ライフサイエンスコーパス: diacetate

1 mino-5-methylamino-2',7'-difluorofluorescein diacetate).

2 using 2',7'-dichloroflorescin diacetate (DCF-diacetate).

3 e determined using 2',7'-dichlorofluorescein diacetate.

4 5-(and -6)-carboxy 2',7'-dichlorofluorescein diacetate.

5 itive fluorescent marker, diaminofluorescein diacetate.

6 5,6-carboxy-2',7'-dihydrodichlorofluorescein diacetate.

7 n the enantiotopic C-O single bonds of a gem-diacetate.

8 s was measured with 2',7'-dichlorofluorescin diacetate.

9 cells with 51Cr or 5-chloromethylfluorescein diacetate.

10 fluorescent probe, 2',7'-dichlorofluorescein diacetate.

11 ation of preloaded 2',7'-dichlorofluorescein diacetate.

12 ith the symplastic tracer carboxyfluorescein diacetate.

13 ere measured using 2',7'-dichlorofluorescein diacetate.

14 er molecule 2',7'-dichlorodihydrofluorescein diacetate.

15 -yl acetates through the intermediacy of gem-diacetates.

16 ing) to test the efficacy of a chlorhexidine diacetate 10% weight per volume (w/v) dental coating (CH

17 or 2,3-diallyl-5,6-dimethyl-1,4-hydroquinone diacetate (16) formed silylated fused bicyclic complexes

18 Acetylation of the diacetate 2 followed by acid-catalyzed elimination and r

19 eta)-3-hydroxycholestane-4,6-diene-1,25-diol diacetate (2) is described.

20 nsfer enzymes leads to an optimized match of diacetate 20 with PPL.

21 enzymatic desymmetrization of advanced meso diacetate 20, through PPL-mediated ester hydrolysis.

22 Racemic diacetate 21 showed a strong activity against KB-3-1 cel

23 C-3 in diltiazem, the 3-monoacetate (8) and diacetate (3) derivatives of 2 were prepared.

24 were also labeled with 6-carboxyfluorescein diacetate (6-CFDA) as an internal standard.

25 e transport kinetics of 6-carboxyfluorescein diacetate (6-CFDA), which is processed in hepatocytes in

26 poxy bisketal 6 or the 5 alpha,6 alpha-epoxy diacetate 7 followed by dehydration of the 6 beta-propar

27 l [(+/-)-7], into enantiomerically pure (+)-diacetate 8 and (-)-monoacetate 9.

28 symmetric allylic alkylation reaction of gem-diacetate 9 with azlactone 10.

29 omo isomers were isolated as the ring closed diacetates 9b and 11 by fractional crystallization.

30 r both FM4-64 and carboxydichlorofluorescein diacetate (a vacuolar luminal vital stain), had a pronou

31 4,5-diaminofluorescein diacetate, a cell-permeable fluorescent molecule, was us

32 Using dichlorofluorescein diacetate, a detector of endogenous oxidative stress, it

33 loromethyl-2',7'-dichlorodihydrofluorescence diacetate acetyl ester (CM-H(2)DCFDA) assay.

34 hloromethyl-2',7'-dichlorodihydrofluorescein diacetate, acetyl ester (CM-H2-DCFDA).

35 chlormethyl-2',7'-dichlorodihydrofluorescein diacetate, acetyl ester (CM-H2DCF-DA), and high levels p

36 loromethyl-2',7'-dichlorodihydrofluorescence diacetate, acetyl ester assay, respectively.

37 hloromethyl-2',7'-dichlorodihydrofluorescein diacetate, acetyl ester in preloaded neutrophils.

38 chloromethyl-2',7'-dichlorodihydrofluorescin diacetate, acetyl ester, in a concentration- and time-de

39 ndividual carotenoid molecules, while lutein diacetate aggregates resemble nematic liquid crystals.

40 sorption and CD spectra of lutein and lutein diacetate aggregates, which have previously been describ

41 In addition, the separated 2,4-diacetates also provide short access to all four anomeri

42 at were loaded with diaminofluorofluorescein diacetate, an intracellular fluorescence probe for NO, e

43 orescence microscopy with diaminofluorescein diacetate, an NO probe, and Fluo-3, a Ca(2+) probe.

44 ifferences in 2'7'dichlorodihydrofluorescein diacetate and 4,5-diaminofluorescein diacetate fluoresce

45 oxidative stress (2',7'-dichlorofluorescein-diacetate and Amplex Red analysis), and phagocytosis (St

46 fluorescent NO probe 4,5-diaminofluorescein diacetate and by the 2,3-diaminonaphthalene method.

47 determined using dichlorodihydrofluorescence diacetate and cytochrome c, were rapidly and significant

48 Only a few nanograms per liter of ethynodiol diacetate and desogestrel in water would be needed for f

49 mino,4-aminomethyl-2',7'-difluorofluorescein diacetate and diamino-rhodamine-4M, respectively.

50 oxidation of both dichlorodihydrofluorescein diacetate and dihydroethidium.

51 hloromethyl-2',7'-dichlorodihydrofluorescein diacetate and dihydrorhodamine 123, respectively.

52 oth the enantiotopic leaving groups of a gem-diacetate and enantiotopic faces of the enolate of an az

53 fluorescent probe 2',7'-dichlorofluorescein diacetate and flow cytometry.

54 l microbiota using 2',7'-dichlorofluorescein diacetate and flow cytometry.

55 e fluorescent probe 2',7'-dichlorofluorescin diacetate and laser-scanning confocal microscopy.

56 e 5, which upon treatment with iodosobenzene diacetate and magnesium oxide in the presence of a rhodi

57 mino-5-methylamino-2',7'-difluorofluorescein diacetate, and this effect was reversed by SR141716A.

58 Using dichlorodihydrofluorescein diacetate as a probe, we found that the NQO1 transfectan

59 bacterial esterase staining with fluorescein diacetate as well as colony-forming unit counts from inf

60 ed by a fluorescent 2',7'-dichlorofluorescin diacetate assay, and >85% reduction in HIF2-alpha mRNA a

61 totoxicity, 2',7'-dichlorodihydrofluorescein diacetate assay, and Western blot were used to investiga

62 duction determined by the dichlorofluorescin diacetate assay.

63 panetricarboxylate), or CDA (1,1-cyclohexane diacetate) at pH values between 7 and 8 yields baroresis

64 short, scalable syntheses of an L-iduronate diacetate C-4 acceptor, and also L-iduronate C-4 accepto

65 ye, carboxy-H(2)-dichloro-dihydrofluorescein diacetate (carboxy-H(2)-DCFDA), to determine whether ROS

66 5-(and 6)-carboxy-2',7'-dichlorofluorescein diacetate (CDCFDA).

67 ime-dependent decrease in carboxyfluorescein diacetate (CFDA) fluorescence was then quantitatively an

68 The fluorescent probes, carboxyfluorescein diacetate (CFDA) for cytoplasmic esterase activity and d

69 hloromethyl-2',7'-dichlorodihydrofluorescein diacetate (CM-H(2)DCFDA), spin-trap electron paramagneti

70 TC-GC) and carboxy-4',5'-dimethylfluorescein diacetate (CMFD), which are fluorescent substrates for t

71 the organic anion 5-chloromethylfluorescein diacetate (CMFDA) was reduced in KO hepatocytes, as well

72 effectively controlled by the chlorhexidine diacetate content and pH.

73 terium tuberculosis labeled with fluorescein diacetate could be accomplished rapidly by using flow cy

74 (6-amidoethyl)triphenylphosphonium Zinpyr-1 diacetate (DA-ZP1-TPP), is essentially nonfluorescent in

75 mino-5-methylamino-2',7'-difluorofluorescein diacetate (DAF) as a fluorescent NO-sensor that locates

76 fluorescent indicator 4,5-diaminofluorescein diacetate (DAF-2 DA) during stimulation of the cervical

77 cific fluorescent dye 4,5-diaminofluorescein diacetate (DAF-2 DA) were treated with lysophosphatidic

78 membrane-permeable dye diaminofluorescein-2/diacetate (DAF-2/DA) that, once intracellular, bound NO

79 NO detection system, 4,5-Diaminofluorescein diacetate (DAF-2/DA), for the direct detection of NO pro

80 itric oxide indicator 4,5-diaminofluorescein diacetate (DAF-2DA) specifically labels the bulbus arter

81 use of fura 2-AM and 4,5-diaminofluorescein diacetate (DAF-2DA), respectively, in microtissue strips

82 luorescence probe diaminodifluorofluorescein diacetate (DAF-FM DA), and the subsequent fluorescent DA

83 luorescence probe diaminodifluorofluorescein diacetate (DAF-FM DA), and the subsequent NO production

84 mino-5-methylamino-2',7'-difluorofluorescein diacetate (DAF-FM DA).

85 mino-5-methylamino-2',7'-difluorofluorescein diacetate (DAF-FM DA).

86 mino-5-methylamino-2',7'-difluorofluorescein diacetate (DAF-FM), we visualized NO production in indiv

87 ating SS-RBC with 2', 7'-Dichloro-fluroescin Diacetate (DCF)-labeled PMN.

88 cence microscopy of 2',7'-dichlorofluorescin diacetate (DCF)-loaded cells showed that IL-1alpha incre

89 epG2) were quantified by dichlorofluorescein diacetate (DCF-DA) dye assay, whereas changes in express

90 metry analysis using 2',7'-dichloroflorescin diacetate (DCF-diacetate).

91 es (ROS) with the use of dichlorofluorescein diacetate (DCFDA), dihydroethidium, and cerium chloride.

92 loromethyl-2',7'-dichlorodihydro-fluorescein diacetate (DCFdA).

93 on of intracellular 2',7'-dichlorofluorescin diacetate (DCFH) dye increased under 2% O(2), indicating

94 cal microscopy with 2',7'-dichlorofluorescin diacetate (DCFH) or using electron microscopy with ceriu

95 ing microscopy, using 2,7-dichlorofluorescin diacetate (DCFH-DA) as a probe.

96 cein AM assay, and 2',7'-dichlorofluorescein diacetate (DCFH-DA) was used to determine intracellular

97 ment procedures with compound 37 yielded the diacetate derivative 39.

98 uorescent probes (dichlorodihydrofluorescein diacetate, dihydroethidium, and MitoSOX Red) in conjunct

99 g the fluorescent probes dichlorofluorescein diacetate, dihydrorhodamine 123, and 2,3-diaminonapthale

100 acrocycle 1,4,7,10-tetraazacyclododecane-1,7-diacetate (DO2A) to the corresponding lanthanide aquo io

101 isting of 1,4,7,10-tetraazacyclododecane-1,7-diacetate (DO2A) was constructed with the goal of improv

102 sured with 2',7'-dicholorodihydrofluorescein diacetate dye assay.

103 was assayed using 2',7'-dichlorofluorescein diacetate dye, inducible nitric oxide synthase levels de

104 asured with 2',7'-dichlorodihydrofluorescein diacetate dye.

105 aldehydes in the presence of ethylenediamine diacetate (EDDA) is reported.

106 were measured with 2', 7'-dichlorofluorescin diacetate; emissions of the oxidized product were detect

107 ad Candida in the coculture with fluorescein diacetate (FDA) and propidium iodide (PI), respectively,

108 antituberculosis agents by using fluorescein diacetate (FDA) staining and flow cytometry.

109 assessed sputum microscopy with fluorescein diacetate (FDA, evaluating M. tuberculosis metabolic act

110 easured as an increase in dichlorofluorescin diacetate fluores-cence) and that similar changes were n

111 OI)-induced 2',7'-dichlorodihydrofluorescein diacetate fluorescence and Northern blot analysis of hem

112 rescein diacetate and 4,5-diaminofluorescein diacetate fluorescence levels.

113 mino-5-methylamino-2',7'-difluorofluorescein diacetate fluorescence mainly determined NO production,

114 mino,4-aminomethyl-2',7'-difluorofluorescein diacetate fluorescence originated from mitochondria.

115 R-stimulated increase in dichlorofluorescein diacetate fluorescence was abolished with catalase but r

116 ation, assessed from 2,7-dichlorofluorescein diacetate fluorescence.

117 ecies were measured with dichlorofluorescein diacetate fluorescence.

118 cells was labeled with tetra-methylrhodamine diacetate followed by the formation of tumor cell-neutro

119 mino-5-methylamino-2',7'-difluorofluorescein diacetate for NO activity in isolated mesenteric resista

120 ime ester (23d) with a polymer-bound iodosyl diacetate gave the spiroisoxazoline (24) and represents

121 assay and 2',7'-dicholorodihydrofluorescein diacetate (H(2)DCFDA) dye assay, respectively.

122 hloromethyl-2',7'-dichlorodihydrofluorescein diacetate (H(2)DCFDA) probe and flow cytometry.

123 etry using 2', 7'-dichlorodihydrofluorescein diacetate (H(2)DCFDA) showed an increase in oxidative st

124 xidation of 2',7'-dichlorodihydrofluorescein diacetate (H2DCFDA) by human 5-LOX.

125 e assay and 2',7'-dichlorodihydrofluorescein diacetate (H2DCFDA) dye assay, respectively.

126 -4H-pyrans was accomplished with iodobenzene diacetate (IBD) and N-chlorosuccinimide (NCS) reagents i

127 3), DDQ, CAN, [Cp(2)Fe][PF(6)], phenyliodine diacetate, IBX).

128 orescence of 2',7'-dihydrodichlorofluorescin diacetate in HAEC, an indicator of ROS production.

129 dant sensitive dye 2',7'-dichlorofluorescein diacetate in murine macrophage J774.1 cells.

130 nes from styrenes mediated by phenyliodonium diacetate in the presence of molecular oxygen and N-hydr

131 xidation-sensitive probe, dihydrofluorescein diacetate, indicating a shift in the intracellular redox

132 ellular activation of PKC with phorbol 12,13-diacetate induced a pharmacological potentiation of the

133 the fluorescent tracer 5-carboxyfluorescein diacetate into the cytoplasm, and quantified its interce

134 ocytes to metabolize and excrete fluorescein diacetate into visible bile canaliculi.

135 escence NO indicator (4,5-diaminofluorescein diacetate), intracellular NO was measured in the endothe

136 (-)-cryptocaryolone and (-)-cryptocaryolone diacetate is presented herein.

137 DCFH2-DA (2',7'-dichlorodihydrofluorescein diacetate) is the most widely used fluorogenic probe for

138 A fructose-derived diacetate ketone has been shown to be an effective catal

139 l-Glutamate-N,N-diacetate (L-GLDA) was recently introduced in the United

140 d chemiluminescence) and elevated NO (DAF-FM diacetate) levels in NOS1(-/-) myocytes.

141 quantitated by the 2',7'-dichlorofluorescein diacetate method.

142 S; mitosox red and 2',7'-dichlorofluorescein diacetate), NADPH, NADP(+) and ATP contents (spectrophot

143 doxybenzoate can be further converted to the diacetate or a bis(trifluoroacetate) derivative by treat

144 ns of a palladium catalyst and iodosobenzene diacetate or copper(II) salts, respectively, represent t

145 of hypervalent iodine reagents (phenyliodine diacetate or Dess-Martin periodinane) allows the rapid a

146 5-carboxyl group from 5-carboxy-fluorescein diacetate or from Oregon green diacetate or from Oregon

147 y-fluorescein diacetate or from Oregon green diacetate or from Oregon green diacetoxymethylester are

148 rwent oxidative cyclization with iodobenzene diacetate or iodosobenzene in the presence of Rh2(OAc)4,

149 rogen (OR, 2.7; 95% CI, 1.1-6.2), ethynodiol diacetate (OR, 2.6; 95% CI, 1.4-4.7), or triphasic dosin

150 cein diacetate, Oregon green carboxylic acid diacetate, or Calcein AM.

151 on using hydroethidine, dicarboxyfluorescein diacetate, or MitoSOX.

152 th the fluorogenic dyes - carboxyfluorescein diacetate, Oregon green carboxylic acid diacetate, or Ca

153 (1S,2S)-, or cis-1,2-diaminocyclohexane; X = diacetate, oxalate, malonate, methylmalonate, cyclobutan

154 nitric oxide [NO] via 4,5-diaminofluorescein diacetate oxidation).

155 sured by the rates of 2,7-dichlorofluorescin diacetate oxidation.

156 mixture dibutyryl cAMP (Bt(2)cAMP) + phorbol diacetate (PDA) stimulated the p38, c-jun NH(2)-terminal

157 al mixture (dibutyryl (Bt2)cAMP plus phorbol diacetate (PDA)) induces promoters I.3/II.

158 In control slices, Mg(2+) and phorbol 12,13-diacetate (PDAc), a protein kinase C activator, strongly

159 ions between anilide 1 and phenyliodine(III) diacetate (PIDA) through hypervalent iodine mediated C(s

160 For the initiator phenyliodine(III) diacetate (PIDA), voltammetric data demonstrate that the

161 nveniently constructed via phenyliodine(III) diacetate (PIDA)-mediated intramolecular oxidative annul

162 A phenyliodine(III) diacetate (PIDA)-mediated, highly efficient and tandem a

163 ene (PhIO) or the combination of iodobenzene diacetate (PIDA)/molecular iodine (I2), under mild react

164 xcitotoxicity was measured using fluorescein diacetate/propidium iodide (FDA/PI) cell viability assay

165 not affect islet viability (>90% fluorescein diacetate/propidium iodide) or the insulin secretion pro

166 tative viability microscopy with fluorescein diacetate, quantitative culture, and acid-fast auramine

167 Phorbol 12,13-diacetate reduced VEGF mRNA levels while down-regulating

168 nd 4-amino-5-methylamino-2',7'-difluorescein diacetate, respectively, using fluorescence microscopy.

169 s hydroethidine and 2',7'-dichlorofluorescin diacetate, respectively, were used to monitor the intrac

170 th the NO-imaging probe diaminofluorescein 2 diacetate revealed that UVA-induced NO release occurs in

171 attributed to the increase of chlorhexidine diacetate solubility at lower pH.

172 ative burst activity with dichlorofluorescin diacetate staining) and adhesion (integrin cell surface

173 Yet the reagent, carboxyfluorescein diacetate, still possesses a free carboxyl group whose i

174 se-catalyzed enzymatic desymmetrization of a diacetate substrate, 10, was employed as a key component

175 orbent spot (ELISpot) and carboxyfluorescein diacetate succinimide ester (CFSE) proliferation assays

176 Injection of carboxyfluorescein diacetate succinimide ester-labeled CTL demonstrated mar

177 donors were labeled with carboxy-fluorescein diacetate succinimidyl diester dye to enable high-resolu

178 cells were stained with carboxy-fluorescein diacetate succinimidyl ester (CFDA SE), after which imag

179 Platelets labeled with carboxyfluorescein diacetate succinimidyl ester (CFDASE) and leukocytes lab

180 n, and the generation of carboxy-fluorescein diacetate succinimidyl ester (CFSE) labeled CD4CD25FOXP3

181 strain, as determined by carboxyfluorescein diacetate succinimidyl ester (CFSE) labeling of the cell

182 lation was determined by carboxy-fluorescein diacetate succinimidyl ester (CFSE) staining and ELISA a

183 divided, as evaluated by carboxyfluoresccin diacetate succinimidyl ester (CFSE) staining.

184 e labeled with 5-(and 6-)-carboxyfluorescein diacetate succinimidyl ester (CFSE) to track cell divisi

185 uclear cells stained with carboxyfluorescein diacetate succinimidyl ester (CFSE) were cultured with B

186 metry after labeling with carboxyfluorescein diacetate succinimidyl ester (CFSE), dioctadecyl-tetrame

187 , or the fluorescent dye carboxy-fluorescein diacetate succinimidyl ester (CFSE), their division hist

188 ned migratory profiles of carboxyfluorescein diacetate succinimidyl ester (CFSE)-labeled T lymphocyte

189 Carboxyfluorescein diacetate succinimidyl ester (CFSE)-stained splenocytes

190 f alum adjuvant including carboxyfluorescein diacetate succinimidyl ester (CFSE).

191 fluorescent dye 5- and 6-carboxyfluorescein diacetate succinimidyl ester and bromodeoxyuridine incor

192 ll suppression assays and carboxyfluorescein diacetate succinimidyl ester assays were used to assess

193 r agonists were tested in carboxyfluorescein diacetate succinimidyl ester assays.

194 by flow cytometry using carboxy-fluorescein diacetate succinimidyl ester dye and cytometric bead arr

195 ured as proliferation by carboxy-fluorescein diacetate succinimidyl ester dye dilution and cytokine s

196 ration (thymidine uptake, carboxyfluorescein diacetate succinimidyl ester dye dilution) and cytotoxic

197 using the fluorescent dye carboxyfluorescein diacetate succinimidyl ester indicated that imatinib mes

198 ewis(BN) lymphocytes were carboxyfluorescein diacetate succinimidyl ester labeled and adoptively tran

199 iferation, as defined by 5-carboxyfluoresein diacetate succinimidyl ester labeling, or an increase in

200 n B was determined by the carboxyfluorescein diacetate succinimidyl ester measurement of division.

201 died by thymidine uptake, carboxyfluorescein diacetate succinimidyl ester staining, and Luminex techn

202 tion, the fluorescein dye carboxyfluorescein diacetate succinimidyl ester was used.

203 were dyed with CFDA-SE (carboxy fluorescein diacetate succinimidyl ester) and labeled with (131)I-io

204 nt marker CFSE (5-(and-6)-carboxyfluorescein diacetate succinimidyl ester) to track the mitotic recor

205 of the membrane-permeable dye, Oregon Green diacetate succinimidyl ester, and a membrane-permeable b

206 orescent label, 5-(and-6)-Carboxyfluorescein Diacetate Succinimidyl Ester, and size exclusion chromat

207 e-binding dye, 5-(and -6)-carboxyfluorescein diacetate succinimidyl ester, to allow a quantitative me

208 T cells were 5-(and-6-)-carboxyfluorescein diacetate succinimidyl ester- (CFSE) labeled to allow de

209 der cells was assessed in carboxyfluorescein diacetate succinimidyl ester-based assays.

210 plex class I typing, and carboxy-fluorescein diacetate succinimidyl ester-based mixed lymphocyte resp

211 ow cytometric analysis of carboxyfluorescein diacetate succinimidyl ester-labeled B cells costained f

212 of adoptively transferred carboxyfluorescein diacetate succinimidyl ester-labeled beta-cell antigen-s

213 Carboxyfluorescein-diacetate succinimidyl ester-labeled CBA/Ca strain CD8+

214 We generated carboxy-fluorescein diacetate succinimidyl ester-labeled CD4+CD25 high FOXP3

215 Transfer of 5,6-carboxyfluorescein diacetate succinimidyl ester-labeled donor cells showed

216 T-cells in recipients of carboxyfluorescein diacetate succinimidyl ester-labeled donor T-cell infusi

217 e experiments, 5- (and 6)-carboxyfluorescein diacetate succinimidyl ester-labeled human CD4+ T cells

218 Carboxyfluorescein diacetate succinimidyl ester-labeled human platelets wer

219 6 weeks postinfection), carboxy-fluorescein diacetate succinimidyl ester-labeled naive ovalbumin-spe

220 Phagocytosis of human carboxyfluorescein diacetate succinimidyl ester-labeled platelets by PAEC/P

221 d by adoptive transfer of carboxyfluorescein diacetate succinimidyl ester-labeled T cells across a pa

222 nt host mice by injecting carboxyfluorescein diacetate succinimidyl ester-labeled T cells into mice d

223 red by the retention of 5-carboxyfluorescein diacetate succinimidyl ester-labeled T cells on FLS mono

224 y transferred 5- (and -6)-carboxyfluorescein diacetate succinimidyl ester-labeled T cells.

225 oliferation capacities of carboxyfluorescein diacetate succinimidyl ester-positive lymphocytes from t

226 ine)- and CFSE [5-(and 6)-carboxyfluorescein diacetate succinimidyl ester]-labeled lymphocytes showed

227 on and labeled using 5(6)-carboxyfluorescein diacetate succinimidyl-ester (CMFSE).

228 5-(and-6)-carboxy-2',7'-dichlorofluorescein diacetate, succinimidyl ester "mixed isomers" (CCFSE) dy

229 hymidine (3H-TdR) uptake, carboxyfluorescein diacetate, succinimidyl ester (CFDA-SE) assays; the regu

230 ls labeled with 5-(and-6)-carboxyfluorescein diacetate, succinimidyl ester (CFSE) were adoptively tra

231 Adoptive transfer of carboxyfluorescein diacetate, succinimidyl ester (CFSE)-labeled naive CD4(+

232 d by adoptive transfer of carboxyfluorescein diacetate, succinimidyl ester-labeled TEa T cell recepto

233 Carboxyfluorescein diacetate, succinimidyl ester-labeled Tg361 cells were a

234 mononuclear cells using a carboxyfluorescein-diacetate-succinimidylester (CFSE) dilution assay.

235 d CFSE(bright) (5-(and-6)-carboxyfluorescein diacetate succinmidyl ester) (nondivided) and activation

236 hloromethyl-2',7'-dichlorodihydrofluorescein diacetate that arsenite induces, within 5 min after trea

237 n the synthesis blocked the N-acetate as a N-diacetate, the N-sulfonates as azido groups, and the ami

238 The esterase converted the diacetate to chloramphenicol, thus inhibiting spirochete

239 d by oxidation of dichlorodihydrofluorescein diacetate to dichlorofluorescein and hydroethidium to et

240 f cyclohexa-2,4-diene-1,2-diylbis(methylene) diacetate to various carbasugars is described.

241 stent to demonstrate delivery of fluorescein diacetate, using applied tension, to an ex vivo esophagu

242 The former diacetate was converted to the conformationally locked (

243 e fluorochrome probe 2'7'-dichlorofluorescin diacetate was used to measure cytosolic oxidant activity

244 ve fluorescent dye, 2',7'-dichlorofluorescin diacetate, was significantly elevated in TGF-alpha/c-myc

245 OS-sensitive probe 2',7'-dichlorofluorescein diacetate, we found that antisense suppression of AOX re

246 ratios of calcium fluoride to chlorhexidine diacetate were 8/2, 5/5, and 2/8.

247 and carboxylated dichlorodihydrofluorescein diacetate were used as probes to measure mitochondrial m

248 ared by an enzymatic asymmetrization of meso-diacetate with acetyl cholinesterase, radical cyclizatio