ライフサイエンスコーパス: 1H-NMR

1 1H NMR analysis of the photoproducts indicates that the

2 1H NMR and CD spectroscopic studies provided significant

3 1H NMR and gas chromatography-mass spectrometry analysis

4 1H NMR and sedimentation velocity experiments carried ou

5 1H NMR before and after disinfection revealed an approxi

6 1H NMR data supports a similar conformation in solution.

7 1H NMR experiments reported here verify this model based

8 1H NMR experiments showed that deblocking of the two new

9 1H NMR has been used to investigate the mode of binding

10 1H NMR indicates that both Ni2+ binding sites form squar

11 1H NMR provided no evidence for dissociation of 1 in sol

12 1H NMR shows a PGH-dependent 18.1 ppm signal that is con

13 1H NMR spectra of aldohexopyranosyl rings containing 13C

14 1H NMR spectra of biofluids provides a wealth of biochem

15 1H NMR spectra were measured for two groups of urine sam

16 1H NMR spectrochemical titrations at concentrations belo

17 1H NMR spectroscopic studies show that these artificial

18 1H NMR spectroscopic studies suggested the coordinating

19 1H NMR spectroscopic techniques such as standard 1D spec

20 1H NMR spectroscopy proves to be a powerful technique fo

21 1H NMR spectroscopy was used to determine the rate of (i

22 1H NMR spectroscopy, identification of the catalyst stru

23 1H NMR studies confirmed that the PDPA cores of these co

24 1H NMR studies indicate that the stacked conformation pe

25 1H NMR studies of aqueous solutions of peptide 3a show a

26 1H NMR studies show downfield alpha-proton chemical shif

27 1H NMR was used to investigate the molecular structure,

28 1H NMR, 81Br NMR, and MS techniques indicated the format

29 1H NMR, mass spectrometry, and HPLC analyses confirmed t

30 1H-NMR analysis of the culture supernatants of the Cj092

31 1H-NMR spectroscopy showed that the reducing end of Arab

32 On the basis of 113Cd, 1H NMR, and circular dichroic spectroscopies, we have sh

33 rfused with 13C-labeled substrates using 13C/1H-NMR isotopomer analysis after 30 minutes of low-flow

34 15N-1H NMR and platelet adhesion studies show that the pepti

35 ical correlation between one-dimensional 19F/1H NMR spectroscopic data sets collected in parallel to

36 abundance and DMSO titration monitored by 1D 1H NMR verified the existence of an intramolecular hydro

37 Here, we describe 1D 1H NMR screening of a group of 79 mouse homologue protei

38 d thus far is as low as 1 sample/34 s for 1D 1H NMR.

39 tein targets, 63% yielded A- or B-quality 1D 1H NMR spectra.

40 Based on the 1D 1H NMR spectra, the proteins are classified into four gr

41 metabolic composition of the sample using 1D 1H NMR spectroscopy.

42 or Structural Genomics, one-dimensional (1D) 1H NMR spectroscopy is routinely used to characterize th

43 2D 1H-1H NMR TOCSY provided evidence of covalent binding of th

44 bound U46619 were further demonstrated by 2D 1H NMR experiments using the transferred NOE technique.

45 tiary structure of mr3a was determined by 2D 1H NMR in combination with a standard distance-geometry

46 rotein (G alpha s-Ct), were determined by 2D 1H NMR spectroscopy.

47 mmon secondary structures (as revealed by 2D-1H NMR spectroscopy), providing a basis for their intera

48 A 1H NMR control experiment proved that the compounds clea

49 previous studies used deuterated buffers, a 1H NMR observable leading electrolyte, tetramethylammoni

50 The accompanying 1H NMR paper shows that the conformation of active site

51 Upon Ni2+ addition 1H NMR changes in chemical shifts indicate the imidazole

52 In addition, 1H NMR NOE studies and X-ray analysis on the synthetic a

53 was accomplished by extensive use of 11B and 1H NMR spectroscopy.

54 in solid form, and characterized by 13C and 1H NMR.

55 4, for which a = 0.025 according to 19F and 1H NMR spectroscopy.

56 een confirmed by circular dichroism (CD) and 1H NMR.

57 Multiple X-ray crystallographic and 1H NMR spectroscopic studies demonstrate that 2,6-disubs

58 crystallography, magnetic resonance (EPR and 1H NMR) spectroscopy, as well as magnetic studies in sol

59 lated and characterized by UV-vis, FTIR, and 1H NMR spectroscopies, and also molecular modeling.

60 clohexadiene as evidenced by UV/vis, IR, and 1H NMR spectra.

61 The ESI-MS and 1H NMR data provided evidence for the formation of mixed

62 flight mass spectrometry (MALDI-TOF MS), and 1H NMR studies, Tl+ and Cs+ react with 1 via formation o

63 LC, GLC, and HPLC) and spectral (UV, MS, and 1H NMR) methods.

64 sis of its chemical hydrolysis products, and 1H NMR spectroscopy.

65 methods (a new molecular docking program and 1H NMR spectroscopy) have been used to study the electro

66 time-of-flight tandem mass spectroscopy and 1H NMR.

67 D.+ groups and have a weak ESR spectrum, and 1H NMR data show that the former is a ground-state singl

68 al use of analytical ultracentrifugation and 1H NMR spectroscopy of both human and mouse TREM-1, we h

69 UV-vis and 1H NMR spectroscopy show that Ge(TPP) is an aromatic Ge(

70 uinuclidine 11 and Dabco 12 using UV-vis and 1H NMR spectroscopy.

71 nt was completed by methylation analysis and 1H-NMR.

72 confirmed using pH-sensitive electrodes and 1H-NMR, respectively, and effects on Vc were measured us

73 With this approach, 1H NMR spectra can be acquired for microgram (nanomole)

74 the aromatic ring-current effect, as well as 1H NMR cross-relaxation rates, locate the hydroxyphenyl

75 mate linear relationship between the average 1H NMR shift and the sum of the NICS values.

76 Both 1H NMR spectroscopic and voltammetric experiments clearl

77 Using both 1H NMR and visible-circular dichroism (CD) spectroscopy,

78 The broadened 1H NMR spectrum of 2 indicates the presence of a triplet

79 Subsequent analysis of 5-13 by 1H NMR spectroscopy demonstrated that the locked residue

80 a = 0.23 by UV-visible titration and 0.21 by 1H NMR spectroscopy.

81 he enantiopurity of chiral primary amines by 1H NMR spectroscopic analysis is described here.

82 Analysis by 1H NMR spectroscopy revealed that the reactions were eff

83 by solid-phase extraction before analysis by 1H NMR spectroscopy.

84 ct of the epimerase reaction was analyzed by 1H NMR spectroscopy, which revealed that tracts of adjac

85 The products were analyzed by 1H NMR spectroscopy.

86 investigated by 1H and 19F NMR for 4 and by 1H NMR and UV-visible absorption spectroscopy for 3.

87 Characterization by 1H NMR and CD spectroscopies of the resulting aptamers,

88 -c, were recrystallized and characterized by 1H NMR and 13C NMR as well as X-ray crystallography; COS

89 liamson ether synthesis and characterized by 1H NMR and GC/MS.

90 Its structure was characterized by 1H NMR spectroscopy and mass spectrometry as well as by

91 ptide synthesis methods and characterized by 1H NMR spectroscopy.

92 v) at 25 degrees C, and was characterized by 1H NMR spectroscopy.

93 These pigments were characterized by 1H NMR, 13C NMR, absorbance/fluorescence spectroscopy, m

94 s are soluble and have been characterized by 1H NMR, 13C NMR, MALDI-TOF, and UV-vis spectroscopy.

95 The peptide has been characterized by 1H NMR, and 170 ROE-derived constraints were used to cal

96 e resulting polymer (1) was characterized by 1H NMR, GPC, FT-IR, and UV-vis and had a number average

97 tein 2 were synthesized and characterized by 1H NMR.

98 cta acid nanocapsule, which was confirmed by 1H NMR and EPR spectroscopy.

99 xylate-containing compounds was confirmed by 1H NMR spectroscopy.

100 The nitrate binding was confirmed by 1H NMR titration of receptor solutions, using tetrabutyl

101 V) complexes was too inert to be detected by 1H NMR up to 400 K.

102 yclic and acyclic products, as determined by 1H NMR analysis.

103 accharides in this pattern was determined by 1H NMR and electrospray ionization mass spectroscopy.

104 High-resolution structures as determined by 1H NMR and NOE-restrained molecular dynamics simulations

105 ucture of this domain has been determined by 1H NMR at 800 MHz.

106 es between the Delta EL values determined by 1H NMR spectroscopy and those determined by EPR or MCD l

107 tion and in the solid state as determined by 1H NMR spectroscopy or thermogravimetric analysis.

108 id residues in peptides can be determined by 1H NMR, provided resonances can be resolved for carbon-b

109 absolute configurations were established by 1H NMR spectroscopy.

110 (3R)-beta-phenylalanine were established by 1H NMR, and the configuration of each hydrogen was assig

111 yde gives the anti,syn triol exclusively (by 1H NMR); addition of HMPA to the reaction or replacement

112 etics of the conversion process, followed by 1H NMR between 21 and 70 degrees C in DMSO solution, yie

113 + AH (S = CD3CN, MH+ = [Ru(tpy)(bpy)H]+), by 1H NMR measurements.

114 G2 was identified by 1H NMR and mass spectrometry as having a structure simil

115 As indicated by 1H NMR spectroscopy, the structure of this ion is fluxio

116 histomum epiclitum have been investigated by 1H NMR on the cyanomet form in order to elucidate the di

117 ene derivatives in CB[7] was investigated by 1H NMR spectroscopy and calorimetric and voltammetric te

118 namic product distributions were measured by 1H NMR, before and after acid-catalyzed equilibration.

119 erium incorporation that can be monitored by 1H NMR spectroscopy, with kcat/Km = 0.26 M-1 s-1.

120 ct absence of dioxygen has been monitored by 1H NMR spectroscopy.

121 ectation was confirmed by its observation by 1H NMR spectroscopy.

122 llow these reactive p-QDMs to be observed by 1H NMR spectroscopy at room temperature.

123 back conversion into oH2@C60 was observed by 1H NMR.

124 lid-state) kinetic data that are obtained by 1H NMR spectroscopy at various reaction times.

125 e diastereomers of photolabile precursors by 1H NMR indicates that isomerization of the hemiacetal an

126 trate and analyzing the reaction products by 1H NMR spectroscopy and mass spectrometry.

127 The wild-type CPS as revealed by 1H NMR had 60-70% O-acetylated ManNAc residues that cont

128 ylphosphonate ligands for -X as was shown by 1H NMR (X = -S-(CH2CH2O)4OCH3) and XPS (X = -Cl).

129 re highly water-soluble (>10 mM) as shown by 1H NMR spectroscopy (D2O) and UV-vis absorption spectros

130 ion of polymeric nanomicelles was studied by 1H NMR longitudinal relaxation time (T1) and light scatt

131 no-2, and alpha-conotoxin GI were studied by 1H NMR to identify structural features which might facil

132 nd forms a dimer in solution as suggested by 1H NMR and X-ray crystallographic analyses.

133 Detection of CAD by 1H-NMR with >99% confidence was therefore very weak comp

134 ucosyl-Gb5), were unambiguously confirmed by 1H-NMR spectral analysis.

135 Da) equilibrium that can also be detected by 1H-NMR spectroscopy.

136 The protein is identical [as judged by 1H-NMR spectroscopy, midpoint redox potential (+ 365 mV)

137 variables in a set of spectra (in this case 1H NMR spectra) to generate a pseudo-two-dimensional NMR

138 e, which was confirmed by its characteristic 1H NMR spectrum.

139 ning NMR techniques were employed to collect 1H NMR spectra of the corresponding cells.

140 tional automerization) coupled with computed 1H NMR shift values should aid in the future characteriz

141 latility, ease of handling, and a convenient 1H NMR handle make this acid an attractive alternative t

142 rge complexation shifts of the corresponding 1H NMR resonances, enabling specific triplet sequences t

143 s described including X-ray crystallography, 1H NMR, 13C NMR, HMQC, UV-visible, HPLC, MALDI-MS, and e

144 was characterized by X-ray crystallography, 1H NMR, UV-vis, FTIR, and elemental analysis.

145 remarkable and complicated solvent-dependent 1H NMR spectrum that suggests the existence of hydrogen

146 (d,p) calculations and temperature-dependent 1H NMR spectroscopy, the predominant conformation of 1 h

147 Moreover, detailed 1H NMR solution studies of 1, 3, 4, 6, and 7 indicate th

148 One-dimensional 1H NMR and DQF-COSY experiments identified two distinct

149 One-dimensional 1H NMR spectra of fresh growth medium were compared with

150 One-dimensional and two-dimensional 1H NMR measurements show that Fe(2+) interacts preferent

151 Two-dimensional 1H NMR spectroscopy over a range of temperature through

152 Solution two-dimensional 1H NMR studies have been carried out on cyanide-inhibite

153 d gradient-dependent changes in the distinct 1H NMR gamma CH3 Val E11 signal of MbO2 in perfused rat

154 CDCl3 with TFA showed progressive downfield 1H NMR chemical shifts for H8 (larger) and H2 (smaller).

155 On the basis of the downfield 1H NMR spectrum in solution, His 57 is not protonated at

156 Dynamic 1H NMR spectroscopic measurements and line-shape simulat

157 ttles have been examined by means of dynamic 1H NMR spectroscopy, which reveals that the movements of

158 Decreased SMR intensities in 1D 13C-edited 1H NMR spectra of 13C-labeled proteins upon addition of

159 now report a very convenient isotope-edited 1H NMR-based assay that can be used to probe the transfe

160 This enables 1H NMR signal connectivities between close-eluting metab

161 ent of major 31P signals to their equivalent 1H NMR spectra, e.g., for phosphorylcholine and phosphor

162 greement between calculated and experimental 1H NMR shifts is excellent for 3 in the absence of count

163 16CH3 positions, respectively, by high-field 1H NMR spectroscopy (eqs 1-3).

164 s in NMR titrations, along with 15N-filtered 1H NMR and selective NOE experiments, identified two mix

165 Finally, 1H NMR spectroscopy and side-by-side comparisons of the

166 aining the different mismatches derived from 1H NMR measurements of the imino proton exchange rates.

167 However, 1H NMR and EPR spectroscopy show that the electronic pro

168 However, 1H NMR finds two residues, His207 and likely Arg208 in c

169 me, the application of directly coupled HPLC 1H NMR spectroscopy to confirm the identification of the

170 reagents at producing chiral recognition in 1H NMR spectra is demonstrated with sodium mandelate, th

171 of commonly used drugs detected routinely in 1H NMR spectra of urine in a human population study.

172 oncluded that effective and very informative 1H NMR studies of the effect of either substrate binding

173 (12), was isolated at -15 degrees C, and its 1H NMR spectrum was recorded at that temperature.

174 rated in situ, does not show a signal in its 1H NMR and reacts relatively slowly with CO.

175 dimeric molten globule, as indicated by its 1H-NMR features and fluorescent binding of 1-anilino-8-n

176 hypothalamus allowed the measurement of its 1H-NMR.

177 al origins were also identified, which makes 1H NMR a convenient and efficient tool, complementary to

178 Here we have analyzed a series of MAS 1H NMR spectra (spin-echo, one-dimensional, and diffusio

179 e investigated if magic angle spinning (MAS) 1H NMR can be used as a tool for detection of liquid-ord

180 Variable-temperature FTIR, MAS-1H NMR, UV-vis spectra, and XRD all indicate that the th

181 rombin with the inhibitors, but in a 600 MHz 1H NMR spectrum of the inhibition adduct at pH 6.7 and 3

182 ial of SHY is illustrated using both 600-MHz 1H NMR and UPLC-TOFMS data obtained from control rat uri

183 Comparison of the mutant N2OR 1H NMR spectra recorded in H2O and D2O indicates that th

184 dative deamination was confirmed by 13C NMR, 1H NMR, mass spectrometry, and chemical tests.

185 model are fully consistent with the observed 1H NMR data.

186 A significant advantage of 1H NMR over other detection methods is the high specific

187 were determined from line shape analysis of 1H NMR spectra [methanol-d4: deltaH++ = 47(1) kJ/mol; de

188 experiments are applied to the assignment of 1H NMR spectra of oligosaccharides, using as an example

189 On the basis of 1H NMR data and X-ray crystallographic evidence, we now

190 Comparison of 1H NMR shifts with those of model compounds allows evalu

191 products were accomplished by correlation of 1H NMR, UV-vis, and EPR spectroscopies.

192 the first quantum chemical investigations of 1H NMR hyperfine shifts in the blue copper proteins (BCP

193 Pattern matching of 1H NMR data was particularly valuable.

194 isomerization have been measured by means of 1H NMR in deuterated solvents at 298.2 K.

195 The pattern of 1H NMR-detected dipolar shifts due to the paramagnetic a

196 According to results of 1H NMR dipolar echo spectroscopy, the broadening of MAS

197 Multivariate analysis of 1H-NMR spectra of blood sera was reported previously to

198 and within four human populations, based on 1H NMR spectroscopy.

199 The data on 1H NMR spectroscopic titrations with Ag+ together with t

200 isolated in such small quantities that only 1H NMR analysis was possible.

201 systematic procedure to decipher first-order 1H NMR multiplets is described.

202 ed an approximately 2% change in the overall 1H NMR signals supporting a significant change in the DO

203 For the sake of comparison, a parallel 1H NMR-based metabolomic analysis was also conducted on

204 ss spectrometry (in-line LC-MS), variable-pH 1H NMR spectroscopy, and, where applicable, X-ray crysta

205 Preliminary 1H NMR and 31P NMR studies indicate that these isoprosta

206 Our preliminary 1H NMR studies of oxidized and reduced T4MOC revealed th

207 Preliminary 1H-NMR studies of recombinant zeta chain suggested that

208 We present 1H-NMR spectra that reveal (NEt4)[MoO(S2)2picolinate] (M

209 rve volume microcoil, thereby enabling rapid 1H NMR spectral acquisition of atenolol (experimental ti

210 Evidence for this SSHB is found in X-ray, 1H NMR, and fractionation factor data.

211 g investigation we have used high-resolution 1H NMR spectroscopy to characterize 24-h urine specimens

212 ped using proton nuclear magnetic resonance (1H NMR) and the ERETIC method to enable quantification b

213 ution hydrogen-1 nuclear magnetic resonance (1H NMR) spectra and characterize the magnesium and alumi

214 n vivo by proton nuclear magnetic resonance (1H NMR) spectroscopy as a diagnostic marker.

215 Proton nuclear magnetic resonance (1H NMR) spectroscopy can detect mobile lipids in vivo.

216 pplied to proton nuclear magnetic resonance (1H-NMR) spectra of human serum can correctly diagnose no

217 ton signal using nuclear magnetic resonance (1H-NMR).

218 mational search was guided by the respective 1H NMR and electronic circular dichroism spectra of the

219 dependence of the observed hyperfine-shifted 1H NMR signals of mutant N2OR were recorded over the tem

220 veral sharp, well-resolved hyperfine-shifted 1H NMR signals were observed in the 60 to -10 ppm chemic

221 s and UV/visible, EPR, and hyperfine-shifted 1H NMR spectroscopic methods.

222 ronic spectrum of CuAbeta, hyperfine-shifted 1H NMR spectrum of CoAbeta, and molecular mechanics calc

223 We describe a simple 1H NMR analysis that permits the stereochemistry of beta

224 Extensive assignments by solely 1H NMR 2D methods reveal a structure that is very strong

225 Solution 1H NMR has been used to assign a major portion of the he

226 Solution 1H NMR has been used to characterize the active site mol

227 Solution 1H NMR has been used to investigate the axial bonding of

228 Solution 1H NMR has been utilized to define the active site molec

229 Solution 1H NMR spectroscopic studies, however, provide evidence

230 Solution 1H NMR spectroscopic titrations have shown the two host

231 Solution 1H NMR spectroscopy and mass spectrometry are utilized t

232 Solution 1H NMR spectroscopy has been used to determine the relat

233 is cyanoglobin were investigated by solution 1H NMR to establish the extent to which, and the manner

234 strate the practicality of detailed solution 1H NMR investigation of the manner in which substrate bi

235 Extensive solution 1H NMR binding studies, thermodynamic investigations, an

236 The solution 1H NMR spectra of dihydrodiazocinone 1a with phenyl moie

237 The heme substituent 1H NMR chemical shifts of NP2-D1A and those of its imida

238 vel of theory in addition to low temperature 1H NMR studies.

239 rmediates in the reaction by low-temperature 1H NMR experiments, with increased fluorine content.

240 constants were determined by low-temperature 1H NMR spectroscopy.

241 n with the results from variable temperature 1H NMR and IR measurements, the existence of conformers

242 Variable-temperature 1H NMR spectroscopy demonstrates that their central [1,3

243 Variable-temperature 1H NMR spectroscopy has been used to identify and quanti

244 ogy in the solid state, variable-temperature 1H NMR studies implicate equilibria in solution, possibl

245 Variable-temperature 1H NMR studies on the more soluble octyl derivative 2 sh

246 tained for this 109 kDa enzyme indicate that 1H NMR spectroscopy in combination with heteronuclear me

247 The 1H NMR chemical shifts of lipid signals were identical t

248 The 1H NMR hyperfine shift pattern for the substrate and axi

249 The 1H NMR spectra of the analogue peptides were completely

250 The 1H NMR spectrum shows a pattern consistent with mobile h

251 As follows from the 1H NMR dilution, diffusion NMR, and vapor pressure osmom

252 With a terminal sulfinyl group, the 1H NMR signals arising from the CH2 group of the diaster

253 It is shown that the difference in the 1H NMR chemical shift of a protic hydrogen in DMSO and C

254 ly produce the largest nonequivalence in the 1H NMR spectra of the substrates.

255 4]resorcarene, and several resonances in the 1H NMR spectra typically exhibit enantiomeric discrimina

256 ylene unit of the beta-hydroxy ketone in the 1H NMR spectra.

257 The single low-field line in the 1H NMR spectrum is assigned by site-directed mutagenesis

258 A decreased SMR intensity in the 1H NMR spectrum of a protein mixture compared to the add

259 P appears with PPACK, which is absent in the 1H NMR spectrum of a solution of the enzyme between pH 5

260 t-butyl group chemical shift observed in the 1H NMR spectrum of this enantiomer measured in the prese

261 A comparison of the 1H NMR monitored temperature titration of the delta-meth

262 Detailed analysis of the 1H NMR spectra (including variable-temperature data for

263 Measurements of the 1H NMR spectra and relaxation rates were used to study t

264 An informative analysis of the 1H NMR spectra of the cis adducts synthesized and compar

265 omparative (Delta delta(SR)) analysis of the 1H NMR spectral data of these two esters.

266 The anomeric (H1) region of the 1H NMR spectrum is band-selected in the F1 dimension.

267 leading to an unequivocal assignment of the 1H NMR spectrum of the hexasaccharide.

268 Only the 1H NMR assignments of the bound ligand are essential.

269 hereby form a C3nu symmetrical receptor: the 1H NMR resonance for the amide N-H protons of the pyridi

270 aromatic Ge(II) porphyrin complex, while the 1H NMR spectrum of Ge(TPP)(py)2 clearly indicates the pr

271 but exhibits some loss of dispersion in the 1H-NMR spectrum.

272 The final dyads were characterized by their 1H NMR, mass, and UV-vis spectra.

273 ibit a weak paratropic ring current in their 1H NMR spectra and are oxygen sensitive.

274 -resolved diastereotopic resonances in their 1H NMR spectra, thus enabling the enantiopurity of the p

275 xhibit significant spectral overlap in their 1H NMR spectra.

276 arrays of chemical shifts (deltas) in their 1H NMR spectra.

277 bility of the method, it has been applied to 1H NMR spectra of urine from a metabonomic study of a mo

278 tion, reducing the average error relative to 1H NMR to 7.1%.

279 hieved an average error of 11.4% relative to 1H NMR.

280 The unique 1H NMR signal of the Fe-bound HNO at 14.8 ppm allows def

281 We have used 1H NMR spectroscopy to determine the high-resolution str

282 Using 1H NMR to characterize Fe2+ binding within the duplex CG

283 ucurbit[n]uril (CB[n]), where n = 6-8, using 1H NMR competition experiments referenced to absolute bi

284 es and their pK(a) values were deduced using 1H NMR.

285 wo EBRIT-BTM compounds were determined using 1H NMR and extensive computer simulations.

286 Manuka honey profiling using 1H NMR is shown to be a possible alternative to chromato

287 e evaluated for binding RNA tetraloops using 1H NMR spectroscopy and fluorescence techniques.

288 ization via a combination of diode array UV, 1H NMR, FT-IR spectroscopy, and mass spectrometry has be

289 chieved via a combination of diode array UV, 1H NMR, FT-IR spectroscopy, and time-of-flight mass spec

290 meters enabled the on-flow collection of UV, 1H NMR, IR, and mass spectra not only for pure 20-hydrox

291 spectrometers allowed the collection of UV, 1H NMR, IR, and mass spectra together with atomic compos

292 nal differentiation are found in the varying 1H NMR, UV-vis, and circular dichroism spectral properti

293 anosine tri-O-pentanoate (32) was probed via 1H NMR complexation studies in 5% DMSO-d6-chloroform-d.

294 urn in skeletal muscle, we performed in vivo 1H NMR on mice 3 days after burn trauma; and ex vivo, hi

295 enzyl)methyl spacers have been studied by VT 1H NMR spectroscopy.

296 ve been studied by variable temperature (VT) 1H NMR spectroscopy.

297 These observations are consistent with 1H NMR data for the neutral DAC-NO complex that indicate

298 In this work, cITP coupled with 1H NMR detection is used to study electrophoretic migrat

299 n of the photoreleased diazeniumdiolate with 1H NMR spectroscopy and by NO quantification measurement

300 l alcohol, tetrahydrofuran, and toluene with 1H NMR spectroscopy.