ライフサイエンスコーパス: diethylamino

1 Treatment with NSC23766 (N(6)-[2-[[4-(diethylamino)-1-methylbutyl]amino]-6-methyl-4-pyrimidiny

2 e of stereoselectivity was developed using 3-diethylamino-1-propanol (deapH) in lieu of BnOH and NEt(

3 imetric sensor using synthesized 3', 6'- bis(diethylamino) -2- ((3,4,5 trimethyl benzylidene) amino)s

4 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoic acid, an inhibito

5 eceptor antagonist JNJ-31020028 (N-(4-(4-[2-(diethylamino)-2-oxo-1-phenylethyl]piperazin-1-yl)-3-fluo

6 3',6'-bis(diethylamino)-2-{[(1E)-(4,5-dimethyl-2-furyl)methylene]a

7 m in some food samples, which used 3',6'-bis(diethylamino)-2-{[(1E)-(4-ethoxyphenyl) methylene] amino

8 The deprotonation of pentacarbonyl[(3-diethylamino-2,4-dimethyl)cyclobut-2-ene-1-ylidene]chrom

9 lculations were performed on pentacarbonyl[3-diethylamino-2,5-dimethyl)cyclopent-2-ene-1-ylidene]chro

10 the parent compound 4-guanidinophenyl (E)-4-diethylamino-2-hydroxy-alpha-methylcinnamate hydrochlori

11 ylation reactions to generate MEGX and omega-diethylamino-2-hydroxymethyl-6-methylacetanilide.

12 yeast actin by a sulfhydryl reagent CPM [7-(diethylamino)-3-(4'-maleimidophenyl)-4-methylcoumain] wa

13 yl)-2-(dimethylamino)naphthalene (BADAN), 7-(diethylamino)-3-(4'-maleimidylphenyl)-4-methylcoumarin (

14 The modification of Cys(154) with 7-(diethylamino)-3-(4'-maleimidylphenyl)-4-methylcoumarin (

15 6-(4-(Diethylamino)-3-nitrophenyl)-5-methyl-4,5-dihydropyridaz

16 by site-directed mutagenesis, labeled with 7-diethylamino-3-((((2-iodoacetamido)ethyl)amino)carbonyl)

17 on maxima of a solvatochromic fluorophore (7-diethylamino-3-((((2-maleimidyl)ethyl)amino)carbonyl) co

18 of the enzyme was developed by conjugating 7-diethylamino-3-((((2-maleimidyl)ethyl)amino)carbonyl)cou

19 te maleimide, SDSM) and membrane-permeable 7-diethylamino-3-(4'-maleimidyl)-4-methylcoumarin (CPM).

20 nal sarcoplasmic reticulum is labeled with 7-diethylamino-3-(4'-maleimidylphenyl)-4-methylcoumarin (C

21 ar quantities of the fluorogenic maleimide 7-diethylamino-3-(4'-maleimidylphenyl)-4-methylcoumarin (C

22 de, 3-(N-maleimidopropionyl)-biocytin, and 7-diethylamino-3-(4'-maleimidylphenyl)-4-methylcoumarin al

23 th the fluorescent monofunctional reagents 7-diethylamino-3-(4'-maleimidylphenyl)-4-methylcoumarin an

24 and ryanodine receptor type 1 (RyR1) with 7-diethylamino-3-(4'-maleimidylphenyl)-4-methylcoumarin, a

25 ry-based peptide sequencing, we identified 7-diethylamino-3-(4'-maleimidylphenyl)-4-methylcoumarin-th

26 NMT1 and NMT2 based on detection of CoA by 7-diethylamino-3-(4-maleimido-phenyl)-4-methylcoumarin.

27 ET) between a protein fusion LuxP-EGFP and 7-diethylamino-3-[N-(2-maleimidoethyl)carbamoyl]coumarin (

28 For the first-time 7-Diethylamino-3-thenoylcoumarin (DETC) is used as the pho

29 cer dye, rhodamine B ([9-(2-carboxyphenyl)-6-diethylamino-3-xanthenylidene]-diethylammonium chloride)

30 -ylidene]chromi um (1d) and pentacarbonyl[(3-diethylamino-4-methyl-2-phenyl)cyclobut-2-ene-1-ylidene]

31 Appp-S-(7-diethylamino-4-methyl-3-(4-succinimidylphenyl)) coumarin

32 ey contained 156 mmol/kg Cu-I, 10 mmol/kg 9-(diethylamino)-5-[4-(15-butyl-1,13-dioxo-2,14-dioxanodecy

33 The lipid soluble fluorophore Nile Red (9-diethylamino-5-benzo[alpha]phenoxazinone) is used to flu

34 can be replaced by a triazole system, the 5-(diethylamino)acetamido substituent found in 8a is requir

35 spontaneously NO-releasing salts 1a (R(2)N = diethylamino) and 1b (R(2)N = pyrrolidino) to prodrugs 2

36 In particular, the MediaChrom bearing a diethylamino as an electron-donating group and a trifluo

37 Here, we describe diethylamino-azo-diethylamino (DAD), a third-generation

38 4-(Diethylamino)benzaldehyde (DEAB) has been extensively re

39 azobisisobutyronitrile (AIBN), 4,4'-bis(N,N-diethylamino)benzophenone (BDEBP, a derivative of Michle

40 methylbenzophenone, 2-adamantanone, 4,4'-bis(diethylamino)benzophenone, and 1,2-diphenylcyclopropen-3

41 The 3-(diethylamino)benzyl (DEABn) group has been studied for r

42 The two most potent compounds 10-[4'-(N-diethylamino)butyl]-2-chlorophenoxazine (10B) and 10-[4'

43 For example, the introduction of a [4-(diethylamino)butyl]amino side chain into the 2-position

44 merization process which afforded 7,7'-bis(((diethylamino)carbonyl)oxy)-6,6'-diiodo-8,8'-biquinolyl (

45 The hemicyanine hybrid containing the 7-(diethylamino)coumarin (ACou) donor attached to the catio

46 Sphingolipid phosphate analogues bearing 7-(diethylamino)coumarin (DECM) and 4-bromo-5-hydroxy-2-nit

47 of glycine was covalently coupled to the 7-(diethylamino)coumarin (DECM) caging group.

48 ith the fluorescent probe 3-(bromoacetyl)-7-(diethylamino)coumarin (PgammaBC, Pgamma-24-45BC) have be

49 gh molecular weight carbonylated LPP with 7-(diethylamino)coumarin-3-carbohydrazide (CHH) and analyze

50 direct reaction of protein carbonyls with 7-(diethylamino)coumarin-3-carbohydrazide (CHH).

51 at Cys197 with N-[2-(1-maleimidyl)ethyl]-7-(diethylamino)coumarin-3-carboxamide (MDCC).

52 We present the synthesis of [7-(diethylamino)coumarin-4-yl]methyl (DEACM)-caged phosphor

53 protein MDCC-PBP, N-(2[1-maleimidyl]ethyl)-7-diethylamino-coumarin-3-carboxamide phosphate binding pr

54 ethylamino)-cyclopropenium chloride and tris(diethylamino)-cyclopropenium iodide reveal the presence

55 In this study, a plausible mechanism for bis(diethylamino)cyclopropenylidene (Et-BAC)-catalyzed synth

56 Here, we describe diethylamino-azo-diethylamino (DAD), a third-generation photoswitch that

57 diazen-1-ium-1,2-diolate (13 and 18), 1-(N,N-diethylamino)diazen-1-ium-1,2-diolate (14 and 19), or ni

58 thione (GSNO) or diethylammonium (Z)-1-1(N,N-diethylamino)diazen-1-ium-1,2-diolate (DEA NONOate) to h

59 red unless the nitric oxide generator 1-(N,N-diethylamino)diazen-1-ium-1,2-diolate (DEANO) was also a

60 ctile response to the NO donor sodium 1-(N,N-diethylamino)diazen-1-ium-1,2-diolate was not altered.

61 Using the NO generator 1-(N,N-diethylamino)diazen-1-ium-1,2-diolate, we were able to g

62 photochemistry of the sodium salt of 1-(N,N-diethylamino)-diazen-1-ium-1,2-diolate (3) has been inve

63 on with cGMP-elevating agents such as 2-(N,N-diethylamino)-diazenolate-2-oxide diethylammonium salt (

64 rmed with NO or the NO donors NOC9 or 2-(N,N-diethylamino)-diazenolate-2-oxide.sodium salt.

65 erivatization of protonated analytes by (N,N-diethylamino)dimethylborane in a Fourier transform ion c

66 solation of a disulfide intermediate (Z)-2-[(diethylamino)disulfan-yl]-2-[(1H-pyrazol-5-yl)imino]acet

67 sence of acid, heating a solution of (Z)-2-[(diethylamino)disulfanyl]-2-[(1,3-dimethyl-1H-pyrazol-5-y

68 xtension of n-electron delocalization by the diethylamino electron-donating group endows the S(1)' st

69 2-(Diethylamino)ethanethiol (DEAET) and 2-(dimethylamino)et

70 of 2-(dimethylamino)ethanethiol (DMAET), 2-(diethylamino)ethanethiol (DEAET), and 2-mercaptoethanol

71 e deprotection of aromatic methyl ethers, 2-(diethylamino)ethanethiol, is reported.

72 that progesterone, imipramine and 3-beta-[2-(diethylamino)ethoxy]androst-5-en-17-one (U18666A) strong

73 ic delivery of (1R-1-benzo thiophen-5-yl-2[2-diethylamino)-ethoxy] ethanol hydrochloride (T-588) prev

74 ties), our initial lead, T3.5 (3-chloro-6-(2-diethylamino-ethoxy)-10-(2-diethylamino-ethyl)-acridone)

75 The 2-(diethylamino) ethyl methacrylate based copolymeric nanog

76 uscarinic receptor antagonist aprophen [(N,N-diethylamino)ethyl 2,2-diphenylpropionate], were synthes

77 moresponsive synthetic hydrogels based on 2-(diethylamino)ethyl acrylate, which support long-term hum

78 utyl acrylate) and pH-responsive poly(2-(N,N-diethylamino)ethyl methacrylate) (PDEAEMA) side chains a

79 well-defined styrene-functionalized poly(2-(diethylamino)ethyl methacrylate) macromonomer as a react

80 he deprotecting reagent and the byproduct 2-(diethylamino)ethyl methyl sulfide into the aqueous phase

81 lthio)phenyl)(naphthalen-1-yl)methanone O-2-(diethylamino)ethyl oxime (MND) exhibited the best safety

82 for HS disaccharides analysis, 6-amino-N-(2-diethylamino)ethyl quinoline-2-carboamide (AMQC).

83 ich protect mice against 4.2 LD(50) of S-(2-(diethylamino)ethyl) O-isobutyl methanephosphonothioate w

84 Melanin targeted N-(2-(diethylamino)ethyl)-18F-5-fluoropicolinamide was used as

85 le by Bu and colleagues (1) introduces N-[2-(diethylamino)ethyl]-(18)F-5-fluoropicolinamide ((18)F-P3

86 In this study, N-[2-(diethylamino)ethyl]-4-(18)F-fluorobenzamide ((18)F-FBZA)

87 hylamino)ethyl]benzenesulfonamides and N-[2-(diethylamino)ethyl]benzenemethanesulfonamides have been

88 and two compound classes consisting of N-[2-(diethylamino)ethyl]benzenesulfonamides and N-[2-(diethyl

89 One such benzamide, N-(2-diethylamino-ethyl)-4-(4-fluoro-benzamido)-5-iodo-2-meth

90 .5 (3-chloro-6-(2-diethylamino-ethoxy)-10-(2-diethylamino-ethyl)-acridone), demonstrates unique syner

91 I) (4-NEt(2) -sal(2) 323)]ClO(4) (2), with a diethylamino group on the ligand, was used to combine th

92 te portion of aprophen by replacement of the diethylamino group.

93 hyl-(R)-4-(2-(3,4-dichlorophenyl)acetyl)-3-((diethylamino)methyl)piperazine-1-carboxylate ((11)C-EKAP

94 agents, (12)C4-, (12)C2(13)C2-, and (13)C4-5-diethylamino-naphthalene-1-sulfonyl chloride (DensCl), i

95 can regulate calcium signaling, including 8-(diethylamino)octyl-3,4,5-trimethoxybenzoate and 2-aminoe

96 um chelators 3,4,5-trimethoxybenzoic acid 8-(diethylamino)-octyl ester (TMB-8) and 2-[(2-bis-[carboxy

97 bitor of intracellular Ca2+ mobilization, 8-(diethylamino)-octyl-3,4,5-trimethoxybenzoate hydrochlori

98 e), the intracellular Ca(2+) channel (8-(N,N-diethylamino)-octyl-3,4,5-trimethoxybenzoate), CaM (N-(6

99 elator, or with the combined presence of [8-(diethylamino)-octyl-3,4,5-trimethoxybenzoate, HCl] (TMB)

100 1 micromol/ 3,4,5-trimethoxybenzoic acid 8-[diethylamino]octyl ester, an intracellular Ca2+ antagoni

101 tion, adding R 2NN(O)NO-GlcNAc (where R 2N = diethylamino or pyrrolidin-l-yl and GlcNAc = N-acetylglu

102 n of Fe(II) with 2-(5-bromo-2-pyridylazo)-5-(diethylamino)-phenol (Br-PADAP).

103 ative of 3-thiolflavone (3TF), namely, 2-(4-(diethylamino)phenyl)-3-mercapto-4H-chromen-4-one (3NTF),

104 FM4-64 [N-(3-triethylammoniumpropyl)-4-(6-(4-diethylamino)phenyl)-hexatrienyl)pyridinium dibromide].

105 pound, N-(3-triethylammoniumpropyl)-4-(6-(4-(diethylamino)phenyl)hexatrie nyl )pyridinium dibromide (

106 tracer N-(3-triethylammoniumpropyl)-4-(6-(4-(diethylamino)phenyl)hexatrienyl)pyridinium dibromide.

107 FM4-64 [N-(3-triethylammoniumpropyl)-4-(6-(4-diethylamino)phenyl)hexatrienyl)pyridinium dibromide] dy

108 /2-chloro-(epsilon-amino-Lys(75))-[6-[4-(N,N-diethylamino)phenyl]-1 ,3,5-triazin-4-yl]calmodulin] sho

109 ts using 2-chloro-(amino-Lys(75))-[6-[4-(N,N-diethylamino)phenyl]-1,3,5-triazin-4-y l]calmodulin (TA-

110 The most potent hit compound, N-[4-(diethylamino)phenyl]-5-methyl-3-phenylisoxazole-4-carbox

111 n, 2-chloro-(epsilon-amino-Lys75)-[6-(4-N, N-diethylamino-phenyl)-1,3,5-triazin-4-yl]-calmodulin (TA-

112 sized by the reaction of Pb-oleate with tris(diethylamino)phosphine selenide are highly sensitive to

113 cid in the reaction can also react with tris(diethylamino)phosphine to create bis(diethylamido)phosph

114 nd (1)H NMR show that water reacts with tris(diethylamino)phosphine to create bis(diethylamido)phosph

115 two expected contributing structures, and 2-(diethylamino)propane and 1,8-diazabicyclo[6.3.1]dodecane

116 The most potent analogue, 2,9-bis{[3-(diethylamino)propyl]amino}-5-methylbenzofuro[3,2-c]quino

117 observed following reaction with 1-ethyl-3-[(diethylamino)propyl]carbodiimide.

118 d 3 and the monosubstituted compounds 2-(N,N-diethylamino)pyrene (1) and 2-cyanopyrene (2) have been

119 our approach, we synthesized 2-cyano-7-(N,N-diethylamino)pyrene (3), a pyrene analogue of the widely

120 ffinity labeling (PAL) agent, 5-azido-2-(N,N-diethylamino)pyridine, was studied in aprotic and protic

121 derivatives or 1,3,5-benzenetriamine and 4-(diethylamino)salicylaldehyde, while a second series resu

122 es used the fluorescent DAT substrate, 4-[4-(diethylamino)-styryl]-N-methylpyridinium iodide (ASP(+))

123 double labeled with a fluorescent dye, 4-(4-diethylamino-styryl)-N-methylpyridinium iodide, for NTs

124 ed is a benzo[a]phenoxazone dye containing a diethylamino substituent at the 9-position.

125 The diethylamino-substituted derivative has a proton associa

126 esis of a new tricyclic cytidine analogue, 8-diethylamino-tC (8-DEA-tC), that responds to DNA duplex

127 peridyl) and (1-NEt2-2-BH2-C6H4)2 (3; NEt2 = diethylamino), were synthesized, and their structural fe