ライフサイエンスコーパス: ethylenediamine

1 tyl)-N'-(7-nitrobenz-2-oxa-1,3-diazol-4 -yl) ethylenediamine).

2 sionally reduced 1D van der Waals solid TiS2(ethylenediamine).

3 ldehyde followed by reductive amination with ethylenediamine.

4 re made by a reaction of K4Ge9 with SbPh3 in ethylenediamine.

5 scavenger N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine.

6 rived from oligonucleotide 5'-phosphates and ethylenediamine.

7 uced from the robust Strecker synthesis with ethylenediamine.

8 er intercalation of guest species such as Li-ethylenediamine.

9 romium(III) perchlorate and pH adjusted with ethylenediamine.

10 halcogen, and tmeda is N,N,N',N'-tetramethyl-ethylenediamine.

11 fected by N,N,N',N'-Tetrakis(2-pyridylmethyl)ethylenediamine.

12 t in solutions composed of alkali metals and ethylenediamine.

13 Eu 2][mu-eta (1),eta (1)-en] structure [en = ethylenediamine].

14 l deoxyinosines and the appropriate diamine (ethylenediamine, 1,3-diaminopropane, 1,4-diaminobutane).

15 ), cis-[Pt(NH(3))(cyclohexylamine)](2+), [Pt(ethylenediamine)](2+), cis-[Pt(NH(3))(cyclobutylamine)](

16 f the type 2-aminobenzoyl-GGX(1)X(2)RKX(3)GQ-ethylenediamine-2,4- dinitrophenyl, where P(2), P(2)', a

17 fluorogenic peptide 2-aminobenzyl-GGFLRKVGQ-ethylenediamine-2,4-dinitrophenol at the R-K bond, exhib

18 port here that with 2-aminobenzoyl-GGFLRKHGQ-ethylenediamine-2,4-dinitrophenyl as substrate, ATP and

19 uorogenic substrate 2-aminobenzoyl-GGFLRKHGQ-ethylenediamine-2,4-dinitrophenyl is increased 2-7-fold

20 ,2-cyclohexanediamine (2a), or N,N'-dimethyl-ethylenediamine (3) is reported.

21 hen to amides with terminal diamines such as ethylenediamine, 4,4'-methylenebis(cyclohexylamine), and

22 red: N,N'-bis-(2,2-dimethyl-2-mercaptoethyl) ethylenediamine (4SS), 1-carboxy-N-N'-bis(2,2-dimethyl-2

23 rboxy-N-N'-bis(2,2-dimethyl-2- mercaptoethyl)ethylenediamine (5SS), and N,N'-bis(2,2- dimethyl-2-merc

24 -9-ylamino)ethyl]-1,3-dimethylthiourea, en = ethylenediamine), a bifunctional platinum-acridine conju

25 le with N,N,N',N'-tetrakis (2-pyridylmethyl) ethylenediamine, a specific Zn(2+) chelator, whereas non

26 N,N,N',N'-tetrakis (2-pyridylmethyl)ethylenediamine, a zinc chelator, completely blocked per

27 at TPEN [N,N,N',N'-tetrakis (2-pyridylmethyl)ethylenediamine], a zinc chelator, protected against neu

28 ue 6 or 6' using galactose oxidase, a dansyl ethylenediamine acceptor fluorophore was coupled to eith

29 cence of N-iodoacetyl-N'-(5-sulfo-1-naphthyl)ethylenediamine (AEDANS) conjugated to Cys(374) of actin

30 4 and an N-iodoacetyl-N'-(5-sulfo-1-napthyl) ethylenediamine (AEDANS) moiety covalently attached to t

31 ic acid or TMU, 552 M(-1)), and theophylline ethylenediamine (aminophylline, 596 M(-1)).

32 s by diamine coordination using tetramethyl- ethylenediamine and (-)-sparteine.

33 -Ge(9)(4-), made from K(4)Ge(9) dissolved in ethylenediamine and 2,2,2-crypt(4,7,13,16,21,24-hexaoxa-

34 azo dye is then separated from N-(1-napthyl)ethylenediamine and quantified by reversed-phase HPLC.

35 duced into the abasic sites by reaction with ethylenediamine and reduction of the aldimine bonds form

36 s of two pillaring agents i.e., the flexible ethylenediamine and the relatively rigid 1,4-diazabicycl

37 ate complex [Co(en)2 O2 CO](+) Cl(-) (en=1,2-ethylenediamine) and (S)-[H3 NCH((CH2 )n NHMe2 )CH2 NH3

38 ystal structures of [CdSe(en)(0.5)] (4; en = ethylenediamine) and [CdSe(pda)(0.5)] (5) are 3-D networ

39 antagonist, aminophylline (AMO; theophylline ethylenediamine) and, for the first time to our knowledg

40 zoic acid and EDDnp is N-(2, 4-dinitrophenyl)ethylenediamine)) and 0.24 x 10(4) M-1 s-1 (Abz-Tyr-Gly-

41 itle compound starting from methyl acrylate, ethylenediamine, and dimethyl malonate is reported.

42 -aminobenzoyl-GGFLRKHGQ-N-(2,4-dinitrophenyl)ethylenediamine as substrate, ATP and triphosphate incre

43 10 mol % of copper(I) iodide and 20 mol % of ethylenediamine as the catalyst in dioxane at 110 degree

44 Electric discharges also produce ethylenediamine, as do NH(4)CN polymerizations.

45 rt beta5i-selective inhibition by asparagine-ethylenediamine (AsnEDA)-based compounds and present the

46 chelator N,N,N',N'-Tetrakis(2-pyridylmethyl)ethylenediamine augmented TLR4-mediated production of IF

47 reported on a novel series of antimalarial, ethylenediamine-based inhibitors of protein farnesyltran

48 es catalyzed by Pd(OAc)2 and bis-benzylidene ethylenediamine (bbeda) is a landmark methodology in tra

49 chelator N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine blocked InsP3R ubiquitination, suggestin

50 )-N'-(acetyl 4,4'-pyridylpyridinium iodide)] ethylenediamine (BPP+), which contains a molecular recog

51 e (CEM) -based anion suppressor and Tris and ethylenediamine buffers using an anion-exchange membrane

52 ine samples of [Co(en)3Cl3]2.NaCl.6H2O (en = ethylenediamine, C2H8N2) doped with Cr(III) in varying c

53 -pentanedionato)(N,N-diethyl-N',N'-dimethyl- ethylenediamine)cadmium(II), Cd(hfa)(2)()(N,N-DE-N',N'-D

54 ototypical porous metal-organic framework to ethylenediamine can effectively retain a variety of weak

55 pH/concentration gradients from a mixture of ethylenediamine, citrate, and phosphate by manipulating

56 ered that adducts formed by [(eta(6) -THA)Ru(ethylenediamine)Cl][PF6 ] (THA=5,8,9,10-tetrahydroanthra

57 xaammine cobalt (III) chloride (Cohex), tris(ethylenediamine) cobalt(III) chloride (Coen), and cobalt

58 d), iodo substitution with lithium acetylide ethylenediamine complex (LiAEDA, HMPA, -5 degrees C), an

59 DANS [N'-iodoacetyl-N'-(1-sulfo-5-n-naphthyl)ethylenediamine]/DABMI [4-(dimethylamino)-phenylazopheny

60 of the bis-diamine ligand N,N'-di-tert-butyl-ethylenediamine (DBED) with O(2) is a functional and spe

61 secondary diamine ligand N,N'-di-tert-butyl-ethylenediamine (DBED), [(DBED)Cu(MeCN)](X) (1.X, X = CF

62 secondary diamine ligand, N,N'-di-tert-butyl-ethylenediamine (DBED).

63 G-actin quenched the fluorescence of dansyl ethylenediamine (DED) attached to Gin-41 by more than 50

64 binding enhanced the fluorescence of dansyl ethylenediamine (DED) attached to Gln41 on the DNase I b

65 Actin labeled at Gln-41 with dansyl ethylenediamine (DED) via transglutaminase reaction was

66 ages modified with the cation N , N -diethyl-ethylenediamine (DEED).

67 re then smoothly deprotected by heating with ethylenediamine derivatives, resulting in a general proc

68 rged cathodic working voltage window through ethylenediamine-derived functional groups, and the enhan

69 nts were both sensitive to the iron chelator ethylenediamine di(o-hydroxyphenylacetic acid) and resis

70 rowth in medium containing the iron chelator ethylenediamine di-o-hydroxyphenylacetic acid, reduced s

71 on media containing the iron chelator EDDA [ethylenediamine-di(o-hydroxyphenyl acetic acid)].

72 um in which iron is chelated by transferrin, ethylenediamine-di(o-hydroxyphenyl-acetic acid), or othe

73 in to growth inhibition by the iron chelator ethylenediamine-di(o-hydroxyphenylacetic acid).

74 ld be activated by a synthetic iron chelator ethylenediamine-di(o-hydroxyphenylacetic) acid, indicati

75 pticase soy broth with 1.5% NaCl (TSBS) plus ethylenediamine-di-(o-hydroxyphenylacetic) acid (EDDA)],

76 ynyloxy)-salicylaldehydes in the presence of ethylenediamine diacetate (EDDA) is reported.

77 sions of relaxation agents (oxygen or nickel ethylenediamine diacetic acid) with spin labels are meas

78 sis by MALDI-TOF MS using the N-(1-naphthyl) ethylenediamine dihydrochloride (NEDC) matrix.

79 ue employing sulfanilamide and N-(1-naphthyl)ethylenediamine dihydrochloride as color reagents where

80 lfanilic acid that reacts with N-(1-naphthyl)ethylenediamine dihydrochloride forming an orange-colore

81 ons containing sulfanilamide/N-(1-naphthyl)- ethylenediamine dihydrochloride or 2,2'-azinobis (3-ethy

82 inking and construction of a GO framework by ethylenediamine (EDA) and (2) the amine-enrichment modif

83 ter of (45.3 +/- 3.7) nm) in the presence of ethylenediamine (EDA) as a stabilizing agent and gold na

84 l of the chiral auxiliary by extraction with ethylenediamine (EDA), due to the kinetic stability of t

85 thesis of dendrimers and dendrons containing ethylenediamine (EDA), piperazine (PPZ), and methyl 2,2-

86 obenzoic acid (Abz) and N-(2,4-dinitrophenyl)ethylenediamine (EDDnp) as fluorophore and quencher grou

87 This was achieved using ethylenediamine electrodeposited on a glassy carbon elec

88 2780 human ovarian cancer cells contained XY=ethylenediamine (en) and extended polycyclic arenes.

89 Reaction of an ethylenediamine (en) solution of the Zintl phase precurs

90 Ethylenediamine (en) solutions of K4Pb9 react with tolue

91 K(4)Sn(9) dissolves in ethylenediamine (en) to give equilibrium mixtures of the

92 general formulas {[Pt(L)Cl]2(mu-pz)}(2+) (L, ethylenediamine, en; (+/-)-1,2-propylenediamine, 1,2-pn;

93 dies were covalently linked to CNT-SPE by an ethylenediamine film strategy.

94 /- 0.03; N,N'-diethyl-N,N'-bis(3-sulfopropyl)ethylenediamine for which log Ka1m = 5.75 +/- 0.03 and l

95 -dimensional hybrid organic/inorganic TiS(2)(ethylenediamine) framework when synthesized from molecul

96 An ethylenediamine functionalized glycidyl methacrylate (GM

97 etyl)-N'-(7-nitrobenz-2-oxa-1, 3-diazol-4-yl)ethylenediamine, further indicated that both agonist and

98 idene)-N,N'-bis(2,2-dimethyl-3- amino-propyl)ethylenediamine) (Ga-[3-ethoxy-ENBDMPI])(+), as a candid

99 n of 4 (7 Li/mol) in t-butanol/n-propylamine/ethylenediamine gave n-decanal 12 in 36% yield.

100 marin and N-iodoacetyl-N'-(5-sulfo-1-naphtyl)ethylenediamine has shown that the reactivity of the SH1

101 d structure calculations confirm that TiS(2)(ethylenediamine) has a direct band gap.

102 tical absorption spectra of alkali metals in ethylenediamine have provided evidence for a third oxida

103 -hydroxyethyl) glycine (HeGly), hydroxyethyl-ethylenediamine (HEEDA), and DEA, secondary amines commo

104 iamino-diphenyl sulphone, DAP) and (naphthyl)ethylenediamine hydrochloride (NED) with nitrite in acid

105 ensitive to hydrolytic cleavage catalyzed by ethylenediamine hydrochloride.

106 id, glucose, ammonia, caffeine, methylamine, ethylenediamine, hydroxylamine, n-butylamine, adenosine,

107 probe N-(iodoacetyl)-N'-(1-sulfo-5-naphthyl)ethylenediamine (IAEDANS).

108 r TPEN (N,N,N',N'-tetrakis-[2-pyridylmethyl]-ethylenediamine), indicating that SNc dopaminergic neuro

109 minoethyl)N-(2-hydroxy-2-nitrohydrazino)-1,2-ethylenediamine) inhibited apoptosis and caspase 3 activ

110 e-activity data for these second generation, ethylenediamine-inspired PFT inhibitors were rationalize

111 n-salen, i.e., mu-oxo N,N'- bis(salicylidene)ethylenediamine iron (Fe(Salen)), but not other metal sa

112 f the quinoxaline system located outside the ethylenediamine kappa pharmacophore allows the fine-tuni

113 relative to that of the previously reported ethylenediamine-linked coumarin nucleotides.

114 ched to the 3'-position of the ribose via an ethylenediamine linker.

115 propyl)piperazine series, compounds with the ethylenediamine moiety (8-11, 15-17) showed 6-20-fold hi

116 negatively charged proteins, is covered with ethylenediamine molecules attached onto a dextran surfac

117 Following a previously reported protocol, ethylenediamine molecules were grafted onto these sites

118 s phase with N,N'-bis(4-methoxysalicylidene) ethylenediamine (MSE) and determination by FAAS.

119 The desired N4O2 ligands, (ethylenediamine)-N,N'-bis[propyl[(2-hydroxy-3-methoxyben

120 opyl[(2-hydroxy-3-methoxybenzyl)imino]] and (ethylenediamine)-N,N'-bis[propyl[2-hydroxy-4,6-dimethoxy

121 s [Pt4(en)4(N intersectionN)4][CF3SO3]8 (en= ethylenediamine, N intersectionN = 4,4'-bipyridine deriv

122 class of antimalarial compounds, hexadentate ethylenediamine-N, N'-bis[propyl(2-hydroxy-(R)-benzylimi

123 ate iron chelator N, N'-bis(2-hydroxybenzyl) ethylenediamine-N, N'-diacetic acid monosodium salt (NaH

124 s N,N'-bis [2-hydroxy-5(carboxyethyl)benzyl] ethylenediamine-N,N'- diacetic acid, TATE is octreotate,

125 -(N,N'-bis-[2-hydroxy-5-(carboxyethyl)benzyl]ethylenediamine-N,N'-diac etic acid) ((68)Ga-PSMA) PET/C

126 , and N,N'-bis(2,2- dimethyl-2-mercaptoethyl)ethylenediamine-N,N'-diacetic acid (6SS).

127 (IV) coordination by N,N'-di(o-hydroxybenzyl)ethylenediamine-N,N'-diacetic acid (HBED) at different p

128 late iron chelator N, N'-bis(2-hydroxybenzyl)ethylenediamine-N,N'-diacetic acid (HBED) for the chroni

129 e Ti(IV) compound of N,N'-di(o-hydroxybenzyl)ethylenediamine-N,N'-diacetic acid (HBED) is cytotoxic t

130 ioxamine B (DFOB) or N,N'-Di(2-hydroxybenzyl)ethylenediamine-N,N'-diacetic acid (HBED)) and a reducta

131 ally administered N,N'-bis (2-hydroxybenzyl) ethylenediamine-N,N'-diacetic acid (HBED), a synthetic i

132 h as (68)Ga-labeled N,N'-bis(2-hydroxybenzyl)ethylenediamine-N,N'-diacetic acid (HBED)-PSMA-11, are p

133 ed N,N'-bis[2-hydroxy-5-(carboxyethyl)benzyl]ethylenediamine-N,N'-diacetic acid (HBED-CC)-based PET t

134 ous ligand EDDASS, N,N'-bis(2-mercaptoethyl) ethylenediamine-N,N'-diacetic acid, which does not conta

135 gents, nitrilotriacetic acid (NTA) and [S,S]-ethylenediamine-N,N'-disuccinic acid ([S,S]-EDDS), for t

136 he use of a new and strong complexing agent, ethylenediamine-N,N'-disuccinic acid (EDDS) in the homog

137 Complexation of Fe by ethylenediamine-N,N'-disuccinic acid (EDDS) leads to sta

138 d this investigation to include the study of ethylenediamine-N,N'-tetramethylphosphonic acid (EDTPA),

139 ylate iron chelator N, N-bis(2-hydroxybenzyl)ethylenediamine-N,N-diacetic acid (HBED) for the chronic

140 oacetyl)-N'-(7-nitrobenz-2-oxa-1, 3-diazolyl)ethylenediamine (NBD) whose emission properties are sens

141 cetyl)-N'-(7-nitrobenz-3-oxa-1,3-diazol-4-yl)ethylenediamine (NBD)-fluorophore-labeled antithrombins

142 cts with sulfanilamide (SA) and N-(1-napthyl)ethylenediamine (NNED) to form a stable azo dye.

143 n2+ and N,N,N',N'-tetrakis-(2-pyridylmethyl)-ethylenediamine on acid-elicited currents suggest contri

144 In all cases 1 mol of ethylenediamine or N, N'-dimethylethylenediamine per gra

145 by TPEN (N,N,N',N'-tetrakis [2-pyridylmethyl]ethylenediamine) or soluble Fas ligand (CD95), was obser

146 The ethylenediamine platinum(II) moiety, herein called Lx, w

147 accumulation of the DDP analog [3H]dichloro(ethylenediamine)-platinum(II) into whole cells derived f

148 Replacing the ethylenediamine portion of aminoethylglycine peptide nuc

149 ve substitution of the phenylthioaminal with ethylenediamine producing 2 in a 45% overall yield.

150 However, addition of Pd(en)Cl2 (en, ethylenediamine) promotes a high-affinity interaction wi

151 or TPEN (N,N,N',N'-tetrakis(2-pyridylmethyl) ethylenediamine), reagents that exhibit strong transitio

152 common protecting chelating ligands such as ethylenediamine saw a Pd3L2 to Pd6L8 rearrangement occur

153 cond generation inhibitors, wherein the core ethylenediamine scaffold was varied in order to examine

154 On the basis of a 4-fold substituted ethylenediamine scaffold, the inhibitors are structurall

155 on was prepared from As7(3-) and Ni(COD)2 in ethylenediamine solutions and isolated as the Bu4P+ salt

156 Reactions of ethylenediamine solutions of K4Bi5 with Ni(PPh3)2(CO)2 y

157 new mixed-valent compound Fe3Se4(en)2 (en = ethylenediamine) synthesized from elemental Fe and Se.

158 HS chains bound to P-selectin are eluted by ethylenediamine tetraacetic acid (EDTA), but only at hig

159 was directed toward an isothiocyanatobenzyl-ethylenediamine tetraacetic acid (EDTA)-protein conjugat

160 eve the same efficacy as the chelating agent ethylenediamine tetraacetic acid.

161 Fresh ethylenediamine-tetraacetic acid blood was obtained and

162 (153)Sm-ethylenediamine tetramethylene phosphonic acid ((153)Sm-

163 xture comprised of 1,2-ethanedithiol and 1,2-ethylenediamine that possesses the remarkable ability to

164 ilane (AMPTS), N-[3-(trimethoxysilyl)propyl]-ethylenediamine (TMSPEDA), N-[3-(trimethoxysilyl)propyl]

165 acid-treated carbon was further modified by ethylenediamine to attach -NH2 surface functional groups

166 oxidant [Pt(en)(2)Cl(2)](2+) (where "en" is ethylenediamine) to oxidize disulfide bonds under condit

167 Sn94- reacts with Pt(PPh3)4 in ethylenediamine/toluene solvent mixtures in the presence

168 Zintl ion precursors react with Pd(PPh3)4 in ethylenediamine/toluene/PBu4(+) solutions to give crysta

169 N,N'-bis-(2-pyridylmethyl)-N,N'-dimethyl-1,2-ethylenediamine; TPA = tris-(2-pyridylmethyl)amine] cata

170 (2+) with N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine (TPEN) abolished SD, implying that Zn(2+

171 plex CuBr/N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine (TPEN) as a versatile and highly active

172 c chelator N,N,N'-tetrakis-(2'-pyridylmethyl)ethylenediamine (TPEN) potently blocked Vpx-mediated SAM

173 chelator N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine (TPEN) significantly delayed both Ca(2+)

174 zinc chelator NNNN-tetrakis(2-pyridylmethyl)ethylenediamine (TPEN) to induce apoptosis, DFO does not

175 t cation chelator, tetrakis-(2-pyridylmethyl)ethylenediamine (TPEN) to probe the effects of lowering

176 lied with N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine (TPEN), a heavy metal ion chelator.

177 N,N,N'N'-tetrakis(-)[2-pyridylmethyl]-ethylenediamine (TPEN), a specific zinc chelator, but no

178 chelator, N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine (TPEN), induced burst-like channel activ

179 chelator N,N,N',N'-tetrakis(2-pyridylmethyl)-ethylenediamine (TPEN), suggesting a role for chelatable

180 elator, N,N,N',N'-tetrakis-(2-pyridylmethyl) ethylenediamine (TPEN), we demonstrated a requirement fo

181 compound N,N,N',N'-tetrakis(2-pyridyl-methyl)ethylenediamine (TPEN), which chelates heavy metals such

182 helator, N,N,N'N'-tetrakis (2-pyridylmethyl) ethylenediamine (TPEN), which instead induced dramatic a

183 a coli to N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine (TPEN).

184 2+ with N,N,N',N'-tetrakis (2-pyridylmethyl) ethylenediamine (TPEN).

185 tion using N,N,N'-tetrakis-(2'-pyridylmethyl)ethylenediamine (TPEN).

186 chelator N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine (TPEN).

187 helator N,N,N',N'-tetrakis-(2-pyridylmethyl)-ethylenediamine (TPEN; 1 microM) suggesting the absence

188 d silanization with N-(trimethoxysilylpropyl)ethylenediamine triacetic acid on aluminum to provide a

189 he formally D3 symmetric [Co(en)3](3+) (en = ethylenediamine) trication were among the first chiral i

190 several types of compounds with lithium and ethylenediamine using low molecular weight amines as sol

191 in one post-modification reaction with N-Boc-ethylenediamine via reductive amination.

192 formation of imidazolines from a nitrile and ethylenediamine was also explored.

193 2(DBED)2(O)2](2+) (DBED = N,N'-di-tert-butyl-ethylenediamine) was shown to perform aromatic hydroxyla

194 talysts, whereas some diamines, most notably ethylenediamine, were excellent catalysts.

195 fluorophenyl moieties of 1 were reacted with ethylenediamine, whereas the deprotected alkyne function

196 he presence of 0.25 equiv of tetramethyl-1,2-ethylenediamine with 3,6-bis(dimethylamino) chalcogenoxa

197 stages of the polymerization of methanal and ethylenediamine within the interlayer of sodium montmori

198 1,4-benzenedithiol, and benzenehexathiol in ethylenediamine yield bright yellow [Pb2(S2C6H2S2)(en)]n

199 anium with Ni(COD)2 and/or Ni(PPh3)2(CO)2 in ethylenediamine yielded the Ni-centered heteroatomic 10-