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PEPTID PROTECTION AGAINST TOXIC INFLUENCE OF UV RADIATION
专利权人:
ХЕЛИКС БАЙОМЕДИКС ИНК. (US)
发明人:
ЧЖАН Лицзюань (US),ФАЛЛА Тимоти Дж. (US)
申请号:
RU2012125260/10
公开号:
RU2012125260A
申请日:
2010.11.18
申请国别(地区):
RU
年份:
2013
代理人:
摘要:
1. A method of reducing the activity of an activated kinase of a control point of a cell cycle, where the specified method comprises exposing the specified kinase to a control point of a peptide, where the specified peptide sequence is SEQ ID NO: 2, 3, 5, 6, 8, or 10.2. The method of claim 1, wherein said peptide is SEQ ID NO: 10.3. The method of claim 1, wherein said peptide is SEQ ID NO: 2, 3, 5, 6, or 8.4. The method of claim 1, wherein said peptide is amidated at its carboxy terminus. The method of claim 1, wherein said control point kinase is a control point kinase-2 (Chk2). The method of claim 1, wherein said checkpoint kinase is activated as a result of DNA damage caused by ultraviolet radiation. The method of claim 1, wherein said checkpoint kinase is present in human skin. A method of treating mammalian skin to reduce toxicity associated with exposure to ultraviolet light, wherein said method comprises applying a peptide to said skin, wherein said peptide sequence is SEQ ID NO: 2, 3, 5, 6, 8, or 10.9. The peptide composed by the sequence of SEQ ID NO: 3, 5, 6, 8 or 10.10. The peptide of claim 9, wherein said peptide is SEQ ID NO: 10.11. The peptide of claim 9, wherein said peptide is SEQ ID NO: 3, 5, 6, or 8.12. The peptide of claim 9, wherein said peptide is amidated at its carboxy terminus. The peptide of claim 12, wherein said peptide is SEQ ID NO: 10.14. The peptide of claim 12, wherein said peptide is SEQ ID NO: 3, 5, 6, or 8.15. A composition comprising the peptide of claim 9 and a pharmaceutically acceptable carrier. The composition of claim 15, wherein the composition is in the form of an aerosol, emulsion, liquid, lotion,1. Способ снижения активности активированной киназы контрольной точки клеточного цикла, где указанный способ включает воздействие на указанную киназу контрольной точки пептида, где указанная пептидная последовательность представляет собой SEQ ID NO:2, 3, 5, 6, 8 или 10.2. Способ по п.1, где указанный пептид представляет собой SEQ I
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