ライフサイエンスコーパス: ethylenediamine

1 interstitial [Fe(en)(3)](2+) complexes (en = ethylenediamine).

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

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

4 ldehyde followed by reductive amination with ethylenediamine.

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

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

7 rived from oligonucleotide 5'-phosphates and ethylenediamine.

8 uced from the robust Strecker synthesis with ethylenediamine.

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

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

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

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

13 t in solutions composed of alkali metals and ethylenediamine.

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

15 itopic acceptor cis-[(en)Pd(NO(3))(2)] [en = ethylenediamine].

16 In this study, single-crystalline CdSe(ethylenediamine)(0.5) and Mn(2+)-doped nanosheets are sy

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

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

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

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

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

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

23 196.0 degrees C (+/-1.8)]; poly(EDMA-co-GMA)-Ethylenediamine [235.9 degrees C (+/-6.1)]; poly(EDMA-co

24 ,2-cyclohexanediamine (2a), or N,N'-dimethyl-ethylenediamine (3) is reported.

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

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

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

28 -9-ylamino)ethyl]-1,3-dimethylthiourea, en = ethylenediamine), a bifunctional platinum-acridine conju

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

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

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

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

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

34 4 and an N-iodoacetyl-N'-(5-sulfo-1-napthyl) ethylenediamine (AEDANS) moiety covalently attached to t

35 cyanate with (1R,2R)-1,2-bis(2-hydroxyphenyl)ethylenediamine afforded a new thiourea chiral solvating

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

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

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

39 by reacting (1R,2R)-1,2-bis(2-hydroxyphenyl)ethylenediamine and 3,5-bis(trifluoromethyl)phenyl isoth

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

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

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

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

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

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

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

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

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

49 10 mol % of copper(I) iodide and 20 mol % of ethylenediamine as the catalyst in dioxane at 110 degree

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

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

52 We recently reported asparagine ethylenediamines (AsnEDAs) as immunoproteasome inhibitor

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

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

55 The resulting method uses ethylenediamine-based ligands and can be used to achieve

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

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

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

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

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

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

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

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

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

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

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

67 The Benkeser reduction with lithium in ethylenediamine converts arenes to a mixture of cyclohex

68 layer of a polyamidoamine dendrimer, with an ethylenediamine core from the fourth generation.

69 MAM is a branched polymeric compound with an ethylenediamine core linked to repeating PAMAM units tha

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

95 s previously shown that capping of MOFs with ethylenediamine (EDA) can effectively retain small gaseo

96 ges of CND formation from arginine (Arg) and ethylenediamine (EDA) under hydrothermal conditions.

97 detect only 1,3-diaminopropane (DAP) and 1,2-ethylenediamine (EDA) vapors, belonging to industrially

98 on of hydrothermally treated citric acid and ethylenediamine (EDA) with various precursor ratios usin

99 of molecular precursors (arginine (Arg) and ethylenediamine (EDA)) and making use of microwave-assis

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

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

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

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

104 2780 human ovarian cancer cells contained XY=ethylenediamine (en) and extended polycyclic arenes.

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

106 of capturing the hypho- [Sn(2)Sb(5)](3-) in ethylenediamine (en) solution.

107 Ethylenediamine (en) solutions of K4Pb9 react with tolue

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

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

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

111 /- 0.03; N,N'-diethyl-N,N'-bis(3-sulfopropyl)ethylenediamine for which log Ka1m = 5.75 +/- 0.03 and l

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

113 An ethylenediamine functionalized glycidyl methacrylate (GM

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

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

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

117 235.9 degrees C (+/-6.1)]; poly(EDMA-co-GMA)-Ethylenediamine-Glutaraldehyde [255.4 degrees C (+/-2.7)

118 picolinic acid groups appended on either an ethylenediamine (H(4)TPAEN) or a trans-1,2-cyclohexyldia

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

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

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

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

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

124 ensitive to hydrolytic cleavage catalyzed by ethylenediamine hydrochloride.

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

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

127 oxidase (IdaA) to further degrade EDDA into ethylenediamine in a two-step oxidation.

128 scheme is the use of lithium, t-butanol, and ethylenediamine in THF (nontraditional Birch reduction c

129 of model substrates using lithium metal and ethylenediamine in THF under various atmospheric conditi

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

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

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

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

134 hydroxy)salicylidene-1,2-bis(4-methoxyphenyl)ethylenediamine]iron(III) complexes was evaluated on hum

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

136 pioid receptor (KOR) agonists comprising the ethylenediamine KOR pharmacophore in a perhydroquinoxali

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

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

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

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

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

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

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

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

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

146 (III) complex of N,N,N'-tris(2-pyridylmethyl)ethylenediamine-N'-acetate (tpena) react with hypochlori

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

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

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

150 phores and high-affinity synthetic chelator (ethylenediamine-N,N'-bis-2-hydroxyphenylacetic acid, EDD

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

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

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

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

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

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

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

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

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

160 (N,N'-bis [2-hydroxy-5-(carboxyethyl)benzyl]ethylenediamine-N,N'-diacetic acid) [(68)Ga]Ga-PSMA(HBED

161 (N,N'-bis [2-hydroxy-5-(carboxyethyl)benzyl]ethylenediamine-N,N'-diacetic acid) shows potential as a

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

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

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

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

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

167 a single high-dose administration of (153)Sm-ethylenediamine-N,N,N',N'-tetrakis(methylene phosphonic

168 ium N,N-bis[2-hydroxy-5-(carboxyethyl)benzyl]ethylenediamine-N,N-diacetic acid ([(68)Ga]Ga-PSMA-11) i

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

170 e (TMSPEDA), forming the hybrid (silylpropyl)ethylenediamine@nanocellulose (SPEDA@nanocel), which was

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

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

173 cent probe 7-nitrobenz-2-oxa-1,3-diazol-4-yl-ethylenediamine (NBD).

174 nteracted with the fluorophore N-(1-naphthyl)ethylenediamine (NEDa) as a Lewis acceptor-donor pair.

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

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

177 transport the fluorescent P-gp probes BODIPY-ethylenediamine or LDS 751, while they were transported

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

179 rt a Birch reduction promoted by lithium and ethylenediamine (or analogs) in tetrahydrofuran at ambie

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

181 zed sodium alginate grafted with rhodamine B ethylenediamine (ORE) and chitosan grafted with fluoresc

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

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

184 Replacing the ethylenediamine portion of aminoethylglycine peptide nuc

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

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

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

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

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

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

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

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

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

194 standard for Birch and Birch-type (lithium, ethylenediamine, t-BuOH, THF) reductions, the atmosphere

195 ous fluoride-containing dentifrice with 2.6% ethylenediamine tetra acetic acid (EDTA) as an anti-tart

196 ous fluoride-containing dentifrice with 2.6% ethylenediamine tetra-acetic acid (EDTA) as an antitarta

197 ing (SRP) alone versus SRP combined with 24% ethylenediamine-tetra acetic acid (EDTA) gel in removing

198 d in negative ionization mode using disodium ethylenediamine tetraacetic acid (EDTA) dihydrate to che

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

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

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

202 antioxidants (Duralox-MANC, erythorbate and ethylenediamine-tetraacetic acid (EDTA)), (ii) incubatio

203 Fresh ethylenediamine-tetraacetic acid blood was obtained and

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

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

206 (nanocel) with N-[3-(trimethoxysilyl)propyl]ethylenediamine (TMSPEDA), forming the hybrid (silylprop

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

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

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

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

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

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

213 (2+) with N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine (TPEN) abolished SD, implying that Zn(2+

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

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

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

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

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

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

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

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

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

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

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

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

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

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

228 2+ with N,N,N',N'-tetrakis (2-pyridylmethyl) ethylenediamine (TPEN).

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

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

231 IONPs) stabilized with trimethoxysilylpropyl-ethylenediamine triacetic acid (EDT) were developed as a

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

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

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

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

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

237 2(DBED)2(O)2](2+) (DBED = N,N'-di-tert-butyl-ethylenediamine) was shown to perform aromatic hydroxyla

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

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

240 eneimine derivative from ethylene glycol and ethylenediamine which are much safer, environmentally be

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

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

243 1,4-benzenedithiol, and benzenehexathiol in ethylenediamine yield bright yellow [Pb2(S2C6H2S2)(en)]n

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