Analgesia with minimal tolerance and dependence by a mu opioid receptor agonist that also binds filamin A
US8722851B2 · kind B2 · utility
13Cited by
1References
20Claims
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Key dates
| Filing date | Oct 31, 2008 |
| Grant date | May 13, 2014 |
| Priority date | — |
| Expiry date | Sep 6, 2031 |
Classification
- Technology area (CPC C)Chemistry; Metallurgy
- CPC primaryC07K14/665
- WIPO fieldBiotechnology
- WIPO sectorChemistry
Abstract
A composition and method are disclosed that utilize an isolated polypeptide or analog thereof to inhibit the interaction of a mu-opioid receptor with filamin A. A contemplated polypeptide has an amino acid residue sequence illustrated by the formula: W-[X1X2X3 . . . X43X44X45]nValAlaX48GlyLeu[X51X52X53 . . . X94X95X96]m-Y, wherein the various elements are defined elsewhere. A contemplated method can be used to select a VAKGL-binding compound.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.