ライフサイエンスコーパス: acetate

1 or GPR43 (the metabolite-sensing receptor of acetate).

2 to commercial white glue based on poly(vinyl acetate).

3 raction of a population initiating growth on acetate.

4 m hexanoate and 1-butyl-3-methyl-imidazolium acetate.

5 y(acrylic acid) hydrogels containing calcium acetate.

6 temperatures and are promoted by copper(II) acetate.

7 two alternative carbon sources, glucose and acetate.

8 plementation with the short-chain fatty acid acetate.

9 as glucose to fermentation products such as acetate.

10 ection of 2.50 g of all-rac-alpha-tocopheryl acetate.

11 trogenase isoform on succinate compared with acetate.

12 iet, or normal chow supplemented with sodium acetate.

13 is in solutions containing 0.01-1.0 M sodium acetate.

14 of 24 days, without formation of methane or acetate.

15 racene when applied before phorbol myristate acetate.

16 s, acetonitrile, acetone, toluene, and ethyl acetate.

17 necrosis factor-alpha, and phorbol myristate acetate.

18 vely for butanal, 2-phenyethanol and isoamyl acetate.

19 nd the Diels-Alder cycloaddition of a dienol acetate.

20 2)H(2)-labelled glucose and (2)H(3)-labelled acetate.

21 e being the common intermediate precursor of acetate.

22 dantly to prevent the accumulation of excess acetate.

23 rated an increase in the production of ethyl acetate.

24 erved in response to phorbol 12-myristate 13-acetate.

25 o D (9-12) are methyl 2,2-bis(1H-indol-3-yl) acetates.

26 ols and in six-member ring rearrangements of acetates.

27 his case, estradiol, 1 mg, and norethindrone acetate, 0.5 mg, once daily) in women with fibroid-assoc

28 pants concurrently used topical prednisolone acetate 1% 4x daily for 3 months, 3x daily for a month,

29 by measuring the (13)C polarization of ethyl acetate-1-(13)C, i.e., the product of pairwise addition

30 f pairwise addition of parahydrogen to vinyl acetate-1-(13)C, resulting from zero-crossing magnetic f

31 ndomly assigned (1:1) to receive abiraterone acetate (1000 mg) once daily orally plus prednisone (5 m

32 ection was found to be a mixture of ammonium acetate 2 mM/acetonitrile (60/40 ; v/v).

33 he wines contained a higher concentration of acetates (257 mg L(-1) to 547 mg L(-1)) and ethyl and me

34 The thiol content (3-sulfanylhexyl acetate (3SHA) and 3-sulfanylhexan-1-ol (3SH)) was usual

35 l metabolite galiellalactone (1) was, as its acetate 4, discovered to undergo a substitution reaction

36 Acetate, a precursor of acetyl coenzyme A (CoA) (a produ

37 signaling inhibitors (ARSi) like abiraterone acetate (Abi) and enzalutamide (Enza) or a functional dr

38 yst to a catalytically relevant Ni(II)(aryl) acetate acceptor was observed.

39 and eugenol, phenethyl alcohol, 2-phenethyl acetate, acetic, isobutyric, isovaleric, hexanoic and oc

40 rious carboxylate-directing groups including acetate, acrylates, pivalates, benzoate or its derivativ

41 bidopsis thaliana), two distinctly localized acetate-activating enzymes, ACETYL-COA SYNTHETASE (ACS)

42 -bioreduction following electron donor (e.g. acetate) addition.

43 g and pungent smell and taste, while isoamyl acetate adds intense 'fruity' and 'banana' odours.

44 ent ions of protonated monomers of alcohols, acetates, aldehydes, ketones, and ethers were produced i

45 and used as chiral auxiliary for asymmetric acetate aldol reaction to generate initial chirality in

46 r and ethanol prior to extraction with ethyl acetate, all MK-7 will be made accessible prior to analy

47 imines) to afford functionalized 2-pyridinyl acetates (alpha-pyridyl acetates) or teraryl motifs by a

48 Additionally, the pyrolysis of vitamin E acetate also produces carcinogen alkenes and benzene for

49 Here we show that alcohol and its metabolite acetate alter the functional state of T follicular helpe

50 flow rate and various electrolytes (ammonium acetate, ammonium bicarbonate, ammonium formate, and pip

51 ls were studied: (1) TAC-deoxycorticosterone acetate and (2) Lepr(db/db).

52 capillaries for complexes in 100 mM ammonium acetate and 100 mM triethylammonium acetate and for stre

53 penylbenzene markers (chavibetol, chavibetol acetate and 4-allyl-1,2-phenylene diacetate).

54 xibility to maintain physiological levels of acetate and a metabolic mechanism for the recovery of ca

55 sters when treated with stoichiometric allyl acetate and a palladium catalyst.

56 elated to the VOO off-flavor (ethanol, ethyl acetate and acetic acid) was also shown.

57 HILIC mobile phase contained 25 mM ammonium acetate and allowed identifying impurities at levels dow

58 imene, alpha- gurjnnene, germacrene-D, hexyl acetate and aromadendrene was the major constituents of

59 ot respond to structurally related molecules acetate and beta-hydroxybutyrate or cofactors NAD(+) and

60 sing lactate and the short-chain fatty acids acetate and butyrate and then alter transcription of col

61 amaldehyde, eugenol, caryophyllene, cinnamyl acetate and cinnamic acid are the major compounds found

62 Samples were extracted with ethyl acetate and cleaned up with primary secondary amine and

63 Plastid-localized ACS metabolizes cellular acetate and contributes to the de novo biosynthesis of f

64 ssociated with hyperaccumulation of cellular acetate and decreased accumulation of acetyl-CoA-derived

65 ammonium acetate and 100 mM triethylammonium acetate and for streptavidin in 200 mM ammonium acetate

66 of the selection of taxa adapted to grow on acetate and form aggregates.

67 Dp3sam with chloride, acetate and formate as counter ions were employed to stu

68 ally required metabolic changes required for acetate and glycerol cross feeding affect dozens of chem

69 ere we use metabolic modeling to ask whether acetate and glycerol cross-feeding are especially likely

70 same environment, but only cross-feeding of acetate and glycerol has been experimentally observed.

71 roduction of short chain fatty acids (mainly acetate and lactate) and favoring growth of the benefici

72 acilli effectively fermented MOS to generate acetate and propionate as main short chain fatty acids.

73 One bacterial functional capacity in the acetate and propionate biosynthesis pathway was identifi

74 One bacterial functional capacity in the acetate and propionate biosynthesis pathway was identifi

75 ial effects seem to be mediated by increased acetate and reduced TMA production by gut microbiota, th

76 caproate (55% of all carbon), as a result of acetate and subsequent n-butyrate elongation.

77 roducts of bacterial fermentation, including acetate and succinate.

78 Acetate and the related metabolism of acetyl-coenzyme A

79 a condensation reaction between progesterone acetate and thiosemicarbazone hydrochloride.

80 on of 2-(4-oxo-2-thioxothiazolidin-5-ylidene)acetates and alpha,alpha-dicyanoolefines under ultrasoun

81 methyl, cyclopentyl methyl, benzyl, phenyl, acetate, and acetamide groups, which smoothly produced t

82 els of high-density lipoprotein cholesterol, acetate, and apolipoprotein A1 were associated with incr

83 lose (MC) core with anthocyanidin and sodium acetate, and chitosan/gallotannin-based shell.

84 on from a mixed substrate (lactose, lactate, acetate, and ethanol).

85 ts, incubated them with labeled palmitate or acetate, and measured production of TCA cycle metabolite

86 e carbon sources included methanol, ethanol, acetate, and their ternary mixture.

87 the IFN-1 receptor (IFNAR) was essential for acetate antiviral activity in pulmonary epithelial cell

88 er CO(2)-derived substrates, wheat straw and acetate, are also demonstrated to be effective in produc

89 tailor-made for each targeted metal) and one acetate arm arranged in a dissymmetrical manner, have be

90 The reaction is carried out in ethyl acetate as a solvent.

91 The reaction utilizes Cu(II) acetate as an environmentally benign catalyst in combina

92 atic/heteroaromatic aldehydes using ammonium acetate as an ideal promoter under neat conditions, whic

93 Using methylene green and thionine acetate as redox mediators and myoglobin as the analyte,

94 ial cerebral spinal fluid (aCSF) using ethyl acetate as the extraction phase.

95 oxazole derivatives from catechols, ammonium acetate as the nitrogen source, and aldehydes (nontoxic

96 to their higher total content of esters and acetates, as well as a greater colour intensity due to a

97 ABA-glucose ester (ABA-GE) and low indole-3-acetate aspartate (IAA-Asp) and isopentenyladenine (iP)

98 ions were effectively avoided using ammonium acetate at ionic strengths above 0.1 M.

99 For example, in the presence of ammonium acetate, at low flow rates, lower charge states of prote

100 ion of two unexpected catalytic cycles, with acetate being only the precatalyst.

101 labeled with DOTATATE by heating in a sodium acetate buffer and 4-(2-hydroxyethyl)-1-piperazineethane

102 liquid chromatography solvent with (14)NH(3)-acetate buffer and in solvent with the buffer modified w

103 dium chloride, gallic acid and pH 5.0 sodium acetate buffer system.

104 orts growth as fast as the Mo-nitrogenase on acetate but not on the more oxidized substrate succinate

105 These protective effects were mimicked by acetate, but not by butyrate supplementation.

106 chamber stiffness in TAC-deoxycorticosterone acetate, but not in Lepr(db/db) mice.

107 l biological product norcarnitine as well as acetate, butyrate, and caproate.

108 Important metabolites such as acetate, butyrate, and propionate are generated at relat

109 Dietary fructose is converted to acetate by the gut microbiota(9), and this supplies lipo

110 Ethyl acetate can be defined a green and bio-based solvent.

111 ted equine estrogens and medroxyprogesterone acetate (CEE+MPA) resulted in increased risk of coronary

112 en the weak Lewis acid tetra-n-butylammonium acetate (CH(3) COOTBA) and P atoms promotes the average

113 CPM-107 contains Mg(2) -acetate chains crosslinked into a 3D net by terephthalat

114 f the gene encoding butyryl-coenzyme A (CoA):acetate-CoA-transferase, a major enzyme in butyrate meta

115 From baseline, serum acetate concentrations were increased by the Prot (beta:

116 The diene methyl ethers or acetates, constructed from the Li-Br exchange/addition r

117 ethanol content, acetaldehyde content, ethyl acetate content and higher alcohols content were evaluat

118 age in hepatocytes and microorganism-derived acetate contribute to lipogenesis.

119 found in ethanol, cyclopentanone, and methyl acetate; conversely, an alpha-diisobutylene and methyl f

120 e is essential for antibody binding, while O-acetate could be equally accommodated at three and four

121 rious methoxylated benzannulated cyclononene acetates could be employed as substrates.

122 de, chloride, trifluoromethyl, ester, nitro, acetate, cyanide, and ether groups.

123 l concentrations demonstrate the activity of acetate-degrading hyperthermophiles.

124 nocytic THP-1 cells, phorbol 12-myristate 13-acetate-differentiated human macrophages, and aortic smo

125 s in THP-1 cells and phorbol-12-myristate-13-acetate-differentiated macrophages in response to lipopo

126 Depot medroxyprogesterone acetate (DMPA) and vaginal dysbiosis have been implicate

127 harmacokinetics of depot medroxyprogesterone acetate (DMPA) are unknown.

128 able contraceptive depot medroxyprogesterone acetate (DMPA) is associated with bone mineral density l

129 onal contraceptive depot medroxyprogesterone acetate (DMPA) may be associated with an increased risk

130 ) or injectable (interferon-beta, glatiramer acetate) DMTs.

131 ethyl Ester (L-NAME) and Deoxycorticosterone Acetate (DOCA) rat models.

132 ttenuate hypertension in deoxycorticosterone acetate (DOCA)-salt rats, a renin-independent model of h

133 ted the role of CXCR6 in deoxycorticosterone acetate (DOCA)/salt-induced inflammation and fibrosis of

134 cane, nonanoic acid, 2-(2-butoxyethoxy)ethyl acetate, (E)-2-undecanal and (S)-germacrene D, were iden

135 crystal structure of AbyA5, the first of an acetate-eliminating enzyme, reveals a deviant acetyl est

136 Mechanistically, we show that acetate enhances innate immune responses by acting on bo

137 mercaptans, 3-mercaptohexanol (3MH) and its acetate ester (3MHA), were seen in the wines.

138 tal ciders), 2-phenylethanol, and some minor acetate esters (higher in the bi-varietal ciders).

139 the presence of specific volatiles (such as acetate esters and higher alcohols) may be indicative of

140 es, from aryl carboxylates (e.g., pivalates, acetates, etc.), aryl carbamates and carbonates, to aryl

141 PX and acetaldehyde diethyl acetal, isobutyl acetate, ethyl isovalerate and guaiacol for CRE.

142 mpare the biological activities of the ethyl acetate (EtOAc), methanolic (MeOH) and aqueous extracts

143 Allograft mice receiving supplemental sodium acetate exhibited similar protection from rejection, and

144 higher in butanol extract, whereas the ethyl acetate extract had the highest inhibitory effect on hea

145 total flavonoid content were found in ethyl acetate extract, methanol extract possessed the stronges

146 ipid radicals were measured ex situ in ethyl acetate extracts of model systems and extrudates by the

147 Interestingly, CFS and crude ethyl acetate extracts of PUFSTP35 (Bacillus licheniformis KT9

148 domized to 0.1% nepafenac or 1% prednisolone acetate eye drops in both eyes.

149 However, concomitant administration of acetate fails to fully revert the increase in autophagy

150 odic electroactive biofilms (EABs) formed by acetate-fed microbial communities.

151 genic genes, and the generation of microbial acetate feeds lipogenic pools of acetyl-CoA.

152 promotes the release of IL-1beta; in ILC3s, acetate-FFAR2 augments expression of the IL-1 receptor,

153 In neutrophils, acetate-FFAR2 signaling accelerates their recruitment to

154 nd filtration), or ethyl alcohol and isoamyl acetate (final product).

155 n of the desired products using DCM or ethyl acetate, followed by subjecting the recovered aqueous so

156 ies, likely providing growth substrate (e.g. acetate) for the hgcA-carrying microorganisms responsibl

157 ed DOCA-salt-butyrate, and treated DOCA-salt-acetate, for 5 weeks.

158 The ethyl acetate fraction inhibited in vitro alpha-glucosidase (p

159 This study was designed to investigate ethyl acetate fraction of Chinese olive fruit extract (CO-EtOA

160 we demonstrate the twin metabolic origins of acetate from the oxidation of ethanol and the nonoxidati

161 arbohydrates, oxoacetonitriles, and ammonium acetate gave densely functionalized pyrroles in 75-96% y

162 the current study was to fabricate Cellulose Acetate/Gelatin (CA/Gel) electrospun mat loaded with ber

163 rophilic intermediate by water generated via acetate group participation during [3,3]-acyloxy rearran

164 study has shown that the vaping of vitamin E acetate has the potential to produce exceptionally toxic

165 was carried out using supersaturated sodium acetate heat packs and results compared to those using a

166 chromatin acts as an important reservoir of acetate in cancer cells.

167 art and leg consumed ketones, glutamate, and acetate in direct proportionality to circulating levels,

168 Thus, the activation of acetate in distinct subcellular compartments provides pl

169 cose in freshwater, anaerobic respiration of acetate in marine sediment, hydrogenotrophic methanogene

170 in transesterification of geraniol and vinyl acetate in the gas phase and maintains the initial activ

171 The formed acetate in turn stimulated straight chain elongation, bu

172 r, relative to ammonium formate and ammonium acetate in water-rich methanol modifier, the ammonium hy

173 aqueous solvents sodium hydroxide and sodium acetate, in contrast to conventional isocratic elution,

174 Phorbol-myristate-acetate-induced formation of neutrophil extracellular tr

175 erplasia during 12-O-tetradecanoylphorbol-13-acetate-induced inflammation.

176 Propionate and butyrate, but not acetate, inhibited IgE- and non-IgE-mediated human or mo

177 The acetate-initiated aliphatic isocyanate trimerization to

178 -localized ACN1 enables the incorporation of acetate into organic acids and amino acids.

179 us using isotopic labeling with 1-(13) C(1) -acetate intravenous infusion, followed by measurement of

180 different chemical ionization methods, i.e., acetate-ion-based (CH(3)COO(-)) and aminium-ion-based (n

181 g ex vivo stimulation with phorbol myristate acetate/ionomycin, PSC patients showed significantly inc

182 w concentrations of fluoride, carbonate, and acetate ions, weakly to phosphate ions, but not to the o

183 diate that is critically stabilized by added acetate ions.

184 Conversion from pyruvate to acetate is activated under hypoxic conditions, and ACS r

185 We found that administration of acetate is remarkably beneficial in ameliorating disease

186 At acidic pH, a planar triangular molecule (acetate) is present in the SBC.

187 ate, ethyl butanoate, ethyl octanoate, ethyl acetate, isoamyl acetate, isobutanol, 2-methyl-1-butanol

188 ate, ethyl octanoate, ethyl acetate, isoamyl acetate, isobutanol, 2-methyl-1-butanol, 2-phenylethanol

189 : no denaturation was induced using ammonium acetate (kosmotropic), whereas ammonium formate and bica

190 e(III) reduction rates were also higher with acetate/lactate (0.53 mg Fe(II) in 6 days) than with OMS

191 eduction after 100 days was the highest with acetate/lactate (43 +/- 3.5% of total Fe present in the

192 RNA amplicon sequence analyses revealed that acetate/lactate mainly enriched Geobacter, while in situ

193 tially more dissolved As was detected in the acetate/lactate setups, after 100 days, higher concentra

194 l Fe(III) reduction than highly bioavailable acetate/lactate, it ultimately has the potential to mobi

195 ed in OMC and OMS, respectively, compared to acetate/lactate-amended setups (6.3 +/- 0.7 mug As/L).

196 etate-producing bacterial population and gut acetate levels, improved colonic integrity, normalized e

197 ess of TBA and the reaction with the formate/acetate ligands bound within the pores, whereas the larg

198 However, after removal of the formate and acetate ligands by reaction with methanol to form esters

199 node OH groups are formed as formate and/or acetate ligands present initially on the nodes react wit

200 mammary tumors driven by medroxyprogesterone acetate (M) and 7,12-dimethylbenz[a]anthracene (D) recap

201 ld type rats, we used the methylzoxymethanol acetate (MAM) model to determine whether POM may indirec

202 Oral administration of acetate mediated interferon-beta (IFN-beta) response by

203 activity of neighbouring adipocytes through acetate-mediated modulation of their thermogenic capacit

204 ocytes isolated from TAC-deoxycorticosterone acetate mice.

205 chamber stiffness in TAC-deoxycorticosterone acetate mice.

206 ndent with best performance for alcohols and acetates, moderate performance for ketones, and worst pe

207 gh-fiber diet or supplementation with sodium acetate modified alloimmunity in a kidney transplant mod

208 ties of bis (1,10-phenanthroline) silver (I) acetate monohydrate (Ag-Phen), toward A549 lung cancer c

209 tradiol +/- 10(-7) mol/L medroxyprogesterone acetate (MPA) +/- 1 IU/mL thrombin pretreatment for 4 ho

210 hese same estrogens plus medroxyprogesterone acetate (MPA) among participants with an intact uterus w

211 n (CEE) plus 2.5 mg/d of medroxyprogesterone acetate (MPA) and 8102, placebo.

212 esized that clearance of medroxyprogesterone acetate (MPA) would increase when given with rifampicin

213 ACETYL-COA SYNTHETASE (ACS) in plastids and ACETATE NON-UTILIZING1 (ACN1) in peroxisomes, function r

214 le starting materials, Morita-Baylis-Hillman acetates of acetylenic aldehydes as C4 synthons, and sim

215 a-derived metabolite, short-chain fatty acid acetate, on an acute mouse model of CDI.

216 rates, while on the inferior carbon source (acetate) only a small fraction of the population manages

217 noids derived from double-knockout mice with acetate or dichloroacetate restored stem cells.

218 nt amine incorporation using either ammonium acetate or HMDS.

219 ond axial position using an innocent ligand (acetate or hydroxyl) to prepare dual-action and triple-a

220 mmation induced by topical phorbol myristate acetate or imiquimod, reduced the inflammation from eryt

221 For either dietary Pb source (Pb acetate or NIST SRM 2710a), low dietary P level markedly

222 g activity was sensitive to addition of zinc acetate or the zinc chelators 1,10-o-phenanthroline and

223 onalized 2-pyridinyl acetates (alpha-pyridyl acetates) or teraryl motifs by a simple Lewis base switc

224 t-butyl nitrone (PBN) bearing a hydroxyl, an acetate, or an acetamide substituent on the N-tert-butyl

225 t diet amended with Pb as a soluble salt, Pb acetate, or in a soil matrix (NIST SRM 2710a).

226 nd its enzymatic cost, while growth rate and acetate overflow were accurately simulated for two E. co

227 ensis and one, or several, of the syntrophic acetate oxidizers Syntrophaceticus schinkii, [ Clostridi

228 Following addition of sodium 1-(13) C-acetate, parahydrogen bubbling within a microtesla magne

229 isted dissociation of the trimeric palladium acetate [Pd(3)(OAc)(6)] is found to be crucial for these

230 al efficiency (MEE) were measured with (11)C-acetate PET/CT.

231 to polyethylene terephthalate-ethylene vinyl acetate (PET-EVA) substrates by a temperature-driven app

232 Using a mobile phase of 0.2 M ammonium acetate (pH 6.9), several proteins (i.e., myoglobin, car

233 nd at a potential of about 1.1 V in ammonium acetate (pH 7.0) and 1.25 V in ammonium hydrogen carbona

234 or C-S bond cleavage, affording 2-pyridinyl acetates, Ph(3)P-catalyzed [4 + 2] annulation leads to f

235 easure several priority toxicants: vitamin E acetate, plant oils, medium-chain triglyceride oil, coco

236 deaths (275 [46%] of 597 in the abiraterone acetate plus prednisone group and 343 [57%] of 602 in th

237 aemia (four [1%] patients in the abiraterone acetate plus prednisone group and none in the other grou

238 e hypertension (125 [21%] in the abiraterone acetate plus prednisone group vs 60 [10%] in the placebo

239 5 mg) once daily orally and ADT (abiraterone acetate plus prednisone group) or matching placebos plus

240 The combination of abiraterone acetate plus prednisone with ADT was associated with sig

241 who crossed over from placebo to abiraterone acetate plus prednisone) and hypokalaemia (70 [12%] vs t

242 were activated with phorbol-12-myristate-13-acetate (PMA) and differentiated into M1 macrophages wit

243 Ionomycin and phorbol 12-myristate 13 acetate (PMA) are used to trigger NETosis.

244 potent PKC activator phorbol 12-myristate 13-acetate (PMA) at 10 nM concentration reduced the intensi

245 toxicity induced by phorbol 12-myristate 13-acetate (PMA) more effectively than SOPD-NAC and several

246 PKC activation using phorbol 12-myristate 13-acetate (PMA) on hERG channels expressed in human embryo

247 entiated in vitro by phorbol-12-myristate-13-acetate (PMA) treatment to produce platelet-like-particl

248 ivation of NF-kappaB2 with phorbol myristate acetate (PMA) upregulated fermentative glycolysis and in

249 ed in suppression of phorbol 12-myristate 13-acetate (PMA)/ionomycin-driven activation of a luciferas

250 d carbonic anhydrase activity (p-nitrophenyl acetate, pNPA) is effectively ablated.

251 tivation of PKC with phorbol-12-myristate-13-acetate potentiated the Ci-VSP-induced decline in Kv7.5

252 patic ACSS2, which generates acetyl-CoA from acetate, potently suppresses the conversion of bolus fru

253 cohols using fluoride or silanolate, allylic acetate precursors to 5-membered rings display distinct

254 dition of three equivalents of isocyanate to acetate prior to product formation, we found that the un

255 BFM increased acetate-producing bacterial population and gut acetate l

256 urther improvements could be achieved if the acetate-producing EEO was minimized and limitations of e

257 We conclude that microbiota-derived acetate promotes host innate responses to C. difficile t

258 elial cells and 12-O-tetradecanoylphorbol-13-acetate promotes the outgrowth of these cells, we found

259 Short chain fatty acids (SCFAs; e.g., acetate, propionate, and butyrate) are produced by micro

260 e, we investigated the effects of the SCFAs (acetate, propionate, and butyrate) on mast cell-mediated

261 pulmonary epithelial cell lines and for the acetate protective effect in RSV-infected mice.

262 Using the MAM (methylazoxymethanol acetate) rat model of schizophrenia and saline-treated c

263 ned a large collection of nonphotosynthetic (acetate-requiring) DNA insertional mutants of Chlamydomo

264 of fast exchange with respect to the (13) C acetate resonance, but we find that relaxation dynamics

265 llylic alkylation of trans-1,3-diphenylallyl acetate revealed a stepwise increase/decrease in ee, wit

266 II (angiotensin II) and deoxycorticosterone acetate-salt induced hypertension.

267 sized and converted into their corresponding acetate salts (compounds 11, 12, and 13).

268 s that performed similarly to ethylene-vinyl acetate shoe materials in quasi-static loading.

269 s validated in terms of specificity (methoxy/acetate signal), linearity (range 0.05-5.00 mg per assay

270 In trimethylammonium acetate solutions and in soft source conditions, the pro

271 ic repeat (CRISPR)-mediated gene editing and acetate supplementation of the culture media.

272 Interestingly, acetate supplementation rescues both histone acetylation

273 hain elongation, but the resulting lower net acetate supply rate towards straight chain elongation le

274 Photolysis of trenbolone acetate (TBA) metabolites in the presence of various nit

275 vious literature, we hypothesized that serum acetate, the main SCFA in circulation, increases on all

276 faster growth based on the V-nitrogenase on acetate, the wild-type strain uses exclusively the Mo-ni

277 TORC2 in promoting acetyl-CoA synthesis from acetate through acetyl-CoA synthetase 2 (ACSS2).

278 hyl 2-[2,3,4-trimethoxy-6-(1-octanoyl)phenyl]acetate (TMPA), and three high-throughput screening hit

279 yltropiporphyrins reacted with palladium(II) acetate to give stable palladium(II) complexes, demonstr

280 1), and butyrate and ammonia outputs and the acetate to propionate ratio were decreased (P < 0.001) w

281 The contribution of labeled palmitate or acetate to the TCA cycle was reduced in organoids derive

282 en promoted by 12-O-tetradecanoyl-phorbol-13-acetate (TPA).

283 nz[a]anthracene/12-O-tetradecanoylphorbol-13-acetate two-stage skin carcinogenesis mouse model.

284 e best staining was achieved with the uranyl acetate (UA) solution, which has been the election metho

285 Butanal and isoamyl acetate underwent metabolic reactions, which decreased t

286 tion, which improved delta(u) for release of acetate up to 7-fold, while retaining all the other exce

287 progesterone receptor modulator, ulipristal acetate (UPA), as a potential treatment for PMDD.

288 n (FldA) from Methanosarcina acetivorans, an acetate-utilizing methane-producing microbe of the domai

289 Vitamin E acetate (VEA) has recently been identified as a potentia

290 "direct" (13) C hyperpolarization of (13) C-acetate via signal amplification by reversible exchange

291 Vitamin E acetate was associated with EVALI in a convenience sampl

292 Vitamin E acetate was identified in BAL fluid obtained from 48 of

293 compounds (butanal, 2-phenyethanol, isoamyl acetate) was studied from a liquid medium into the coffe

294 n order from parahydrogen to (13) C spins of acetate weakly bound to the catalyst, under conditions o

295 Increases in acetate were associated with decreases in insulin and gl

296 (human) in aqueous solution (150 mM ammonium acetate) were investigated using a variable temperature

297 hy plasticity induced by the odorant geranyl acetate (which is attractive) shows no CP although it in

298 tment with the zonulin antagonist larazotide acetate, which specifically increases intestinal barrier

299 tate and for streptavidin in 200 mM ammonium acetate with no charge reduction.

300 ction of beta-ketosulfones with nitroallylic acetates yields tetrasubstituted sulfonyl furans through