ライフサイエンスコーパス: hydrogen cyanide

1 athway involving decomposition to ketene and hydrogen cyanide.

2 cetylene, ethylene, ethane, diacetylene, and hydrogen cyanide.

3 nergy organic compounds such as cyanamide or hydrogen cyanide.

4 Hydrogen cyanide, a gaseous molecule, is produced by whi

5 his process is studied here for the cases of hydrogen cyanide, acetylene, and cyanoacetylene in heliu

6 r dioxide, acrylonitrile, cyanogen chloride, hydrogen cyanide, acrolein, formaldehyde, and ethyl para

7 re equilibrium mixture of cometary material, hydrogen cyanide and acetylene were produced with yields

8 oday, and might have been formed solely from hydrogen cyanide and formaldehyde.

9 ses are presumed to have been available from hydrogen cyanide and other nitrogenous species formed in

10 be derived by the reductive homologation of hydrogen cyanide and some of its derivatives, and thus t

11 taldehyde, hexanoic acid, hydrogen sulphide, hydrogen cyanide, and methyl phenol, were found to be si

12 Avoidance of hydrogen cyanide as a by-product also improves process s

13 ment key literature results and suggest that hydrogen cyanide--"Blausaure"--was that feedstock.

14 spatial distributions of carbon dioxide and hydrogen cyanide, both considered to be products of come

15 we show that these sugars can be formed from hydrogen cyanide by ultraviolet irradiation in the prese

16 The results obtained bring evidence that hydrogen cyanide can be adsorbed onto aerosol liquid wat

17 tion by endogenous plant enzymes can release hydrogen cyanide causing potential toxicity issues for a

18 lar, the self-assembly of exclusively linear hydrogen cyanide chains is observed, even when the folde

19 Deuterated hydrogen cyanide (DCN) was detected in a comet, C/1995 O

20 s operates catalytically to disproportionate hydrogen cyanide, first generating the sugars and then s

21 eaction of an imine or imine equivalent with hydrogen cyanide, followed by nitrile hydrolysis-is an e

22 tissue disruption leads to release of toxic hydrogen cyanide gas, which can deter herbivore feeding.

23 Prunasin may be degraded to hydrogen cyanide, glucose, and benzaldehyde by the actio

24 osed of micrometre-sized particles of frozen hydrogen cyanide (HCN ice).

25 Respiration was inhibited by two gases, hydrogen cyanide (HCN) and nitric oxide (NO), whose appe

26 ent results in prebiotic chemistry implicate hydrogen cyanide (HCN) as the source of carbon and nitro

27 e inferred deuterium/hydrogen (D/H) ratio in hydrogen cyanide (HCN) is (D/H)HCN = (2.3 +/- 0.4) x 10(

28 The chemistry of hydrogen cyanide (HCN) is believed to be central to the

29 The abundance of HNC relative to hydrogen cyanide (HCN) is very similar to that observed

30 en or chlorine (and other halogens) can form hydrogen cyanide (HCN) or hydrogen chloride (HCl) and th

31 CL activity in FRD1 contributes to increased hydrogen cyanide (HCN) production by this isolate.

32 Quantification of hydrogen cyanide (HCN) production from laboratory isolat

33 Additionally, direct measurement of hydrogen cyanide (HCN) production showed that P. aerugin

34 lity, biofilm formation, quorum sensing, and hydrogen cyanide (HCN) production.

35 We investigated if gaseous hydrogen cyanide (HCN) was a marker of BCC infection.

36 odium cyanide in aqueous solution at pH 7.4, hydrogen cyanide (HCN) was found to degas from the solut

37 asis of their detection of ammonia (NH3) and hydrogen cyanide (HCN) when the sample oven was heated t

38 tratosphere, using satellite observations of hydrogen cyanide (HCN), a tropospheric pollutant produce

39 ydrogen peroxide (H2O2), nitric acid (HNO3), hydrogen cyanide (HCN), hydroxymethyl hydroperoxide, per

40 including the H2S-oxidation pathway and the hydrogen cyanide (HCN)-assimilation pathway.

41 reactive hydroxynitrile that releases toxic hydrogen cyanide (HCN).

42 denotes a chemical defensive strategy where hydrogen cyanide (HCN, hydrocyanic or prussic acid) is p

43 met Hyakutake with an abundance (relative to hydrogen cyanide, HCN) similar to that seen in dense int

44 e, hydrochloric acid, cyanogen chloride, and hydrogen cyanide in negative polarity are investigated.

45 ndicate a similar stability of formamide and hydrogen cyanide in solution as well as their relatively

46 -driven, six-electron catalytic reduction of hydrogen cyanide into methane and likely also ammonia.

47 Hydrogen cyanide is a ubiquitous gas in the atmosphere a

48 Our results imply that hydrogen cyanide is the sole or primary toxic factor pro

49 e-body dissociation of sym-triazine to three hydrogen cyanide molecules.

50 one of the two-membered products acetylene, hydrogen cyanide, or N2.

51 The higher order hydrocarbons and hydrogen cyanide peak sharply in abundance and are undet

52 , carbon metabolism in Escherichia coli, and hydrogen cyanide production in the plant beneficial stra

53 Pseudomonas aeruginosa, including alginate, hydrogen cyanide production, and type IV pilus-mediated

54 Hydrogen cyanide serves as a deterrent against herbivore

55 ion mutation in a gene encoding a subunit of hydrogen cyanide synthase (hcnC) eliminated nematode kil

56 eruginosa PAO1 strain with a mutation in the hydrogen cyanide synthase gene cluster was much less tox

57 osition of cyanohydrins in order to generate hydrogen cyanide upon tissue damage.

58 after impact, whereas those for methanol and hydrogen cyanide were unchanged.