ライフサイエンスコーパス: dimethyl sulfide

1 on of organosulfur compounds (OSCs), such as dimethyl sulfide.

2 te with levels of isoprene, monoterpenes, or dimethyl sulfide.

3 nisole < ether-sulfides < dialkyl sulfides < dimethyl sulfide.

4 erexpressing methionine-gamma-lyase produced dimethyl sulfide.

5 avage pathway to the climatically active gas dimethyl sulfide(3,4).

6 es of domoic acid, a marine algal toxin, and dimethyl sulfide, a volatile precursor to cloud condensa

7 ne adducts were similar to that observed for dimethyl sulfide adducts.

8 Dimethyl sulfide, an alternate substrate for thioether S

9 amined as borane carriers in comparison with dimethyl sulfide and 1,4-oxathiane: tert-butyl methyl su

10 of tissue disintegration, and the release of dimethyl sulfide and dimethyl disulfide was related to t

11 The oxidation of dimethyl sulfide and dimethyl selenide, two-electron oxi

12 depletion, as well as the rapid oxidation of dimethyl sulfide and mercury in the Antarctic boundary l

13 substitutions with the neutral nucleophiles dimethyl sulfide and triethylamine and the bromination w

14 by biotin or the nonphysiological products, dimethyl sulfide and trimethylamine.

15 reased hydrogen sulfide (H2S), methanethiol, dimethyl sulfide, and carbon disulfide concentrations.

16 o coordinate various ligands like imidazole, dimethyl sulfide, and carbon monoxide depending on the r

17 oprene (C(5)H(8)), methyl bromide (CH(3)Br), dimethyl sulfide, and oxygen (O(2)), which increased sub

18 itrite to a water-soluble phosphine (tppts), dimethyl sulfide, and the biological thiols cysteine (Cy

19 Both the alternate substrate, dimethyl sulfide, and the competitive product inhibitor,

20 Significant amounts of dimethyl sulfide are emitted from cruciferous vegetables

21 hat procellariiform seabird species that use dimethyl sulfide as a foraging cue selectively forage on

22 controlled to release increasing amounts of dimethyl sulfide as the supply of DMSP exceeds cellular

23 tron ionization (EI) were: carbonyl sulfide, dimethyl sulfide, carbon disulfide, 2-methylthiophene, 3

24 riethylsilane, cycloheptatriene, or a borane-dimethyl sulfide complex.

25 obial nitrate reductase, selenate reductase, dimethyl sulfide dehydrogenase, ethylbenzene dehydrogena

26 l)-R-pyridinium) with dimethylplatinum-micro-dimethyl sulfide dimer.

27 sulfur compounds detected were methanethiol, dimethyl sulfide, dimethyl disulfide, and dimethyl trisu

28 sulfoniopropionate (DMSP) cleavage, yielding dimethyl sulfide (DMS) and acrylate, provides vital carb

29 reactivity with aldehydes and the effects of dimethyl sulfide (DMS) and Saharan dust on aerosol pH; a

30 ide to form water oxide and the oxidation of dimethyl sulfide (DMS) by hydrogen peroxide to form dime

31 Dimethyl sulfide (DMS) is a key compound in global sulfu

32 Dimethyl sulfide (DMS) is produced in large quantities a

33 The production of the marine trace gas dimethyl sulfide (DMS) provides 90% of the marine biogen

34 Oceanic emissions of volatile dimethyl sulfide (DMS) represent the largest natural sou

35 methanethiol (MeSH), ethanethiol (EtSH), and dimethyl sulfide (DMS) were assessed in wines post-bottl

36 P lyases cleave DMSP, producing acrylate and dimethyl sulfide (DMS), a climate-active gas with roles

37 The presence of dimethyl sulfide (DMS), either as a component originatin

38 e conversion of dimethyl sulfoxide (DMSO) to dimethyl sulfide (DMS), reversibly, in the presence of s

39 Oceans dominate emissions of dimethyl sulfide (DMS), the major natural sulfur source.

40 ntermediates in the atmospheric oxidation of dimethyl sulfide (DMS), was generated by flash pyrolysis

41 BlMGL) produced the sulfur volatile compound dimethyl sulfide (DMS).

42 sms(2,3) and the major precursor for gaseous dimethyl sulfide (DMS).

43 nism by which anthropogenic SO(2) and marine dimethyl sulfide emissions generate secondary biogenic a

44 terised by a high level of sulfur compounds (dimethyl sulfide, ethanethiol), and ester and alcohol co

45 While transgenic lines emitted dimethyl sulfide from leaves and roots, no sulfur-contai

46 the olefin followed by brief treatment with dimethyl sulfide gave a mixture of diastereomeric ozonid

47 none 12c in CH2Cl2 and reductive workup with dimethyl sulfide generated unstable beta-formyl ester 21

48 ived metabolites, including volatile esters, dimethyl sulfide, glycerol and mannoproteins with harves

49 Dimethyl sulfide has been studied in the context of glob

50 ules of keystone significance: saxitoxin and dimethyl sulfide in marine communities and tetrodotoxin

51 lent yield and enantiomeric excess by borane-dimethyl sulfide in the presence of a chiral oxazaboroli

52 e that the ability of DMSOR to be reduced by dimethyl sulfide is lost upon mutation of Tyr-114 and th

53 own to arise on extended aerobic exposure to dimethyl sulfide, is susceptible to a further degradativ

54 y a compensatory (100-fold) up-regulation in dimethyl sulfide metabolic enzymes.

55 y, the release of acetone, carbon disulfide, dimethyl sulfide, nitromethane, pentane, 3-methylfuran,

56 um carbonate precipitation and production of dimethyl sulfide, often blooms in mid-latitude at the be

57 usly shunts as much as 59% of DMSP uptake to dimethyl sulfide production.

58 reaction in which the accumulating product, dimethyl sulfide, reacts with oxidized enzyme to yield t

59 our results, we postulate a heme-based redox/dimethyl sulfide sensory function of MA4561 and propose

60 , converting phosphines to phosphine oxides, dimethyl sulfide to dimethyl sulfoxide, and dibenzylamin

61 uch faster than the corresponding adducts of dimethyl sulfide, which are currently used extensively.