U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Pyridones as antidandruff agents

Patent 4185106 Issued on January 22, 1980. Estimated Expiration Date: Icon_subject January 22, 1997. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

2742393

2922793

3236733

3269904

3644626

3655897

3883545

Process for the manufacture of 1-hydroxy-2-pyridones
Patent #: 3968118
Issued on: 07/06/1976
Inventor: Lohaus ,   et al.

Process for the preparation of 1-hydroxy-pyridones Patent #: 3972888
Issued on: 08/03/1976
Inventor: Lohaus ,   et al.

Inventors

Assignee

Application

No. 05/605210 filed on 08/15/1975

US Classes:

514/336, Additional hetero ring containing514/348, Chalcogens bonded directly to at least two ring carbons of the six-membered hetero ring514/351, Nitrogen attached indirectly to the six-membered hetero ring by nonionic bonding546/283.4, The additional hetero ring is five-membered546/290, Chalcogen bonded directly to ring carbon of the six-membered hetero ring546/294, Chalcogen bonded directly to chalcogen546/295, Halogen bonded directly to the six-membered hetero ring by nonionic bonding546/300, Nitrogen attached indirectly to the six-membered hetero ring by nonionic bonding546/301, Chalcogen attached indirectly to the six-membered hetero ring by nonionic bonding546/302, Halogen attached directly or indirectly to the six-membered hetero ring by nonionic bonding546/303Halogen attached directly or indirectly to the six-membered hetero ring by nonionic bonding

Examiners

Primary: Thomas, James O. Jr.
Assistant: Clarke, Vera C.

Attorney, Agent or Firm

International Class

A61K 31/44 (20060101)

Foreign Application Priority Data

1972-07-11 DE

Abstract

A cosmetic composition comprising a content of an 1-hydroxy-2-pyridone of the general formula ##STR1## in which R1 stands for hydrogen, alkyl of 1 to 17 carbon atoms, alkenyl of 2 to 17 carbon atoms, cycloalkyl of 5 to 8 carbon atoms, bicycloalkyl of 7 to 9 carbon atoms, cycloalkyl-alkyl of 1 to 4 alkyl carbon atoms, the cycloalkyl groups being optionally substituted by alkyl groups of 1 to 4 carbon atoms, aryl, aralkyl of 1 to 4 alkyl carbon atoms, aryl-alkenyl of 2 to 4 alkenyl carbon atoms, aryloxy-alkyl or arylthio-alkyl of 1 to 4 alkyl carbon atoms, benzhydryl, phenylsulfonyl-alkyl of 1 to 4 alkyl carbon atoms, furyl or furyl-alkenyl of 2 to 4 alkenyl carbon atoms, the aryl groups being optionally substituted by alkyl of 1 to 4 carbon atoms, by alkoxy of 1 to 4 carbon atoms, by nitro, cyano or halogen atoms, R2 stands for hydrogen, alkyl of 1 to 4 carbon atoms, alkenyl or alkinyl of 2 to 4 carbon atoms, halogen atoms or benzyl, R3 stands for hydrogen, alkyl of 1 to 4 carbon atoms or phenyl, and R4 stands for hydrogen, alkyl of 1 to 4 carbon atoms, alkenyl of 2 to 4 carbon atoms, methoxy-methyl, halogen or benzyl, and/or salt thereof, which may be used as an anti-dandruff agent.

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