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 litis was induced in mice by dextran sulfate sodium salt.

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

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

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

8 more than 3 times that of the corresponding sodium salt.

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

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

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

12 ydrolyzed to the corresponding water-soluble sodium salts.

13 nge of carbonyl compounds and tosylhydrazone sodium salts.

14 ctively, and subsequently converted to their sodium salts.

15 loids or colloids, and most crystalloids are sodium salts.

16 ultaneous bio-reduction approach to selenium sodium salts.

17 in corn stover hydrolysates containing high sodium salts.

18 in xylose or glucose-mixed medium containing sodium salts.

19 on is the dominant mode of transport for 1:1 sodium salts.

20 Potassium salts are more effective than sodium salts.

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

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

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

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

25 42, 546 nm, 1% extinction coefficient of the sodium salt = 244 2).

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

27 8.0) containing 0.9ml of N-lauroylsarcosine (sodium salt, 30% [w/v] solution) per 100ml of buffer.

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

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

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

31 8-bromoguanosine 3',5'-cyclic monophosphate sodium salt (8-Br-cGMP), or pioglitazone dose-dependentl

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

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

34 6] (1), has been prepared by the reaction of sodium salt and CsF in dichloromethane and water.

35 The combination of sodium salt and DHB sublimation was found to be an effec

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

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

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

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

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

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

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

43 We identified sodium salts as the primary yeast inhibitors, and evolve

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

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

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

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

48 Adding sodium salts before PEF application intensified structur

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

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

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

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

53 owing to the relatively lower solubility of sodium salts compared to its alkaline cousins (Li, K, an

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

55 ate framework ZIF-8 by impregnation with the sodium-salt-containing ionic liquid (IL) (Na(0.1)EMIM(0.

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

57 articles with poly[styrene-alt-(maleic acid, sodium salt)(Cu ferrite oxide-polymer) by a simple one-s

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

59 ihydrochloride (nor-BNI) and dibutyryl-cAMP, sodium salt (DB-cAMP) as two phenotypic modulators of pr

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

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

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

63 The combination of sodium salt doping of a tissue section along with the su

64 1,2-dioleoyl-sn-glycero-3-[phospho-l-serine] sodium salt (DOPS), indicating that the anionic lipids D

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

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

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

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

69 ]dioxin-2-yl-methoxy)-1-butanesulfonic acid, sodium salt (EDOT-S).

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

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

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

73 te neurotransmitter), and phenylacetic acid (sodium salt form; treatment of urea cycle disorder).

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

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

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

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

78 9 in three steps using a modification of the sodium salt glycosylation method.

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

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

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

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

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

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

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

86 The dicarboxylic acids are isolated as sodium salts in high yields (up to 77%) by direct precip

87 iran 160 mg (free acid; equivalent to 170 mg sodium salt) in adults was associated with the highest p

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

89 romotes oleoyl-L-alpha-lysophosphatidic acid sodium salt-induced integrin-mediated TGF-beta1 activati

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

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

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

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

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

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

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

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

98 ol and 2,3-dimercapto-1-propanesulfonic acid sodium salt monohydrate) led to polymers 2d and 2f, resp

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

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

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

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

103 X-ray diffraction analysis of the sodium salt, [{Na(+) (18-crown-6)(THF)(2) }(3) {Na(+) (1

104 ed electric field (PEF: 10 kV) combined with sodium salts (NaCl, Na(2)CO3, NaH2PO4) to investigate ho

105 o-fused heterocycles using readily available sodium salts (NaCl/NaBr/NaI) as halogen source and K(2)S

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

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

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

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

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

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

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

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

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

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

116 nsuccessful, leading to the isolation of the sodium salt of a cyclotrialuminene, Na(2)[AlAr(iPr6)](3)

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

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

119 Sodium salt of aryl sulfinic acid reacts with enynone in

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

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

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

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

124 MI was induced in animals and borax, a sodium salt of boron, was administered for 7 days, p.o.,

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

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

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

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

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

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

131 reclinical studies, and the synthesis of the sodium salt of HST5040 for clinical trials.

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

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

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

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

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

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

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

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

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

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

142 The sodium salt of polymethacrylic acid is the most effectiv

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

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

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

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

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

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

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

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

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

152 The sodium salts of allyldimethylsilanol and 2-butenyldimeth

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

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

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

156 via supramolecular complexation between the sodium salts of calixarene derivatives and crown ether s

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

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

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

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

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

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

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

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

165 .8%), sodium (total sodium/salt: TLS, -6.4%; sodium/salt per 100 g/ml: NS: -7.8%), fat (total fat: NS

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

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

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

169 as a lead compound, further improved as the sodium salt PPAP53, drastically enhancing solubility.

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

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

172 Sodium salt reduction in cereal products has been one of

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

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

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

176 included if they investigated the effects of sodium/salt restriction as compared to no restriction on

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

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

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

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

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

182 cket-plug recognition occurs over "other" in sodium salt solutions while precisely the reverse occurs

183 The use of (i) a reduced-sodium salt substitute, Pansalt(R) (NaCl 57%, other salt

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

185 nation of two additives (a lithium salt or a sodium salt, such as NaI).

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

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

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

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

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

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

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

193 4-butylazobenzyl-4'-triazologlucuronic acid sodium salt thus synthesized can be isomerized from its

194 S, -3%; NS, -3.5%; NW, -3.8%), sodium (total sodium/salt: TLS, -6.4%; sodium/salt per 100 g/ml: NS: -

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

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

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

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

199 oriented channels, a chromophore (resorufin sodium salt) was successfully embedded into the channels

200 4H-pyrido[1,3]oxazin-4-one precursors (imide sodium salts) was developed and led to the desired triaz

201 Various sodium salts were tested for their capability to ionize

202 er-protecting groups are saponified to their sodium salts, which after ion exchange underwent quantit

203 alysis reveals a polymeric structure for the sodium salt with the anionic units connected by [B-Br-Na

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

205 ry intake of potassium and widespread use of sodium salts with anions other than chloride as food add

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

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