ライフサイエンスコーパス: nitroso compound

1 e structure of the acyl group of the acyloxy nitroso compound.

2 ites because of the increased formation of N-nitroso compounds.

3 he acidic medium of stomach to form N- and C-nitroso compounds.

4 nous production of mutagenic aldehydes and N-nitroso compounds.

5 ma by reducing the endogenous formation of N-nitroso compounds.

6 excess carboxylic acid gives various acyloxy nitroso compounds.

7 Processed meats contain N-nitroso compounds.

8 , we report that appropriately substituted C-nitroso compounds act solely as donors of neutral nitric

9 Calculated results reveal that the unbound nitroso compound acts as a better proton transferring ag

10 es to conjugated dienes in the presence of a nitroso compound (additive) was studied quantum mechanic

11 ar hetero-Diels-Alder cycloadduct of an acyl nitroso compound and a 9,10-dimethyl anthracene derivati

12 Dietary N-nitroso compounds and endogenous nitrosation are importa

13 Cured meat increased nitroso compounds and lipoperoxidation in human stools (

14 jor defense against the carcinogenicity of N-nitroso compounds and other alkylators.

15 lative DNA damage rates of three mutagenic N-nitroso compounds and styrene.

16 ction of nitroaromatics to the corresponding nitroso compounds and, subsequently, to hydroxylamine pr

17 amines, polycyclic aromatic hydrocarbons, N-nitroso compounds, and heme iron.

18 combined forming the corresponding nitro and nitroso compounds, and the most reactive cis/syn isomer

19 Aromatic C-nitroso compounds (Ar-N horizontal lineO) and related sp

20 ay increase cancer risk as HCAs, PAHs, and N-nitroso compounds are carcinogenic in animal models.

21 After metabolic activation, many N-nitroso compounds are converted into a diazoacetate inte

22 C-Nitroso compounds are sources of biologically active neu

23 Together, these results identify acyloxy nitroso compounds as a new class of HNO donors.

24 stry of nitrile oxides, oximes, oxazete, and nitroso compounds as well as S(N)Vin reactions.

25 Many N-nitroso compounds can be metabolically activated to give

26 Some N-nitroso compounds can be metabolically activated to yiel

27 We report a method of S-nitroso compound detection using cavity ring-down measur

28 Nitrite (NO2(-)) and nitroso compounds (E-NO, E = RS, RO, and R2N) in mammali

29 addition of nitrile oxide to form a bicyclic nitroso compound, followed by a retro-ene reaction of th

30 These results suggest that nitroso compounds form a general class of thiol-modifyin

31 Humans are exposed to N-nitroso compounds from both endogenous and exogenous sou

32 cient condensation of sulfinic acid and aryl nitroso compounds has been transformed into a chemoselec

33 exogenous alkylating agents, particularly N-nitroso compounds, has been associated with increased in

34 Various N-nitroso compounds have been associated with neural tube

35 S-Nitroso compounds have received much attention in biolog

36 Several pathways, involving the nitroso compound in a free or bound state to the gold-al

37 approximately 5 pmol of S(15)NO groups for S-nitroso compounds in aqueous solutions.

38 ondary or tertiary amines and amides, form N-nitroso compounds in the presence of nitrite.

39 is important for understanding the role of S-nitroso compounds in vivo.

40 These acyloxy nitroso compounds inhibit glyceraldehyde 3-phosphate deh

41 ncludes the observed nitroxide radical and C-nitroso compound intermediates has been forwarded to exp

42 ethod for the synthesis of gem-difluorinated nitroso compounds is described.

43 The most common method to assay biological S-nitroso compounds is to chemically or photochemically re

44 N-Nitroso compounds, known animal carcinogens, are formed

45 g-down detection allows the measurement of S-nitroso compound levels from pico- to nanomole amounts.

46 as new species that react similarly to acyl nitroso compounds, making them useful synthetic intermed

47 These results suggest that N-nitroso compounds may influence the risk of ESCC in men,

48 te, 40 +/- 6 nM S-nitroso, and 33 +/- 6 nM N-nitroso compounds (n = 4-8).

49 The prototypic aromatic C-nitroso compound, nitrosobenzene (NB), was shown previou

50 iron, heterocyclic amines, and endogenous N-nitroso compounds (NOC) are proposed to explain this eff

51 a precursor in the endogenous formation of N-nitroso compounds (NOC), which are possible bladder carc

52 Humans are exposed to preformed N-nitroso compounds (NOCs) and endogenous NOCs.

53 been linked to the formation of genotoxic N-nitroso compounds (NOCs) and lipid peroxidation products

54 Metabolic activation of some N-nitroso compounds (NOCs), an important class of DNA dama

55 e exposed to both endogenous and exogenous N-nitroso compounds (NOCs), and many NOCs can be metabolic

56 , heterocyclic aromatic amines (HAAs), and N-nitroso compounds (NOCs).

57 t appeared that the moderate basicity of the nitroso compound plays a crucial role to reduce the acti

58 e, via rearrangement of the O-nitrene to a C-nitroso compound (R'ON --> O=NR'), and subsequent tautom

59 N-nitroso compounds represent a common type of environment

60 Five S-nitroso compounds, S-nitroso-N-acetyl-dl-penicillamine,

61 A resin-bound nitroso compound sequestered a single unexpected compone

62 rates of addition of radicals to nitrones or nitroso compounds (spin traps; STs).

63 exposure may also lead to the formation of N-nitroso compounds that can act as alkylating agents.

64 agents and highly acidic conditions, form N-nitroso compounds that have been found to be teratogenic

65 Humans are exposed to N-nitroso compounds through environmental exposure and end

66 ree radicals, consists of using a nitrone or nitroso compound to "trap" an unstable free radical as a

67 The lower rate of conversion of the (C7-R)-nitroso compound to the corresponding oximes compared wi

68 The conversion of the (C8-S)-nitroso compound to the E/Z-oximes was approximately 8 t

69 leophilic addition of the protein thiol to a nitroso compound to yield an N-hydroxysulfenamide, which

70 Addition of these acyloxy nitroso compounds to AhpC C165S yields a sulfinic acid a

71 yzed radical addition with in situ-generated nitroso compounds to prepare sterically hindered amines

72 EPR spectroscopic evidence showed that the nitroso compound trapped other transient intermediates t

73 No corresponding nitroso compound was formed in reactions involving l-dop

74 everse isomerization from the oxime to the C-nitroso compound was observed.

75 adicals and leads initially to a diamagnetic nitroso compound, which is transformed into a persistent

76 Nitrate and nitrite are precursors of N-nitroso compounds, which induce tumors of the pancreas i

77 cs of Diels-Alder reactions for a variety of nitroso compounds with dienes were explored with density