ライフサイエンスコーパス: final product

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

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

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

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

5 steps until a termination event produces the final product.

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

7 ntributed to the antioxidant activity of the final product.

8 ion strategies on their concentration in the final product.

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

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

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

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

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

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

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

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

17 amic selection of stable nanoclusters as the final product.

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

19 in controlling the concave morphology of the final product.

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

21 igration and deprotonation that generate the final product.

22 which determined the stereochemistry of the final product.

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

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

25 traction protocols with the exception of the final product.

26 GMIB with trifluoroacetic acid delivered the final product.

27 de specific combinations of chirality in the final product.

28 dox event to release triplet dioxygen as the final product.

29 surprisingly, predicts that graphane is the final product.

30 e pattern of the side chain structure of the final product.

31 onservation and partial cDNAs to predict the final product.

32 g a late transition state that resembles the final product.

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

34 hable steps to produce Fe(3+)Fbp(PO(4)) as a final product.

35 is the frequency at which errors pervade the final product.

36 of S-[6-xH]H4F with formaldehyde to form the final product.

37 ons and paramagnetic particles to purify the final product.

38 enone, displacing the first GSH to give the final product.

39 on) to increase the complexity of the mature final product.

40 ophenol only to 2,6-dichloro-p-quinol as the final product.

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

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

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

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

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

46 he complex technology were measurable in the final product.

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

48 crambled and incorrectly folded forms in the final product.

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

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

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

52 ated into the target unsymmetrical thioether final products.

53 intermediates along the reaction pathway to final products.

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

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

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

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

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

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

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

61 lver cathode then catalyzes formation of the final products.

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

63 the crystal growth pathway and morphology of final products.

64 ed disulfides and dimerized peptide as major final products.

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

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

67 UV-observable diphenylalkyl radicals as the final products.

68 zymatic steps between initial substrates and final products.

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

70 ng a gapped circle and a displaced strand as final products.

71 s were used to prepare key intermediates and final products.

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

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

74 functioning to convert these precursors into final products.

75 of three adjacent stereogenic centers in the final products.

76 arbene and the naphthylcarbenes leads to the final products.

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

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

79 Neither of the final products (1a,b) matched the natural substance by T

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

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

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

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

84 both the initial substrate, CTFbeta, and the final product, Abeta40/42, of gamma-secretase.

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

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

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

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

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

90 -fold increase in the rate of release of the final product, an AP-site with a 3'-nick, and that it do

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

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

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

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

95 to precisely define the stoichiometry of the final product and to ensure that atomic-scale diffusion

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

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

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

99 Both the final products and intermediates for each shape exhibit

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

101 offers the advantages of facile isolation of final products and monosubstitution of unprotected nucle

102 (~39 Mt) produced each year never reaches a final product, and a detailed discussion of these high y

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

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

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

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

107 and subsequent oxidation to form the +30 Da final product are catalyzed by the heme cofactor, most p

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

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

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

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

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

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

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

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

116 zyme, as well as the subsequent formation of final product as a function of time.

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

118 astereomeric/enantiomeric composition of the final product as well as to identify any remaining E/Z i

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

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

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

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

123 tion of dioxygen at E(1/2) = 0.38 V with the final products being an approximate 50% mixture of H(2)O

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

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

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

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

128 ts which are stable or decompose to give the final products by two different pathways.

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

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

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

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

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

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

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

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

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

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

139 Moreover, the final product contains two consecutive stereogenic cente

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

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

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

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

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

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

146 The final product emerges in yields of 12.5% and 20.3% from

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

148 phosphine from the site trans to Si, but the final product, fac-(PMe(3))(3)Ru(SiR(3))H(3) (SiR(3) = S

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

150 scovering materials or understanding how the final products form.

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

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

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

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

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

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

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

158 97%, and the efficiency of conversion to the final product glycerol was 78% during the operational pe

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

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

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

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

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

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

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

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

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

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

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

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

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

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

173 structural intermediate in activation, and a final product, in which the anaphylatoxin domain has und

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

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

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

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

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

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

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

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

182 The final product is precipitated and washed, and the radioa

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

184 e carbinolamine (or gem-diamine) to give the final product is the rate-determining step in this syste

185 The most likely path to the final products is found to be via oxidation of Pd(HSO4)(

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

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

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

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

190 FAS coupled system, [(3)H]palmitic acid, the final product, is readily detected by scintillation prox

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

192 s starting from small synthetic templates to final product lengths of several hundreds to thousands o

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

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

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

196 roduct from both starting materials, and the final product mixture reflects, in part, coupling of met

197 oreover, separation of the diastereoisomeric final product mixture shows a different cytostatic activ

198 The final product mixture was composed of two atropisomeric

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

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

201 sed to explain the diastereomer ratio in the final products obtained via the oxathiaphospholane appro

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

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

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

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

206 could be restored if prostaglandin E(2), the final product of COX-2 activity, was added simultaneousl

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

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

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

210 oxidation, oxazolone appears to be a stable final product of guanine oxidation, and, if formed in vi

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

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

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

214 The final product of the assembly reaction is a bi-dodecamer

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

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

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

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

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

220 e ATIC convert the intermediate AICAR to the final product of the pathway, IMP.

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

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

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

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

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

230 four fragments simultaneously (for a 10.8 kb final product), offering an additional improvement on th

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 The final product QH(2) is higher in energy at the proximal

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

239 nutrients can reduce desired yields or alter final product quality.

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

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

242 t viscosity on the kcat values suggests that final product release is rate-limiting in the wild-type

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

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

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

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

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

248 ctive, with the alpha and beta groups in the final product showing a strong preference for the trans

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

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

255 of isobutane to produce the C-O bond of the final product, tert-butyl alcohol.

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

257 his chemistry on Wang resin, which led to 18 final products that were cleaved from polymer beads with

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

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

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

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

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

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

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

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

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 This intermediate is converted to the final products via reductive amination with an appropria

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 e effectiveness of NH(3) cleavage leading to final products was also followed by MALDI-TOF in success

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

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 d the difficulties in removing DPCP from the final products, we switched to the oxathiaphospholane ap

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

279 The final products were analyzed via two-dimensional chromat

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

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

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

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

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

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

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

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

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

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

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

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

295 GSTM2-2 catalyze the conversion of COMC-6 to final product with similar efficiencies (K(m) = 0.08-0.3

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

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

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

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

300 which connect these three structures to the final product, (Z,Z)-1,3-cycloheptadiene.