ライフサイエンスコーパス: amino

1 port the diastereoselective synthesis of a 3-amino-1,2,4-oxadiazine (AOXD) scaffold.

2 )((aq)), NTO was quantitatively reduced to 3-amino-1,2,4-triazol-5-one following first-order kinetics

3 ic testing of 90 in rats revealed that the 5-amino-1,3,4-oxadiazole analogues may have limited brain

4 gent reverses the regioselectivity to give 5-amino-1,3-oxazoles, in comparison with the previously re

5 d nitrene transfers to ynamides to furnish 4-amino-1,3-oxazoles.

6 reported a series of novel substituted N-(4-amino-2-chlorophenyl)-5-chloro-2-hydroxybenzamide analog

7 n of the heterocyclic aromatic amine (HAA) 2-amino-3,4-dimethylimidazo(4,5-f)quinoline (MeIQ).

8 iscovery of TNO155, (3S,4S)-8-(6-amino-5-((2-amino-3-chloropyridin-4-yl)thio)pyrazin-2-yl)-3-methyl-2

9 We tested whether alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA

10 activity of oligodendrocyte NMDARs and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA

11 ve aminotransferase inactivator (1R,3S,4S)-3-amino-4-fluoro cyclopentane-1-carboxylic acid (1), in th

12 The continuous generation of the 7-amino-4-methylcoumarin (AMC) from substrates specific to

13 isage that our reported protocol to access 7-amino-4-methylcoumarin derivatives will find use toward

14 ted in the discovery of TNO155, (3S,4S)-8-(6-amino-5-((2-amino-3-chloropyridin-4-yl)thio)pyrazin-2-yl

15 The composition of beer wort in terms of amino acid (AA) content affects the final product qualit

16 tivation to support T cell growth even under amino acid (AA) replete conditions.

17 The alteration of modified amino acid (MAA) profiles in biological samples is relat

18 Amino acid 159 of the envelope (E) protein is reportedly

19 fast' proteins, respectively, based on their amino acid absorption rate.

20 port the first application of the system for amino acid analysis coupled to an extraction unit in ord

21 Our data support the model that the amino acid and growth factor signaling pathways converge

22 l amino acids, and a conditionally essential amino acid and its precursor.

23 e that allowed us to assemble their complete amino acid and nucleotide sequences.

24 in of type P(N) SadP adhesin showed that the amino acid asparagine 285, which is replaced by an aspar

25 le fermentation product (isocaproate) and an amino acid associated with tissue damage (taurine), whic

26 A biosynthesis genes, and a gene controlling amino acid availability.

27 n developed to identify regions with LCRs or amino acid bias, but most of them as stand-alone applica

28 s essential for biological processes such as amino acid biogenesis, iron-sulfur cluster formation, an

29 ynthase (DAH7PS), at the gateway to aromatic amino acid biosynthesis in Mycobacterium tuberculosis, w

30 xylic acid cycle, balancing anaplerosis from amino acid breakdown.

31 on remains uncertain but does not involve an amino acid change in FAN1.

32 s carrying the parC mutation conferring S83I amino acid change.

33 The highest-affinity variant contained seven amino acid changes and bound to the RBD 170-fold more ti

34 Amino acid changes in the hypervariable part of G protei

35 he domain provides a binding platform for 21 amino acid CIF peptide ligands, which are tyrosine sulfa

36 Here we investigate amino acid code for fuzzy binding in terms of the entrop

37 equences are characterized by a less diverse amino acid composition compared to typically observed se

38 ictions to gain insights on the interplay of amino acid composition, structure, self-association, and

39 prion protein (PrP(C)) molecules varying in amino acid composition.

40 2-targeted pTyr residues exist in a specific amino acid context that allows selective binding.

41 imulations and state-dependent non-canonical amino acid cross-linking.

42 C have impaired growth in the absence of the amino acid cysteine and that gigC regulates the expressi

43 is interaction is promoted during oxygen and amino acid depletion and protects LRS from degradation.

44 ar to non-polar molecule, while for the VP4, amino acid differences at position D195G was radical in

45 ng penicillin G (pcbAB, pcbC and penDE) show amino acid divergence between the Fleming strain and bot

46 Amino acid exporters were identified in MAGs identified

47 Amino acid fragments from such hydrated protein films ar

48 between structural water and strain-specific amino acid groups is fundamental to the stabilisation of

49 angiotensin system to regulating intestinal amino acid homeostasis and the gut microbiome.

50 hr518Met mutation altered a highly conserved amino acid in the MYRF protein and three of four algorit

51 to predicted self-regulatory intramolecular amino acid interactions between the SnoaL_2 domain and t

52 ketoimine rather than an alpha,beta-dehydro-amino acid intermediate during C(alpha)-thioether bridge

53 led by demonstrating that for ABCG2 a single amino acid is essential for engaging and initiating tran

54 , we demonstrate that the mammalian Expi293F amino acid labelling kit is suitable for preparation of

55 Each ingredient affected plasma amino acid levels in a singular manner when fed individu

56 ary administration of high protein increases amino acid levels in the gut and promotes pathogen colon

57 Correspondingly, amino acid levels were increased 2 weeks after tendon re

58 in skeletal muscle may contribute to reduced amino acid metabolism and insulin resistance in MHD pati

59 is might impair glucagon's action on hepatic amino acid metabolism and lead to hyperaminoacidemia and

60 Amino acid metabolism in different cells and their cross

61 Protein rebalancing and amino acid metabolism were focal points of the metabolic

62 oid and phytol metabolism, a limited role in amino acid metabolism, and dual sets of the SUF pathway

63 uding AOX, TCA cycle, fatty acid metabolism, amino acid metabolism, organic acid metabolism, and ethy

64 whole-body protein turnover, and splanchnic amino acid metabolism.

65 transcriptional activation and that this 90-amino acid mini-protein is cell permeable and can inhibi

66 has recently emerged as a mild approach for amino acid modification, generating a sizable toolbox of

67 The amino acid moiety was included on the grounds that it ma

68 Each of the identified single amino acid mutations result in impaired shRNA-mediated s

69 Amino acid positions in the HA protein that may be invol

70 pth structural analyses to identify key ACE2 amino acid positions including 30, 83, 90, 322, and 354

71 The kinase-specific positional amino acid preferences are learned using a bidirectional

72 t-chain fatty acids, nitrogen recycling, and amino acid production.

73 rial encapsulation affected the volatile and amino acid profile of the wines, while the biogenic amin

74 Amino acid propensities at a site change in the course o

75 This study describes the use of amino acid quantitation and amino-acid-specific isotope

76 olates of the same emm type had an identical amino acid replacement.

77 Virtually all analyzed strains had single amino acid replacements in penicillin-binding protein 2X

78 L-Tryptophan is an essential amino acid required for protein synthesis.

79 inase K (PK), an N-terminal truncation up to amino acid residue 209 altered the conformation of the S

80 Here, we focused on the amino acid residue at position 8 (P8) of the proteolytic

81 Here, we show that a single amino acid residue in CD28 drove T cell exhaustion and h

82 sequences annotated to indicate whether the amino acid residue is located within a hinge-bending reg

83 eolytic cleavage site of MuV F, because this amino acid residue shows a striking variability dependin

84 ighly reactive and footprint broadly several amino acid residue side chains on the time scale of subm

85 m was characterized and named ToPI1, with 33 amino acid residues and three disulfide bonds.

86 y activity, we propose that those C-terminal amino acid residues are a potentially targetable motif o

87 When these amino acid residues are individually mutated, the necros

88 g entire genes, and orthologs for which most amino acid residues are polymorphic.

89 e designed a systematic approach to identify amino acid residues crucial for the expression and stabi

90 d light on this issue, we exchanged selected amino acid residues in a highly conserved stretch within

91 enthalpy of unfolding provides the number of amino acid residues nu participating in the unfolding re

92 the structure of apo-hGGT reveal movement of amino acid residues within the active site as the substr

93 s, to calculate the digestible indispensable amino acid score (DIAAS).

94 (TFs) regulated by the Ssy1-Ptr3-Ssy5 (SPS) amino acid sensing system and have been proposed to have

95 tated peptide peaks with their corresponding amino acid sequence by database search and subsequent MA

96 11 teleost Sws2 photopigments for which both amino acid sequence information and experimentally measu

97 ted how natural interstrain variation in the amino acid sequence of gO influences the biology of HCMV

98 oop of approximately 20 residues in the ExoU amino acid sequence.

99 3a, respectively, and translated these into amino acid sequences and used for genotype variation ana

100 sequences and protein information, including amino acid sequences, are included.

101 existing tools can not perform alignment of amino acid sequences, which could prove useful in variou

102 gions (IDRs), are modulated by the nature of amino acid side chains as well as by local solvent expos

103 vestigated the stability of the conventional amino acid side-chain-protecting groups, t-Bu, Boc, Trt,

104 ain a conserved helicase core domain and key amino acid sites affecting helicase function, which shar

105 pended on extracellular macromolecules as an amino acid source by activating endocytosis to sustain c

106 HPF1, an accessory factor that switches the amino acid specificity of PARP1 and PARP2 from aspartate

107 This structural feature means that each amino acid spends sufficient time in the pore for sensit

108 Th17 cells that led to the induction of the amino acid starvation response and altered cellular fatt

109 f Gln4p inhibited growth, and induced a GCN4 amino acid starvation response, indicative of uncharged

110 ex, and prevents Rag dimer activation during amino acid starvation.

111 Here, we identify a single amino acid substitution (M159I) that fundamentally alter

112 e, virtually all emm12 isolates had a single amino acid substitution in penicillin-binding protein PB

113 escribe a new mouse model featuring a single amino acid substitution in the coiled-coil motif of BRCA

114 her SSB folds and creation of truncation and amino acid substitution mutants, we provide the first ev

115 Clinical trial data revealed that PA amino acid substitutions at residue 38 (I38T/F/M) reduce

116 plasticity in PR with resistance-associated amino acid substitutions by formation of optimal sulfur

117 e methods provides insight into how specific amino acid substitutions distant from the active site in

118 The location of a number of encoded amino acid substitutions in hemagglutinin-esterase fusio

119 g and requires a particular investigation of amino acid substitutions in the context of protein struc

120 cell viability assays, we report that point amino acid substitutions in the trigger loop, a flexible

121 For VP7 neutralization epitopes, amino acid substitutions observed at positions T91A/V, S

122 able increase in stability with as few as 18 amino acid substitutions suggests that this bovinization

123 Three GmVTL1a amino acid substitutions that block nitrogen fixation in

124 ng with interspecies chimeras and individual amino acid substitutions, to identify regions required f

125 be associated with oil synthesis (27 genes), amino acid synthesis (four genes) and the tricarboxylic

126 sis, the tricarboxylic acid (TCA) cycle, and amino acid synthesis/catabolism.

127 Here, we apply bioorthogonal non-canonical amino acid tagging (BONCAT) to visualize and quantify ba

128 tidine produces a vibrational-probe-equipped amino acid that can readily be incorporated into any pep

129 der Mer (vdM)-that maps the backbone of each amino acid to statistically preferred positions of inter

130 nsporter-mediated histidine uptake, system L amino acid transporter activity and Na(+) K(+) -ATPase a

131 orter-mediated histidine uptake and system L amino acid transporter activity were similar in sarcolem

132 Amino acid transporter-mediated histidine uptake and sys

133 clude a glycine-proline-hydroxyproline (GPO) amino acid triad are biomimetic analogs of the collagen

134 86%), and liver (47%) is predominantly a 129-amino acid truncated mature frataxin (79-207) in which t

135 om gut bacterial metabolism of the essential amino acid tryptophan, in regulating intestinal barrier

136 oadly considering LCRs as regions with fewer amino acid types compared to an average composition.

137 Targeting LAT1-mediated amino acid uptake is a potentially useful immunosuppress

138 distinct, if uncertain, roles in protein and amino acid utilization.

139 44,604 single codon changes encoding 14,160 amino acid variants in Hsp90 and quantified growth effec

140 (DMS) datasets probing the effects of single amino acid variation on enzyme activity and steady-state

141 rch over a template database of fixed-length amino acid words to determine estimated class-membership

142 tural relationships (e.g. distances ligand - amino acid).

143 including monosaccharides, disaccharides, an amino acid, and a steroid.

144 sis revealed changes in pathways involved in amino acid, glucose, and TCA cycle metabolism.

145 ant heme proteins that degrade the essential amino acid, l-tryptophan (Trp), along the kynurenine pat

146 erated by the brain, D-serine, an endogenous amino acid, offers new hope as a therapeutic agent for r

147 to confirm the central role of GLR3.3 in the amino acid-elicited cytosolic Ca(2+) increase in Arabido

148 The first amino acid-Fmoc-O-TIPS-beta-tyrosine-was prepared in 78%

149 curement for quantification of this critical amino acid.

150 ve measurement of the excluded volume of the amino acid.

151 strain was already inhibited by 1 mM of the amino acid.

152 /MLL4 human sequences, we mapped a short ~80-amino-acid UTX stabilization domain (USD) that promotes

153 Neuregulin protein 1 (NRG1) is a large (> 60-amino-acid) natural peptide ligand for the ErbB protein

154 We identify an amino-acid-binding pocket that is formed by transmembran

155 i-synthetic organism creation, and unnatural-amino-acid-containing protein synthesis.

156 lation, the reduced charging of tRNA(Gln) in amino-acid-deprived cells also leads to specific depleti

157 We found that the cleavage site in this 1192-amino-acid-long fragment is located between amino acids

158 ribes the use of amino acid quantitation and amino-acid-specific isotope ratio analysis of scalp hair

159 ; P = 0.04; eta2p = 0.31] and branched-chain amino acids (BCAAs) [between-group difference (95% CI):

160 24 bp in length with an ORF that encodes 434 amino acids (molecular mass of 46.9 kDa).

161 an open reading frame (ORF) that encodes 539 amino acids (molecular mass of 62.7 kDa); dsRNA2 dsRNA i

162 These results show that amino acids 93-111 in SNAP25 act as a flexible molecular

163 -amino-acid-long fragment is located between amino acids 961-971.

164 Rather, amino acids alanine, phenylalanine, glutamic acid, valin

165 t is, the predominance of "left-handed" or l-amino acids and "right-handed" or d-sugars, is a unique

166 nt in metabolic pathways (eg, branched chain amino acids and arginine biosynthesis) and virulence gen

167 orphology of the subpopulations, and 20 free amino acids and glucose in EV subpopulations were identi

168 indings indicate that sequential inputs from amino acids and growth factors trigger PA production req

169 lipins, and the metabolism of carbohydrates, amino acids and indol- and alkaloid-derivatives.

170 -to-tail cyclized, composed of proteinogenic amino acids and lack disulfide bonds; they are also know

171 sent entities of the protein-ligand complex (amino acids and ligands) and the edges represent structu

172 During this process, most amino acids and monosaccharides kept increasing, and acc

173 ment of dopegal in the reaction with several amino acids and neuropeptides.

174 ameters and fluorescence spectra of aromatic amino acids and nucleic acids (AAA + NA), tryptophan res

175 the generation of unnatural gamma-quaternary amino acids and other valuable synthetic targets.

176 tional modifications (PTMs) affecting single amino acids and peptides.

177 ation, which results in the truncation of 45 amino acids and shifts the localization of ClVST1(97) to

178 Isolated aromatic amino acids and short peptides provide benchmark cases t

179 olines, phosphatidylcholines, acylcarnitine, amino acids and sphingomyelins; Lyso.PC.a.C18.0, PC.ae.C

180 he diastereoselective synthesis of unnatural amino acids and the late-stage derivatization of a tripe

181 res seemed dependent on both their number of amino acids and their proximity with the supported lipid

182 The N-acyl amino acids are a family of bioactive lipids with pleiot

183 s gateways, seven different diol-convertible amino acids are converted to diols including 1,3-propane

184 Eighteen of the 20 amino acids are each encoded by more than one synonymous

185 In comparison, all of the other 17 amino acids are encoded by either 4, 3, 2, or 1 codon.

186 Reduced amounts of amino acids are found in the guts of conventionally rais

187 Peptides and free amino acids are naturally generated in dry-cured ham as

188 hich depend critically on the details of how amino acids are packed.

189 study focused on understanding the specific amino acids around the receptor binding site (RBS) that

190 lved in the biosynthesis of nonproteinogenic amino acids as building blocks of natural products and a

191 nique cross-linked position pair for every 7 amino acids at a 1% false discovery rate.

192 Two splice variants of MPST, differing by 20 amino acids at the N terminus, give rise to the cytosoli

193 mydial response mechanisms acting when other amino acids become limiting, we tested the efficacy of p

194 we demonstrate that increasing extracellular amino acids beyond the nutritional need of HLCs and HepG

195 We first validate that amino acids buried within the structural core are networ

196 and avian H3N2 influenza viruses encoded 61 amino acids but were truncated after introduction into d

197 ein-deprived diet enriched in free essential amino acids can 1) promote the brown fat thermogenic pro

198 vian ANP32A proteins harbor an additional 33 amino acids compared to human ANP32A proteins, which are

199 gSPY-MYC(3), 2) its functional dependence on amino acids critical for OGT activity, and 3) its abilit

200 omatis, has a limited capacity to synthesize amino acids de novo and therefore must obtain oligopepti

201 lite 3-MOB along with related branched-chain amino acids demonstrated strong predictability for famil

202 sequence enables the formation of sulfonated amino acids during embryo development in the egg at no c

203 talytically active hexamers to generate free amino acids from human hemoglobin and are drug targets f

204 l as the interfacial adhesive roles of other amino acids have been understudied.

205 other tRNAs retain charging of their cognate amino acids in a manner that is dependent upon intact ly

206 stry with pulsed stable isotope labelling of amino acids in cell culture to quantify the host proteom

207 beling approach using stable isotope-labeled amino acids in cells (pSILAC), phosphoproteomics, and a

208 eater changes in the reducing sugar and free amino acids in fermented cocoa beans.

209 probes that can discriminate enantiomers of amino acids in organic media or aqueous solution are dis

210 vity toward indole, phenyl, or hydroxyphenyl amino acids in plant AAADs.

211 years, suggesting that the low abundances of amino acids in Tagish Lake cannot be ascribed to fluid c

212 xons 7 and 8 is predicted to delete critical amino acids in the ATP-binding site.

213 nds, organic acids, water soluble sugars and amino acids in three onion varieties ('Shallot', 'Chata'

214 theless, the lower TID of sulphur-containing amino acids in tofu than in soya milk induced a signific

215 to enable incorporation of the rare cognate amino acids into the growing peptide chain at a rate of

216 x dynamic allostery: three distinct aromatic amino acids jointly communicate occupancy to the active

217 Specific glycan sites and amino acids located at the tip of the HA molecule enhanc

218 d bacteriocytes, where it produces essential amino acids needed by hosts.

219 We demonstrate that the 33 amino acids of chicken ANP32A and the PB2 627 domain of

220 r becomes unstable when fused to the last 10 amino acids of SpxA2 but remained stable when fused to t

221 The inhibitory effects of amino acids on Pro- and Ala-stimulated R(N) were mitigat

222 ite (imidazolide) and can covalently bind to amino acids other than cysteine on target proteins such

223 genotypes, most likely because of chelating amino acids present in the murine nutrient solution.

224 Site-specific replacement of active-site amino acids revealed the presence of a water-coordinatin

225 is associated with reorganization of further amino acids structurally transforming a loop adjacent to

226 orrelation is at play between a small number amino acids that either favour or disfavour hinge-bendin

227 mTOR complex 1 (mTORC1) senses amino acids to control cell growth, metabolism, and auto

228 In this study, we used a set of unnatural amino acids to fully map the substrate preferences of Gr

229 ng-range interaction patterns between k-mers amino acids to predict protein crystallizability.

230 omic distances, and positioning of catalytic amino acids to rationalize the underlying electronic rea

231 The true ileal digestibility (TID) of their amino acids was determined in minipigs, to calculate the

232 ing intermediates separated by as few as two amino acids were detected using focused-ion-beam-modifie

233 uctures of inactive MCR lacking the modified amino acids were indistinguishable from the fully modifi

234 m combines the natural catabolism of charged amino acids with a catalytically efficient and thermodyn

235 ship for binding using a series of unnatural amino acids with different lengths of hydrophobic side c

236 esis of previously identified phosphorylated amino acids within CHT7.

237 y of ZikV-NS5 appears to be dispensable, the amino acids Y25, K28, and K29 that are involved in NS5 o

238 s, which are tags of minimal size (ca. 15-20 amino acids) affording high-affinity lanthanide ion bind

239 les (e.g. proteins, dyes, drugs, biomarkers, amino acids) based on application of the alternating ele

240 o that of other genera, but much longer (418 amino acids).

241 ethanolamines, 5 ceramides, 3 branched chain amino acids, and 9 neurotransmitters).

242 ridoxine/vitamin B6, taurine, some essential amino acids, and a conditionally essential amino acid an

243 vels of very low-density lipoprotein (VLDL), amino acids, and citrate.

244 linking studies with site-specific unnatural amino acids, and species-specific activity of AimB.

245 potential of end-to-end learning for single amino acids, as compared to more classical manually-cura

246 0.046-0.002), including five gamma-glutamyl amino acids, beta-citryl-glutamate, N-acetyl-aspartyl-gl

247 reveals that necrocytosis provides not only amino acids, but sugars, fatty acids and nucleotides for

248 this method, including enantiomerically pure amino acids, enabling us to explore structural diversity

249 ; secreted glutamine and other nitrogen-rich amino acids, indicating active protein breakdown, at a r

250 s the decoding of some triplets of these two amino acids, leading to reduced translation efficiency.

251 Together with other hydrophobic amino acids, the phenylalanines act as the channel's gat

252 Among amino acids, we find that cysteine is most toxic for mit

253 signal intensity for polar molecules such as amino acids, which has important implications for SIMS i

254 mechanisms towards cysteine thiols and other amino acids.

255 ble of modifying almost all of the canonical amino acids.

256 eased urinary concentrations of the cationic amino acids.

257 puree resulted in high levels of total free amino acids.

258 e complex, bioactive metabolites from simple amino acids.

259 encoding a putative membrane protein of 127 amino acids.

260 ls of nutrients such as glucose, lipids, and amino acids.

261 s intracellular, but not circulating, N-acyl amino acids.

262 rotein (CP) comprising ~260 rather than ~180 amino acids.

263 a handful of the most reactive proteinogenic amino acids.

264 vity with IA derived from L-Glu and aromatic amino acids.

265 nts with (1)O(2) comparable to those of free amino acids.

266 oved by enriching the linker with functional amino acids.

267 cing industrially important C3-C5 diols from amino acids.

268 alogues were synthesized by conjugating with amino acids.

269 ubtle molecular differences among all twenty amino acids.

270 gin of life there were only seven primordial amino acids: Valine (coded by GUX [X = U, C, A or G]), a

271 ectars contain nitrogenous compounds such as amino acids; however, little is known about the role(s)

272 Puromycin is an amino-acyl transfer RNA analog widely employed in studie

273 Here, we show that a second-generation amino-acyl tRNA synthetase (aaRS)/tRNA(CUA) pair for sit

274 establish the stereochemistry of the vicinal amino alcohol motif embedded within the targets.

275 g product, dibenzosuberenone, bearing a beta-amino-alpha-ketone group was secured by X-ray crystallog

276 n, an unstable metabolic intermediate, alpha-amino-beta-carboxymuconate-epsilon-semialdehyde (ACMS),

277 that both arylation and alkylation of alpha-amino C(sp3)-H bonds occurs via the sequence of nickel o

278 [(CAAC)(2)Be](+*) (2) [CAAC = cyclic (alkyl)(amino)carbene], prepared by oxidation of a zero-valent b

279 Cyclic (alkyl)- and (aryl)-(amino)carbenes (CAACs and CAArCs) are stronger sigma-don

280 tical process in the metabolism of bioactive amino compounds.

281 condensation of readily available ynones and amino crotonates under very mild conditions.

282 00-times stronger than the cis photoisoform (amino-cSS).

283 induction for the most efficient diether and amino ether ligands prove to be foreseeable by modeling

284 strategy for the monoprotodeboration of beta-amino gem-bis(boronate) precursors.

285 on can be greatly enhanced by employing a 3'-amino group at the 3'-end of each oligonucleotide, in co

286 t nucleophilic attack by the substrate alpha-amino group on the sn-2 ester to form a cyclic tetrahedr

287 reaction between a sulfonyl fluoride and an amino group.

288 crosslinking with glutaraldehyde (GA) on the amino groups of the 3D-Au-PAMAM-p-ABA-SPCE, where tau pr

289 der mild conditions to provide valuable beta-amino ketones with unprecedented ease.

290 ethod is based on the electrosynthesis of an amino moiety-bearing polymer layer on the graphene chann

291 odeposition using an equivalent mixture of 4-amino-N,N,N-trimethylanilinium and 4-aminobenzenesulfona

292 oxy-5-[(6-[(18)F]fluoro-pyridine-3-carbonyl)-amino]-pentyl)-ureido)-pentanedioic acid), or (18)F-JK-P

293 -2-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]amino]propanoic acid) is a naturally occurring caffeoyl

294 oenergetics in the colonic epithelium with 5-amino salicylic acid, a PPAR-gamma (peroxisome prolifera

295 hylamino) -2- ((3,4,5 trimethyl benzylidene) amino)spiro [isoindoline-1,9'-xanthen] -3-one (BTSIXO) c

296 For example, the OH stretch of an amino-substituted analogue is red-shifted by roughly 50

297 ets, including microbial necromass biomarker amino sugars and SOC, from two long-term agricultural fi

298 l-regulated kinase 1/2 (ERK1/2), p38 and Jun amino-terminal kinase (JNK), which consequently potentia

299 ructural probing revealed that the RNA binds amino-tSS about 100-times stronger than the cis photoiso

300 binds the trans isoform of a stiff-stilbene (amino-tSS)-a rapidly and reversibly photoisomerizing sma