ライフサイエンスコーパス: isomer

1 arpane-type tricycle (from the E-geometrical isomer).

2 ations correctly identify as the most stable isomer.

3 he thermodynamically less favorable branched isomer.

4 0.7 kcal mol(-1) more stable than the trans isomer.

5 ity for the (R) isomer compared with the (S) isomer.

6 the reaction path, when compared to the beta-isomer.

7 tection to favor the synthesis of the I(9)aa isomer.

8 onitoring the electrical conductance of each isomer.

9 stability of the metastable cyclophanediene isomer.

10 m the cis,cis (ccMA) to the cis,trans (ctMA) isomer.

11 ess of fit, which can be used to distinguish isomers.

12 ne, toluene, ethylbenzene, and (BTEX) xylene isomers.

13 h the calculated relative stabilities of the isomers.

14 es ranging from 1.05 to 1.26 y for different isomers.

15 rentiate those of alpha2,6-sailoglycopeptide isomers.

16 midine, which exists as a mixture of Z and E isomers.

17 S calibration for phospholipid and bile acid isomers.

18 or rac- (R(P)R(P)R(P)R(P)/S(P)S(P)S(P)S(P)) isomers.

19 ility for misinterpretation of conformers as isomers.

20 ere analyzed for 24 PFASs including branched isomers.

21 inc complexes stabilized by different ligand isomers.

22 d state-selectively cooling two nuclear spin isomers.

23 ble that is made up of different topological isomers.

24 pecific MS/MS transitions for individual PAH isomers.

25 ketochlorin and all five beta,beta'-diketone isomers.

26 ly similar but electronically very different isomers.

27 ional moieties, producing stereoselective dl-isomers.

28 ale determination of fourteen hexagonal grid isomers.

29 nones with high stereoselectivity toward (E) isomers.

30 s of both lipid C=C location and sn-position isomers.

31 mers had shorter half-lives than linear PFOS isomers.

32 separation and identification of subresidue isomers.

33 the stability of both arene and aryl hydride isomers.

34 Photorelease of the naturally occurring isomer 1,5-(PP)(2)-InsP(4) led to an immediate and conce

35 ggest that the lifetime of the most abundant isomer, 1,2-IHN, is shortened significantly by a water-m

36 formation), while the lifetime of a similar isomer, 4,3-IHN, is not.

37 Cans leached BPA (<5865 ng L(-1)), three BPF isomers (8.2-1286 ng L(-1)) and BPAP (1.6 ng L(-1)), whi

38 a correlation between double bond positional isomer abundance and the hormone receptor status of the

39 ies that suggest FA synthase activity and FA isomer abundances are significantly altered within breas

40 ipid isomer standards, including sn backbone isomers, acyl chain isomers, and double-bond position an

41 of anomeric glycans and linkage sialoglycan isomers, alpha2,3 and alpha2,6, were identified by the c

42 ectrometry (MS/MS) analyses of the separated isomers also distinguish these isomeric forms of cyclosp

43 However, IM-based isomer analysis may be complicated by the presence of mu

44 n affording a 50/50 mixture of cis and trans isomers and (2) a direct nucleophilic substitution leadi

45 arisons and contrasts between 2,3,5,6TMP-TQS isomers and active and inactive enantiomers of other TQS

46 The advantages include near-bistable isomers and an increased separation of the n -> pai* ban

47 ng the fine structural alterations within FA isomers and often limited to global profiling of lipids

48 racterization due to its ability to separate isomers and provide collision cross section (CCS) values

49 s-adducts were all-[6,6]- or [6,6][6,6][5,6]-isomers and that some showed mutual isomerization or rem

50 carbene labeling produces subresidue peptide isomers and the intensity changes of these isomers in re

51 ity resolving power for better separation of isomers and to acquire additional structural information

52 ne/C(2) hydrocarbons, normal alkanes, alkane isomers, and alkane/alkene/alkyne and C(8) alkylaromatic

53 s, including sn backbone isomers, acyl chain isomers, and double-bond position and stereoisomers, is

54 ch to simplify complex mixtures, disentangle isomers, and elucidate their geometries.

55 nnosidic glycan anomers, sialoglycan linkage isomers, and regioisomers of afucosylated and fucosylate

56 sent as 9-cis, 11-cis, 13-cis, and all-trans isomers, and the total levels were higher in neural reti

57 he remarkable property that the newly formed isomer appears in the excited state rather than in the g

58 c and torsional strains present in the trans isomer are responsible for this unexpected relative cis/

59 Both endo- and exo-ring-protonated isomers are calculated to have an exceptionally low bond

60 teraction (C-H...pai), only two enantiomeric isomers are formed (secondary structure).

61 The desired syn or anti isomers are isolated independently in good yields and ex

62 minating the subtle structural difference of isomers are urgently needed.

63 ures of dibromo(bromovinyl)borane with the Z-isomer as a major product (up to 85%).

64 a) to form the 5-OHBza-ribotide (5-OHBza-RP) isomer as the sole product.

65 In solution, ([Co(L1)](2+) ) forms two isomers as shown by (1) H NMR spectroscopy.

66 rmalis constitutively overproduce glycolipid isomers associated with high temperature to levels unatt

67 onstrating remarkable thermal stability of Z isomers at high temperatures and liquid-phase stability

68 Quantitation of lipid structure isomers at multiple levels of specificity is achieved an

69 ws that the reactivity changes of subresidue isomers at Phe399 can identify the interactive nuances b

70 timal kinetic separation of all three xylene isomers at room temperature.

71 en-bond network is disrupted, as seen in the isomer, at high scan rates (~1000 mV s(-1)) a chemically

72 ors in ambient air among a range of possible isomers based on fingerprint fragment ions.

73 The deciphering of multiple structural isomers based on the monosaccharides composition (stereo

74 These isomers become protonated in 58 mus and 3.2 ms, respecti

75 neration of unusually high levels of the cis-isomer by irradiation with green/yellow light as well as

76 ion, we have probed differences between each isomer by using gas-phase hydrogen-deuterium exchange (H

77 daptively molecular discrimination of xylene isomers by employing a NbOF(5)(2-)-pillared metal-organi

78 identification and discrimination of glycan isomers by providing different fragmentation pathways to

79 fferentiation of individual disulfide-bonded isomers by traditional high-performance liquid chromatog

80 22) H(14) ) along with its benzo[a]tetracene isomer (C(22) H(14) ) is unraveled by probing the elemen

81 eas MoBA compounds decomposed faster via the isomer (C(6)H(4), O)(C, N, Ph) formed by P-stereomutatio

82 ne- 3', 5'- cyclic monophosphorothioate, Sp- isomer (cAMPS) gradients move faster and split more read

83 rically shielded and hence more reactive exo-isomer can be generated through oxidation of a stable Fe

84 t metal ions simultaneously, the looser 3(1) isomer can bind only either one copper(I) ion or one lut

85 Unfortunately, the presence of such isomers can make the detection and identification of the

86 hat the barriers for insertion of individual isomers cannot be determined.

87 , or combined) for generating liquid-state Z isomers capable of storing thermal energy.

88 of PFAS class, chain length, and structural isomers changed with depth and distance from the FTA, su

89 ific NulOs, of which there are several known isomers characterized.

90 ricarboxylic acids, and tetracarboxylic acid isomers, commonly called BPCAs.

91 loss in duplex thermal stability for the (R) isomer compared with the (S) isomer.

92 Interestingly, the cis isomer could not be detected in inner prolines, in line

93 The isomers could be differentiated by TIMS-MS and also iden

94 By obtaining conformational isomer crystals of gold nanoclusters, we investigate cry

95 DMS, we demonstrate the separation of three isomers: CycA and CycH (cyclosporin H), which are enanti

96 avelength range of 360-410 nm, whereas the E-isomer cyclization (Phi(c) = 0.006-0.008) and cyclorever

97 High-resolution separation of glycan isomers differentiating from positional, linkage, branch

98 d workflows for molecular identification and isomer differentiation.

99 Here we report the preparation of rare sugar isomers directly from biomass carbohydrates through site

100 re used to interpret observations of the IHN isomer distribution in ambient air.

101 e and perchlorate, which in turn affects the isomer distribution of the receptor under UV-light irrad

102 Analysis of solution phase isomer distributions and single-crystal X-ray structures

103 ecting the eta(2)-benzene and phenyl hydride isomers, due to the relatively flat energy landscape.

104 polyprotein forms two competing topological isomers during its biosynthesis at the ribosome-transloc

105 te of isoprene-derived hydroxy nitrate (IHN) isomers during the OH-initiated oxidation of isoprene af

106 rgonidin-3-malonylglucoside and two to three isomers each of cyanidin-3-dimalonylglucoside, peonidin-

107 isomerization of the (E)-azobenzene to its Z isomer enhances diol binding, and the magnitude of this

108 Furthermore, isomer equilibration is much faster than migratory inser

109 ntidepressants and the FDA approval of its s-isomer, Esketamine (Spravato), the first mechanistically

110 whereas oxazolidines were produced as trans-isomers exclusively.

111 results with computation, we show that each isomer exerts intrinsic control by affecting distinct st

112 olefinic bond location, the alpha- and beta- isomer exhibit dramatically different ignition temperatu

113 l of the absorption bands (490 nm), both the isomers exhibit more efficient photoisomerization (Phi(Z

114 The results showed that both isomers exhibited two deprotonation steps.

115 Coriander contains petroselinic acid, an isomer fatty acid of oleic acid.

116 2D NMR studies indicate that the isolated isomers for 2-(1'-cycloalkenyl)thiophenes having five-,

117 major products were four tris- and one tetra-isomers for both Y(3)N@I(h)-C(80) and Gd(3)N@I(h)-C(80).

118 In the E isomer form, the chiral m-BTA monomers intercalate into

119 tructural information that can differentiate isomers from conformers.

120 method allows relative quantification of FA isomers from heterogeneous biological tissue sections, y

121 ctrospray ionization (DESI) MS imaging of FA isomers from human tissue sections.

122 tions leading to the production of these cis-isomers from trans-violaxanthin remain poorly understood

123 n and beta-hydroxy-beta-ketodihydroporphyrin isomers, generally in regioselective manner, and sets of

124 Bacillus anthracis is composed entirely of d-isomer glutamic acid, whereas nonpathogenic Bacillus spe

125 ion of NAs in the samples, the C(8)H(14)O(2) isomer group appeared to be a reasonable indicator of th

126 reas the concentrations of the individual NA isomer groups ranged between 0.2 and 44 mg L(-1).

127 In total, we detected 55 unique NA isomer groups, out of the 181 screened homologous groups

128 NAs in the samples varied between 14 and 44 isomer groups.

129 , but they are far apart in the unfolded 1,4-isomer (H...H distance ~ 7 angstrom).

130 Branched PFOS isomers had average half-lives ranging from 1.05 to 1.26

131 Branched PFOS isomers had shorter half-lives than linear PFOS isomers.

132 oxide (D(2)O) at 298 K, whereas the 4,3-IHN isomer has been observed to hydrolyze much less efficien

133 Each isomer has vastly different light-switching properties:

134 aldehyde (H(2)CS) and its thiohydroxycarbene isomer (HCSH).

135 This study proposed that besides HMS, its isomer hydroxymethyl sulfite (HMSi), which has not been

136 e accumulation of nonphysiological porphyrin isomer I metabolites.

137 Glyceollin isomers I, II, and III are the major pathogen-elicited s

138 Moreover, identification of structural isomers in a single DOM sample was achieved.

139 e so-far-undescribed existence of two stable isomers in cyclic iodonium salts substituted with alipha

140 e isomers and the intensity changes of these isomers in response to ligand binding can be exploited t

141 ic separation of over 20 high-mannose glycan isomers in ribonuclease B and a diverse range of hybrid

142 wed an absence or reduction of two EOM ether isomers in seeds.

143 of the equilibration of the methyl ethylene isomers in the presence of excess ethylene showed the is

144 allows selective access to either the trans isomer (in generally good to excellent yield with very h

145 n of three AD, BC-propenones (mixture of Z,E-isomers) in CH(3)CN containing InCl(3) and In(OTf)(3) at

146 bles quantitative analysis and resolution of isomers, including from ion mobility spectrometry.

147 ifferent adduct distribution for the E and Z isomers, indicating that the covalent bis-functionalizat

148 he active isomer of JQ1 but not its inactive isomer inhibits IL-1beta-induced RA-FLS activation and p

149 tive conversion of the cryptand to the E,E,Z isomer inside CB[8].

150 vibrational fingerprints of specific glycan isomer ions.

151 int energy computations reveals that the cis isomer is 0.7 kcal mol(-1) more stable than the trans is

152 ubstituent, the high selectivity for the cis isomer is also driven by repulsive electrostatic interac

153 vity of the new conditions yielding the anti isomer is rationalized by invoking a reactive rotamer fe

154 both Pai enantiomers are available, only one isomer is required-the order of nucleophile addition con

155 alating steps in which the ground-state keto-isomer is tautomerized to an enol and then ionized by so

156 at the formation of one of these topological isomers is linked to PRF.

157 formed during the combustion of each of the isomers is needed.

158 mbiguous identification of sialoglycopeptide isomers is still needed.

159 d M have been revised to four constitutional isomers, isolated as two mixtures of dioxobacteriochlori

160 e rapid formation of the catalytically inert isomer kick-starts replication through the template-dire

161 nce of heterogeneous composition, ubiquitous isomers, lability of post-translational glycan modificat

162 variations in glycosylation profiles at the isomer level, with confident assignment of each isomeric

163 orphyrins could be obtained as the only type isomers, likely due to a minimization of the steric stra

164 o store thermal energy in their metastable Z isomer liquid phase and release the energy by optically

165 eoretical studies, the heterocyclopentadiene isomer may be regarded as a rather unreactive closed-she

166 provides rapid, quantitative results for PAH isomer measurements in soil samples.

167 lated analogs, namely, toluene, three xylene isomers, mesitylene, and anisole, and determined their c

168 For a complex trisaccharide isomer mixture, HRdm was able to resolve 5 out of 6 comp

169 /Z)-ratios of 75 and 23%, rhodoxanthin (E/Z)-isomer mixtures in acetone revealed color hues (CIE-h de

170 Lyotropic aggregation of rhodoxanthin (E/Z)-isomer mixtures in acetone/water yielded red (CIE-h degr

171 to the corresponding 5-hydroxy-gamma-lactone isomer myrocin C (1) are also detailed.

172 The radicals are divided into two groups of isomers, named open (O-) and closed (C-), based on the r

173 l. reported a few complexes featuring an NHC isomer, namely an imidazol-5-ylidene, also termed abnorm

174 namically less stable than its acyclic ether isomer (O-CF(3)).

175 namine (3), which is supposedly a positional isomer of 1.

176 s, covering shares of the (all-E)-configured isomer of 19-91%.

177 ha7 mutant by the ago-PAM GAT107 (the active isomer of 4BP-TQS).

178 ntiomers, and isocyclosporin A (a structural isomer of CycA and CycH).

179 de with dihydrodaidzein (DHD) and a putative isomer of DHD.

180 Moreover, a skeletal isomer of exotine A that likely originates from a 1,2-al

181 We demonstrate that the active isomer of JQ1 but not its inactive isomer inhibits IL-1b

182 ase in length when switching from the E to Z isomer of m-BTA in the copolymer with inert a-BTA.

183 t and by C-C and P-C bond formation to a new isomer of phosphaallenes, 10, which features a strained

184 significantly better antagonist than the (+) isomer of the allosteric activation of both wild-type al

185 nd (1,2'-bipyl), the monocationic structural isomer of the prototypical 2,2'-bipyridine ligand (2,2'-

186 C-C bond coupling products are identified as isomers of [H(3)C-Pt-H(CO(2))](-) by a synergy between a

187 etry measurements revealed that two isobaric isomers of a dimeric oxidation product were formed.

188 vergent, gram-scale synthesis of four stereo-isomers of a mycolic acid and its glucose ester.

189 Using three isomers of a synthetic non-nucleoside triphosphate, we d

190 ee isomers of fluoroamphetamine and two ring-isomers of both MDA and MDMA, we demonstrate the ability

191 e characterization of double bond positional isomers of charge inverted dication.FA complexes and the

192 Four cyanobutadiene isomers of considerable interest to the organic chemistr

193 For the first time, four isomers of cyanidin-3-malonylglucoside, four isomers of

194 For the tested sets with up to five isomers of di- to heptasaccharides, the root-mean-square

195 Ferulic acid and isomers of di-ferulic acid (DFA) were not significantly

196 ndard HPLC and MS analysis of conformational isomers of disulfide-rich peptides and proteins.

197 ical biomimetic sensor for discrimination of isomers of ethambutol (ETB) employing square wave voltam

198 Using three isomers of fluoroamphetamine and two ring-isomers of bot

199 of intact proteoforms, including positional isomers of glycated species in a single run.

200 1 +/- 0.2 mM for the ortho-, meta-, and para-isomers of methoxyphenol, respectively.

201 to the qualitative distinction of structural isomers of ortho-, meta-, and para-fluorotoluene.

202 isomers of cyanidin-3-malonylglucoside, four isomers of pelargonidin-3-malonylglucoside and two to th

203 properties with respect to three structural isomers of phenylpropanol.

204 ferential distribution of Delta9 and Delta11 isomers of phosphatidylcholines in mouse brain and in hu

205 Also identified were isomers of pyridine dicarboxylic acids and tricarboxylic

206 rein the single and double reductions of all isomers of the beta,beta'-diketones, generating hydroxyc

207 B[8] was found to be able to encapsulate the isomers of the cryptand by forming a Matryoshka-type com

208 under UV-light irradiation, stabilizing the isomers of the cryptand with Z-configurations.

209 Both isomers of the methyl ethylene complex can be generated

210 (TIMS-MS), several 2- and 3-disulfide-bonded isomers of the mu-conotoxin PIIIA were investigated for

211 two temperature-driven, mutually convertible isomers of the nanoclusters open up an avenue to employ

212 For this purpose, disulfide isomers of three peptides bearing two intramolecular dis

213 the small energy differences between E and Z isomers of trisubstituted alkenes (compared with 1,2-dis

214 arbon-carbon double bond (C=C db) positional isomers of unsaturated phospholipids (PL) in tissue sect

215 nation of alkynes to access both the E and Z isomers of vinyl fluorides.

216 ABA is derived from the cleavage of 9-cis-isomers of violaxanthin and neoxanthin, which are oxygen

217 metallocycle discriminates between the three isomers of xylene with liquid-phase selectivity in the o

218 In the cases of toluene and the three isomers of xylene, benzylic C-H activation is also possi

219 The behaviour of CD-CuMOF for ETB isomers on GCE is postulated to be an artificial enzyme

220 e report that the separation of glycopeptide isomers on porous graphitic carbon (PGC)-LC was signific

221 ckel(II) complexes with the R(P)S(P)S(P)R(P) isomer only, in which the orientation of the lone pairs

222 ngthy precursor syntheses, the separation of isomers, or impractical limitations of the scale.

223 r spin orientations, giving rise to the spin isomers ortho- and para-hydrogen.

224 The separation of xylene isomers (para-, meta-, orth-) remains a great challenge

225 The separation of xylene isomers, particularly p- and m-xylenes, is vital for the

226 ny point across the single peptide oxidation isomer peak, greatly simplifying data acquisition and da

227 hogenic Bacillus species produce mixed d-, l-isomer PGAs.

228 tal synthesis revealed that the natural levo-isomer possesses the R absolute configuration, not S.

229 single-crystal X-ray structures reveals that isomer preference in the crystal lattice is due to gener

230 d protection from 5' exonuclease and the (S) isomer provided protection from 3' exonuclease in the co

231 The (R) isomer provided protection from 5' exonuclease and the (

232 and stereoselective decomposition of their E-isomer provided pure (Z)-(2-bromovinyl)boronates in 57-6

233 f the symmetric C8b-C8c dimer to the C3c-C8b isomer, providing rapid entry into the vitisin core.

234 Multi-functionalization and isomer-purity of fullerenes are crucial tasks for the de

235 The IHN isomer ratio (1,2-IHN to 4,3-IHN) in a high NO(x) enviro

236 s gave (3-8, 19, and 34) in 30-74% yield and isomer ratios in the range 6.7:1 to >50:1.

237 Higher binding constants for the Z isomer relative to the E isomer were observed with all d

238 ble bond, whereas the heterocyclopentanediyl isomer represents an open-shell singlet biradical with i

239 While chromatographic methods provide isomer resolution, such strategies are cost and time int

240 M and 8.52 x 10(-8) M for RR-ETB and SS-ETB isomers respectively.

241 The abundance of lipid isomers revealed by this workflow is found to vary signi

242 preliminary data as a diagnostic ligand, the isomer rhPSMA-7.3 is a promising candidate for potential

243 he discovery of a stereospecific Resolvin D6-isomer (RvD6si) that drives the process.

244 This low-temperature pathway can launch isomer-selective routes to aromatic structures through s

245 ucture that not only increases difficulty in isomer separation but can also introduce the possibility

246 ilarity in physicochemical properties of the isomers sharing the same amino acid sequence.

247 l that the alkylated Fe has an unusually low isomer shift, which reflects the highly covalent Fe-C bo

248 PFOA, PFHxS, and linear PFOS isomers showed average half-lives of 1.77, 2.87, and 2.9

249 ereomer remains static even at 373 K, the RR isomer shows a slow rotational process of the phenylene

250 omise to deeper understand PL metabolism and isomer-specific functions in health and disease.

251 e potential of the technique to expose local isomer-specific metabolism of PLs.

252 MALDI TIMS-MS separation of lipid isomer standards, including sn backbone isomers, acyl ch

253 ion is encoded through switching between two isomer states by applying a voltage signal to the molecu

254 Among the various regio-isomers synthesized, those carrying the hydroxyl at the

255 anoscale, leads to a higher yield of desired isomers than catalysts with platinum particles inside th

256 ase of stereoselective activity of cis/trans isomers that can discriminate between structurally relat

257 In the folded 1,6-isomer, the two t-butyl groups are in close proximity (H

258 hallenge due to the large number of possible isomers, the absence of a chromophore, the high charge d

259 ty of aNHCs, relative to that of their nNHCs isomers, they were used for small molecules activation,

260 an retarding the transformation of the minor isomer through repulsive steric forces.

261 ospace/sites can adapt the shape of specific isomers through geometric deformation and/or the rotatio

262 ng ZU-61 to effectively differentiate xylene isomers through multiple C-H...F interactions.

263 most abundant components, carvacrol and its isomer, thymol, were shown to block virus-target cell fu

264 and that MAR efficiently reduced all muconic isomers to adipic acid.

265 oach, wherein we designed several structural isomers to maximize coordination of endogenous carbonate

266 served empirical formulae limit the observed isomers to those which are nearly circular with high aro

267 Photoisomerization to the Z isomer transforms the intercalator into a chain capper,

268 scrimination of alpha2,3/alpha2,6-sialylated isomers, unambiguous identification of sialoglycopeptide

269 e islets of Langerhans associated with lipid isomer upregulation and depletion.

270 us to relatively quantify peptide oxidation isomers using an ETD MS/MS spectrum acquired at any poin

271 rence (DeltaEp (SS-RR) = 108 mV) between ETB isomers using SWV showing a clear distinction in the rac

272 Here, we report the discrimination of xylene isomers via refinement of the pore size in a series of p

273 ate facile discrimination of several JWH-018 isomers via SERS even when MS and MS(2) spectra are indi

274 f 2,3,5,6TMP-TQS and determined that the (-) isomer was a significantly better antagonist than the (+

275 The Z-isomer was found to be emissive, while the origin of the

276 of a mixture of branched and linear nitrile isomers was also demonstrated to underline the value of

277 constants for the Z isomer relative to the E isomer were observed with all diols investigated, includ

278 -p-coumaric acid, sesaminol and matairesinol isomers were found among all the compounds detected.

279 Ignition characteristics for both isomers were found to be strongly dependent on the kinet

280 tive compounds led to the discovery that (S)-isomers were more potent than their corresponding (R)-en

281 ed to analyze the natural product; all other isomers were prone to ring opening and/or ring expansion

282 t flavonoid content, mainly catechin and its isomers, whereas half-rate fertilizer (330 Kg/ha), prese

283 ingly, imidazolidines were formed as the cis-isomers, whereas oxazolidines were produced as trans-iso

284 n was dependent on the phenyl group in the Z-isomer, which stabilizes the Franck-Condon state, result

285 fullerene cage results in a large number of isomers, which are generally employed as isomeric mixtur

286 ody ratio (DAR) species, and drug positional isomers, which must be monitored to ensure the safety an

287 the release of the cryptand as a major E,E,E isomer, while other studied anions were ineffective in t

288 8-pendants in cis-configuration and a second isomer with 1,4-pendants in trans-configuration.

289 X-ray crystallographic studies show one isomer with 1,8-pendants in cis-configuration and a seco

290 It is the second C(7)H(7) isomer with a five-membered ring yet to be detected, the

291 t an additional loss process for the 1,2-IHN isomer with a time constant of about 6 h best explains o

292 at chloride loss is 1000 times faster in the isomer with the NHC trans to chloride.

293 ce two temperature-responsive conformational isomers with complete reversibility, which forms the bas

294 ng number of possible proteoforms, including isomers with different PTM positions.

295 ept, in situ separation and imaging of lipid isomers with distinct spatial distributions were perform

296 hod, we identified 44 cell membrane O-glycan isomers with MS/MS, and, among them, we unambiguously ch

297 he energetic ordering of the different water isomers with respect to the uncorrected DFAs, the result

298 higher concentrations of FAHFAs particularly isomers with the ester bond at the 9(th) carbon due to d

299 with very high diastereomeric excess) or cis isomer (with yields and diastereoselectivity ranging fro

300 information about alterations in double bond isomers within these samples.