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nitrile hydratase activity
Known as:
NHase activity
, 3-cyanopyridine hydratase activity
, nitrile hydro-lyase activity
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Catalysis of the reaction: an aliphatic amide = a nitrile + H2O. [EC:4.2.1.84]
National Institutes of Health
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nitrile hydratase
Papers overview
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Highly Cited
2017
Highly Cited
2017
Iridium-Catalyzed Reductive Strecker Reaction for Late-Stage Amide and Lactam Cyanation.
Ángel L. Fuentes de Arriba
,
E. Lenci
,
M. Sonawane
,
Odilon Formery
,
D. Dixon
Angewandte Chemie
2017
Corpus ID: 22675892
A new iridium-catalyzed reductive Strecker reaction for the direct and efficient formation of α-amino nitrile products from a…
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Highly Cited
2013
Highly Cited
2013
Lactic acid bacteria convert glucosinolates to nitriles efficiently yet differently from enterobacteriaceae.
J. Mullaney
,
W. Kelly
,
T. McGhie
,
J. Ansell
,
J. Heyes
Journal of Agricultural and Food Chemistry
2013
Corpus ID: 7571879
Glucosinolates from the genus Brassica can be converted into bioactive compounds known to induce phase II enzymes, which may…
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Highly Cited
2012
Highly Cited
2012
A genetically encoded norbornene amino acid for the mild and selective modification of proteins in a copper-free click reaction.
E. Kaya
,
M. Vrábel
,
Christian A Deiml
,
S. Prill
,
Viviana S. Fluxá
,
T. Carell
Angewandte Chemie
2012
Corpus ID: 34582781
Highly Cited
2010
Highly Cited
2010
New synthesis of 1-substituted-1H-indazoles via 1,3-dipolar cycloaddition of in situ generated nitrile imines and benzyne.
C. Spiteri
,
S. Keeling
,
J. Moses
Organic Letters
2010
Corpus ID: 29572029
A new synthesis of 1-substituted-1H-indazoles via 1,3-dipolar cycloaddition of nitrile imines to benzyne is described. The…
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Highly Cited
2009
Highly Cited
2009
Synthesis and pharmacological evaluation of 1,3,4-oxadiazole bearing bis(heterocycle) derivatives as anti-inflammatory and analgesic agents.
B. Jayashankar
,
K. M. Lokanath Rai
,
N. Baskaran
,
H. Sathish
European journal of medicinal chemistry
2009
Corpus ID: 12252474
Highly Cited
2005
Highly Cited
2005
An entry to a chiral dihydropyrazole scaffold: enantioselective [3 + 2] cycloaddition of nitrile imines.
M. Sibi
,
L. Stanley
,
C. Jasperse
Journal of the American Chemical Society
2005
Corpus ID: 28270589
We have developed a versatile strategy to access dihydropyrazoles in highly enantioenriched form. Dipolar cycloaddition of…
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Highly Cited
2002
Highly Cited
2002
Sulforaphane and its glutathione conjugate but not sulforaphane nitrile induce UDP-glucuronosyl transferase (UGT1A1) and glutathione transferase (GSTA1) in cultured cells.
G. Basten
,
Y. Bao
,
G. Williamson
Carcinogenesis
2002
Corpus ID: 2621227
Glucoraphanin in Brassica vegetables breaks down to either sulforaphane or sulforaphane nitrile depending on the conditions, and…
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Highly Cited
2002
Highly Cited
2002
Novel sigma receptor ligands. Part 2. SAR of spiro[[2]benzopyran-1,4'-piperidines] and spiro[[2]benzofuran-1,4'-piperidines] with carbon substituents in position 3.
C. Maier
,
B. Wünsch
Journal of Medicinal Chemistry
2002
Corpus ID: 44297748
Several spiro[[2]benzopyran-1,4'-piperidines] and spiro[[2]benzofuran-1,4'-piperidines] were synthesized and evaluated for their…
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Highly Cited
2001
Highly Cited
2001
Comparison of the bioactivity of two glucoraphanin hydrolysis products found in broccoli, sulforaphane and sulforaphane nitrile.
Nathan V. Matusheski
,
E. Jeffery
Journal of Agricultural and Food Chemistry
2001
Corpus ID: 929037
Epidemiological and laboratory studies suggest that dietary broccoli may prevent or delay a variety of cancers. Broccoli and…
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Highly Cited
1986
Highly Cited
1986
Biologically active derivatives of gossypol: synthesis and antimalarial activities of peri-acylated gossylic nitriles.
R. Royer
,
L. Deck
,
N. M. Campos
,
L. A. Hunsaker
,
D. V. Vander Jagt
Journal of Medicinal Chemistry
1986
Corpus ID: 7983474
A series of peri-acylated gossylic nitriles were synthesized from gossypol dioxime by treatment of the dioxime with the…
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