ライフサイエンスコーパス: butanone

1 reaction of the enolate ion of 3-mercapto-2-butanone.

2 nogen, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone.

3 ts of 4-(methylnitrosoamino)-1-(3-pyridyl)-1-butanone.

4 nogen, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone.

5 ene or 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone.

6 doacetate, 1,3-dibromoacetone, and 1-bromo-2-butanone.

7 ced by 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone.

8 )P and 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone.

9 on of two of the compounds, 2-propanol and 2-butanone.

10 appetitive olfactory learning in response to butanone.

11 androsterone to approximately 940-fold for 2-butanone.

12 molecule(-1) s(-1) for 3-methyl-3-nitrooxy-2-butanone.

13 ly depended on the proportions of hexane and butanone.

14 inary solvent system, composed of hexane and butanone.

15 cleavage in 2-butanol partial oxidation to 2-butanone.

16 wo ion peaks, corresponding to benzene and 2-butanone.

17 thyl salicylate, naphthalene, benzene, and 2-butanone.

18 inogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone.

19 obtained with dimethyl methylphosphonate and butanone.

20 carcinogen 4-methylnitrosamino-1-3-pyridyl-1-butanone.

21 [e.g., 4-[methylnitrosamino]-1-(3-pyridyl)-1-butanone].

22 , trans-2-hexenal (0.49-17.49%), 3-hydroxy-2-butanone (0.08-7.39%), 1-hexanol (0.56-16.39%), 1-octano

23 ohexanol (23 mV; 2575th, 19-38), 3-hydroxy-2-butanone (16 mV, 9-26), 3-methylbutanal (20 mV; 14-26),

24 ring-containing ketones, such as 4-phenyl-2-butanone (1a) and 1-phenyl-1,3-butadione (2a), were redu

25 acetaldehyde, acetic acid, ethyl acetate, 2-butanone, 2,3,-butanedione, and acetone, or the monoterp

26 bon disulfide, dimethyldisulfide, acetone, 2-butanone, 2,3-butanedione, 6-methyl-5-hepten-2-one, indo

27 GC-MS identified 2-butanol, 2-butanone, 2-pentanone and 1-propanol to be possibly elev

28 2-butanone, 2-pentanone, 2-heptanone and 3-methyl-1-butano

29 2-butanone, 2-pentanone, 2-heptanone and 3-methyl-1-butano

30 The longer-chain ketones butanone, 2-pentanone, 3-pentanone, and 2-hexanone were

31 methylpyrazine, 2-vinylpyrazine, 3-hydroxy-2-butanone, 3-(methylsulfanyl)-propanal, and 5-methyl-2-fu

32 methyl 2-propenal), four ketones (acetone, 2-butanone, 3-buten-2-one, and 6-methyl-5-hepten-2-one), o

33 sugar damage to DNA: glycolate, 3-hydroxy-2-butanone, 3-phenylbutyraldehyde, and alpha-hydroxy-gamma

34 lose 5-phosphate (Ru5P) to l-3,4-dihydroxy-2-butanone 4-phosphate and formate.

35 RibB (3,4-dihydroxy-2-butanone 4-phosphate synthase) is a magnesium-dependent

36 he Escherichia coli gene for 3,4-dihydroxy-2-butanone 4-phosphate synthase, a key enzyme for riboflav

37 previously shown to code for 3,4-dihydroxy-2-butanone-4-phosphate synthase (DHBP synthase), an enzyme

38 The enzyme 3,4-dihydroxy-2-butanone-4-phosphate synthase (DHBPS) catalyzes one of t

39 taining GTP cyclohydrase and 3,4-dihydroxy-2-butanone-4-phosphate synthase activities.

40 rotein GTP cyclohydrolase II/3,4-dihydroxy-2-butanone-4-phosphate synthase and a negative regulator o

41 his bacterial gene encodes the 4-dihydroxy-2-butanone-4-phosphate synthase enzyme of the riboflavin b

42 -ray crystal structures of L-3,4-dihydroxy-2-butanone-4-phosphate synthase from Magnaporthe grisea ar

43 ioning GTP cyclohydrolase II-3,4-dihydroxy-2-butanone-4-phosphate synthase, an enzyme essential for r

44 dependent OH radical reaction of 4-hydroxy-2-butanone (4H2B) is presented.

45 significantly higher amounts of 3-hydroxy-2-butanone (acetoin), 6-methyl-5-hepten-2-one (sulcatone),

46 -methyl-1-butanol, 3-methyl-1-butanol, and 2-butanone after storage.

47 The use of benzene as a dopant with 2-butanone allowed one to see two ion peaks, corresponding

48 nogen 4-(methylnitrosamino)-1-(3-pyridyl)-1- butanone also had a low incidence (16.7%) of ER methylat

49 Methyl-2-buten-1-ol (prenol) and 3-Hydroxy-2-butanone (AMC) were selected for further behavioral assa

50 droxylation, 4-(methylamino)-1-(3-pyridyl)-1-butanone (aminoketone), can be converted to the potent t

51 2) enables an efficient direct conversion of butanone ammoximation to butanone oxime, showing a high

52 and octanal), sauce-like flavor (3-hydroxy-2-butanone and 2-furfural), and sweet, caramel (2,3-octane

53 eduction of such challenging substrates as 2-butanone and 3-hexanone.

54 2-Butanone and 3-methyl-1-butanol were identified in Lacto

55 2-Butanone and 3-methyl-1-butanol were identified in Lacto

56 orea and Ruminococcus and higher levels of 2-butanone and 4-methyl-2-pentanone compared to CTRLs.

57 s (TC) 4-(methylnitrosamino)-I-(3-pyridyl)-1-butanone and benzo(a)pyrene.

58 otein bound with small molecules 4-hydroxy-2-butanone and FK506.

59 am for 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone and N'-nitrosoanabasine.

60 gens 4-(methylnitrosamino)-1-(3-pyridinyl)-1-butanone and N-nitroso nornicotine were also detected.

61 (TSNA) 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone and N-nitrosonornicotine by repairing O(6)-[4-o

62 exhaust, oil refining, and gasoline leaks (2-butanone and xylenes), and plastics (acetone and styrene

63 3) cm(3) molecule(-1) s(-1) for 3-nitrooxy-2-butanone, and (2.6 +/- 0.9) x 10(-13) cm(3) molecule(-1)

64 anol, 3,7-dimethyl-1,3,6-octatriene, hydroxy butanone, and 1-octen-3-ol perceived aroma for longan.

65 same conditions, cycloheptanone, 3-methyl-2-butanone, and 2-butanone were converted to dienes.

66 m enolates derived from acetone, pinacolone, butanone, and 3-methyl-2-butanone to give fair to good y

67 ncies of alpha-nitrooxyacetone, 3-nitrooxy-2-butanone, and 3-methyl-3-nitrooxy-2-butanone have been d

68 ncluding 2- and 3-methylbutanal, 3-hydroxy-2-butanone, and 6-methyl-5-hepten-2-one.

69 ains: ethyl butyrate (EB), propionic acid, 2-butanone, and ethyl acetate.

70 anal, 2-pentylfuran, 2-heptanone, nonanal, 2-butanone, and heptanal, while stored samples were associ

71 g. hexanal, (E)-2-nonenal, (E)-2-heptenal, 2-butanone, and hexadecane), lipids, myoglobin, total vola

72 ake of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone, and nicotine, respectively, in relation to lun

73 otine, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone, and volatiles.

74 entanedione) or the absence of a keto group (butanone) are not ODR-10 agonists.

75 (5 mol %) and oxalic acid (10 mol %) with 2-butanone as a solvent for the racemization of a range of

76 migration as evident from the formation of 2-butanone as the major product via the enol 2-hydroxy-2-b

77 e obtained in high yields and selectivity in butanone by changing the ligand to 1,3,5,7-tetramethyl-2

78 four analytes (methanol, ethanol, acetone, 2-butanone) by systematically varying the oscillating freq

79 during prolonged starvation, nor butanol or butanone, compounds closely related to BOH, had an effec

80 ceae, 4-methyl-2-pentanone, 1-butanol, and 2-butanone could discriminate NAFLD patients from CTRLs.

81 ion of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone could occur in humans.

82 . vaginalis T016 with >/=20 mM 1,4-diamino-2-butanone (DAB) to inhibit ODC resulted in growth arrest,

83 transformant was inhibited by 1, 4-diamino-2-butanone (DAB), a known inhibitor of eukaryotic ODC.

84 panone (7a) was reduced with lower ee than 2-butanone derivatives.

85 sm for 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone detoxification.

86 curves were produced for ethanol, acetone, 2-butanone, ethyl acetate and eucalyptol, yielding R(2) >

87 g 4-(N-methyl-N-nitrosamino)-1-(3-pyridyl)-1-butanone-exposed hamsters revealed that MUC1 mRNA increa

88 unds (acetaldehyde, diacetyl, acetoin, and 2-butanone) followed a sigmoidal trend described by the mo

89 tudied by varying the volume ratio of hexane/butanone from 85:15 to 45:55.

90 trooxy-2-butanone, and 3-methyl-3-nitrooxy-2-butanone have been determined at room temperature at 100

91 well as hydroxy acetone (HA) and 1-hydroxy-2-butanone (HB) as donor substrates, in each case using gl

92 ospira and higher levels of 1-pentanol and 2-butanone in NAFL patients compared to CTRLs.

93 ion of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone-induced pulmonary adenoma formation by myo-inos

94 ocking 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone-induced short-term O(6)-methylguanine and long-

95 mine, 4-(methylnitrosoamino)-1-(3-pyridyl)-1-butanone, is activated to lung DNA methylating and pyrid

96 Adaptation to one odorant, butanone, is disrupted by ODR-1 overexpression.

97 amine, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone, is one of the most potent and abundant procarc

98 tivity even for the hydrazone derived from 2-butanone (methyl vs ethyl, 91% ee).

99 THF was analyzed for a series of ketones (2-butanone, methyl acetoacetate, and N,N-dimethylacetoacet

100 The rate constants for the reduction of 2-butanone, methylacetoacetate, N, N-dimethylacetoacetamid

101 ion of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) (0.05 ng/L) and 4-(methylnitrosamino)-1-(

102 ncluding (methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) and 4-(methylnitrosamino)-1-(3-pyridyl)-1

103 ure of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) and benzo[a]pyrene (BaP) in A/J mice.

104 amines 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) and N'-nitrosonornicotine (NNN) can under

105 amines 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) and N-nitrosonicotine (NNN) are potent ca

106 amines 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) and NNN and the addictive alkaloid nicoti

107 inogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) and vinyl carbamate (VC) during mouse lun

108 nogens 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) and vinyl carbamate, and the occupational

109 samine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) by measuring the frequency of NNK-induced

110 samine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) by s.c. injection at a dose of 1.5 mg/kg

111 cromol 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) given by gavage once weekly for 8 weeks.

112 inogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) in a 2-year bioassay.

113 ced by 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) in male F344 rats that had been fed eithe

114 inogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) in people who had stopped smoking: 4-(met

115 inogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) induces Ca(2+) signalling, a mechanism th

116 inogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) into DNA-altering compounds that cause lu

117 samine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) is an important component in cigarette sm

118 samine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) is formed by nitrosation of nicotine and

119 samine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) is formed by nitrosation of nicotine and

120 samine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) is of particular interest due to its pote

121 samine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) is the most potent carcinogen contained i

122 ion by 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) or vinyl carbamate (VC) resulted in a sig

123 samine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) reproducibly induces pulmonary adenocarci

124 inogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) were previously shown to be highly persis

125 inogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) within DNA duplexes representing p53 muta

126 inogen 4-(methylnitrosamino)-I-(3-pyridyl)-1-butanone (NNK), 4ebp1(-/-)/4ebp2(-/-) mice showed increa

127 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK), a tobacco-specific lung carcinogen, is b

128 (NNN), 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK), and 4-(methylnitrosamino)-1-(3-pyridyl)-

129 nogen, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK), and its inhibition by black tea have bee

130 N) and 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK), are human carcinogens with No Significan

131 samine-4-(methylnitrosamino)-1-(3 pyridyl)-1-butanone (NNK), BEAS-2B cells exhibited evidence of tran

132 e.g., 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK), have not been elucidated.

133 amine, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK), in the canine trachea.

134 amine, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK), is a chemical carcinogen thought to be i

135 he NOC 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK), O(6)-methyl-dG (O(6)-Me-dG) and O(6)-pyr

136 amine, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK), selectively induces lung tumors in F344

137 inogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK), the inflammatory agent lipopolysaccharid

138 ole in 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK)-induced lung cancer by producing carcinog

139 ine on 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK)-induced lung tumor progression from adeno

140 ncy on 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK)-induced lung tumorigenesis.

141 inogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK).

142 amine, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK).

143 inogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK).

144 samine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK).

145 inogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK).

146 tes of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK).

147 , and (4-methylnitrosoamino)-1-(3-pyridyl)-1-butanone (NNK).

148 samine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK).

149 inogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK); and r-1-,t-2,3,c-4-tetrahydroxy-1,2,3,4-

150 sed to 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone, NNK, a potent carcinogen in tobacco smoke.

151 4-(acetoxymethylnitrosamino)-1-(3-pyridyl)-1-butanone (NNKOAc), enhanced the tumorigenic activity of

152 4-(acetoxymethylnitrosamino)-1-(3-pyridyl)-1-butanone (NNKOAc).

153 irect conversion of butanone ammoximation to butanone oxime, showing a high conversion rate of 80.2%

154 ose of 4-(methylnitrosamino)-I-(3-pyridyl)-1-butanone (P = 0.03) per cigarette than noncarriers.

155 entanone (PF-2M3P), and perfluoro-3-methyl-2-butanone (PF-3M2B) using outdoor atmospheric simulation

156 .1 g/mol), 4-aminopiperidine, 3,3-dimethyl-2-butanone (pinacolone) and methylisobutyl ketone for whic

157 luding 4-(methylnitrosamino)-I-(3-pyridyl)-1-butanone plus benzo(a)pyrene.

158 found to modify the kinetic parameters for 2-butanone reduction by R-HPCDH in a saturable fashion, wi

159 , and increasing the enantioselectivity of 2-butanone reduction to a theoretical value of 100% (S)-2-

160 ypentan-2-ones or 1,4 bis-phenyl-substituted butanones, respectively.

161 samine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone results in accumulation of Bcl2 in the nucleus

162 samine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone results in accumulation of Bcl2 in the nucleus,

163 ation leading to the eventual formation of 2-butanone than for the other two pathways.

164 lectivity for producing (S)-2-butanol from 2-butanone that was unaffected by modulators that interact

165 onated monomers and proton-bound dimers of 2-butanone, the limits of detection are 1.3 ppt(v) and 57

166 sion of 4-hydroxy-4-(6-methoxy-2-naphthyl)-2-butanone to 6-methoxy-2-naphthaldehyde and acetone.

167 ase the selectivity for the CBS reduction of butanone to 80% enantiomeric excess (ee), the highest po

168 cetone, pinacolone, butanone, and 3-methyl-2-butanone to give fair to good yields of 2H-1,2-benzothia

169 An Oscillospira decrease coupled to a 2-butanone up-regulation and increases in Ruminococcus and

170 The effect of proportions of hexane and butanone was first studied by varying the volume ratio o

171 The optimal mixture ratio of hexane to butanone was found to be 65:35.

172 D or L dibenzoyl tartaric acid (DBTH2) in a butanone/water or 2-pentanone/water solution.

173 , cycloheptanone, 3-methyl-2-butanone, and 2-butanone were converted to dienes.

174 rcinogen 4-methylnitrosamino-1-(3-pyridyl)-1-butanone were hypermethylated at the p16 gene promoter;

175 nder Dakin-West conditions, forms 4-phenyl-2-butanone when the reaction is catalyzed by 1-methylimida

176 -LPC at 60 degrees C in the presence of 30 % butanone, where the synthesis rate was 100 times higher

177 the Corey-Bakshi-Shibata (CBS) reduction of butanone, which constitutes the classic and prototypical

178 te the partial oxidation of 2-butanol into 2-butanone with near 100% selectivity at low oxygen covera

179 nogen, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone, with a catalytic efficiency much greater than