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naftifine
Known as:
1-Naphthalenemethanamine, N-methyl-N-(3-phenyl-2-propenyl)-, (E)-
, Naftifina
, naftifine [Chemical/Ingredient]
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A topical, synthetic allylamine derivate similar to terbinafine with broad-spectrum antifungal activity. Naftifine can be fungicidal or fungistatic…
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National Institutes of Health
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Related topics
Related topics
10 relations
Broader (2)
Allylamine
Antifungal Agents
Hypersensitivity
Mycoses
Naftifine hydrochloride 0.02 MG/MG Topical Gel [Naftin]
Naftifine hydrochloride 10 MG/ML Topical Cream [Naftin]
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Narrower (2)
Naftifine hydrochloride
Naftin
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2013
Highly Cited
2013
In-vitro Activity of 10 Antifungal Agents against 320 Dermatophyte Strains Using Microdilution Method in Tehran
P. Adimi
,
S. Hashemi
,
+6 authors
P. Kordbacheh
Iranian journal of pharmaceutical research
2013
Corpus ID: 14818529
Dermatophyte fungi are the etiologic agents of skin infections commonly referred to as ringworm. These infections are not…
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Review
2012
Review
2012
A Review of its Pharmacological Properties and Therapeutic Potential in the Treatment of Onychomycosis and Other Superficial Fungal Infections
M. Haria
,
H. Bryson
2012
Corpus ID: 195698417
Various sections of the manuscript reviewed by: Y.M. Clayton, Institute of Dermatology, St Thomas' Hospital, London, England; A…
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Highly Cited
2011
Highly Cited
2011
Substrate-directable Heck reactions with arenediazonium salts. The regio- and stereoselective arylation of allylamine derivatives and applications in the synthesis of naftifine and abamines.
P. Prediger
,
L. Barbosa
,
Y. Génisson
,
C. R. Correia
Journal of Organic Chemistry
2011
Corpus ID: 33103975
The palladium-catalyzed, substrate-directable Heck-Matsuda reaction of allylamine derivatives with arenediazonium salts is…
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Highly Cited
1997
Highly Cited
1997
In‐vitro Permeability of the Human Nail and of a Keratin Membrane from Bovine Hooves: Prediction of the Penetration Rate of Antimycotics through the Nail Plate and their Efficacy
D. Mertin
,
B. Lippold
The Journal of pharmacy and pharmacology
1997
Corpus ID: 25739538
In contrast to the partition coefficient octanol/water the molecular size of penetrating drugs has a noticeable influence on the…
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Highly Cited
1993
Highly Cited
1993
IN VITRO SUSCEPTIBILITY OF DERMATOPHYTES TO ANTIFUNGAL DRUGS: A COMPARISON OF TWO METHODS
A. Macura
International Journal of Dermatology
1993
Corpus ID: 12110157
Background. There is an evidence that some fungal strains are resistant to certain antimycotic drugs with resulting therapeutic…
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Review
1990
Review
1990
Pharmacology of the allylamines.
J. Birnbaum
Journal of American Academy of Dermatology
1990
Corpus ID: 4868732
Highly Cited
1986
Highly Cited
1986
Synthesis and structure-activity relationships of naftifine-related allylamine antimycotics.
A. Stütz
,
A. Georgopoulos
,
W. Granitzer
,
G. Petrányi
,
D. Berney
Journal of Medicinal Chemistry
1986
Corpus ID: 39649139
Naftifine (1) is the first representative of the new antifungal allylamine derivatives. Its biological activity is strictly bound…
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Highly Cited
1984
Highly Cited
1984
Allylamine derivatives: new class of synthetic antifungal agents inhibiting fungal squalene epoxidase.
G. Petrányi
,
N. Ryder
,
A. Stütz
Science
1984
Corpus ID: 21017549
A new class of synthetic antifungal agents, the allylamines , has been developed by modification of naftifine , a topical…
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Highly Cited
1981
Highly Cited
1981
In vivo antimycotic activity of naftifine
G. Petrányi
,
A. Georgopoulos
,
H. Mieth
Antimicrobial Agents and Chemotherapy
1981
Corpus ID: 26731698
Naftifine, a new antifungal agent belonging chemically to the allylamines, was tested for its in vivo activity after topical…
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Highly Cited
1981
Highly Cited
1981
In vitro activity of naftifine, a new antifungal agent
A. Georgopoulos
,
G. Petrányi
,
H. Mieth
,
J. Drews
Antimicrobial Agents and Chemotherapy
1981
Corpus ID: 29077696
Naftifine exhibits an interesting in vitro spectrum of activity against dermatophytes (38 strains; minimal inhibitory…
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