WO2008114976A8 - Spinorphin derivatives as potent and selective human p2x3 receptor antagonist - Google Patents
Spinorphin derivatives as potent and selective human p2x3 receptor antagonist Download PDFInfo
- Publication number
- WO2008114976A8 WO2008114976A8 PCT/KR2008/001476 KR2008001476W WO2008114976A8 WO 2008114976 A8 WO2008114976 A8 WO 2008114976A8 KR 2008001476 W KR2008001476 W KR 2008001476W WO 2008114976 A8 WO2008114976 A8 WO 2008114976A8
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- peptide
- spinorphin
- receptor antagonist
- potent
- human
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/06—Linear peptides containing only normal peptide links having 5 to 11 amino acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Life Sciences & Earth Sciences (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
The present invention relates to a spinorphin derivative useful as a potent and selective human P2X3 receptor antagonist. More particularly, the present invention provides a spinorphin derivative useful as a potent and selective human P2X3 receptor antagonist selected from peptide AVVYPWT, peptide LAVYPWT, peptide LVAYPWT, peptide LVVAPWT and/ or cyclic peptide LWYPWT. Human P2X3 receptor antagonist has been developed on the electrophysiological evaluation of spinorphin peptide derivatives, truncated peptide analogues, cyclic peptides and a retroinverso peptide at human P2X3 receptors to determine the channel blocking activity.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020070026408A KR100880370B1 (en) | 2007-03-19 | 2007-03-19 | Spinorphin derivatives as potent and selective human P2X3 receptor antagonist |
KR10-2007-0026408 | 2007-03-19 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2008114976A1 WO2008114976A1 (en) | 2008-09-25 |
WO2008114976A8 true WO2008114976A8 (en) | 2009-11-05 |
Family
ID=39766051
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/KR2008/001476 WO2008114976A1 (en) | 2007-03-19 | 2008-03-17 | Spinorphin derivatives as potent and selective human p2x3 receptor antagonist |
Country Status (2)
Country | Link |
---|---|
KR (1) | KR100880370B1 (en) |
WO (1) | WO2008114976A1 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20110201642A1 (en) * | 2008-11-03 | 2011-08-18 | John Blunt | Bioactive Compounds |
CN115327000B (en) * | 2022-10-12 | 2022-12-27 | 深圳市海滨制药有限公司 | Method for detecting 4-methylenepiperidine in efinaconazole |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5367053A (en) * | 1993-05-19 | 1994-11-22 | Houghten Pharmaceuticals, Inc. | Opioid peptide inhibitors |
EP1453849A4 (en) | 2001-11-09 | 2006-03-01 | Algos Therapeutics Inc | Antisense modulation of purinoreceptor p2x3 |
-
2007
- 2007-03-19 KR KR1020070026408A patent/KR100880370B1/en not_active IP Right Cessation
-
2008
- 2008-03-17 WO PCT/KR2008/001476 patent/WO2008114976A1/en active Application Filing
Also Published As
Publication number | Publication date |
---|---|
WO2008114976A1 (en) | 2008-09-25 |
KR20080085245A (en) | 2008-09-24 |
KR100880370B1 (en) | 2009-02-03 |
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