ライフサイエンスコーパス: carbodiimide

1 ylaminopropyl) carbodiimide, a water-soluble carbodiimide.

2 up in the presence of an activator such as a carbodiimide.

3 ilitated by 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide.

4 tion with a positively charged water-soluble carbodiimide.

5 nt with N-ethyl-1-3-[3-(dimethylamino)propyl]carbodiimide.

6 lamine and 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide.

7 -linked by 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide.

8 itated by 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide.

9 linked with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide.

10 eaction with 1-ethyl-3-[(diethylamino)propyl]carbodiimide.

11 ic cross-linker, N- ethyl-3-(3-diaminopropyl)carbodiimide.

12 e plates by 1-ethyl-3(3-dimethylaminopropyl) carbodiimide.

13 zirine, which photorearranges to give methyl carbodiimide.

14 azone and 1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide.

15 inked to apoptotic leukocytes using ethylene carbodiimide.

16 yl- and silylnitrile imines) or rearrange to carbodiimides.

17 sceptibility of the V-PPase to inhibition by carbodiimides.

18 s and the C horizontal lineN double bonds of carbodiimides.

19 he photoisomerization of nitrile imines into carbodiimides.

20 which upon thermolysis isomerize to bridging carbodiimides.

21 Carbodiimide 10, cyanamide 12, N-cyanomethyleneimine 13,

22 Using carbodiimide, (111)In-DOTA-ChL6 (DOTA is dodecanetetraac

23 via thermolysis of the pyridannulated enyne-carbodiimides 14, 19, and 23 were established.

24 sphorane 14 produced in situ the benzoenynyl carbodiimides 15.

25 lso produced in situ the benzannulated enyne-carbodiimides 25, which on thermolysis gave the isoquino

26 Thermolysis of the enyne-carbodiimide 42 having a methoxymethyl substituent at th

27 dinitrogen and sulfur to form the respective carbodiimides 5a,b as sole photoproducts.

28 the quantum yields for the formation of the carbodiimides 5a,b were modest and showed little change

29 Thermolysis of the enyne-carbodiimides 7 having the central carbon-carbon double

30 rd 32 by conducting thermolysis of the enyne-carbodiimide 7e in the presence of 5 equiv of dimethylph

31 talyzed by 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide, a water-soluble carbodiimide.

32 f PEDF with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide abolished it, implicating the PEDF aspartic

33 We have utilized labeling with carbodiimide-activated [14C]AGA to identify peptides 120

34 derivatized protein, and (ii) binding of the carbodiimide-activated terminal phosphate group of the C

35 The carbodiimide activation of carboxylate groups occurs onl

36 d through a streptavidin-biotin bridge via a carbodiimide activation protocol.

37 Reactions with ketenes and carbodiimides afford four-membered anionic heterocycles

38 o syngeneic splenic leukocytes with ethylene carbodiimide (Ag-coupled splenocytes [Ag-SP]) has been d

39 d with 1-ethyl-3-[3-(trimethylammonio)propyl]carbodiimide and [35S]sulfanilic acid.

40 omethane, benzophenone and N,N'-di-isopropyl carbodiimide and by density functional theory.

41 Ugi treated with carbodiimide and glycine ethyl ester produced five discr

42 ed to a dendrimer in a reaction catalyzed by carbodiimide and imidazole.

43 nas and optic nerves were fixed overnight in carbodiimide and labeled with an antiserum to histamine

44 SA) using N-ethyl-N'-(3-dimethylaminopropyl) carbodiimide and N-hydroxysuccinimide (EDC/NHS) chemistr

45 a simple 1-ethyl-3-(3-(dimethylamino)propyl)-carbodiimide and N-hydroxysuccinimide (EDC/NHS) chemistr

46 e by using 1-Ethyl-3-(3-dimethylaminopropyl)-carbodiimide and N-Hydroxysuccinimide coupling reagents,

47 oteins with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide and N-hydroxysuccinimide revealed that carb

48 mutagenesis and chemical cross-linking using carbodiimide and N-hydroxysuccinimide.

49 reagents, 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide and sulfo-N-hydroxysuccinimide.

50 orm an amide derivative with a water-soluble carbodiimide and the electrophoric amine, AMACE1; (3) pu

51 to succinylated hemocyanin by water-soluble carbodiimide and was used as an immunogen to produce pol

52 [4+2] annulation of thioimidates with vinyl carbodiimides and an alkyne hydroamination employing 2-a

53 nd Ph(Me)C(H)Bpin, and (ii) hydroboration of carbodiimides and pyridine to form N-boryl formamidines

54 , alkyne, N 2, alkene, diazene, azide, CO 2, carbodiimide, and Bronsted acid containing substrates.

55 cal mol(-1) for hydrazoic acid, nitrilimine, carbodiimide, and ketenimine, respectively.

56 ction with 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide, and the peptide quenched the fluorescence

57 ndency to chemically and thermally eliminate carbodiimide, and the scarcely observed ring expansion b

58 oup of N-DNW using ethyl(dimethylaminopropyl)carbodiimide as the coupling agent and N-hydroxysuccinim

59 ng ethylenedicysteine with glucosamine, with carbodiimide as the coupling agent.

60 tal-mediated catalytic addition of amines to carbodiimides as an atom-economical alternative to the c

61 ides, are converted to phosphoramidates with carbodiimide assistance.

62 nic acid mono methyl esters with diisopropyl carbodiimide at ambient temperature leads to clean stere

63 alizing the PA sorbent with oligo dT20 using carbodiimide-based amide linker chemistry.

64 intact tissues, we developed a method using carbodiimide-based chemistry to stably retain RNAs in cl

65 The usual strategy has employed carbodiimide-based condensing reagents for activation of

66 e reaction of 3-azidopropanoic acid with the carbodiimide-based coupling reagent DIC leads to a six-m

67 d gold electrode surface by the formation of carbodiimide bond.

68 itrile imines isomerize to the corresponding carbodiimides both thermally and photochemically.

69 ss-linker, 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide, can link the N-terminal G-S extension of t

70 covalently attached onto the electrode using carbodiimide chemistry between the carboxylic groups of

71 ferent length covalently immobilized through carbodiimide chemistry on the surface of rGO-CMC-modifie

72 which can also be functionalized by classic carbodiimide chemistry with N-hydroxysuccinimide (NHS).

73 Using the simple and versatile carbodiimide chemistry, Abs were attached to the carboxy

74 Using carbodiimide chemistry, functionalized probe DNA strands

75 were coupled to phosphorylated primers using carbodiimide chemistry.

76 ovalent immobilization of antibodies through carbodiimide chemistry.

77 of proteins to the particles using standard carbodiimide chemistry.

78 and then conjugating the anti-A IgG through carbodiimide chemistry.

79 lucose transporter-1 (GLUT-1) antibodies via carbodiimide chemistry.

80 Here, we show that carbodiimides constitute a simple class of chemical fuel

81 e quantum dots (QDs) on carboxylated GRs via carbodiimide coupling chemistry, followed by the immunor

82 amenable to covalent modification via simple carbodiimide coupling chemistry, which is achieved by fu

83 by plasma activating the PMMA and the use of carbodiimide coupling chemistry.

84 band UV exposure of the polymer surface, (2) carbodiimide coupling of amine-terminated oligonucleotid

85 mines to glutamic acid side chains through a carbodiimide coupling reaction.

86 F through a 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide coupling reaction.

87 was covalently conjugated to afGQDs through carbodiimide coupling reaction.

88 covalently tethered onto gold electrodes via carbodiimide coupling to cysteamine-modified gold electr

89 Carbodiimide coupling, cooper-mediated 'click' coupling,

90 NS1 comparing copper free click coupling to carbodiimide coupling, one of the most common approaches

91 opylene carbonate) (PEG-PCC) copolymer using carbodiimide coupling, which self-assembled into micelle

92 Both mAbs were conjugated to SarAr using carbodiimide coupling.

93 otide probes to these surface groups through carbodiimide coupling.

94 om carboxyl-coated polystyrene particles via carbodiimide coupling.

95 ugated to simple amino acids and peptides by carbodiimide coupling.

96 ii) stabilization of fragile sialic acids by carbodiimide coupling; (iii) release of N-glycans by PNG

97 oint at the end of a PEG chain combined with carbodiimide-coupling to attach two TA groups per PEG ch

98 ubes covalently attached to chitosan via the carbodiimide crosslinker EDC followed by chitosan electr

99 A carbodiimide crosslinker was used for crosslinking radio

100 immobilizing Con A on a 5MHz gold crystal by carbodiimide crosslinking chemistry.

101 olving an intramolecular ring closure of the carbodiimide-derived phosphazene intermediate is given.

102 Contrary to its oxide analogue, iron carbodiimide does not require heavy treatments (such as

103 venous injection of peptide-pulsed, ethylene carbodiimide (ECDI)-fixed splenic antigen-presenting cel

104 therapy that utilizes infusions of ethylene carbodiimide (ECDI)-treated donor splenic antigen-presen

105 re bound by the cross-linking agent ethylene carbodiimide (ECDI).

106 donor splenocytes cross-linked with ethylene carbodiimide (ECDI-SPs) has been demonstrated to effecti

107 ated with 1-ethyl-3-(3'-dimethylaminopropyl)-carbodiimide (ECDI-SPs) provide permanent donor-specific

108 Analogs of syndecan-1 were produced by carbodiimide (EDAC) conjugation of glycosaminoglycan (GA

109 Ib-2) using 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDAC), which modifies acidic amino acid re

110 density of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) activated anti-LCN2 capture antibodie

111 inking with 1-ethyl-3-(dimethylamino-propyl)-carbodiimide (EDC) allowed the isolation of a BPL:apo-BC

112 , involving 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) and 1-cyano-4-dimethylaminopyridinium

113 ss-linker 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide (EDC) and analyzed by gel electrophoresis.

114 resence of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) and imidazole.

115 activator 1-ethyl-3-(3-dimethylamino)propyl)carbodiimide (EDC) and the catalyst 1-hydroxybenzotriazo

116 gomers with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) in the presence of linear plasmid DNA

117 roups with 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) or 2-chloro-1-methylpyridinium iodide

118 to BSA by 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) to form GAMP(CNBr)AH-BSA and GAMP(CDA

119 1-Ethyl 3-[3-(dimethylamino)propyl]carbodiimide (EDC) was found to promote formation of sto

120 ter-soluble 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) was used to cross-link proteins with

121 s-linker, 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide (EDC), and the Paracoccus membranes were us

122 g UV-ozone, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC), and treated with N-hydroxysuccinimid

123 -linker, l-ethyl-3-[3-(dimethylamino) propyl]carbodiimide (EDC), cross-linked the ND8-G-actin complex

124 ed reagent, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC), in a concentration-dependent and sub

125 ss-linker 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide (EDC), referred to as EDC-actin.

126 h a novel, 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC)-mediated, chemical cross-linking step

127 e through N-ethyl-N'-(3-dimethylaminopropyl) carbodiimide (EDC)-N-hydroxy succinimide (NHS) chemistry

128 ing agent 1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide (EDC).

129 ss-linker 1-ethyl-3-[3-dimethyl-aminopropyl]-carbodiimide (EDC).

130 with ADH and 1-ethyl-3(3-dimethylaminopropyl carbodiimide (EDC).

131 ocol with 1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide (EDC).

132 We discovered that using the soluble carbodiimide, EDC, to cross-link RNA to nylon membranes

133 opyl ester of methionine (MIPE), mediated by carbodiimide EDCI, 1, and HOBt, 2, have been studied in

134 In particular, iron carbodiimide, FeNCN, can be efficiently used as negative

135 nostaining for the cysteinyl leukotrienes in carbodiimide-fixed cells, we show, for the first time, t

136 ated epitopes, by i.v. injection of ethylene carbodiimide-fixed peptide-pulsed APCs, either before di

137 reatment with Ag (peptide)-coupled, ethylene carbodiimide-fixed syngeneic splenocytes (Ag-SP) is a po

138 istration of myelin peptide-pulsed, ethylene carbodiimide-fixed syngeneic splenocytes, but not solubl

139 reaction proceeds through the formation of a carbodiimide, followed by a sequential addition--dehydra

140 pling to a keto function and a water-soluble carbodiimide for coupling to a carboxyl function.

141 (LNA) and 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide for cross-linking the RNA to the membrane.

142 rea intermediates that, in the presence of a carbodiimide-functionalized resin, cyclize to benzazoles

143 The use of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide HCl (EDC) has recently been investigated fo

144 resence of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDAC) and then hybridized wi

145 tion using 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDC) and physical adsorption

146 MBs using 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDC) chemistry.

147 YiiP with 1-ethyl-3-[3-dimethylaminopropyl] carbodiimide hydrochloride (EDC) resulted in a dimeric c

148 fied with 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide hydrochloride (EDC), is not associated with

149 ied using 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide hydrochloride (EDC), Mn2+ is photooxidized

150 g reagent, 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (EDC), to localize regions of

151 ng reagent, 1-ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride (EDC), was used to covalently

152 e optimized 1-ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride (EDC)-catalyzed amide bond fo

153 loped a new 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDCI)-mediated oxazole rearr

154 sue with 1-ethyl-3-[3-(dimethylamino)propyl]-carbodiimide hydrochloride and (ii) removing highly abun

155 MTP) using 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride and N-hydroxysulfosuccinimide

156 s-linked by 1-ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride to probe for the aggregation

157 nol using 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide hydrochloride.

158 nopril by 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide hydrochloride/N-hydroxysuccinimide coupling

159 Using the method of water-soluble carbodiimide-induced chemical ligation, four 27-member o

160 proximity was assessed by the efficiency of carbodiimide-induced cross-linking and the orientation b

161 activated thiourea through the formation of carbodiimide intermediate.

162 The five-membered ring carbodiimide is a stable structure, possibly isolable.

163 ture of this reaction is that no part of the carbodiimide is incorporated into the transient species;

164 d actinide-catalyzed addition of alcohols to carbodiimides is presented.

165 enimines 5 with various heterocumulenes like carbodiimides, isocycanates, isothiocyanates and ketenim

166 Monosubstituted carbodiimides isomerize thermally to the corresponding c

167 cted to locate the transition states between carbodiimides isomers.

168 ron compound, several other transition-metal carbodiimides M(x)(NCN)y with M=Mn, Cr, Zn can cycle suc

169 s on the CNTs' tips that were modified using carbodiimide mediated coupling between the carboxylic ac

170 Carbodiimide mediated couplings with amines were then us

171 conjugated to bovine serum albumin (BSA) by carbodiimide-mediated chemistry, a key step in the reali

172 After carbodiimide-mediated cross-linking, Lys-3 of thymosin b

173 -coupling reactions for building blocks, and carbodiimide-mediated esterification for building up the

174 onjugates of Vi and OAcP were synthesized by carbodiimide-mediated synthesis with adipic acid dihydra

175 oxal, and 1-cyclohexyl-3-(2-morpholinoethyl)-carbodiimide metho-p-toluene sulfonate (CMCT) offers the

176 nd including 1-cyclohexyl(2-morpholinoethyl) carbodiimide metho-p-toluene sulfonate (CMCT) reactiviti

177 s include 1-cyclohexyl-3-(2-morpholinoethyl) carbodiimide metho-p-toluene sulfonate (CMCT; to probe U

178 l sulfate, 1-cyclohexyl-3-(2-morpholinoethyl)carbodiimide metho-p-toluene sulfonate, and kethoxal; co

179 cans with 1-cyclohexyl-3-(2-morpholinoethyl) carbodiimide metho-p-toluene sulfonate, dimethyl sulfate

180 ate (DMS), 1-cyclohexyl-3-(2-morpholinoethyl)carbodiimide metho-p-toluenesulfonate (CMCT), and beta-e

181 ulfate and 1-cyclohexyl-3-(2-morpholinoethyl)carbodiimide metho-p-toluenesulfonate probing, mutate-an

182 hoxal, and 1-cyclohexyl-3-(2-morpholinoethyl)carbodiimide metho-p-toluenesulfonate, can be combined i

183 repared by employing an N-hydroxysuccinimide/carbodiimide method.

184 The sensitivity of enzyme to water-soluble carbodiimide modification of carboxyl groups prompted ev

185 Carbodiimide modification of EmrE has been studied using

186 fferent substrate analogs to protect against carbodiimide modification of Glu269, it is suggested tha

187 in the presence of ethyl(dimethylaminopropyl)carbodiimide / N-hydroxysuccinimide (EDC/NHS) between th

188 ix-sense-selective polymerization of achiral carbodiimide, N-(1-anthryl)-N'-octadecylcarbodiimide (1)

189 s-linked with 1-ethyl-3-(dimethylaminopropyl)carbodiimide/N-hydroxylsulfosuccinimide in a 1:1 complex

190 accomplished using 3-(3-dimethylaminopropyl) carbodiimide/N-hydroxysuccinimide (EDC/NHS) coupling to

191 ing by 1-ethyl-3-(3-dimethylaminopropyl) and carbodiimide/N-hydroxysuccinimide (EDC/NHS) was adopted

192 e N-cyclohexyl-N'-(4-(dimethylamino)naphthyl)carbodiimide (NCD-4) fluorophore, whereas tryptophan is

193 razoic acid (NH=N=N), nitrilimine (NH=N=CH), carbodiimide (NH=C=NH), or ketenimine (NH=C=CH2) plus on

194 of imidoylnitrenes, which also rearrange to carbodiimides or add intramolecularly to aryl substituen

195 Using carbodiimide polyesterification, these stress-responsive

196 provides a pathway involving O2 to give the carbodiimide product whereas homogeneous metal ion catal

197 was 75-fold higher compared with traditional carbodiimide protein coupling.

198 with primary amines (H2N-R') and O2 to give carbodiimides (R-N=C=N-R') at room temperature and above

199 CHO-H4PteGlun were cross-linked to SHMT by a carbodiimide reaction to Lys-450 which resides in a stre

200 the desired antibody was carried out by the carbodiimide reaction.

201 a significant proportion of the decrease in carbodiimide reactivity occurs specifically in a nanopep

202 In contrast, carbodiimide reactivity of mutant Glu269-->Asp that exhi

203 that substrate protects the permease against carbodiimide reactivity.

204 ciency, MMOH and MMOR were cross-linked by a carbodiimide reagent and analyzed by specific proteolysi

205 The reaction is mediated with water-soluble carbodiimide reagent and is assumed to result in a prima

206 ocyanate and imidoyl isothiocyanate-thioacyl carbodiimide rearrangements.

207 Computational studies of alicyclic carbodiimides (RN horizontal lineC horizontal lineNR) (r

208 ing differential labeling by a water-soluble carbodiimide, seven specific carboxylates in RIalpha wer

209 e first time, that treatment of capsule with carbodiimide significantly reduced recognition by capsul

210 tamethylcyclopentadienyl, 1b) with different carbodiimide substrates RN horizontal lineC horizontal l

211 somerization, or C-C coupling of the applied carbodiimide substrates, respectively, to form unusual m

212 ion of the corresponding benzannulated enyne-carbodiimides, such as 10, followed by a formal intramol

213 ation with 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide that irreversibly immobilizes the microRNA

214 d utilizes 1-cyclohexyl-3-(2-morpholinoethyl)carbodiimide to derivatize pseudouridine residues.

215 linked using 1-ethyl-3(dimethylamino-propyl) carbodiimide to generate a catalytically active heterodi

216 yde and N-ethyl-1-3-[3-(dimethylamino)propyl]carbodiimide to investigate the organization of the poly

217 ked with 1-ethyl-3-[3(dimethylamino) propyl] carbodiimide to prevent shortening.

218 s were treated with N,N'-dicyclohexyl-[(14)C]carbodiimide to radiolabel the D61 residue on less than

219 diphenylketene and bis(2,6-diisopropylphenyl)carbodiimide to yield the anionic four-membered heterocy

220 ates, isothiocyanates, and in situ-generated carbodiimides to form zwitterionic intermediates that un

221 , produced by the formal [2 + 2] addition of carbodiimides to the P=N bond, have been isolated and ch

222 with EDC (1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide) to prevent shortening, with FHS.

223 vation chemistries, and we demonstrated that carbodiimide treatment under aqueous conditions results

224 ovalent modification of carboxyl groups with carbodiimides using electrospray ionization mass spectro

225 electrochemical activity of transition-metal carbodiimides versus lithium and sodium.

226 aryl) catalytically metathesize C=N bonds of carbodiimides via an addition/elimination mechanism that

227 ted when 1-ethyl-3-[3-(dimethylamino)-propyl]carbodiimide was used as cross-linking agent, whereas th

228 This reagent, N-(2,2-diethoxyethyl)carbodiimide, was convenient to prepare and was stable u

229 cross-linker ethyl-3-(3-dimethylaminopropyl)carbodiimide, we obtained cross-linked heterodimers of b

230 ng reagent, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide were identified after trypsin digestion of

231 upled with cardiac myosin by use of ethylene carbodiimide, were administered intravenously before dis

232 rosslinking agent before the addition of the carbodiimide, which allowed for the shell crosslinking t

233 th the chemical cross-linking agent ethylene-carbodiimide, which effectively modulate Th1/Th17 diseas

234 oss-linked by 1-ethyl-3-(dimethylaminopropyl)carbodiimide, while subunits a and E could be cross-link

235 astereoselective [4 + 2]-annulation of vinyl carbodiimides with chiral N-alkyl imines has been develo

236 on of anionic secondary phosphine boranes to carbodiimides yields both chiral and achiral phosphaguan