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Benzamidines
Known as:
Benzamidines [Chemical/Ingredient]
Amidines substituted with a benzene group. Benzamidine and its derivatives are known as peptidase inhibitors.
National Institutes of Health
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Related topics
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2-aminobenzamidoxime
3,4,5-trihydroxybenzamidoxime
3,5-dipentadecyloxybenzamidine hydrochloride
4'-amidinophenyl-4-chloroanthranilic acid
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antagonists & inhibitors
aspects of radiation effects
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Structure-based design, synthesis and evaluation in vitro of arylnaphthyridinones, arylpyridopyrimidinones and their tetrahydro derivatives as inhibitors of the tankyrases.
Katerina P Kumpan
,
Amit Nathubhai
,
+6 authors
M. Threadgill
Bioorganic & Medicinal Chemistry
2015
Corpus ID: 39443207
Highly Cited
2012
Highly Cited
2012
Copper-catalyzed synthesis of quinazolines in water starting from o-bromobenzylbromides and benzamidines.
C. Malakar
,
A. Baskakova
,
J. Conrad
,
U. Beifuss
Chemistry
2012
Corpus ID: 37804608
Water makes it possible: The Cu(2)O-catalyzed reaction between easily available o-bromobenzylbromides and benzamidines by using…
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Highly Cited
2012
Highly Cited
2012
Copper catalyzed N-arylation of amidines with aryl boronic acids and one-pot synthesis of benzimidazoles by a Chan-Lam-Evans N-arylation and C-H activation/C-N bond forming process.
Jihui Li
,
S. Bénard
,
L. Neuville
,
Jieping Zhu
Organic Letters
2012
Corpus ID: 23176070
Mono-N-arylation of benzamidines 1 with aryl boronic acids 2 was effectively achieved in the presence of a catalytic amount of Cu…
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Highly Cited
2010
Highly Cited
2010
Direct synthesis of quinazolines through copper-catalyzed reaction of aniline-derived benzamidines.
Y. Ohta
,
Yusuke Tokimizu
,
S. Oishi
,
N. Fujii
,
H. Ohno
Organic Letters
2010
Corpus ID: 29986819
A novel synthesis of 2-phenyl-4-[(triisopropylsilyl)methyl]quinazolines from monosubstituted arenes has been developed. Treatment…
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Highly Cited
2002
Highly Cited
2002
A new catalytic cross-coupling approach for the synthesis of protected aryl and heteroaryl amidines.
Carrie L Kusturin
,
L. S. Liebeskind
,
W. Neumann
Organic Letters
2002
Corpus ID: 28405445
[reaction: see text] A new method for the synthesis of protected benzamidines is described. The commercially available 1,3-bis…
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Highly Cited
2001
Highly Cited
2001
Structure-based approach for the discovery of bis-benzamidines as novel inhibitors of matriptase.
I. Enyedy
,
Sheau-Ling Lee
,
Angera H. Kuo
,
Robert B. Dickson
,
C. Lin
,
Shaomeng Wang
Journal of Medicinal Chemistry
2001
Corpus ID: 25008156
Matriptase, a trypsin-like serine protease, which may be involved in tissue remodeling, cancer invasion, and metastasis. Potent…
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Highly Cited
2001
Highly Cited
2001
Thermodynamic analysis of binding of p-substituted benzamidines to trypsin.
R. Talhout
,
J. Engberts
European Journal of Biochemistry
2001
Corpus ID: 32991113
Understanding the structural basis of inhibitor-enzyme interactions, important for the design of new drugs, requires a complete…
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1987
1987
Hepatic microsomal N-demethylation of N-methylbenzamidine. N-dealkylation vs N-oxygenation of amidines.
B. Clement
,
M. Zimmermann
Biochemical Pharmacology
1987
Corpus ID: 23276011
1983
1983
The N-oxidation of benzamidines in vitro.
B. Clement
Xenobiotica; the fate of foreign compounds in…
1983
Corpus ID: 37454032
The enzymic N-oxidation of a series of N-unsubstituted basic benzamidines (I) to a new type of metabolite, the amidoximes (II…
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1978
1978
Inhibition of four human serine proteases by substituted benzamidines.
J. Andrews
,
D. Roman
,
D. Bing
Journal of Medicinal Chemistry
1978
Corpus ID: 41034588
A series of substituted benzamidines has been examined for their inhibitory activity against the human serine proteases--trypsin…
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