ライフサイエンスコーパス: di-

1 he reactions are compatible with various 1,1-di- and 1,1,3-trisubstituted allenes and N-hydroxyanilin

2 ether+10% tris-(2-ethylhexyl) phosphate+10% di-(2-ethylhexyl) phosphate; pH of the sample solution,

3 NMR experiments showed them to be N(1),N(10)-di-(E)-caffeoyl-N(5)-p-(E)-coumaroyl spermidine, N(1)-(E

4 the hydrophilicity and peptide length of 153 di- to tetrapeptides.

5 nd injection of 8-OH-DPAT [(+/-)-8-hydroxy-2-di-(n-propylamino) tetralin hydrobromide; 5-HT(1A) agoni

6 Of these sites 79% were mono-, 20% di-, and approximately 1% were tri- and tetraphosphopept

7 lished impact on global histone H3 lysine 27 di- and trimethylation (H3K27me2/3), the relevance of th

8 u generated new NHC ligand derived from {1,3-di-(2,6-diethylphenyl)acenaphtho[1,2-d] imidazolium} chl

9 rase SDG8, implicated in histone 3 lysine 36 di- and trimethylation (H3K36me2 and me3), is involved i

10 wed a specific deficit in histone 3 lysine 4 di- and trimethylation, while histone 3 lysine 4 monomet

11 lites of high-molecular-weight phthalates, 4 di-(2-ethylhexyl) phthalate (DEHP) metabolites (Sigma4DE

12 sparity in reaction performance between 4,4'-di- tert-butyl-2,2'-bipyridine (dtbpy)- and 2,2'-bipyrid

13 , the Zr-amido complex FI(2)ZrX(2) (FI = 2,4-di- tert-butyl-6-((isobutylimino)methyl)phenolate, X = N

14 rt-butylphenyl) phosphate (AO168=O), bis(2,4-di- tert-butylphenyl) pentaerythritol diphosphate (AO626

15 2,4-di- tert-butylphenyl) phosphite, bis(2,4-di- tert-butylphenyl) pentaerythritol diphosphite, and t

16 cts, triisodecyl phosphate (TiDeP), tris(2,4-di- tert-butylphenyl) phosphate (AO168=O), bis(2,4-di- t

17 yl) phosphite, triphenyl phosphite, tris(2,4-di- tert-butylphenyl) phosphite, bis(2,4-di- tert-butylp

18 O(-) =anion of triphenylsilanol) and the 2,4-di-(t) Bu-PhO(-) (2,4-di-(t) Bu-PhO(-) =anion of 2,4-di-

19 ylsilanol) and the 2,4-di-(t) Bu-PhO(-) (2,4-di-(t) Bu-PhO(-) =anion of 2,4-di-tertbutylphenol) ligan

20 igand L(N6) , leads to [Dy(III) (L(N6) )(2,4-di-(t) Bu-PhO)(2) ](PF(6) ) (1), [Dy(III) (L(N6) )(Ph(3)

21 proaches for the preparation of 5'-mono-, 5'-di-, and 5'-triphosphorylated nucleosides, also known as

22 We found that in vitro, YvcI converts RNA 5'-di- and triphosphates into monophosphates in the presenc

23 Cy3G) was more instable than delphinidin 3,5-di (Dp3,5dG) and cyaniding 3,5-diglucosides (Cy3,5dG).

24 and improve the electrical conductivity, 2,5-di-(2-thienyl)-1-pyrrole-1-(p-benzoic acid) and chloroau

25 complex, Mn((tbu)dhbpy)Cl, where 6,6'-di(3,5-di- tert-butyl-2-phenolate)-2,2'-bipyridine = [(tbu)dhbp

26 With the EDTA-2D-RP/RP approach, 13 mono-, 6 di-, and 3 triphosphopeptides were identified in the alp

27 ixed dimers with NaHMDS, NaDA, or sodium 2,6-di- tert-butylphenolate, the reactivities of which are e

28 r the double-asymmetric hydrogenation of 2,6-di-(1-phenylethenyl)-4-methylaniline to produce the C2-s

29 of the 4-(nitrophenyl)phenoxyl radical, 2,6-di-(t)butyl-4-(4'-nitrophenyl) phenoxyl radical ((t)Bu2N

30 n the alpha-casein sample, while 19 mono-, 8 di-, 4 tri-, and 3 tetraphosphopeptides were identified

31 ng Cu(I)/Cu(II) as catalyst and K(2)S(2)O(8)/di- tert-butylperoxide as oxidant has been achieved.

32 Three xanthones, 1,3,7-trihydroxy-2,8-di-(3-methylbut-2-enyl)xanthone, 1,3,7-trihydroxy-4,8-di

33 hylbut-2-enyl)xanthone, 1,3,7-trihydroxy-4,8-di-(3-methylbut-2-enyl)xanthone a previously undescribed

34 often associates with the neighboring Lys-9 di- or tri-methylations, they are not required for the a

35 nascent RNAs to initiate histone H3 lysine 9 di- and trimethylation (H3K9me2 and H3K9me3, respectivel

36 Four series of 7,9-di- and 2,7,9-trialkyl guanine derivatives were synthesi

37 aluminum foil (VACNT-Al foil) with poly (9,9-di-(2-ethylhexyl)-fluorenyl-2,7-diyl)-end capped with 2,

38 as alkyl-substituted electrophiles bearing a di- or trisubstituted alkene may be employed.

39 -monomer-based orthometalation followed by a di- or trisolvated arylsodium monomer-based rearrangemen

40 E,Z-configured conjugated diene linked to a di- or triyne chain.

41 ere observed of which 4-sinapoylquinic acid, di- and tri-methoxycinnamoylquinic acids, two isomers of

42 a seven-membered transition state to afford di-, tetra-, and pentapeptides in 78-95% yields.

43 for the reaction of NO(3)(*) with aliphatic di- and tripeptides suggest that attack occurs at all of

44 th weakly activating groups reveal analogous di- and trisolvated monomer-based metalations.

45 rystal phases are observed for the analogous di- and tetracationic compounds without an ion shelterin

46 her, tris-(2-ethylhexyl) phosphate (10%) and di-(2-ethylhexyl)phosphate (10%) as the extraction solve

47 its reactions with aliphatic amino acids and di- and tripeptides, suggesting that attack at the amide

48 is also potentially diastereoselective, and di- and trisubstituted tetraenes often undergo cascade r

49 found that di-isobutyl phthalate (DiBP) and di- n-butyl phthalate (DnBP) were the main PAEs released

50 he likely in vivo substrates are NAD(P)H and di-, poly-, and persulfide derivatives of coenzyme A, al

51 H3 tails mono- and dimethylated on H3K4 and di- and trimethylated on H3K36, an H3 methylation patter

52 Both mono- and di- hydroxyl metabolites were identified for parent HBCD

53 Mono- and di-(18)F-labeled derivatives of phenolsulfonphthalein (p

54 l and allows for synthesizing both mono- and di-, tri-, and poly( p-carboxyphenyl)siloxanes with p-ca

55 or TGs having a combination of saturated and di- or triunsaturated fatty acyls in sn-1 and sn-3 posit

56 ASP-1 associated with UHRF1, G9a, Snail1 and di- and tri-methylated histoneH3 in a CXCL12-dependent m

57 ed with sequences with identical coding and (di-)nucleotide composition but disrupted RNA secondary s

58 ulfate (KS), its desulfated form, as well as di-, tetra- (N-acetyllactosamine and lacto-N-tetraose) a

59 f total anthocyanins and high ratios between di- and tri-substituted forms.

60 lexibility is involved in the switch between di- and pentapeptide hydrolysis.

61 etylase complex have both been shown to bind di- and trimethylated histone H3 Lys-36 stimulated by Ea

62 aches to show that the Set3 PHD finger binds di- and trimethylated states of H3K4 with comparable aff

63 mono- and dimethylated lysines, SFMBT1 binds di- and trimethyl H3K4, both of which are enriched at ac

64 Moreover, several potentially bioactive di- and tripeptides were identified in oryzacystatin pep

65 D,D-carboxypeptidase, which hydrolyzes both di- and pentapeptide.

66 llular exposure of the TLR2 PAMPs carried by di- and triacylated SVLP cores, which indicates subset-d

67 Only SVLPs carrying di- and triacylated lipopeptide cores induced DC activat

68 Syntheses of certain di- and mono-oxygenated derivatives (e.g., 2 and 3, resp

69 regioselective monoepoxidation of conjugated di- and trienes using 30% H2O2 at or below room temperat

70 also methylated other l-histidine-containing di- and tripeptides.

71 en beta-CN derived C-terminal Pro-containing di-, tri, and tetrapeptides which were predicted in sili

72 In contrast, di- and trimethylation of lysine 9 of histone 3 (H3K9) a

73 ng partners giving rise to the corresponding di- or trisubstituted alkenes, typically in high yield a

74 is process is the ability to directly couple di-, tri- and tetrasubstituted alkenyl cyanohydrin pronu

75 molecular mechanism underlying Na(+)-coupled di- and tricarboxylate transport by this family is under

76 Cyclic di- and linear oligo-nucleotide signals activate defense

77 uitous bacterial secondary messenger, cyclic di-(3',5')-guanosine monophosphate (c-di-GMP), represent

78 ke nucleotidyltransferase synthesizes cyclic di- or tri-nucleotide second messengers in response to i

79 ng nucleotides demonstrate that these cyclic di- and trinucleotides activate distinct host receptors

80 ers, including the synthesis of well-defined di- and triblock copolymers.

81 to hydrophobic phthiocerol dimycocerosates, di- and pentaacyl trehaloses and sulfoglycolipids.

82 ssociated alpha-glucosidase that breaks down di- and oligosaccharides to absorbable monosaccharides.

83 Ps can encompass multiple orientations; each di- and triphosphorylated species binds with comparable

84 In this study, we explored di- and tripeptides with beta-lactam electrophilic warhe

85 ubiquitin chain cleavage was comparable for di- and tri-ubiquitin, the Km value was lower for tri-ub

86 orded from m/z 167 and 168 ions obtained for di- and tri-deuterio isotopologues showed peak pairs at

87 ort chain monoglycerides was larger than for di- and triglycerides when Tween 80 was used as surfacta

88 e sulfur directly reacted with MexR, forming di- and trisulfide cross-links between two Cys residues,

89 The method forms di-, tri-, and even tetrasubstituted acetones with high

90 set of covalently linked homo-oligomers from di- to tetramers serve as proof-of-principle test cases.

91 panes and oxepane-containing polyethers from di- and trisubstituted epoxides.

92 fully defined HS saccharide structures (from di- to decasaccharides) permits unambiguous sequence det

93 n the presence or absence of water furnishes di- and trioxidized cyclopentenones, respectively.

94 med over the (1-->5)-beta-d-galactofuranosyl di- and trisaccharide derivatives 12 and 13.

95 , core, and outer arm), and galactosylation (di-, tri-, and tetra-) between striatum and SN N-glycans

96 At transcriptionally active genes, di- and tri-methylated H3K36 inhibit PRC2.

97 I)-mediated isomerization process that gives di- or trisubstituted allylic boronic esters with high E

98 first TEMPO(.) -catalyzed, redox-neutral C-H di- and trifluoromethoxylation of (hetero)arenes.

99 ophila E(z) homolog, were deficient in H3K27 di- and trimethylation, with no detectable replication s

100 Here we show that the levels of H3K27 di- and trimethylation (H3K27me2 and H3K27me3) are reduc

101 K27Ac and H3K36me2, whereas repressive H3K27 di- and trimethylation (H3K27me2/3) marks were globally

102 nes with altered expression as well as H3K36 di- and trimethylation in H3.3K36M cells are enriched in

103 lation (H3K27me3) rarely coexists with H3K36 di- or tri-methylation (H3K36me2/3) on the same histone

104 ithout obvious changes in the levels of H3K4 di- and trimethylation.

105 egions, coupled to a modest decrease in H3K9 di- and trimethylation at the rDNA promoter.

106 rchitecture, with significantly reduced H3K9 di- and tri-methylation at specific chromatin sites.

107 to the DSB, where local levels of histone H4 di- and tri-methylation at lysine 20 (H4K20me2, 3) and H

108 Here, di- and monozinc catalysts, coordinated by bis(imino)dip

109 9) at the expense of broad losses in histone di- and tri-methylation.

110 Homogenous di- and tetravalent dendrimers incorporating the alpha7-

111 ta-fructofuranosidase capable of hydrolyzing di- and trisaccharides containing a terminal, non-reduci

112 ding large hydrophobic peptides, hydrophilic di-/tripeptides and glycopeptides.

113 CZE-MS for the analysis of small hydrophilic di-/tripeptides, large hydrophobic peptides, glycopeptid

114 tes inorganic As(III) into mono- (MAs(III)), di- (DMAs(III)) and tri- (TMAs(III)) methylarsenicals.

115 (sp(3))-H bonds of N-terminal amino acids in di-, tri-, and tetrapeptides without installing a direct

116 Decreases were observed in di- and triacylglycerides, sphingomyelins (SMs), lysopho

117 -Cys60' interprotomer cross-links, including di-, tri- and tetrasulfide bonds, which allosterically i

118 ger-associated molecular patterns, including di- and triacylated lipopeptides.

119 acyl chains across lipid species, including di- and triacylglycerols, phospholipids, cholesteryl est

120 en the accessions were related to metal ion (di-, trivalent inorganic cation) transmembrane transport

121 In this study, we evaluated isosorbide di-(linoleate/oleate) (IDL), which was generated by este

122 or site-specific incorporation of K48-linked di- or tetra-Ub chains onto the side chain of Lys12 of a

123 sine 27 trimethylation and histone H3 lysine di- and trimethylation.

124 The main di- and tribromophenols detected were 2,4-diBP > 2,5-diB

125 dified individual amino acids, Fmoc-modified di- and tripeptides, and Fmoc-modified tetra- and pentap

126 arum AVEF17, leading to high levels of mono, di-, and tri-hydroxy-octadecenoic acids.

127 Mono-, di-, and triPAPs, including several diPAP homologues, we

128 Mono-, di-, and trisubstituted arenes lacking a directing group

129 tive form of the drug (Gemcitabine 5'-mono-, di- and triphosphates) by specific enzymatic activities,

130 des with 1-100 residues and adenosine mono-, di-, and triphosphate nucleotides are used as model poly

131 d azelaic acid) acid with alkylamine (mono-, di-, and trimethylamines), represent those commonly foun

132 ntification and quantification of all mono-, di-, oligosaccharides and cyclitols observed in green te

133 Engineering HMS2 reveals alternative mono-, di- or tri-cistronic and antisense transcription units (

134 A wide range of readily available mono-, di-, and trifluoromethyl heteroaryl sulfones can thus be

135 Histone H3 lysine 4 (H3K4) can be mono-, di-, and trimethylated by members of the COMPASS (comple

136 nd histone residue that could also be mono-, di-, and trimethylated by PRDM9 as efficiently as H3K4.

137 onal assignment of substances bearing mono-, di-, and perfluoroalkyl rather than trifluoromethyl grou

138 um bromide salts (TAA), benzylamines (mono-, di-, and tri-), and illicit drugs (MA, MDEA, and haloper

139 pplied to a variety of alpha- or beta-mono-, di-, and polythiosugar derivatives to synthesize efficie

140 Repressive Complex 2 (PRC2) catalyzes mono-, di-, and trimethylation of lysine 27 on histone H3 (H3K2

141 sociated methyltransferase catalyzing mono-, di-, and trimethylation of lysine 27 on histone H3 (H3K2

142 histone methyltransferase catalyzing mono-, di-, and trimethylation of the H3K4 mark.

143 d to the production of singly charged mono-, di-, and trisaccharide fragments.

144 This protocol comprises mono-, di-, and trisubstituted aliphatic, alpha-amino, and alph

145 ic conversion of structurally diverse mono-, di-, tri-, and tetrasubstituted olefins to N-H aziridine

146 The final mono-, di-, and tetravalent ligands were resistant to enzymatic

147 lysine methyltransferase required for mono-, di-, and trimethylation of this site.

148 paration of side-chain functionalized mono-, di-, and trifluoromethylisoxazoles, for example, fluorin

149 omplex the reaction mixture generated mono-, di- and tri-substituted sugar complexes and their hydrol

150 zuki cross-coupling reactions to give mono-, di-, and trisubstituted bullvalenes.

151 e surfactant, including PEO(n)-glucam mono-, di-, and tristearates as well as free and esterified PEO

152 An array of olefins, including mono-, di-, and trisubstituted olefins, are all smoothly hydrom

153 and broad substrate scope, including mono-, di-, and trisubstituted tertiary, secondary, and primary

154 The separation of myo-inositol mono-, di-, tri-, tetra-, pentakis-, and hexakisphosphate (InsP

155 hat the valency of H3K79 methylation (mono-, di-, and tri-) is determined by nucleosome turnover rate

156 cytosine and uracil (deoxy)nucleoside mono-, di-, and triphosphates by uniport and antiport.

157 unmodified nucleosides and nucleotide mono-, di- and tri-phosphates by capillary electrophoresis coup

158 -49 and 64-124ngmL(-1) for nucleotide mono-, di-, and tri-phosphates, respectively, were found.

159 The ion signal intensities of mono-, di-, and oligohexosylceramides were enhanced by up to 10

160 Here, we synthesized a panel of mono-, di-, and tri-meric fatty acid-conjugated siRNAs to syste

161 The synthesis of mono-, di-, and trifluoromethyl aryl ethers by fluorodecarboxyl

162 ocess was used to prepare a series of mono-, di-, and trifunctionalized mesoporous metal-organic fram

163 analysis to differentiate a panel of mono-, di-, and triglycerides.

164 ed binding to the oligosaccharides of mono-, di-, and trisialylated gangliosides.

165 A range of mono-, di-, and trisubstituted olefins as well as alkyl- and ar

166 resent method allows the synthesis of mono-, di-, and trisubstituted pyrroles with appropriate substi

167 -O(Ar))(2)M(n+) cores with a range of mono-, di-, and trivalent Lewis acids (M(n+)).

168 Manduca sexta), which uses a blend of mono-, di-, and uncommon triunsaturated fatty acid (3UFA) deriv

169 es as electrophiles, a broad range of mono-, di-, tri- and tetrasubstituted alkenes are compatible in

170 All members of this library of mono-, di-, tri-, and tetramethyl-substituted derivatives were

171 irect regioselective incorporation of mono-, di-, tri-, and tetrasubstituted olefins at the alpha-car

172 Various olefins, mono-, di-, and trisubstituted, are epoxidized chemoselectively

173 suggestions of a dinuclear Fe site or mono-, di-, or trinuclear Cu sites.

174 the photolysis of this and six other mono-, di-, and triazastilbenes in solid and solution states.

175 the construction of highly oxygenated mono-, di-, and polycyclic carbocycles from the reaction of dis

176 ifferent phosphoinositide phosphates (mono-, di-, and triphosphorylated inositides), a phosphatidic a

177 iciresinol monoglycoside, pinoresinol mono-, di- and triglycoside, sesaminol, sesaminol triglycoside,

178 ne H3, but not by histones previously mono-, di-, or trimethylated at H3K4.

179 of the Sir proteins to reconstituted mono-, di-, tri-, and tetra-nucleosomal chromatin templates and

180 parate diesel samples into saturates, mono-, di-, and polyaromatics by gas chromatography, with selec

181 The stability of seven mono-, di-, and trihaloacetonitriles was examined under a varie

182 omannose type N-glycans, sialylation (mono-, di-, and tetra-), fucosylation (tri-, core, and outer ar

183 ites can reach a tetra-anionic state, mono-, di-, tri-, and tetra-anionic complexes likely dominate a

184 In this study, mono-, di-, and triPAPs, perfluorinated alkyl acids (PFAAs), sa

185 osphinate) and NODAGA, we synthesized mono-, di-, and trimeric conjugates of the alphavbeta6 integrin

186 osphinate) and NODAGA, we synthesized mono-, di-, and trimeric conjugates of the alphavbeta6 integrin

187 ases comprises 27 members that target mono-, di-, and trimethylated lysine residues of histone (or no

188 ing, catalytic transformations of the mono-, di-, and oligosaccharides.

189 Finally, the mono-, di-, and triglycosylceramides were characterized as gala

190 he successive oxyfunctionalization to mono-, di-, and tetraepoxy derivatives is accomplished using hy

191 els for predicting methylation types (mono-, di-, tri-methylation).

192 ormational ensembles of unacetylated, mono-, di-, tri-, and tetra-acetylated H4 histone tails using R

193 nstructs having controlled valencies (mono-, di-, trivalent in terms of biotin-binding sites) are stu

194 , fluidic and multicompartments) with mono-, di-, and tricomponents configurations were achieved, and

195 brary of 20 CBMs was synthesized with mono-, di-, or trisaccharides at each site for comparison of bi

196 tonitrile was also performed yielding mono-, di- and tri-stearic ester derivatives.

197 ymes that deposit histone H3 Lys4 (K4) mono-/di-/tri-methylation and regulate gene expression in mamm

198 In contrast, most di- and tri-methylation PTMs are enriched on old histone

199 ich are presumed to be PG fragments (muramyl di- and tripeptides).

200 trometry, confirming the presence of muramyl di- and tripeptides in Chlamydia-infected cell lysate fr

201 Cp*(Cl)Ti(N,N-di-(t)Bu-eta(1),eta(2)-diimine) (2), in the presence of

202 ioanisole, diphenyl ether, phenol, naphthol, di- and trimethoxy benzenes, xylene, mesitylene, N,N-dim

203 cil, thymine, and cytosine (deoxy)nucleoside di- and triphosphates by an antiport mechanism and SLC25

204 MS fragmentation, clustered in flavonol-3-O-di-/tri-glycosides-7-O-rhamnosides and other flavonol-gl

205 ioselective redox-relay Heck alkynylation of di- and trisubstituted alkenols to construct propargylic

206 were identified as having reduced amounts of di- and trimethylated myricetins and increased monomethy

207 cages were prepared by the self-assembly of di- or tritopic anilines and 2,6-diformylpyridine subcom

208 e O antigen would be capped by attachment of di- or tri-O-methylated fucose as catalyzed by glycosylt

209 (intra ligand-ligand), (ii) the building of di- or oligonuclear complexes (inter ligand-ligand), (ii

210 presence/absence of specific combinations of di- and trinucleotides, (iii) nucleotide interactions by

211 e MR antagonists based on the conjugation of di- or tripeptides to M(2)R-preferring dibenzodiazepinon

212 hocyanin profiles differently constituted of di- and tri-substituted forms.

213 elective synthesis of either diastereomer of di- and trisubstituted cyclopropanes.

214 d, we compare here the removal efficiency of di-(2-ethylhexyl)phthalate (DEHP) on hands by handwashin

215 Frequency of di-(AG/CT), tri-(AGG/CTT), tetra-(AAAT), penta-(AGAGG),

216 atalysts for the asymmetric hydrogenation of di-, tri-, and tetrasubstituted unfunctionalized alkenes

217 onstrated high microsatellite instability of di- and tetranucleotides (EMAST), and immunohistochemica

218 r the tested sets with up to five isomers of di- to heptasaccharides, the root-mean-square deviation

219 e capacity to recognize a diverse library of di- and tripeptides, making them extremely promiscuous a

220 de into small fragments consisting mainly of di- and tripeptides that ensured the safe breakdown of t

221 on conditions, regioselective methylation of di-, tri-, and tetrasaccharide substrates proceeded in i

222 We prepared a number of di- and trifunctionalized quinolines by selective metala

223 ches that may be used for the preparation of di- or tri-substituted alkenyl nitriles.

224 (JmjC) domain that catalyzes the removal of di- and trimethylation on H3K27.

225 The synthesis of a series of di-, tri-, and tetraalkyl beta-thiolactones and beta-lac

226 This procedure can be used for synthesis of di-, tri-, and tetra-substituted allenes.

227 for chloroacetamide but higher than those of di- and trichloroacetamide.

228 orters (POTs) couple the inward transport of di- or tripeptides with an inwardly directed transport o

229 he large PTR family facilitate the uptake of di- and tripeptides to provide cells with amino acids fo

230 ily, functioning in proton-coupled uptake of di- and tripeptides.

231 This is accomplished by the use of di- or trisubstituted alkenes in stereoretentive process

232 guided pathway to develop a large variety of di- and trinuclear 1,2,4-triazolate-based clusters for u

233 ts flexibility in accommodating a variety of di- and trivalent metals, which can be further utilized

234 ormation was explored for a large variety of di- to tetrasubstituted piperidines with aryl, alkyl, an

235 avoid gluten, or reduce fermentable oligo-, di-, and mono-saccharides and polyols.

236 ate diet and diet low in fermentable oligo-, di-, and monosaccharides and polyols.

237 s, due to high levels of fermentable oligo-, di-, monosaccharides and polyols (FODMAPs).

238 tain fructans, a type of fermentable oligo-, di-, monosaccharides and polyols.

239 ort-chain carbohydrates (fermentable oligo-, di-, monosaccharides, and polyols [FODMAPs]) has been re

240 rt-chain carbohydrates (fermentable, oligo-, di-, monosaccharides, and polyols [FODMAPs]) in subjects

241 A series of three short oligomers (di-, tri-, and tetramers) of cis-2-(aminomethyl)cyclobut

242 Furthermore, the presence of one di- and two monohydroxylated octachlorinated biphenyls (

243 Summed metabolites of butyl phthalates or di-(2-ethylhexyl) phthalates were significantly associat

244 ort of the formation of opioid receptor (OR) di-/oligomers suggests previously unknown mechanisms use

245 e mainly zerovalent, such as thiols, organic di- and polysulfides, or heterocycles.

246 The distinction of oxidized di- and triterpenes, for example, is hindered by the sup

247 iisopentyl phthalate, di-n-pentyl phthalate, di-(2-ethylhexyl) phthalate, di-n-octyl phthalate, diiso

248 This analogue was used to make potent di- and trivalent binders of ASGPR.

249 ic ester, a variety of selectively protected di- and trisaccharide derivatives can be accessed in an

250 The present strategy to provide di- and triaryl carbazoles in one pot involves benzannul

251 iazo compounds and terminal alkynes provides di- and trisubstituted allenes.

252 In the presence of slow reacting di- and tricarboxylic acids (oxalic, malonic, succinic,

253 Agonist stimulation did not alter receptor di-/oligomerization, but increased the mobility of GABA(

254 SHL and EBS recognize di- and trimethylated histone H3 at lysine 4 and bind re

255 Binding studies with two related di- and tetrasaccharides revealed a similar decrease tha

256 distinct mechanisms, including the reported (di-)polar, axial, and a previously undescribed mechanism

257 rs, thus achieving well-defined and resolved di- or tri-BCPs of acrylates.

258 o, taxanes, epothilones, statins, retinoids, di-/triterpenes, noviose deoxysugar, and antibiotics der

259 On the basis of these discoveries, robust di- and triblock copolymer syntheses have been demonstra

260 vosyldiacylglycerols (SQDGs), sphingolipids, di- and tri-acylglycerols (DAGs and TAGs), and sterol de

261 In this way, selectively substituted di-, tri-, tetra-, and pentachloro-BODIPYs 2-5 were prep

262 beta-(1->3)-glucan mimetics and synthesized di-, tri-, and tetramers in an enantiomerically pure for

263 ngineered the native E. coli ACP into tandem di- and tri-domain constructs joined by a naturally occu

264 KDM6A) is a histone demethylase that targets di- and tri-methylated histone H3 lysine 27 (H3K27).

265 nd the stereoselectivity with which terminal di- and trisubstituted tetraenes are known to react bios

266 nosaccharide attachments perform better than di- or trisaccharide glycosides.

267 showed a higher resistance against heat than di- and non-acylated.

268 Computations indicate that di- and trisubstituted tetraenes undergo facile but less

269 SETDB1 reversibly catalyzes the di- and trimethylation of histone 3 (H3) K9 in euchromat

270 The thermal stability for the di- and tri-domain constructs was similar to that of the

271 em products 12 and 14 were isolated from the di- and trimethylated substrates 1k and 1l, respectively

272 tions in kis cause a global reduction in the di- and tri-methylation of histone H3 on lysine 36 (H3K3

273 We found that the di- and trimethylated states both contribute to activati

274 nt activation, and further indicate that the di- and trimethylation states play distinct roles in the

275 ce inhibitors structurally dissimilar to the di- and tripeptide-based HCV protease inhibitors in adva

276 (8), and bionectin A (9)--starting with the di-(tert-butoxycarbonyl) derivative 17 of the trioxopipe

277 yltransferase activity but differed in their di- and trimethylation activities.

278 These di- and tricarboxylates are imported into the cell by th

279 An approach to di- and trihetera[3.3.n]propellanes (n = 2-4 ), advanced

280 /5/7 specifically stimulates NuA4 binding to di- and trimethylated histone H3 Lys-36 and that this bi

281 te and polyM, which were further degraded to di- and trisaccharides.

282 ted anthocyanins was increased from mono- to di- to triglycosyl moieties, possibly due to steric inte

283 By linking of sialylated LAcNAc units to di- and trivalent scaffolds, inhibitors were obtained wi

284 is process shows functional group tolerance; di-, tri-, and tetrasubstituted N-vinylazoles were obtai

285 silver-catalyzed aminations which transform di- and trisubstituted homoallylic carbamates into [4.1.

286 e solute carrier 15 family (SLC15) transport di- and tripeptides as well as peptidomimetic drugs acro

287 based nucleotides, including adenosine tri-, di-, and mono-phosphate, are controlled through their ra

288 LLE using di-(2-ethylhexyl)phosphoric acid (D2EHPA) extracted 97%

289 llows: organic solvent: 1-octanol+2.5% (V/V) di-(2-ethylhexyl) phosphate, applied voltage: 70V, extra

290 road range of acceptors, generating valuable di- and trifluoromethylated cyclopentanes, pyrrolidines

291 A series of various di- and trisubstituted oxazole products bearing differen

292 lly to PtdIns3P, non-specifically to various di- and tri-phosphorylated phosphoinositides, bind both

293 od yields and selectivities, especially with di- and trisubstituted arenes.

294 is indeed a result of complex formation with di- and polyols, specific binding.

295 t the strongest interactions took place with di- and tetra-acetylated peptides derived from the histo

296 VLPs) carrying hydrophobic TLR2 PAMPs within di- and triacylated lipopeptide cores (P2Cys-SVLPs and P

297 ked to the N atom of proline residues within di- and tripeptides.

298 Oxidation of diamino MDI derivatives yields di- and tetraimide functionalized azaacenes with signifi

299 of a broad range of N-allyl amides to form Z-di-, tri-, and tetrasubstituted enamides with exceptiona

300 metabolization to succinyl-ZMP, ZDP, or ZTP (di- and triphosphate derivatives of AICAR) strongly redu