WO2006108686A3 - Bnp agonists - Google Patents
Bnp agonists Download PDFInfo
- Publication number
- WO2006108686A3 WO2006108686A3 PCT/EP2006/003473 EP2006003473W WO2006108686A3 WO 2006108686 A3 WO2006108686 A3 WO 2006108686A3 EP 2006003473 W EP2006003473 W EP 2006003473W WO 2006108686 A3 WO2006108686 A3 WO 2006108686A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- amino acid
- xaa1
- xaa3
- xaa2
- alkyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/575—Hormones
- C07K14/58—Atrial natriuretic factor complex; Atriopeptin; Atrial natriuretic peptide [ANP]; Cardionatrin; Cardiodilatin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/575—Hormones
- C07K14/58—Atrial natriuretic factor complex; Atriopeptin; Atrial natriuretic peptide [ANP]; Cardionatrin; Cardiodilatin
- C07K14/582—Atrial natriuretic factor complex; Atriopeptin; Atrial natriuretic peptide [ANP]; Cardionatrin; Cardiodilatin at least 1 amino acid in D-form
-
- 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
- C07K7/08—Linear peptides containing only normal peptide links having 12 to 20 amino acids
Abstract
The present invention relates to dipeptidyl peptidase resistant BNP agonists, their synthesis and therapeutic applications thereof. In particular the present invention relates to compounds of formula (I): R-Xaa1-Xaa2-Xaa3-Pep-OH ; wherein R is selected from the group comprising hydrogen, acetyl, formyl, or alkyl, wherein Xaa1 is an amino-acid selected from serine, alanine, threonine or asparagine, Xaa2 is a L-amino acid or a D-amino acid, different from L-proline, L-alanine, L-glycine or L-serine, optionally substituted by at least one substituent selected from alkyl, aryl or acyl, and Xaa3 is a L-amino acid or a D-amino acid, optionally substituted by at least one substituent selected from alkyl, acetyl, or aryl, wherein Xaa1, Xaa2, Xaa3 are linked to each other by peptide bonds or pseudo-peptide bonds, and wherein Pep is a peptide sequence comprising not more than 29 amino acid residues said sequence comprising a disulfide linked ring structure said ring comprising between 12 and 20 amino acids, wherein the disulfide bond is formed by two cysteines.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP05447080.2 | 2005-04-14 | ||
EP05447080 | 2005-04-14 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2006108686A2 WO2006108686A2 (en) | 2006-10-19 |
WO2006108686A3 true WO2006108686A3 (en) | 2006-12-21 |
Family
ID=36954070
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2006/003473 WO2006108686A2 (en) | 2005-04-14 | 2006-04-14 | Bnp agonists |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2006108686A2 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009043526A2 (en) * | 2007-09-11 | 2009-04-09 | Mondobiotech Laboratories Ag | Use of a peptide as a therapeutic agent |
US10189884B2 (en) | 2014-04-28 | 2019-01-29 | The Trustees Of The University Of Pennsylvania | Thioamide-modified peptides and uses thereof |
CN112094338B (en) * | 2019-05-14 | 2022-03-25 | 深圳市亚辉龙生物科技股份有限公司 | Amino-terminal brain natriuretic peptide precursor polypeptide and conjugated protein |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000069900A2 (en) * | 1999-05-17 | 2000-11-23 | Conjuchem, Inc. | Protection of endogenous therapeutic peptides from peptidase activity through conjugation to blood components |
WO2004011498A2 (en) * | 2002-07-31 | 2004-02-05 | Conjuchem Inc. | Long lasting natriuretic peptide derivatives |
-
2006
- 2006-04-14 WO PCT/EP2006/003473 patent/WO2006108686A2/en not_active Application Discontinuation
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000069900A2 (en) * | 1999-05-17 | 2000-11-23 | Conjuchem, Inc. | Protection of endogenous therapeutic peptides from peptidase activity through conjugation to blood components |
WO2004011498A2 (en) * | 2002-07-31 | 2004-02-05 | Conjuchem Inc. | Long lasting natriuretic peptide derivatives |
Non-Patent Citations (5)
Title |
---|
AHLUWALIA A ET AL: "Endothelium-derived C-type natriuretic peptide: more than just a hyperpolarizing factor", TRENDS IN PHARMACOLOGICAL SCIENCES, ELSEVIER, HAYWARTH, GB, vol. 26, no. 3, March 2005 (2005-03-01), pages 162 - 167, XP004771640, ISSN: 0165-6147 * |
AMININASAB M ET AL: "Functional and structural characterization of a novel member of the natriuretic family of peptides from the venom of Pseudocerastes persicus", FEBS LETTERS, ELSEVIER, AMSTERDAM, NL, vol. 557, no. 1-3, 16 January 2004 (2004-01-16), pages 104 - 108, XP004485668, ISSN: 0014-5793 * |
BIDZSERANOVA A ET AL: "Structure-activity studies on the effects of atrial natriuretic peptide, brain natriuretic peptide and their analogs on fear-motivated learning behavior in rats", NEUROPEPTIDES, XX, XX, vol. 23, no. 2, October 1992 (1992-10-01), pages 61 - 65, XP002390351, ISSN: 0143-4179 * |
DESCHENES J ET AL: "Development of a selective peptide antagonist for the human natriuretic peptide receptor-B", PEPTIDES, ELSEVIER, AMSTERDAM, US, vol. 26, no. 3, March 2005 (2005-03-01), pages 517 - 524, XP004989568, ISSN: 0196-9781 * |
SCHOENFELD J R ET AL: "Mutations in B-type natriuretic peptide mediating receptor-A selectivity", FEBS LETTERS, ELSEVIER, AMSTERDAM, NL, vol. 414, no. 2, 8 September 1997 (1997-09-08), pages 263 - 267, XP004366327, ISSN: 0014-5793 * |
Also Published As
Publication number | Publication date |
---|---|
WO2006108686A2 (en) | 2006-10-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
IN2014CN02050A (en) | ||
PE20091753A1 (en) | PEPTIDE ANTAGONIST CONJUGATES ANALOGUE TO PUMP | |
CA2651990C (en) | Improved antimicrobial peptides | |
UA103154C2 (en) | Hla-a*-1101-restricted wt1 peptide and pharmaceutical composition comprising thereof | |
SK2052001A3 (en) | Peptide analogues, process for their preparation, pharmaceutical composition containing same, their use and intermediates | |
HU205141B (en) | Process for producing peptide boronic acid derivatives inhibiting trypsin-like protease, as well as pharmaceutical compositions comprising such compounds as active ingredient | |
IL175319A0 (en) | Novel phosphate-binding protein, pharmaceutical compositions containing same and use thereof | |
JP2002530430A (en) | Pharmaceutical composition for inhibiting hepatitis C virus NS3 protease | |
ATE482978T1 (en) | MIMETIC CD4 PEPTIDES AND THEIR USES | |
NZ610732A (en) | Novel angiotensin type 2 (at2) receptor agonists and uses thereof | |
HK1093308A1 (en) | Use of peptides derived from the b beta chain of human fibrinogen for the treatment of shock | |
ATE280827T1 (en) | PENAEIDINE: ANTIMICROBIAL PEPTIDES FROM CRUSTACEANS | |
WO2006108686A3 (en) | Bnp agonists | |
EP0696199A4 (en) | Amidino and guanidino substituted boronic acid inhibitors of trypsin-like enzymes | |
AU2008339610B2 (en) | Methods of peptide modification | |
CA2883531A1 (en) | Stable peptide-based furin inhibitors | |
Debowski et al. | Hybrid analogues of SFTI‐1 modified in P1 position by β‐and γ‐amino acids and N‐substituted β‐alanines | |
Roumelioti et al. | Design, synthesis and biological evaluation of cyclic angiotensin II analogues with 3, 5 side-chain bridges: role of C-terminal aromatic residue and ring cluster for activity and implications in the drug design of AT1 non-peptide antagonists | |
GB0717526D0 (en) | Improvements in or relating to compositions for the treatment or prophylaxis of viral infections | |
US5776903A (en) | Peptide derivatives usable as zinc endopeptidase 24-15 inhibitors | |
CA2720778C (en) | Opiorphin peptide derivatives as potent inhibitors of enkephalin - degrading ectopeptidases | |
EP1730174A4 (en) | Peptide carrier for drug delivery | |
KR900004762A (en) | New peptidase inhibitor | |
TW201730203A (en) | Method for preparation of RADA-16 | |
HK1147210A1 (en) | Anti-hypertensive agent |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWW | Wipo information: withdrawn in national office |
Country of ref document: DE |
|
NENP | Non-entry into the national phase |
Ref country code: RU |
|
WWW | Wipo information: withdrawn in national office |
Country of ref document: RU |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 06753391 Country of ref document: EP Kind code of ref document: A2 |
|
WWW | Wipo information: withdrawn in national office |
Ref document number: 6753391 Country of ref document: EP |