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1 e structure of the acyl group of the acyloxy nitroso compound.
2 , the favoured reaction product was a stable nitroso-compound.
3 nous production of mutagenic aldehydes and N-nitroso compounds.
4 ites because of the increased formation of 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 he acidic medium of stomach to form N- and C-nitroso compounds.
9 , we report that appropriately substituted C-nitroso compounds act solely as donors of neutral nitric
10   Calculated results reveal that the unbound nitroso compound acts as a better proton transferring ag
11 es to conjugated dienes in the presence of a nitroso compound (additive) was studied quantum mechanic
12 ar hetero-Diels-Alder cycloadduct of an acyl nitroso compound and a 9,10-dimethyl anthracene derivati
13                                    Dietary N-nitroso compounds and endogenous nitrosation are importa
14                         Cured meat increased nitroso compounds and lipoperoxidation in human stools (
15 jor defense against the carcinogenicity of N-nitroso compounds and other alkylators.
16 lative DNA damage rates of three mutagenic N-nitroso compounds and styrene.
17 ction of nitroaromatics to the corresponding nitroso compounds and, subsequently, to hydroxylamine pr
18  amines, polycyclic aromatic hydrocarbons, N-nitroso compounds, and heme iron.
19  metabolites, phenols, pesticides, nitro and nitroso compounds, and per- and polyfluoroalkyl substanc
20 combined forming the corresponding nitro and nitroso compounds, and the most reactive cis/syn isomer
21                                   Aromatic C-nitroso compounds (Ar-N horizontal lineO) and related sp
22 ay increase cancer risk as HCAs, PAHs, and N-nitroso compounds are carcinogenic in animal models.
23           After metabolic activation, many N-nitroso compounds are converted into a diazoacetate inte
24                                            C-Nitroso compounds are sources of biologically active neu
25                                              Nitroso-compounds are potentially mutagenic and carcinog
26     Together, these results identify acyloxy nitroso compounds as a new class of HNO donors.
27 stry of nitrile oxides, oximes, oxazete, and nitroso compounds as well as S(N)Vin reactions.
28            Fecal content of apparent total N-nitroso compounds (ATNC), nitrosothiols and nitrosyl iro
29                    To date, the formation of nitroso-compounds by the reaction of nitrite with food c
30                                       Many N-nitroso compounds can be metabolically activated to give
31                                       Some N-nitroso compounds can be metabolically activated to yiel
32                      We report a method of S-nitroso compound detection using cavity ring-down measur
33                         Nitrite (NO2(-)) and nitroso compounds (E-NO, E = RS, RO, and R2N) in mammali
34 addition of nitrile oxide to form a bicyclic nitroso compound, followed by a retro-ene reaction of th
35                   These results suggest that nitroso compounds form a general class of thiol-modifyin
36 oppose the milk mineral-induced reduction of nitroso compound formation.
37 processed meat could be a strategy to reduce nitroso compounds formed endogenously after consumption.
38                      Humans are exposed to N-nitroso compounds from both endogenous and exogenous sou
39 cient condensation of sulfinic acid and aryl nitroso compounds has been transformed into a chemoselec
40  exogenous alkylating agents, particularly N-nitroso compounds, has been associated with increased in
41                                    Various N-nitroso compounds have been associated with neural tube
42                                            S-Nitroso compounds have received much attention in biolog
43              Several pathways, involving the nitroso compound in a free or bound state to the gold-al
44 approximately 5 pmol of S(15)NO groups for S-nitroso compounds in aqueous solutions.
45 n, milk mineral reduced the concentration of nitroso compounds in feces and small intestinal content.
46 ondary or tertiary amines and amides, form N-nitroso compounds in the presence of nitrite.
47 is important for understanding the role of S-nitroso compounds in vivo.
48                                These acyloxy nitroso compounds inhibit glyceraldehyde 3-phosphate deh
49 ncludes the observed nitroxide radical and C-nitroso compound intermediates has been forwarded to exp
50 ethod for the synthesis of gem-difluorinated nitroso compounds is described.
51 The most common method to assay biological S-nitroso compounds is to chemically or photochemically re
52 the most common sources of human exposure to nitroso-compounds is their formation in the acidic envir
53                                            N-Nitroso compounds, known animal carcinogens, are formed
54 g-down detection allows the measurement of S-nitroso compound levels from pico- to nanomole amounts.
55  as new species that react similarly to acyl nitroso compounds, making them useful synthetic intermed
56                 These results suggest that N-nitroso compounds may influence the risk of ESCC in men,
57 te, 40 +/- 6 nM S-nitroso, and 33 +/- 6 nM N-nitroso compounds (n = 4-8).
58                    The prototypic aromatic C-nitroso compound, nitrosobenzene (NB), was shown previou
59  iron, heterocyclic amines, and endogenous N-nitroso compounds (NOC) are proposed to explain this eff
60 a precursor in the endogenous formation of N-nitroso compounds (NOC), which are possible bladder carc
61            Humans are exposed to preformed N-nitroso compounds (NOCs) and endogenous NOCs.
62  been linked to the formation of genotoxic N-nitroso compounds (NOCs) and lipid peroxidation products
63             Sixty-six structurally diverse N-nitroso compounds (NOCs) yielded a range of conversion e
64               Metabolic activation of some N-nitroso compounds (NOCs), an important class of DNA dama
65 e exposed to both endogenous and exogenous N-nitroso compounds (NOCs), and many NOCs can be metabolic
66 roperties, is implicated in the formation of nitroso compounds (NOCs), such as nitrosylheme, nitrosam
67 , heterocyclic aromatic amines (HAAs), and N-nitroso compounds (NOCs).
68 y via endogenous formation of carcinogenic N-nitroso compounds or increased lipid and protein oxidati
69 t appeared that the moderate basicity of the nitroso compound plays a crucial role to reduce the acti
70             Unfortunately, not all ionized N-nitroso compounds produce diagnostic fragment ions and h
71 e, via rearrangement of the O-nitrene to a C-nitroso compound (R'ON --> O=NR'), and subsequent tautom
72                                              Nitroso compounds, R-N=O, are common intermediates in or
73                                            N-nitroso compounds represent a common type of environment
74                                       Five S-nitroso compounds, S-nitroso-N-acetyl-dl-penicillamine,
75                                A resin-bound nitroso compound sequestered a single unexpected compone
76 rates of addition of radicals to nitrones or nitroso compounds (spin traps; STs).
77 exposure may also lead to the formation of N-nitroso compounds that can act as alkylating agents.
78  agents and highly acidic conditions, form N-nitroso compounds that have been found to be teratogenic
79                      Humans are exposed to N-nitroso compounds through environmental exposure and end
80 ree radicals, consists of using a nitrone or nitroso compound to "trap" an unstable free radical as a
81   The lower rate of conversion of the (C7-R)-nitroso compound to the corresponding oximes compared wi
82                 The conversion of the (C8-S)-nitroso compound to the E/Z-oximes was approximately 8 t
83 leophilic addition of the protein thiol to a nitroso compound to yield an N-hydroxysulfenamide, which
84                    Addition of these acyloxy nitroso compounds to AhpC C165S yields a sulfinic acid a
85 yzed radical addition with in situ-generated nitroso compounds to prepare sterically hindered amines
86   EPR spectroscopic evidence showed that the nitroso compound trapped other transient intermediates t
87                             No corresponding nitroso compound was formed in reactions involving l-dop
88 everse isomerization from the oxime to the C-nitroso compound was observed.
89 id pesticide nitenpyram, which forms toxic N-nitroso compounds, was consistent with model compounds,
90 adicals and leads initially to a diamagnetic nitroso compound, which is transformed into a persistent
91      Nitrate and nitrite are precursors of N-nitroso compounds, which induce tumors of the pancreas i
92 ollowed by CAD to differentiate protonated O-nitroso compounds with a pyridine ring from analogous N-
93 cs of Diels-Alder reactions for a variety of nitroso compounds with dienes were explored with density
94 ory studies revealed that RDX was reduced to nitroso compounds without denitration and the concomitan