ライフサイエンスコーパス: NMR spectra

1 data with more than one dimension (e.g., 2D NMR spectra).

2 ning process, could be monitored through the NMR spectra.

3 the appearance of a CO2 peak on the FTIR and NMR spectra.

4 rance of two distinct sets of signals in the NMR spectra.

5 C and (13)C-(15)N magic angle spinning (MAS) NMR spectra.

6 the near-silence of the ITC carbon in (13)C NMR spectra.

7 al intensities in magic-angle spinning (MAS) NMR spectra.

8 they greatly simplify the interpretation of NMR spectra.

9 and provides chemical resolution missing in NMR spectra.

10 of one-dimensional (1D) or multidimensional NMR spectra.

11 he corresponding UV/Vis absorption and (13)C NMR spectra.

12 nts from interleaved natural abundance (13)C NMR spectra.

13 n the gel as can be seen from the (29)Si MAS NMR spectra.

14 f the oligomers gave discrete (1)H and (13)C NMR spectra.

15 scape, yet are often "invisible" in standard NMR spectra.

16 d results in large chemical shift changes in NMR spectra.

17 unprecedented shifts up to -24 ppm in (7) Li NMR spectra.

18 f parahydrogen-originating hydrogens in (1)H NMR spectra.

19 AMEs was achieved based on the recorded (1)H NMR spectra.

20 ing heteronuclear single quantum correlation NMR spectra.

21 ic sorption capacity but also on their (31)P NMR spectra.

22 s of methyl resonances in its (1)H and (13)C NMR spectra.

23 etermined through acquisition of progressive NMR spectra.

24 an algorithm for correcting diffusion-edited NMR spectra.

25 ides in apolar solvents is evidenced in (1)H NMR spectra.

26 of the effects of temperature and solvent on NMR spectra.

27 with changes in near- and far-UV CD and (1)H NMR spectra.

28 interactions on the observed differences in NMR spectra.

29 of the amino acids of CaM in (1)H-(15)N HSQC NMR spectra.

30 ransformations could be observed in FTIR and NMR spectra.

31 ssible through the analysis of routine (13)C NMR spectra.

32 up to 100% according to their LC-MS and (1)H NMR spectra.

33 traction in D2O in order to acquire the (1)H NMR spectra.

34 ed by monitoring signal perturbations in the NMR spectra.

35 ving rise to changes in the luminescence and NMR spectra.

36 pid mixtures from 1D (31)P and 2D (1)H-(31)P NMR spectra.

37 btained from high field magic angle spinning NMR spectra.

38 , which do not contribute to the solid state NMR spectra.

39 ilitates visual inspection of the associated NMR spectra.

40 f time series of nuclear magnetic resonance (NMR) spectra.

41 y (GPC) and (1)H nuclear magnetic resonance (NMR) spectra.

42 The resulting (1)H NMR spectra (600 MHz) were evaluated against a database

43 efold enhancements were observed in the (1)H NMR spectra after sample transfer to high field (9.4 T).

44 (15)N NMR spectra allow the extraction of four H37 pKas and sh

45 (17)O NMR spectra allowed identification and distinction of va

46 direct observation of aggregates via unusual NMR spectra also correlated with promiscuous behavior of

47 NMR spectra also indicate the existence of a minor confo

48 The NMR spectra also show significant peak broadening, indic

49 of the crystal structure of the catalyst and NMR spectra analysis, a bifunctional catalytic model was

50 S models were built on diffusion-edited (1)H NMR spectra and calibrated on HPLC-derived lipoprotein s

51 High resolution (1)H NMR spectra and DFT calculations provided evidence for t

52 VT-NMR spectra and DFT calculations were used to determine

53 (31)P NMR spectra and DFT investigation provide indication tha

54 Comparisons between NMR spectra and molecular dynamics (MD) simulations sugg

55 range of coalescence temperatures in the VT NMR spectra and occurrence of the isosbestic points in t

56 The 5S,6R,9S isomer has NMR spectra and optical rotation identical with those of

57 Solid-state (13)C NMR spectra and single-crystal X-ray diffraction structu

58 (31)P NMR spectra and small-angle X-ray scattering (SAXS) data

59 Collectively, our NMR spectra and the electron micrographs of the purified

60 approach that simulates (13) C multiplets in NMR spectra and utilizes mass increments to obtain long-

61 NMR spectra and X-ray structures of hybrid [n]arenes ind

62 pproaches used for acquiring high-resolution NMR spectra, and discuss the information that these spec

63 characterized by infrared, and multinuclear NMR spectra, and elemental analyses.

64 ully characterized by infrared, multinuclear NMR spectra, and elemental analysis.

65 l coefficients of backbone amide protons, 2D-NMR spectra, and molecular modeling revealed that these

66 uses a combination of conventional 1D and 2D NMR spectra, and residual dipolar couplings (RDCs), is r

67 V-vis) spectra, near-infrared (NIR) spectra, NMR spectra, and two simulated sets, one with correlated

68 Proton NMR spectra are indispensable for structural characteriz

69 usion that the downfield shifts in the (19)F NMR spectra are mainly due to steric interactions betwee

70 Systematic collections of NMR spectra are often analyzed in terms of the changes i

71 for cryo-EM and in the solution phase where NMR spectra are recorded.

72 IR and NMR spectra are used to aid the assignment of the relati

73 One-dimensional (1)H NMR spectra are widely used for metabolic profiling.

74 urement of both liquid-state and solid-state NMR spectra as a function of time.

75 shapes and two-dimensional (1)H-(17)O HETCOR NMR spectra as well as accurate internuclear distance me

76 Its simple NMR spectra, as well as HDFT calculations, indicate that

77 4-hexoxy, 4-OMe, exhibit well-resolved (1)H NMR spectra at 298 K, whereas those containing 3,5-OMe a

78 tive integrations of both peaks in the (15)N NMR spectra at different temperatures to measure the pop

79 presence of p-H(2) generates hyperpolarized NMR spectra because of magnetically inequivalent hydride

80 Starting from nuclear magnetic resonance (NMR) spectra belonging to a small cohort, metabolic NMR

81 rred, and these explain the strongly shifted NMR spectra by spin density contributions at the hydroge

82 econvolution and quantification from complex NMR spectra by using the Bayesian automated metabolite a

83 ermediates below the detection limit of (1)H NMR spectra can be applied also to other classes of cata

84 o- and diastereo-isomers with near-identical NMR spectra can be distinguished and unambiguously assig

85 after dissolving the silica matrix, the (1)H NMR spectra can be resolved for every single component o

86 ty of this para-H2 experiment, the resulting NMR spectra can have hydride signal-to-noise ratios exce

87 From analysis of the NMR spectra collected at various R3Abeta2m to alphaB-cry

88 gnals in one-dimensional and two-dimensional NMR spectra, confirming the ligninolytic capabilities of

89 ls in two- and three-dimensional solid-state NMR spectra, conformation-dependent (15)N and (13)C NMR

90 Al-27) = +12.5 ppm in the (27)Al solid-state NMR spectra, consistent with the mixed octahedral Al/Zn

91 Computational deconvolution of (1)H NMR spectra containing the components for more than one

92 that they possess different melting points, NMR spectra, crystal structures, and stacking patterns i

93 (1)H-NMR spectra datasets of serum, urine, cortex, and stomac

94 NMR spectra demonstrate that for internal Psi-A, Psi-G a

95 yl of W and Ti in (1)H-(1)H multiple-quantum NMR spectra demonstrates that W and Ti species are in cl

96 The NMR spectra display a large (1)H-(19)F J coupling typica

97 H iterative full spin analysis (QM-HiFSA) of NMR spectra distinguished previously unrecognized detail

98 NMR spectra employing a deuterium-labeling approach enab

99 The characteristic signals observed in NMR spectra encode essential information on the structur

100 reverse micelles prepared in pentane yields NMR spectra essentially identical to the protein in free

101 Low-temperature (13)C NMR spectra established that (Z)-1 was dissolved as a tr

102 t of urea with sequential single-pulse (13)C NMR spectra, every second for up to ~2 min.

103 Qualitatively, F508del NMR spectra exhibit significantly more peak broadening t

104 ence Matching), that uses 2D J-resolved (1)H NMR spectra for enhanced information recovery using the

105 NMR spectra for single-stranded C(4) oligonucleotide, mi

106 Proton NMR spectra for the dications showed the presence of enh

107 r polarization (DNP) enable the detection of NMR spectra from low-gamma nuclei with outstanding sensi

108 Previously, it has been shown that (1)H NMR spectra from rat brain extracts can be accurately qu

109 Various algorithms comparing 2D NMR spectra have been explored for their ability to dere

110 High-quality (17)O NMR spectra have been obtained for all three compounds u

111 CONCISE and PCA of NMR spectra have discovered novel states of a well-studi

112 NMR spectra have revealed that ISCU populates two confor

113 he in-line flow cell gives excellent quality NMR spectra having little impact on peak shape.

114 Their similar NMR spectra in chloroform clearly suggest the same 1,3-a

115 predicted and compared with the experimental NMR spectra in order to identify the molecular structure

116 QM computations and NMR spectra in solution confirm the stacked molecular as

117 A detailed analysis of the NMR spectra (including 2D experiments) revealed previous

118 Deuterium NMR spectra indicate that bound cholesterol is approxima

119 erature (1)H, (15)N, and 2-D (1)H-(1)H ROESY NMR spectra indicated rapid exchange of the proton and h

120 (1)H nuclear magnetic resonance ((1)H NMR) spectra indicated that the oxidation of fluorescing

121 Line shape analysis of the NMR spectra indicates that the peptide N-H bonds are til

122 Both mimics fold cooperatively and exhibit NMR spectra indicative of a closely packed conformation,

123 Data processing for 1D NMR spectra is a key bottleneck for metabolomic and othe

124 The use of 1D and 2D NMR spectra is indeed very helpful to investigate the co

125 ation content of nuclear magnetic resonance (NMR) spectra is routinely used to identify and character

126 y to assign disulfide connectivities because NMR spectra lack direct evidence for disulfide bonds.

127 nsing behavior of L was corroborated by (1)H NMR spectra, mass spectrometry, and theoretical calculat

128 tionship between multiplets typical for (1)H NMR spectra must be abandoned.

129 analysis of up to three two-dimensional (2D) NMR spectra, namely, (13)C-(1)H HSQC (heteronuclear sing

130 separation by mathematically dissecting the NMR spectra obtained from chromatographic fractions.

131 han 60 metabolites have been assigned in the NMR spectra obtained from the fresh fecal buffer extract

132 r of a few minutes and the simplicity of the NMR spectra obtained make this approach well-suited to t

133 d J-resolved two-dimensional (J-Res-2D) (1)H NMR spectra obtained on a 600 MHz spectrometer, equipped

134 emonstrate the utility of high-quality (13)C NMR spectra obtained using a custom (13)C-optimized prob

135 pressure NMR probe was used to collect (13)C NMR spectra of (13)C-labeled CO2 reactions with NaOH sol

136 We find that multidimensional solid state NMR spectra of (15)N,(13)C-labeled CA assemblies are rem

137 iring high signal-to-noise ratio solid-state NMR spectra of (17)O nuclear spins and to probe sites on

138 NMR spectra of (S)-alanine and (S)-proline derived compo

139 Here we show that the (19)F NMR spectra of 1 (~1:1 diastereomer mixture prepared by

140 Comparison of the NMR spectra of 1 and 2 with those obtained from a sample

141 (93)Nb solid-state NMR spectra of 1a-3a and (31)P solid-state NMR on their

142 (19)F NMR spectra of 1b and 1c were strongly deshielded compar

143 and their splitting patterns in multinuclear NMR spectra of 2H indicate that the chiral Cu20H11 core

144 The (31)P NMR spectra of 3% CLWMS at pH 12 showed decreased cyclic

145 database of experimental and predicted (1)H NMR spectra of 6000 flavonoids.

146 Line shape analysis of solid state (2)H NMR spectra of a phenylene-d4 isotopologue, obtained as

147 ing NOE-derived distance restraints, and the NMR spectra of a series of designed eta-helices were alt

148 Detailed NMR spectra of all complexes as well as IR and single cr

149 (1)H and (13)C NMR spectra of allyl isothiocyanate (AITC) were measured

150 site residues were assigned by comparing the NMR spectra of ALR bound to oxidized and reduced flavin

151 However, (31)P MAS NMR spectra of analyzed series display a higher number o

152 Here, we use multidimensional NMR spectra of animal and in vitro model tissues as fing

153 ts in the position of peaks commonly seen in NMR spectra of biological samples.

154 l protocol for acquiring high-quality HR-MAS NMR spectra of biological tissues at low spinning rates

155 Using NMR spectra of blood samples, taken at different time po

156 The simulated and experimental NMR spectra of caffeoylquinic acids are in excellent agr

157 NMR spectra of delipidated BmorPBP solutions at the phys

158 NMR spectra of deuterated glycine-2-(13)C revealed inter

159 es of photocatalytic reactions and to obtain NMR spectra of dilute solutions with a single pulse of a

160 Next, NMR spectra of each member of the structural manifold ar

161 Here we show that solution NMR spectra of H-RasGTPgammaS mixed with a functional fr

162 mentation with the one-dimensional (1D)-(1)H NMR spectra of HPLC-TOFMS-SPE-trapped compounds, we eluc

163 g a few identified for the first time in the NMR spectra of human serum.

164 This revises the proton NMR spectra of ieodomycin B.

165 NMR spectra of isolated MOS indicated minimal amounts of

166 We demonstrate with the high quality HR-MACS NMR spectra of micronematodes and tissue biopsy, and ill

167 ain natural abundance (13)C and (15)N CP MAS NMR spectra of microporous organic polymers with excelle

168 me in order to give access to the individual NMR spectra of mixture components.

169 The (1)H, (2)H and (13)C NMR spectra of mixtures of racemic mono- and prochiral b

170 NMR spectra of NBD1 lacking the N-terminal tail, NBD1-De

171 Solid-state NMR spectra of new P-Se heterocycles based on peri-subst

172 veloped for the simulation of (13)C and (1)H NMR spectra of oligo- and polysaccharides and their deri

173 the near-silence of the ITC carbon in (13)C NMR spectra of organic isothiocyanates.

174 compound (the tetramer), comparison with the NMR spectra of other oligomers indicates that they form

175 The NMR spectra of oxytocin and dihydrooxytocin suggest a hi

176 High resolution (13)C NMR spectra of plasma triacylglycerols and glucose provi

177 The imino NMR spectra of pre-let-7 loops and LREs contain resonanc

178 Further, we show that 2D (13)C NMR spectra of protease-cleaved Fc and Fab fragments can

179 It was possible to extract NMR spectra of pure N-glycans that were heavily overlapp

180 NMR spectra of quadrupolar nuclei (I > (1)/2) are often

181 exciting and challenging new applications of NMR spectra of quadrupolar nuclei in the fields of energ

182 OGe)4 environments are expected in (31)P MAS NMR spectra of R3c NASICON samples.

183 observed from chemical shift changes in the NMR spectra of residues in the helices and on the surfac

184 the structural information available in the NMR spectra of saccharides and to advance our understand

185 High-resolution (195)Pt NMR spectra of select regions of the broad (195)Pt powde

186 NMR spectra of several small molecules as well as a prot

187 The NMR spectra of simple binary complexes of the TAZ1 and T

188 n also facilitated the interpretation of the NMR spectra of small molecule models of phenanthriplatin

189 spin parameters against experimental 1D-(1)H NMR spectra of small molecules.

190 (23)Na MAS NMR spectra of sodium-oxygen (Na-O2) cathodes reveals a

191 ilicic acid (Q(1)) can be observed in (29)Si NMR spectra of solutions containing PEG 10000 with inten

192 been suggested to bind to the SRA1 RNA, but NMR spectra of SRA1p in the presence of its 80-nt RNA ta

193 We were able to produce high-quality NMR spectra of substrate bound to microcrystalline LeuT

194 charides was confirmed by comparison of (1)H NMR spectra of synthetic antigens and isolated fragments

195 ce of transmembrane helix 6 (Cys-265), (19)F NMR spectra of the beta2 adrenergic receptor (beta2AR) r

196 The (1)H NMR spectra of the CO and deoxy forms of these mutants i

197 on of the nitroso group were observed in the NMR spectra of the compounds where two distinct intramol

198 esent in a measurable quantity in the (23)Na NMR spectra of the cycled electrodes.

199 The (31)P NMR spectra of the degraded olive oils, which contain OH

200 eteronuclear single quantum coherence (HSQC) NMR spectra of the entire array of wall polymers.

201 two-dimensional (13)C and (15)N solid-state NMR spectra of the formulations while preserving the mic

202 asis of the comparison of the (1)H and (13)C NMR spectra of the individual stereoisomers with literat

203 nal packing is also consistent with (1)H-MAS NMR spectra of the L(o) phase, NMR diffusion experiments

204 high-resolution (17)O (I = 5/2) solid-state NMR spectra of the mixed-conducting solid oxide fuel cel

205 The (19)F NMR spectra of the mono-(18)O-substituted monoanion in w

206 the multiplicity of signals observed in the NMR spectra of the N,N'-(1,4-phenylene)bisphthalimide 11

207 Comparison of NMR spectra of the nonselective NaK and potassium-select

208 In contrast, the NMR spectra of the peptides labeled with (13)C at the sa

209 Re-examination of NMR spectra of the previously reported d-allo-ShK protei

210 (1) H NMR spectra of the protonolysis product of 2 synthesized

211 mical shift differences observed in the (1)H NMR spectra of the racemic and the enantio-enriched comp

212 Subtle differences in the (1)H NMR spectra of the rotaxanes can be related to the prese

213 to remarkably clean homo- and heteronuclear NMR spectra of the serum metabolome that compare favorab

214 The complicated (31)P{(1)H} NMR spectra of the three compounds were simulated, evide

215 The NMR spectra of the three trisaccharides were fully assig

216 es of binding to two sites directly from the NMR spectra of the titrations.

217 NMR spectra of these dynamic complexes thus reflected ap

218 Comparisons of the NMR spectra of three conservative mutations, I63M, L74M,

219 study is based on the analysis of (1)H HRMAS NMR spectra of tomato puree using a combination of parti

220 matic process is introduced to compare (13)C NMR spectra of two (or more) candidate samples of known

221 previously published crystal structures and NMR spectra of various NBD1 mutants, we propose that del

222 lar tensors and peak intensities from 3D MAS NMR spectra of wild-type and the A92E and G94D CypA esca

223 NMR spectra of WT NBD1 reveal significant concentration-

224 e spinning (MAS) nuclear magnetic resonance (NMR) spectra of 5-30 kDa proteins.

225 tionally, we have included predicted MS- and NMR-spectra of thousands of compounds for assignment of

226 restraints from four-dimensional solid-state NMR spectra on extensively deuterated and (1)H back-exch

227 Fidelity of reconstruction of series of NMR spectra or images requires more PCs than needed to p

228 The splitting of signals in the NMR spectra originating from enantiotopic sites in proch

229 corresponding to the two species in the (1)H NMR spectra over a range of temperatures.

230 us set of gauge transformations (CSGT) (13)C NMR spectra prediction by Density Functional Theory (DFT

231 strong peak overlaps in one-dimensional (1D) NMR spectra prevent straightforward quantification throu

232 ured in solution via integration of the (1)H NMR spectra, providing an accurate comparison of the N-h

233 g (NUS) data acquisition and high-resolution NMR spectra reconstruction.

234 Variable-temperature (17)O NMR spectra recorded from 22 to 214 degrees C were inter

235 e that a profiling strategy based on fast 2D NMR spectra recorded in 2.4min is more efficient than th

236 The (1)H NMR spectra recorded in deuterated dichloromethane indic

237 uple this application of PCA to an automated NMR spectra recording and processing protocol and obtain

238 Solid-state (2)H NMR spectra report the folding and orientation of the co

239 The resonance for Met-187 in our NMR spectra reported on the ability of the enzyme to che

240 However, NMR spectra reveal sharp resonances with chemical shifts

241 NMR spectra reveal that EmrE can simultaneously bind and

242 Moreover, NMR spectra revealed that the CaM-F142L-CaMBD interactio

243 The (1)H NMR spectra revealed that the halides formed tight ion-p

244 sis of structural information encoded in the NMR spectra reveals a way to the automated elucidation o

245 In each case, low-temperature (6)Li NMR spectra show stereoisomerically pure homoaggregates

246 NMR spectra show that CusB-NT is mostly disordered in th

247 cross peaks between HPTS and CTAB in the 2D NMR spectra show that HPTS embeds in the interface.

248 Furthermore, (31)P and (2)H solid-state NMR spectra show that liquid crystalline 1,2-dimyristoyl

249 (13)C CP/MAS NMR spectra show that the Fe(CO)3 moiety in polycrystall

250 embranes mimicking the virus envelope, (15)N NMR spectra show that the His-27 tetrad protonates with

251 (31)P NMR spectra show that the peptide retains the lamellar s

252 NMR spectra show that the structural heterogeneity is su

253 The NMR spectra show that the two delta-dicarbonyl sugars ex

254 (HH) and 3J(13C-H) coupling constants in the NMR spectra showed an anti addition with a diastereosele

255 (1)H NMR spectra showed large upfield shifts of the protons i

256 ross-polarization magic angle spinning (13)C NMR spectra showed that CO2 binds chemically to IRMOF-74

257 Their (1)H NMR spectra showed the typical pattern of four atropisom

258 II) protein displays high-resolution in-cell NMR spectra similar to, but not identical to, those of t

259 inite-pulse radiofrequency-driven recoupling NMR spectra, spatial proximities between I32 and V40 as

260 The NMR spectra suggest that the carbohydrate links to hydro

261 a matter of minutes to hours, of solid-state NMR spectra suitable for quantitative analysis of protei

262 NMR spectra support this model and raise the possibility

263 --are the exclusively detectable form in the NMR spectra taken in DMSO-d(6).

264 was confirmed by X-ray crystallography, has NMR spectra that are very similar, but not identical, to

265 acceptability range are qualified to produce NMR spectra that can be considered statistically equival

266 ses by selecting subsets of homogeneous (1)H NMR spectra that contain specific spectroscopic metaboli

267 pulses, very high-resolution proton-based 3D NMR spectra that correlate single-quantum (SQ), DQ and S

268 We present 1H-NMR spectra that reveal (NEt4)[MoO(S2)2picolinate] (Mo-p

269 in two-dimensional and three-dimensional MAS NMR spectra the CL-bound cyt-c displays a spectral resol

270 , complex refractive indices, (1)H and (13)C NMR spectra, thermograms, aerosol and electrospray ioniz

271 Statistical analyses were run on NMR spectra to discriminate patients according to the la

272 resolution 1D (1)H-CPMG and diffusion edited NMR spectra to identify the potential molecular biomarke

273 monstrating the utility of [(1)H,(15)N] HSQC NMR spectra to provide a spectroscopic fingerprint refle

274 l-line-shape (CTLS) approach applied to (1)H NMR spectra to quantify metabolites present in onion spe

275 covered that one-dimensional (13)C and (15)N NMR spectra, together with spectroscopic selections base

276 2D NMR spectra, total correlated spectroscopy and nuclear O

277 ted directly from noninterpreted, complex 2D NMR spectra using principal component analysis (PCA) to

278 ized [1-(13)C]pyruvate during acquisition of NMR spectra using selective excitation to maximize detec

279 Chemometric analysis of the NMR spectra, utilizing both (1)H and (1)H-(13)C HSQC NMR

280 + dipyrromethanedicarbinol routes, and their NMR spectra, UV-vis spectra, X-ray crystal structures, a

281 NMR spectra were acquired by applying the robust, sensit

282 ities of coenzymes and antioxidants in blood NMR spectra were established combining 1D/2D NMR techniq

283 and signal-to-noise ratio (SNR) of the (1)H NMR spectra were evaluated.

284 molecules, for which replicas of their (1)H NMR spectra were generated.

285 (1)H NMR spectra were obtained for the CO and deoxy forms of

286 and above, outstanding quality 2D and 3D MAS NMR spectra were obtained for tubular CA and CA-SP1 asse

287 (+)-1 a-1 b-for those instances in which the NMR spectra were obtained in CD3OD-to their correspondin

288 Overcrowded conventional (1)H HRMAS-NMR spectra were selectively simplified with two NMR pul

289 Hyperpolarized (13)C NMR spectra were used to characterize product tacticity

290 Nuclear magnetic resonance (NMR) spectra were obtained for five cations, and the che

291 l of 36 NMR data sets (corresponding to 1260 NMR spectra) were produced by 30 participants using 34 N

292 ion is constructed from variable-temperature NMR spectra with (13) C-labeled agostic complexes.

293 rmation, allowing then to record single-spin NMR spectra with 13 Hz resolution at room temperature.

294 l NV-based sensor device records single-spin NMR spectra with 13 Hz resolution at room temperature.Di

295 (19)F-T2 NMR spectra with different relaxation delays were record

296 The resulting protein samples yield NMR spectra with improved sensitivity due to the essenti

297 simplify and resolve complex, congested (1)H NMR spectra with many overlapping spin multiplets, while

298 This linked enzyme produced NMR spectra with severe signal overlap and line broadeni

299 mass spectra and nuclear magnetic resonance (NMR) spectra with those of authentic reference standards

300 readily be observed in one-dimensional (1)H NMR spectra without any isotope labeling.