ライフサイエンスコーパス: butanediol

1 ethylene, succinic acid, isobutanol, and 1,4-butanediol.

2 accumulation of by-products acetoin and 2,3-butanediol.

3 cluding the growth promoting VOC (2R,3R)-(-)-butanediol.

4 ansesterification of divinyl adipate and 1,4-butanediol.

5 ntation or indirectly via the dehydration of butanediols.

6 luding ethylene glycol, 1,3-propanediol, 1,4-butanediol, 1,5-petanediol, and 1,6-hexanediol.

7 commercial vitamin D and enantiomers of 1,3-butanediol (23 and 24).

8 Here we systematically developed the 2,3-butanediol (23BD) biosynthetic pathway in Synechococcus

9 s enhanced due to its ability to produce 2,3-butanediol, a neutral fermentation end product, and supp

10 l alcohols, acetaldehyde, ethyl acetate, 2,3-butanediol, acetoin and 2,3-butanedione.

11 icators were 2,3,5,6-tetramethylpyrazine,2,3-butanediol and 4-ethylguaiacol, beta-linalool, 2-,3-dime

12 subtilis that emitted reduced levels of 2,3-butanediol and acetoin conferred reduced Arabidopsis pro

13 wth whereas bacterial mutants blocked in 2,3-butanediol and acetoin synthesis were devoid in this gro

14 In particular, the volatile components 2,3-butanediol and acetoin were released exclusively from tw

15 he known plant growth-promoting volatile 2,3-butanediol and acetoin.

16 nt regulation by the federal government, 1,4-butanediol and gamma-butyrolactone, another precursor of

17 droxybutyrate and a history of ingesting 1,4-butanediol and patients discovered through public health

18 of toxic effects due to the ingestion of 1,4-butanediol and reviewed the related health risks.

19 , were identified as key contributors to 2,3-butanediol and/or mixed acid fermentation as the major m

20 anol and ethyl propanoate; peak 3, (R,R)-2,3-butanediol, and peak 4, nonanoic acid.

21 hesis of butadiene from ethanol, butanol and butanediols, and (iii) the catalytic synthesis of HMF an

22 The health risks of 1,4-butanediol are similar to those of its counterparts, gam

23 DNA-DNA cross-links, 1,4-bis-(guan-7-yl)-2,3-butanediol (bis-N7G-BD) and 1-(guan-7-yl)-4-(aden-1-yl)-

24 which can then form 1,4-bis-(guan-7-yl)-2,3-butanediol (bis-N7G-BD) lesions.

25 DNA conjugates, e.g. 1,4-bis-(guan-7-yl)-2,3-butanediol (bis-N7G-BD), 1-(guan-7-yl)-4-(aden-1-yl)-2,3

26 er system; the addition of water reduces the butanediol concentration, inducing the formation of a di

27 the 1,4-bis(2'-deoxyadenosin-N(6)-yl)-2R,3R-butanediol cross-link arising from N(6)-dA alkylation of

28 zirconia particles and cross-linked with 1,4-butanediol diglycidyl ether (BUDGE).

29 radiolytic markers and isomerisation of 2,3-butanediol during irradiation of food.

30 hermore, pharmacological applications of 2,3-butanediol enhanced plant growth whereas bacterial mutan

31 Peak area RSDs were 2-7% for 2, 3-butanediol, ethanol, glycerol, erythritol, rhamnose, ara

32 cohol esters, namely 3-methyl-1-butanol, 2,3-butanediol, ethyl lactate, 3-methyl-1-butyl acetate, 2-p

33 dicated that B. subtilis grows by mixed acid-butanediol fermentation but that no formate is produced.

34 ma-hydroxybutyrate; gamma-butyrolactone, 1,4-butanediol, flunitrazepam, ketamine, and nitrites.

35 ionally produced pseudo-enantiomerism in 1,3-butanediol generates a chiral response in the frontier e

36 cis-1,2-cyclopentanediol > 2,3-dimethyl-2,3-butanediol > 1,2-propanediol.

37 norbornene-2,2-dimethanol > 3,3-dimethyl-1,2-butanediol > cis-1,2-cyclopentanediol > 2,3-dimethyl-2,3

38 configurational enantiomers of 1,3- and 2,3-butanediols has been examined with a focus on the large

39 Multivariate data analyses revealed that 2,3-butanediol, hexanal, hexanol and cinnamaldehyde contribu

40 yst, does not explain the dehydration of 1,4-butanediol in HTW without catalyst.

41 The doses of 1,4-butanediol ingested ranged from 5.4 to 20 g in the patie

42 we identified cases of toxic effects of 1,4-butanediol involving patients who presented to our emerg

43 1,4-Butanediol is an industrial solvent that, when ingested,

44 -furanacrylic acids (monomer II), with a 1,4-butanediol linker.

45 caused by metabolites such as glycerol, 2,3-butanediol, malic acid, alpha/beta-glucose and phenolic

46 eucine, isoleucine and alanine, and also 2,3-butanediol, methanol, glycerol and isotopic variables we

47 arch, palm oil, or R-3-hydroxybutyrate-R-1,3-butanediol monoester (3HB-BD ester).

48 diet in which D-beta-hydroxybutyrate-(R)-1,3 butanediol monoester [ketone ester (KE)] replaced equica

49 bis-N7G-BD), 1-(guan-7-yl)-4-(aden-1-yl)-2,3-butanediol (N7G-N1A-BD), and 1,N(6)-(1-hydroxymethyl-2-h

50 -N7G-BD) and 1-(guan-7-yl)-4-(aden-1-yl)-2,3-butanediol (N7G-N1A-BD).

51 omatography-mass spectrometry to measure 1,4-butanediol or its metabolite, gamma-hydroxybutyrate, in

52 e dehydrogenase, pyruvate formate-lyase, and butanediol pathways.

53 e regulation enables carbon fixation and 2,3-butanediol production in the absence of light.

54 -butene-1,2-diol metabolism to 3,4-epoxy-1,2-butanediol, rather than from 1,2;3,4-diepoxybutane.

55 fects in eight patients who had ingested 1,4-butanediol recreationally, to enhance bodybuilding, or t

56 An N16961 mutant (SSY01) defective in 2,3-butanediol synthesis showed the same defect in growth th

57 the chemocatalytic conversion of ethanol and butanediols to butadiene, including thermodynamics and k

58 hanism of tetrahydrofuran synthesis from 1,4-butanediol via dehydration in high-temperature liquid wa

59 emic mixture of (RR) and (SS) isomers of 2,3-butanediol was found to trigger ISR and transgenic lines

60 The L(3) phase was the monoolein/butanediol/water system; the addition of water reduces t

61 (R,R) and (S,S)-2,3-butanediol were detected in samples irradiated at 8 kGy,

62 nd glucose, and produces 12.6 g l(-1) of 2,3-butanediol with a rate of 1.1 g l(-1) d(-1) under contin

63 to the phosphorus atom and obtained from d,l-butanediol, with hexafluoroacetone (CCl4, -40 degrees C)