ライフサイエンスコーパス: final product

1 tion), or ethyl alcohol and isoamyl acetate (final product).

2 impact on the quality and production cost of final product.

3 roduct released from EncA to endocrocin as a final product.

4 rter culture reduced the bitter taste of the final product.

5 cies, which directly leads to a weakly bound final product.

6 he complex technology were measurable in the final product.

7 ps with double C-N/C-N bond formation to the final product.

8 teel products in Europe does not end up in a final product.

9 crambled and incorrectly folded forms in the final product.

10 ented graphene nanoribbons on Au(111) as the final product.

11 add sugar to adjust sensory deficits in the final product.

12 of anthocyanins if these remain rich in the final product.

13 s from purple wheat, and to characterize the final product.

14 ripened for 0, 1, 2, 4, and 8days, or in the final product.

15 relationship with physical properties of the final product.

16 in extrusion to enhance fibre content of the final product.

17 steps until a termination event produces the final product.

18 ty of N-ethyl-d-glucamine is retained in the final product.

19 drying methods depends on the purpose of the final product.

20 ntributed to the antioxidant activity of the final product.

21 ion strategies on their concentration in the final product.

22 dapted to the requirements and design of the final product.

23 asing behaviour and thus market value of the final product.

24 intramolecular proton transfer leads to the final product.

25 impact, and a clean, non-thermally-degraded final product.

26 thereby the shape or morphology taken by the final product.

27 Br(-)) as an intermediate and bromate as the final product.

28 ion vessel and 8 h to isolate and purify the final product.

29 s, requiring multiple steps to arrive to the final product.

30 chanism and kinetics lead to M-carbon as the final product.

31 amic selection of stable nanoclusters as the final product.

32 ation observed in the 6-deoxyerythronolide B final product.

33 in controlling the concave morphology of the final product.

34 d forms may not be completely removed in the final product.

35 igration and deprotonation that generate the final product.

36 which determined the stereochemistry of the final product.

37 ure the delivery of a dependable dose in the final product.

38 by donating a proton to the enol to give the final product.

39 traction protocols with the exception of the final product.

40 GMIB with trifluoroacetic acid delivered the final product.

41 degrade product quality, or contaminate the final product.

42 lting in the incorporation of a C-H into the final product.

43 ance genes, and human enteric viruses in the final product.

44 t without affecting the acceptability of the final product.

45 ations for the organoleptic qualities of the final product.

46 l changes occur affecting the quality of the final product.

47 operties, applications, economy, etc. of the final product.

48 lite cultivars with specific end-uses of the final product.

49 affects the chemical characteristics of the final product.

50 egy offers a comparable overall yield of the final product.

51 surprisingly, predicts that graphane is the final product.

52 n intermediate product, and chem158K, as the final product.

53 ms sustained PCE dechlorination to cDCE as a final product.

54 facile C-C reductive elimination to form the final product.

55 functioning to convert these precursors into final products.

56 of three adjacent stereogenic centers in the final products.

57 arbene and the naphthylcarbenes leads to the final products.

58 n process on the chemical composition of the final products.

59 ated into the target unsymmetrical thioether final products.

60 V) self-decay and produces Fe(III) and O2 as final products.

61 s converted into a set of unusually modified final products.

62 he intermediates is not required to form the final products.

63 pecies, which were hydrolyzed in situ to the final products.

64 p) leading to nitric oxide and citrulline as final products.

65 atly increasing the frequency of full-length final products.

66 lver cathode then catalyzes formation of the final products.

67 the crystal growth pathway and morphology of final products.

68 ins nor associated DNA can be present in the final products.

69 ed disulfides and dimerized peptide as major final products.

70 s in one assay with uniform abundance of the final products.

71 omerizes to form H(2)PO(4)(-) and GDP as the final products.

72 RIP processing of full-length substrates to final products.

73 texture and the structural properties of the final products.

74 simplifies the isolation of intermediate and final products.

75 intermediates along the reaction pathway to final products.

76 e the precursors of the mono- and bis-adduct final products.

77 e efficient to remove the urethanes from the final products.

78 sformed to C-Cl, C-Br, C-I, and C-O bonds in final products.

79 action yielded C1-C4 carboxylic acids as the final products.

80 ints during pre-harvest intervals and in the final products.

81 extract, thus imparting lower quality to the final products.

82 Q biosynthetic intermediate, as well as the final product (13)C(6)-coenzyme Q.

83 olase located in family GH105, producing the final product 4-deoxy-beta-l-threo-hex-4-enepyranosyl-ur

84 an antioxidant recovery rate of 89.8%, and a final product 4.75 times richer in the main antioxidants

85 is reaction proceeds through to the Ar-NO(2) final product, a four-electron oxidation, and produces -

86 termediate since it formed in advance of the final product A2E and was consumed as A2E accumulated.

87 In the final product, AA content was close to 300 ug kg(-1).

88 les, the reaction was more inhibited and the final product absorbed less light at 525 nm.

89 source and 100 +/- 4% of electrons into the final product (acetic acid) were achieved after developm

90 as the key intermediate, affording 4 as the final product after a second metal-mediated step.

91 f bisulfite to the ribose, and these are the final products after heating.

92 The final products, after etching the PS, generated a highly

93 f manufacture, starting material source, and final product, all critical forensic evidence.

94 improving the quality by design (QbD) of the final product and reducing manufacturing costs.

95 iels-Alder cycloadduct radical cation to the final product and reforms oxygen.

96 mation of the enzyme prior to release of the final product and reveals novel information regarding th

97 nt purification strategies to obtain a clean final product and thus avoid ambiguities in the source o

98 zed to link the required substituents in the final product and thus completing the total synthesis of

99 ovine breeds compromises the quality of the final product and undervalues the original PDO cheese.

100 set of inputs produced gluconic acid as the final product and yielded an acidic medium, lowering the

101 iform representation of all sequences in the final product and, in turn, enhances the quality of the

102 Both the final products and intermediates for each shape exhibit

103 des only chromatographic purification of the final products and is devoid of chromatography or crysta

104 (~39 Mt) produced each year never reaches a final product, and a detailed discussion of these high y

105 mics of the reactants, all intermediates and final products, and determined their reaction time scale

106 the efficient channeling of intermediates to final products, and if the means for sequestering natura

107 oying on the structure and morphology of the final products, and methods for promoting or preventing

108 product distribution covers about 90% of the final products, and we are able to discriminate between

109 Upon heating to 150 C, the final products are all converted to the remarkably stabl

110 The final products are in the bulk form with crystallite siz

111 In cell-free assays, the final products are markedly inhibitory against HIV RT an

112 More importantly, the final products are nanocrystals with controlled size and

113 urs can be conventionally processed, but the final products are not of acceptable quality.

114 The final products are of interest to chemical biology, with

115 lex facilitates NO oxidation to nitrite; the final products are the reduced heme and Cu(II)-nitrito c

116 judged by the antimicrobial activity of the final product, Arg(280) and Tyr(285) were not.

117 of this four-protein system and identify the final product as (1S,2R)-allocoronamic acid bound in thi

118 h a sequence of steps yields an FHDC for the final product as a function of the initial agonist conce

119 g a home-made tea cup), which represents the final product as ingested by the consumers.

120 sign play important roles in determining the final products, as revealed by atomic force microscopy i

121 which is epoxidized at C5-C6 by AsuE3 to the final product, asukamycin.

122 sis was used to couple the two halves of the final product at a late stage in the synthesis.

123 iable assessment of texture and taste of the final products based on the non-destructive fresh materi

124 hich spontaneously dehydrates to produce the final products, BChlide e or BChlide f The demonstration

125 gives the highest desaturation activity, the final products being phenanthrene (P1) and phenanthrene

126 ts on the impact of each brewing step on the final product, being also very useful for certification

127 th 20-fold less inhibitory activity than the final product BS.

128 he structure and composition not only of the final products but also of the intermediate steps of the

129 leucyl intermediate which is cyclized to the final product by KtzA without redox participation of the

130 ough enhances the nutritional aspects of the final product by the enrichment of several compounds wit

131 egy improved production of amorphadiene, the final product, by twofold over that from inducible or co

132 In this way, the final product can be out of the methane explosive range

133 uels and bulk chemicals, accumulation of the final product can negatively impact the cultivation of t

134 cine seed strains to the distribution of the final product can take several months.

135 hosphorane intermediate the formation of the final products can be accounted for by facile ethyl grou

136 ols for in-process monitoring as well as for final product characterization.

137 lectron transfer to regenerate Ni(I) and the final product CoBS-SCoM.

138 lanations for the increased stability of the final product complex and for its preferential recogniti

139 The final products contained more than 90% CD56(+) cells and

140 After separation, the final product contains greater than 90% fully functional

141 Moreover, the final product contains two consecutive stereogenic cente

142 nstead, the DNA is converted straight to the final products cut on both sides.

143 nating with the carbocation precursor to the final product cyclooctat-9-en-7-ol.

144 The structure of final products depended on the nature of the catalyst.

145 The composition of the final product depends on several factors, such as the fr

146 ion of a piperidinone or an enaminone as the final product depends on which of the two diastereotopic

147 intermediate is apparently converted to the final product, DIP, by an inositol monophosphatase-like

148 forming and breaking processes such that the final product distribution always reflects the thermodyn

149 and termination which might also affect the final product distribution.

150 Striped NPls were observed in the final products, due to stacking faults at the boundary b

151 y, were identified and the structures of the final products elucidated.

152 ions without compromising the quality of the final product, especially in semi-arid areas where irrig

153 ogen, and hydrogen were considered to be the final products for the other one.

154 scovering materials or understanding how the final products form.

155 share a common catalytic mechanism up to the final product formation step, and speculate on the roles

156 on intermediates that are on the pathways to final product formation, and they have identified a new

157 lineNMe(2), dimerization of this to give the final product, formation of the linear diborazane H(3)B.

158 ddition, the reactivity of 2-pyrones and the final products formed is shown to depend on the solvent

159 xyHb consumed over the concentrations of the final products formed.

160 val, 8.1 mg of pure hFGF21 was obtained as a final product from 500 mL of starting culture.

161 sterase that is responsible for removing the final product from the biosynthetic complex and a type I

162 In every case, the release of final products from resin is by a cyclitive cleavage pro

163 free amino group content and the presence of final products from the Maillard reaction.

164 97%, and the efficiency of conversion to the final product glycerol was 78% during the operational pe

165 The final products had a low energy value, ranging from 116

166 and unproductive polymer are removed, so the final product has more uniform binding characteristics.

167 On the level of hybrids, only the final product has to be purified by precipitation or chr

168 Demand for aluminum in final products has increased 30-fold since 1950 to 45 mi

169 ral important experimental parameters on the final products have been explored through systematic stu

170 ectron paramagnetic resonance to measure the final product Hb(II)NO.

171 Colorectal cancer cell cytotoxicities of the final products highlight the impact of the griseusin tet

172 raw material itself, and subsequently to the final products (i.e. pasta).

173 r 98%, respectively, of all particles in the final product, (iii) epithelial cell-tropic DB particles

174 to increase the structural complexity of the final product in a controllable and versatile manner.

175 impart increased enantiomeric excess to the final product in comparison with the analogous single tr

176 Interestingly, (90)Zr, daughter of (90)Y and final product in the decay sequence, is found to be unst

177 of doing so determining the position of the final product in the energy landscape.

178 tantaneous molecular weight confirmations of final products in drug discovery.

179 range of functional groups, and provides the final products in good to excellent yields.

180 rge size ketoenone substrates leading to the final products in high yields and providing excellent st

181 yrimidines 2'o with sodium azide, leading to final products in higher yields, that is, avoiding the i

182 nder Bronsted acid catalysis, giving rise to final products in moderate to good yields.

183 actions were straightforward, leading to the final products in reduced reaction times with improved y

184 Regulatory requirements for the final product include the removal of host cell proteins

185 Key steps to the final products include a Stobbe condensation to form the

186 The final product is a bulk hybrid ceramic-based material wh

187 the first committed step of a pathway by its final product is a classical means of controlling biosyn

188 Consequently, the nutritional value of the final product is compromised requiring double portion si

189 rmediate analogous to 5a (5a-i-DFT), and the final product is displaced from 5a-i-DFT by an associati

190 n the starting material on the colour of the final product is investigated.

191 course of brain development rather than the final product is most disturbed in autism.

192 where tens of grams to hundreds of grams of final product is needed.

193 t, at a 40% drug load, the section where the final product is produced, is situated earlier in the ba

194 nutritional status and that excretion of the final products is highly selective.

195 In both assimilation strategies, one of the final products is malate that is formed by the condensat

196 actants and solvents on the structure of the final products is presented.

197 onversion of intermediate adducts to the two final products is proposed to involve E2, S(N)2', and [2

198 The key step in the elaboration to the final products is the conversion of an intermediate olef

199 Since the salt represents around 4% of the final product, it will therefore strongly influence the

200 a soluble intermediate and then an insoluble final product magnesium iodide.

201 completely disappeared after 15 h, giving a final product mainly composed of monoacylglycerol ethers

202 The efficacy of the final product (MitoCEHC) to lower oxidative stress was t

203 epresents ATCase in the R state bound to the final product molecule, phosphate.

204 would then proceed stereoselectively to the final product obtained as a single diastereomer.

205 uences of construction intermediates and the final product of a gene synthesis project is a critical

206 sition to adenosine-5'-aldehyde as the major final product of aerobic photolysis as well as to adenos

207 pathway, without substantially changing the final product of aggregation.

208 itrifier denitrification pathway (N2O as the final product of AOB denitrification with NO2(-) as the

209 ting process, do not necessarily control the final product of Cr(VI) reduction.

210 oenzyme A, and the synthesis of taurine, the final product of cysteamine oxidation and the second mos

211 s(III) and methylarsenite (MAs[III]), with a final product of dimethylarsenate (DMAs[V]).

212 Indeed, the final product of HO activity in the mosquito midgut, AeB

213 Corticosterone, the final product of hypothalamic-pituitary-adrenal (HPA)-ax

214 ylation of the diacid leads to the pathway's final product of stipitatic acid.

215 assays and plant extracts indicate that the final product of the ALD1-catalyzed reaction is enaminic

216 ion and feedback inhibition by cysteine, the final product of the biosynthesis pathway.

217 poliovirus that are thought to represent the final product of the cell entry pathway.

218 Our results show that the final product of the coagulation cascade is a key determ

219 Even if the final product of the exchange, in both cases, was rock-s

220 spho-3-deoxy-D-manno-2-octulosonic acid, the final product of the Kdo biosynthesis pathway, with a Ki

221 bound structure prior to the release of this final product of the reaction.

222 Ultimately, the final product of these root-driven processes is CO(2), p

223 e drastic and unforeseen consequences in the final products of a reaction.

224 Platelets are the final products of megakaryocyte (MK) maturation.

225 The final products of PheCAP include a phenotype algorithm,

226 lysis control by which the structures of the final products of Pks15/1 are defined, and to scrutinize

227 ne T47D, we have shown that PGE2, one of the final products of the cyclooxygenase-2 (COX-2) pathway,

228 achidonic acid and docosahexaenoic acid, two final products of the enzyme, were reduced in the serum

229 rotaxanes by analyzing the intermediate and final products of various assembly routes by electrophor

230 because they alter the approach, but not the final product, of existing commercial products.

231 contents afterward provides knowledge of the final products only.

232 ructure characterization typically image the final product or laboriously determine the presence of i

233 es purification of neither intermediates nor final product other than extraction into and removal of

234 ible for downstream reactions leading to the final product, polyacyltrehalose (PAT), have not been id

235 vironmentally friendly methodologies and the final product presented acceptable sensory characteristi

236 Cyclooxygenases (COXs) and their final product, prostaglandin E2 (PGE2), are known to pla

237 terms of amino acid (AA) content affects the final product quality, once it is related to the vitalit

238 from the perspective of fish performance and final product quality.

239 on present in the solution with 13 gives the final product Qz.

240 This enrichment exhibited the largest NH2OH:final product ratio (1.92%), followed by N. multiformis

241 iency of this approach and the fact that the final product remains linked to a DNA sequence that full

242 lobal flows of aluminum from liquid metal to final products, revealing for the first time a complete

243 A Rh(I) complex of the final product, [Rh(P(i)Bu(3))(2){eta(2)-(H(2)BNMe(2))(2)

244 revious cooking events with bias towards the final product(s) cooked in the pot, and (3) absorbed lip

245 high throughput evaluation of in-process and final product samples.

246 The consumer acceptance (n=200) of final product showed the sensory scores in the range of

247 is that one construct can generate multiple final products, significantly streamlining the reagent g

248 Furthermore, periodate reactivity of the final product signifies acquisition of a ribose sugar wi

249 t they either are minimized or absent in the final product since their removal is somewhat difficult

250 hanism is proposed to explain the variety of final products starting with structurally very similar r

251 on of catalytic pathways was performed and a final product structure was found that is consistent wit

252 lylethers give different isomers of the same final products, suggesting that a metathetic cascade pat

253 1), 1711.8mgkg(-1) and 2959.2mgkg(-1) in the final product (T0), and after 1 (T1) and 3 (T3) months o

254 The final product takes an octahedral shape, with the surfac

255 truct to a CAR-signalling tail and named the final product TCR-CAR.

256 and fibers contribute to better maintain the final product texture.

257 Treated as a single final product, the rate of formation of the 5'-5' 1,4-GG

258 ound intermediate, its transformation to the final product, the regiochemical and eventual stereochem

259 The final product, the structure of which was confirmed by X

260 detected both assembly intermediates and the final product, the T=3 viral capsid, during reassembly o

261 vident from the structural complexity of the final products, the considerable scope, and the overall

262 As for final products, the highest T-2/HT-2 concentrations were

263 ating groups are often incorporated into the final products, these methods are generally not amenable

264 e latter compound (7) was transformed to the final product through a hydroxy dithioketal cyclization,

265 controls the absolute stereochemistry of the final product through a unique enantiodivergent design.

266 hylfurfural, which affect the quality of the final product through the degradation of the wine aromat

267 d hydroxylation to afford, respectively, the final products tirandamycin A (TirA) and tirandamycin B

268 potential to provide information linking the final products to a particular precursor by the manufact

269 tions in dough are poorly defined but affect final product usage.

270 ature and was cofactor-dependent because the final product was not detected by an anaerobic process.

271 containing 10 carbons and one oxygen of the final product was prepared in 98.6% ee and 39% yield fro

272 s extraction and their concentrations in the final product was validated.

273 of cyanide concentration, intermediates, and final products was analyzed in order to elucidate the re

274 The distribution of final products was controlled by the reaction between CO

275 The in vitro antioxidant activity of the final products was investigated.

276 nhibit their growth and its stability in the final products was proven.

277 he relative importance of these compounds to final product water quality, samples were collected from

278 of the precursor, two intermediates, and the final product were directly identified by the differenti

279 All stereocenters of the final product were established relative to the stereoche

280 The final products were obtained in high to almost quantitat

281 The final products were obtained in moderate to excellent ov

282 Selected final products were reasonably selective ALK5 kinase inh

283 CA) was developed; and all intermediates and final products were structurally confirmed using nuclear

284 nd purified by RP-HPLC; all intermediate and final products were verified by HPLC-MS and NMR analyses

285 n in the bakery chain, its raw materials and final products, were examined.

286 zoquinone, and absence of a labeled carbonyl final product when the reaction is performed in the pres

287 f the 8 biogenic amines were detected in the final products, which could serve as a safety guarantee

288 of the physical ion gels is preserved in the final product, while the tensile strength is increased b

289 ation products with the latter two being the final products, while glutathione sulphenic acid, glutat

290 rtant roles for minimizing mycotoxins in the final products, while the recipe formulation has an impa

291 tions of the H-bond network that lead to the final product, whose gamma-phosphate is not in the previ

292 ou create the first mock-up of a system, the final product will provide a better user experience.

293 orates the bromine activating group into the final product with concomitant borylation of the aryl ha

294 rols and total phenolics, thus originating a final product with enhanced functional properties.

295 gation of the variation of impurities in the final product with reaction time.

296 utomated synthetic strategy that yielded the final product with remarkable purity and molar activity.

297 ficiently by both TPST enzymes, leading to a final product with three sulfotyrosine residues.

298 improving the antioxidant properties of the final product, without changing the nutritional profile.

299 tical mechanistic questions that dictate the final product yields and isomorphic forms.

300 A-templated library synthesis that increases final product yields, simplifies the structure and prepa