melting shifts after treatment with DMSO, 1 or 20 uM staurosporine with five replicates.

299 Without DMSO and [Fe(II)]0 = 300 muM variation of pH yielded dec

300 superlattice of TiS2/[(hexylammonium)x(H2O)y(DMSO)z], with an in-plane lattice thermal conductivity o