US4621090A
Expired / Lapsed
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Antifungal compositions
Assignee: Tosoh Corp
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Filing: 1984-09-13
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Granted: 1986-11-04
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Expires: 2004-09-13
Abstract
Abstract An antifungal composition comprising an effective amount of carbamate derivative having the formula (I): ##STR1## where X is 2-naphthyl, 5-indanyl, 5,6,7,8-tetrahydro-2-naphthyl, 1,4-methano-1,2,3,4-tetrahydro-6-naphthyl, 1,4-ethano-1,2,3,4-tetrahydro-6-naphthyl, 2-quinolyl, or a phenyl group having one or two of the same or different substituents selected from the group of halogen atom, lower alkyl, lower alkenyl, lower alkoxy, lower alkenyloxy, halogenated lower alkyl, lower alkylthio, lower alkylsulfonyl, lower alkylamino, nitro, and methylenedioxy; Y is an oxygen atom or a sulfur atom; Z is lower alkyl group; W is pyridyl group having one or two of the same substituents selected from the group of lower alkyl, lower alkoxy, lower alkenyloxy, and lower alkylamino.
Inventors
- 👤 Kazuo Iwata
- 👤 Tetsuo Takematsu
- 👤 Yuji Nonaka
- 👤 Akira Nakanishi
- 👤 Hideo Morinaka
- 👤 Kenji Tsuzuki
- 👤 Mitsuyuki Murakami
- 👤 Takeshi Uotani
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-30 21:32
CPC Classifications
C; C07; C07D; C07D213/00; C07D213/02; C07D213/04; C07D213/60; C07D213/72; C07D213/75; A; A01; A01N; A01N47/00; A01N47/08; A01N47/10; A01N47/18; A01N47/22; A61; A61P; A61P31/00; A61P31/04; A61P31/10; C07D401/00; C07D401/02; C07D401/12; C07D405/00; C07D405/02; C07D405/12
Claims Analysis
Total Claims: 13
Claim 1
Independent Claim
112 words
A method for controlling fungus, comprising administering an effective amount of a compound of formula (I) ##STR4## wherein X is 2-naphthyl, 5-indanyl, 5,6,7,8-tetrahydro-2-naphthyl, 1,4-methano-1,2,3,4-tetrahydro-6-naphthyl, 1,4-ethano-1,2,3,4-tetrahydro-6-naphthyl, 2-quinolyl, or a phenyl group having one or two of the same or different substituent selected from the group consisting of halogen atoms, lower alkyls, lower alkenyls, lower alkoxys, lower alkenyloxys, halogenated lower alkyls, lower alkylthios, lower alkylsulfonyls, lower alkylaminos, nitro and methylenedioxys; Y is an oxygen atom or a sulfur atom; Z is a lower alkyl group; and W is a pyridyl group having one or two of the same substituents selected from the group consisting of lower alkyls, lower alkoxys, lower alkenyloxys and lower alkylaminos.
Claim 2
Independent Claim
112 words
A method for controlling fungus, comprising administering an effective amount of a compound of formula (I) ##STR4## wherein X is 2-naphthyl, 5-indanyl, 5,6,7,8-tetrahydro-2-naphthyl, 1,4-methano-1,2,3,4-tetrahydro-6-naphthyl, 1,4-ethano-1,2,3,4-tetrahydro-6-naphthyl, 2-quinolyl, or a phenyl group having one or two of the same or different substituent selected from the group consisting of halogen atoms, lower alkyls, lower alkenyls, lower alkoxys, lower alkenyloxys, halogenated lower alkyls, lower alkylthios, lower alkylsulfonyls, lower alkylaminos, nitro and methylenedioxys; Y is an oxygen atom or a sulfur atom; Z is a lower alkyl group; and W is a pyridyl group having one or two of the same substituents selected from the group consisting of lower alkyls, lower alkoxys, lower alkenyloxys and lower alkylaminos.
Claim 3
Dependent Claim
36 words
The method of claim 1, wherein said fungus comprises Trichophyton mentagrophytes, Trichophyton violaceum, Microsporum canis, Microsporum gypseum, Epidermophyton floccosum, Fonsecaea compactum, Phialophora verrucosa, Histoplasma capsulatum, Blastomyces dermatitidis, Aspergillus fumigatus, Aspergillus niger, Fusarium pedrosoi or Cryptococcus neoformans.
Claim 4
Independent Claim
11 words
The method of one of claims 1, comprising administering O-2-naphthyl N-methyl-N-(6-methoxy-2-pyridyl)thiocarbamate.
Claim 5
Independent Claim
11 words
The method of one of claims 1, comprising administering O-5-indanyl N-(6-methoxy-2-pyridyl)-N-methyl-thiocarbamate.
Claim 6
Independent Claim
11 words
The method of one of claims 1, comprising administering O-5,6,7,8-tetrahydro-2-naphthyl (N-(6-methoxy-2-pyridyl)-N-methylthiocarbamate.
Claim 7
Independent Claim
11 words
The method of one of claims 1, comprising administering O-4-ethylphenyl N-(6-methoxy-2-pyridyl)-N-methylthiocarbamate.
Claim 8
Independent Claim
11 words
The method of one of claims 1, comprising administering O-4-bromophenyl N-(6-methoxyl-2-pyridyl)-N-methylthiocarbamate.
Claim 9
Independent Claim
11 words
The method of one of claims 1, comprising administering O-4-chloro-3-methylphenyl N-(6-methoxyl-2-pyridyl)-N-methylthiocarbamate.
Claim 10
Independent Claim
11 words
The method of one of claims 1, comprising administering O-4-trifluoromethyl N-(6-methoxy-2-pyridyl)-N-methylthiocarbamate.
Claim 11
Independent Claim
11 words
The method of one of claims 1, comprising administering O-4-methylthiophenyl N-(6-methoxy-2-pyridyl)-N-methylthiocarbamate.
Claim 12
Dependent Claim
119 words
A composition comprising: (i) an antifungal effective amount of a compound of formula (I) ##STR5## wherein X is 2-naphthyl, 5-indanyl, 5,6,7,8-tetrahydro-2-naphthyl, 1,4-methano-1,2,3,4-tetrahydro-6-naphthyl, 1,4-ethano-1,2,3,4-tetrahydro-6-naphthyl, 2-quinolyl, or a phenyl group having one or two of the same or different substituents selected from the group consisting of halogen atoms, lower alkyls, lower alkenyls, lower alkoxys, lower alkenyloxys, halogenated lower alkyls, lower alkylthios, lower alkylsulfonyls, lower alkylaminos, nitro and methylenedioxys; Y is an oxygen atom or a sulfur atom; Z is a lower alkyl group; and W is a pyridyl group having one or two of the same substituents selected from the group consisting of lower alkyls, lower alkoxys, lower alkenyloxys and lower alkylaminos; and (ii) an inert carrier suitable for antifungal applications.
Claim 13
Dependent Claim
119 words
A composition comprising: (i) an antifungal effective amount of a compound of formula (I) ##STR5## wherein X is 2-naphthyl, 5-indanyl, 5,6,7,8-tetrahydro-2-naphthyl, 1,4-methano-1,2,3,4-tetrahydro-6-naphthyl, 1,4-ethano-1,2,3,4-tetrahydro-6-naphthyl, 2-quinolyl, or a phenyl group having one or two of the same or different substituents selected from the group consisting of halogen atoms, lower alkyls, lower alkenyls, lower alkoxys, lower alkenyloxys, halogenated lower alkyls, lower alkylthios, lower alkylsulfonyls, lower alkylaminos, nitro and methylenedioxys; Y is an oxygen atom or a sulfur atom; Z is a lower alkyl group; and W is a pyridyl group having one or two of the same substituents selected from the group consisting of lower alkyls, lower alkoxys, lower alkenyloxys and lower alkylaminos; and (ii) an inert carrier suitable for antifungal applications.
References Cited (Backward Citations)
No citation records indexed.
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