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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1956 1
1958 1
1960 2
1966 1
1967 1
1973 1
1974 2
1982 1
1984 1
1988 1
1989 1
1990 1
1995 1
1998 1
1999 1
2001 5
2003 4
2004 2
2005 2
2007 7
2008 5
2009 9
2010 5
2011 5
2012 9
2013 9
2014 6
2015 4
2016 3
2017 4
2018 6
2019 5
2020 7
2021 2
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106 results
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Page 1
Benzyl Cyanide Leads to Auxin-Like Effects Through the Action of Nitrilases in Arabidopsis thaliana.
Urbancsok J, Bones AM, Kissen R. Urbancsok J, et al. Front Plant Sci. 2018 Aug 24;9:1240. doi: 10.3389/fpls.2018.01240. eCollection 2018. Front Plant Sci. 2018. PMID: 30197652 Free PMC article.
Treatment with benzyl cyanide led to a dose-dependent reduction of primary root length and total biomass. ...A NIT2RNAi line suppressing several nitrilases was resistant to all tested benzyl cyanide concentrations. When exposed to phenylacetic acid (PA …
Treatment with benzyl cyanide led to a dose-dependent reduction of primary root length and total biomass. ...A NIT2RNAi line s …
Toxicity of benzyl cyanide in the rat.
Guest A, Jackson JR, James SP. Guest A, et al. Toxicol Lett. 1982 Feb;10(2-3):265-72. doi: 10.1016/0378-4274(82)90086-8. Toxicol Lett. 1982. PMID: 7080096
Sublethal oral doses of benzyl cyanide were nephrotoxic causing increased excretion of protein, amino acids and glucose. ...The oral cyanide antidote was ineffective against benzyl cyanide and the intravenous antidote, Kelocyanor (cobalt edetate …
Sublethal oral doses of benzyl cyanide were nephrotoxic causing increased excretion of protein, amino acids and glucose. ...Th …
2-Methyl-3-nitro-benzyl cyanide.
Chen YS, Zhang JH. Chen YS, et al. Acta Crystallogr Sect E Struct Rep Online. 2009 Mar 14;65(Pt 4):o767. doi: 10.1107/S1600536809008484. Acta Crystallogr Sect E Struct Rep Online. 2009. PMID: 21582496 Free PMC article.
An assessment of the release of inorganic cyanide from the fragrance materials benzyl cyanide, geranyl nitrile and citronellyl nitrile applied dermally to the rat.
Potter J, Smith RL, Api AM. Potter J, et al. Food Chem Toxicol. 2001 Feb;39(2):147-51. doi: 10.1016/s0278-6915(00)00125-3. Food Chem Toxicol. 2001. PMID: 11267708
Urinary thiocyanate levels as a biomarker for the generation of inorganic cyanide from benzyl cyanide in the rat. Food and Chemical Toxicology 39, 141-146). In the case of benzyl cyanide, there was a marked increase in urinary thiocyanate levels …
Urinary thiocyanate levels as a biomarker for the generation of inorganic cyanide from benzyl cyanide in the rat. Food …
Urinary thiocyanate levels as a biomarker for the generation of inorganic cyanide from benzyl cyanide in the rat.
Potter J, Smith RL, Api AM. Potter J, et al. Food Chem Toxicol. 2001 Feb;39(2):141-6. doi: 10.1016/s0278-6915(00)00126-5. Food Chem Toxicol. 2001. PMID: 11267707
It was concluded from these results that the recoveries of urinary thiocyanate were such that this anion was suitable for use as a biomarker for the release of cyanide from organonitriles such as benzyl cyanide. Benzyl cyanide (150 mg/kg) admini …
It was concluded from these results that the recoveries of urinary thiocyanate were such that this anion was suitable for use as a biomarker …
Diverse Excretion Pathways of Benzyl Glucosinolate in Humans after Consumption of Nasturtium (Tropaeolum majus L.)-A Pilot Study.
Kühn C, Kupke F, Baldermann S, Klopsch R, Lamy E, Hornemann S, Pfeiffer AFH, Schreiner M, Hanschen FS, Rohn S. Kühn C, et al. Mol Nutr Food Res. 2018 Oct;62(20):e1800588. doi: 10.1002/mnfr.201800588. Epub 2018 Aug 28. Mol Nutr Food Res. 2018. PMID: 30091516
SCOPE: Different metabolic and excretion pathways of the benzyl glucosinolate breakdown products benzyl isothiocyanate and benzyl cyanide are investigated to obtain information about their multiple fate after ingestion. ...In breath, benzyl isot …
SCOPE: Different metabolic and excretion pathways of the benzyl glucosinolate breakdown products benzyl isothiocyanate and …
Effects of ultrasound on the formation of alpha-benzoylbenzyl cyanide from benzyl cyanide and alkylphenyl ketone from alpha-alkylbenzyl cyanide by potassium superoxide in the presence of crown ether.
Yim ES, Park MK, Han BH. Yim ES, et al. Ultrason Sonochem. 1999 Mar;6(1-2):105-9. doi: 10.1016/s1350-4177(98)00036-4. Ultrason Sonochem. 1999. PMID: 11233929 Free article.
Ultrasound accelerates the formation of alpha-benzoylbenzyl cyanide and benzoic acid in the reaction of benzyl cyanide with potassium superoxide in the presence of 18-crown-6. ...Possible mechanisms for the formation of alpha-benzoylbenzyl cyanide from …
Ultrasound accelerates the formation of alpha-benzoylbenzyl cyanide and benzoic acid in the reaction of benzyl cyanide
Heterogeneous Catalytic Hydrogenation of 3-Phenylpropionitrile over Palladium on Carbon.
Lévay K, Tóth KD, Kárpáti T, Hegedűs L. Lévay K, et al. ACS Omega. 2020 Mar 4;5(10):5487-5497. doi: 10.1021/acsomega.0c00125. eCollection 2020 Mar 17. ACS Omega. 2020. PMID: 32201841 Free PMC article.
PPN, which belongs to the homologous series of benzonitrile (BN) and benzyl cyanide (BC), was hydrogenated under mild reaction conditions (30-80 C, 6 bar), over Pd/C, in two immiscible solvents (dichloromethane/water) and using acidic additives (NaH(2)PO(4) and H(2) …
PPN, which belongs to the homologous series of benzonitrile (BN) and benzyl cyanide (BC), was hydrogenated under mild reaction …
Metabolism of organonitriles to cyanide by rat nasal tissue enzymes.
Dahl AR, Waruszewski BA. Dahl AR, et al. Xenobiotica. 1989 Nov;19(11):1201-5. doi: 10.3109/00498258909043172. Xenobiotica. 1989. PMID: 2618074
Vmax values for cyanide release from acetonitrile, propionitrile, butyronitrile, isobutyronitrile, acrylonitrile, benzyl cyanide and succinonitrile were determined for rat nasal and liver microsomal metabolism. 3. Km and Vmax values were determined for nasal …
Vmax values for cyanide release from acetonitrile, propionitrile, butyronitrile, isobutyronitrile, acrylonitrile, benzyl cy
Copper-catalysed synthesis of 3-hydroxyisoindolin-1-ones from benzylcyanide 2-iodobenzamides.
Kavala V, Wang CY, Wang CC, Patil PB, Fang C, Kuo CW, Yao CF. Kavala V, et al. Org Biomol Chem. 2020 Feb 7;18(5):988-998. doi: 10.1039/c9ob02329a. Epub 2020 Jan 16. Org Biomol Chem. 2020. PMID: 31942895
An efficient one-pot two-step sequential reaction for the synthesis of biologically active 3-hydroxyisoindolin-1-one derivatives from 2-iodobenzamide derivatives and various substituted benzyl cyanides in the presence of CuCl and cesium carbonate in DMSO is reported. Furth …
An efficient one-pot two-step sequential reaction for the synthesis of biologically active 3-hydroxyisoindolin-1-one derivatives from 2-iodo …
106 results