ライフサイエンスコーパス: sodium salt

1 hydroxy-2,5-dioxopyrrolidine-3-sulfonic acid sodium salt).

2 -(trimethylsilyl)propionic-2,2,3,3-d(4) acid sodium salt.

3 or 2-(N,N-diethylamino)-diazenolate-2-oxide.sodium salt.

4 (HVFP) of the corresponding p-tosylhydrazone sodium salt.

5 ersion of the sulfate diester to the desired sodium salt.

6 ty in vitreous humor, when compared with its sodium salt.

7 ee) final drug substance as its crystalline sodium salt.

8 ydrolyzed to the corresponding water-soluble sodium salts.

9 nge of carbonyl compounds and tosylhydrazone sodium salts.

10 ctively, and subsequently converted to their sodium salts.

11 Potassium salts are more effective than sodium salts.

12 to a decasaccharide in their common form as sodium salts.

13 rinones ("sulfoglows") are isolated as their sodium salts.

14 ), are isolated as THF-solvated potassium or sodium salts.

15 piked with alpha-naphthyl beta-d-glucuronide sodium salt (1-NAP-GLU) and pyrene-1-sulfate potassium s

16 The NO donor, diethylamine NO complex sodium salt (10-100 microM), activated neurons from both

17 imidin-1-yl]-1-phenylethylamino}butyric acid sodium salt, 10b (elagolix), was identified as a potent

18 the safety and efficacy of 3'-sialyllactose sodium salt (3'SL), an oligosaccharide that occurs natur

19 8.0) containing 0.9ml of N-lauroylsarcosine (sodium salt, 30% [w/v] solution) per 100ml of buffer.

20 s(4-(2-quinolylmethoxy)phenyl)pentanoic acid sodium salt (47.Na) met our design parameters for a drug

21 reoxygenation injected with 7-nitroindazole sodium salt (7-NINA), a selective nNOS inhibitor, immedi

22 hosphate, beta-phenyl-1, N(2)-etheno-8-bromo-sodium salt (8 Br PET cGMP) produced a significant incre

23 8-bromoguanosine 3',5'-cyclic monophosphate sodium salt (8-Br-cGMP), or pioglitazone dose-dependentl

24 enylthio)-guanosine 3,5-cyclic monophosphate sodium salt (8pCPTcGMP), mimicked the extrinsic flow-ind

25 Potassium and sodium salts add selectively to C6 of 6-chloro-8-iodo-9-

26 6] (1), has been prepared by the reaction of sodium salt and CsF in dichloromethane and water.

27 the five basic tastes; sweet, sour, bitter, sodium salt and umami.

28 The photophysics of both the sodium salts and the ethyl esters of the three carboxyla

29 toyl-2-oleoyl-sn-glycero-3-phospho-l-serine (sodium salt)), and ganglioside GM1.

30 f poly(l-lysine HBr) or poly(l-glutamic acid sodium salt), and helical, hydrophobic segments of poly(

31 eraction between bupivacaine and fatty acids sodium salt, and greater surface activity.

32 molecule (9,10-anthraquinone-2-sulfonic acid sodium salt, AQ), through tuning of the charge density i

33 -sulfonamido-1,2,3-triazole-4-carbothioamide sodium salts as the only products.

34 to reduce deposition from samples such as 1% sodium salts (as NaCl) and seawater (approximately 3% di

35 However, the higher doses of glipizide sodium salt attenuated the increments in plasma concentr

36 dministration of the water-soluble glipizide sodium salt attenuates vascular and end-organ dysfunctio

37 ed in formal solutions containing lithium or sodium salts before coating in matrix via air-spray depo

38 ccinate (AOT) in the organogel phase, as the sodium salt, caused marked changes in the peak currents

39 The resulting increase in fecal sodium salts causes an isotonic increase in fecal water

40 ecently, a hydrosoluble chlorine composed of sodium salts chlorine e6, chlorine p6, and purpurine-5 h

41 mino-2-(2-chloro-5-hydroxyphenyl)acetic acid sodium salt (CHPG) an mGluR5 agonist restored sensitivit

42 d]pyrida zin-7- one (13) was prepared by the sodium salt condensation of ethyl 3-cyanopyrrole-2-carbo

43 nsity to orient interfacial water molecules, sodium salts could be placed in the following order: NaS

44 +)-xylose, d-fructose, 1-thio-beta-d-glucose sodium salt, d-(+)-galactose, sorbitol, glycerol, and de

45 ic adenosine monophosphate, N6,O2-dibutyryl, sodium salt (db-cAMP) resulted in reduction of INa to 62

46 t disruption of the afferent taste signal to sodium salts disrupts the normal age-dependent "pruning"

47 eoyl-sn-glycero-3-[phospho-rac-(1-glycerol)] sodium salt (DOPG)</=1,2-dioleoyl-sn-glycero-3-[phospho-

48 1,2-dioleoyl-sn-glycero-3-[phospho-l-serine] sodium salt (DOPS), indicating that the anionic lipids D

49 duction of colitis by either dextran sulfate sodium salt (DSS) or 2,4,6-trinitrobenzene sulfonic acid

50 nduced by azoxymethane (AOM)/dextran sulfate sodium salt (DSS), and highly enriched beta-catenin hot

51 ice were more susceptible to dextran sulfate sodium salt (DSS)-induced colitis than wild type (WT) mi

52 markedly increased by addition of fatty acid sodium salts due to greater oil/water interface area, in

53 mino-2-(2-chloro-5-hydroxyphenyl)acetic acid sodium salt] enhanced the discriminative stimulus effect

54 The deposition of sodium salts followed by a sputtered layer of gold has b

55 + adducts were the dominant ions with 0.5 mM sodium salts for these compounds.

56 transduction component used to discriminate sodium salts from other taste stimuli was deleted in tas

57 Benzaldehyde tosylhydrazone sodium salt gave enantioselectivities of 91 +/- 3% ee an

58 red reaction mixtures of the modified-purine sodium salts generated in a polar solvent and cooled sol

59 s of the benzimidazole nucleosides using the sodium salt glycosylation method.

60 9 in three steps using a modification of the sodium salt glycosylation method.

61 d]pyridazin -7-one (24) was prepared via the sodium salt glycosylation of 5 with (1,3-dihydroxy-2-pro

62 The sodium salt glycosylation of the imidazo[4,5-d]isothiazo

63 thenyl]-4,6-dichloroindole-2-carboxylic acid sodium salt (GV 150526A, 40 mg/kg).

64 ation of diazo compounds from tosylhydrazone sodium salts has been established and applied in sulfur-

65 arboxylic acid (ATA) (IC50=1.4 muM), suramin sodium salt (IC50=3.6 muM), NF 023 hydrate (IC50=6.2 muM

66 to pressure-controlled hemorrhage, glipizide sodium salt improved mean arterial pressure in a dose-de

67 Gelation properties of the corresponding sodium salts in DMF and DMSO are generalized with respec

68 preferentially extracted NaOH over all other sodium salts, including the normally preferred nitrate a

69 In proteomics, dodecyl sulfate (DS(-)) as sodium salt is commonly used in protein solubilization p

70 midine bases with ribose analogues using the sodium salt-mediated glycosylation procedure.

71 binofuranosyl analogues were prepared by the sodium salt method to give both the alpha- and beta-anom

72 orthoformate followed by alkylation via the sodium salt method with a variety of alkylating agents f

73 ure, was coupled with several purines by the sodium salt method.

74 -erythro-pentofuranosyl chloride 5 using the sodium salt method.

75 toyl-sn-glycero-3-phospho-(1'-rac-glycerol) (sodium salt)) micelles show extensive chemical shift dif

76 In the azoxymethane (AOM)/dextran sulfate sodium salt model, PUMA deficiency increased the multipl

77 ino acid glutamate [often in the form of the sodium salt monosodium glutamate (MSG)] and the nucleoti

78 group [2-sulfonatoethyl methanethiosulfonate sodium salt (MTSES)] rescued the cGMP-activated conducta

79 xy-1-methacryloxy)propyl-3,5-dimethylaniline sodium salt (N35A) was synthesized by an addition reacti

80 ydroxy-1-methacryloxy)propyl-4-methylanaline sodium salt (Na-NTG-GMA), the latter being widely used i

81 and poly[2,6-{1,5-bis(3-propoxysulfonic acid sodium salt)}naphthylene]ethynylene (PNES), which helica

82 mino) benzenetellurenyl]propanesulfonic acid sodium salt (NDBT) were evaluated in solution, red blood

83 The aqueous photochemistry of the sodium salt of 1-(N,N-diethylamino)-diazen-1-ium-1,2-dio

84 The sodium salt of 2,5,6-trichlorobenzimidazole (8a) was con

85 furanosyl alpha-chloride derivative with the sodium salt of 2-benzylthio-5,6-dichloroindole (5).

86 With 4-trifluoromethylbenzyl bromide, the sodium salt of 4 gave (4-CF(3)C(6)H(4)CH(2)OCH(2))C(Me)(

87 be mimicked by either amiloride or by the di-sodium salt of 4,4'-dinitrostilbene-2,2'-disulphonic aci

88 FAIRs was synthesized directly from the sodium salt of 5-amino-1-(beta-D-ribofuranosyl)imidazole

89 tion of these compounds are (1) treating the sodium salt of 6, 7-dihydroimidazo[4,5-d][1,3]diazepin-8

90 The sodium salt of 9 was reacted with allyl bromide or acety

91 n of the TDMS approach is demonstrated for a sodium salt of a representative, carboxylated drug molec

92 ound 29, which contains as a substituent the sodium salt of a sulfonic acid, has an ETA IC50 = 0.38 n

93 d decreased colon cancer cell growth and the sodium salt of aspirin also inhibited tumor growth in an

94 nerated from 5-(1-azulenyl)tetrazole and the sodium salt of azulene-1-carbaldehyde tosylhydrazone usi

95 Potassium phthalimide and sodium salt of benzenethiol converted 2-(benzotriazol-1-

96 itiation) with the soluble and nonaggressive sodium salt of BHT (BHT=2,6-di-tert-butyl-hydroxytoluene

97 d in situ by treatment of the tosylhydrazone sodium salt of cinnamaldehyde with transition metal cata

98 Within a total residence time of 9 min, the sodium salt of ciprofloxacin was prepared from simple bu

99 f a range of (enantiopure) epoxides with the sodium salt of diethyl (phenylsulfonyl)methylphosphonate

100 e achieved via the oxidative addition of the sodium salt of ethyl 2-halo-substituted-4-mercaptobenzoa

101 ry using an aqueous electrolyte based on the sodium salt of flavin mononucleotide.

102 n evaluated the effects of the water-soluble sodium salt of glipizide, an inhibitor of ATP-sensitive

103 Finally, we showed that the sodium salt of IQ-1 had favorable pharmacokinetics and i

104 The sodium salt of IQ-1 inhibited LPS-induced TNF-alpha and

105 tion of the drug was developed, based on the sodium salt of MPA (EC-MPS, Myfortic).

106 The conformation of the sodium salt of mycophenolic acid (MPA), a potent inhibit

107 N-reaction of glycidyl methacrylate with the sodium salt of N-(3,5-dimethylphenyl)alanine, which was

108 ociation constants of the hosts bound to the sodium salt of N-acetyl phenylalanine in d(6)-DMSO and i

109 Hence, the sodium salt of N-acetylhomotaurinate (i) is ineffective

110 n reaction of glycidyl methacrylate with the sodium salt of N-reaction of glycidyl methacrylate with

111 eaction of 2,4,6-triaminopyrimidine with the sodium salt of nitromalonaldehyde to afford the key inte

112 mer, sulfated gamma-cyclodextrin family, the sodium salt of octakis(2,3-diacetyl-6-sulfato)-gamma-cyc

113 The sodium salt of polymethacrylic acid is the most effectiv

114 Tolevamer, (GT160-246), is a sodium salt of styrene sulfonate polymer that is under d

115 ded were demonstrated in the presence of the sodium salt of the drug and formulation excipients.

116 s, Na10[Co4(H2O)2(VW9O34)2].35H2O (Na101-V2, sodium salt of the polyanion 1-V2), was synthesized, tho

117 The sodium salt of the resulting [B20H17SH]4- ion has been e

118 butylidene was generated by pyrolysis of the sodium salt of the tosylhydrazone derivative of 3-trimet

119 The effects of the sodium salt of the weak acid lactate on tension and intr

120 a is demonstrated with sodium mandelate, the sodium salt of tryptophan, and doxylamine succinate.

121 o glycosidation by SN2 displacement with the sodium salts of 6-chloropurine or 2-amino-6-chloropurine

122 low the detection of picomole amounts of the sodium salts of a disaccharide, sucrose octasulfate, and

123 The sodium salts of allyldimethylsilanol and 2-butenyldimeth

124 ntrolled through the use of hydrochloride or sodium salts of amino acids to generate a diversity of p

125 ne sulfate, and 2-butenediol sulfate and the sodium salts of benzyl sulfate, methyl sulfate, ethyl su

126 The sodium salts of both released NO in pH 7.4 buffer, with

127 ning nitric and hydrochloric acids and their sodium salts of systematically varied composition, ionic

128 eridine in 50-75% yield by reaction with the sodium salts of the amines in dry tetrahydrofuran at roo

129 Thermal decomposition of the sodium salts of these tosylhydrazones gives carbene-deri

130 Thermal decomposition of the sodium salts of tosylhydrazone derivatives of 1-trimethy

131 The effects of sodium gluconate and other sodium salts on the hydration behaviour and the basic ta

132 Herein, the effect of a series of sodium salts on the lower critical solution temperature

133 ar (10 and 40 mg/kg) injections of glipizide sodium salt or vehicle.

134 )s uccinyl]-(S)-phenylalanine-N-methylamide, sodium salt), p38 MAPK inhibitors do not directly inhibi

135 delivery of polyinosinic-polycytidylic acid sodium salt (poly I:C) to target Toll-like receptor 3 (T

136 Polyriboinosine-polyribocytidylic acid sodium salt (poly(IC)) is a mimic of dsRNA and viral inf

137 eoyl-sn-glycero-3-phospho-(1'-rac-glycerol) (sodium salt)), POPS (1-palmitoyl-2-oleoyl-sn-glycero-3-p

138 vacuum pyrolysis (FVP) of a tosyl hydrazone sodium salt precursor, to give a number of rearrangement

139 rious targets, such as bacteria [fluorescein sodium salt, recombinant green fluorescence protein (rGF

140 milar levels of increased licking to several sodium salts regardless of anion but did not increase li

141 NaCl and Na-gluconate (small and large anion sodium salts, respectively) in isolated taste cells from

142 Substantial and selective suppression of sodium salt responses occurred in a graded manner genera

143 Detection of sodium-salt-rich ice grains emitted from the plume of th

144 ing the transduction pathway responsible for sodium salt sensation, and that these factors may become

145 ophenyl)dimethylsilanolate prepared as their sodium salts showed excellent activity in the coupling r

146 After diclofenac sodium salt solution injection, drug levels declined rap

147 arging of proteins from aqueous ammonium and sodium salt solutions were investigated.

148 Sodium ascorbate, like other sodium salts such as saccharin, glutamate, and bicarbona

149 We found that the specific deletion of sodium salt taste during development produced terminal f

150 thesis that the lack of activity elicited by sodium salt taste impacts the terminal field organizatio

151 of how specific taste stimuli, in this case sodium salt taste, play a role in the maturation of the

152 mice, demonstrating for the first time that sodium salt taste-elicited activity is necessary for the

153 e, enriched with a commercial NA mixture (NA sodium salt; TCI Chemicals), batch biotransformation ass

154 he corresponding methylamine derivative as a sodium salt that was highly unstable but could be trappe

155 ulations disallowing dumping of concentrated sodium salts, the residuals from popular Na-exchange sof

156 4-butylazobenzyl-4'-triazologlucuronic acid sodium salt thus synthesized can be isomerized from its

157 -(p-toluidinyl) naphthalene-6-sulfonic acid, sodium salt (TNS), inherent tryptophan fluorescence, and

158 ium, sodium, and potassium salts tested, the sodium salt was found to give the highest yield and sele

159 The enhanced licking of sodium salts was abolished in the presence of amiloride.

160 Ion-pair extraction of neutral sodium salts was not changed or only mildly enhanced by

161 4H-pyrido[1,3]oxazin-4-one precursors (imide sodium salts) was developed and led to the desired triaz

162 Various sodium salts were tested for their capability to ionize

163 ation of 6-(substituted-imidazol-1-yl)purine sodium salts with 2-deoxy-3,5-di-O-(p-toluoyl)-alpha-D-e

164 can be activated by halide abstraction with sodium salts, with the resulting catalyst [kappa(5) -((1

165 cribed phosphocitrate in a mixed calcium and sodium salt, yet to be tested in a guinea pig osteoarthr