Methods and materials for reducing cysts and kidney weight in mammals with polycystic kidney disease
US-2017333530-A1 · Nov 23, 2017 · US
US10947289B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10947289-B2 |
| Application number | US-201514806487-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 22, 2015 |
| Priority date | Jan 23, 2013 |
| Publication date | Mar 16, 2021 |
| Grant date | Mar 16, 2021 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present invention provides a modified atrial natriuretic peptide that exhibits prolonged duration in blood and maintains cGMP elevating activity. The present invention provides a modified peptide in which at least one sugar substance is linked directly through a glycosidic bond or via a linker structure to at least one hANP peptide, or a pharmaceutically acceptable salt thereof, a medicament comprising the modified peptide or the salt thereof as an active ingredient, etc.
Opening claim text (preview).
The invention claimed is: 1. A modified peptide or a pharmaceutically acceptable salt thereof, wherein the modified peptide has a structure of wherein hANP is hANP(1-28) consisting of the amino acid sequence of SEQ ID NO: 1 and is bonded at the N terminus of the amino acid sequence to the linker structure through an amide bond; and SG is a sugar substance of following formula wherein Gxx is GlcNAc and “O/N-L” represents binding to the linker structure through an O-glycosidic bond. 2. The modified peptide or pharmaceutically acceptable salt according to claim 1 , wherein the pharmaceutically acceptable salt is a trifluoroacetate salt or an acetate salt. 3. A medicament comprising a modified peptide or a pharmaceutically acceptable salt according to claim 1 . 4. The medicament according to claim 3 , wherein the medicament is an agent for treating or alleviating a cardiovascular disease. 5. The medicament according to claim 4 , wherein the medicament is an agent for management of a medical condition after the onset of acute heart failure. 6. A medicament comprising a modified peptide or a pharmaceutically acceptable salt according to claim 1 . 7. The medicament according to claim 6 , wherein the medicament is an agent for treating or alleviating a cardiovascular disease. 8. The medicament according to claim 7 , wherein the medicament is an agent for management of a medical condition after the onset of acute heart failure. 9. A method for treating or alleviating a cardiovascular disease comprising administering the modified peptide or a pharmaceutically acceptable salt according to claim 1 to a patient in need thereof. 10. A method for management of a medical condition after the onset of acute heart failure comprising administering the modified peptide or pharmaceutically acceptable salt according to claim 1 to a patient in need thereof. 11. A method for treating or alleviating a cardiovascular disease comprising administering the modified peptide or a pharmaceutically acceptable salt according to claim 2 to a patient in need thereof. 12. A method for management of a medical condition after the onset of acute heart failure comprising administering the modified peptide or pharmaceutically acceptable salt according to claim 2 to a patient in need thereof.
Medicinal preparations containing peptides (peptides containing beta-lactam rings A61K31/00; cyclic dipeptides not having in their molecule any other peptide link than those which form their ring, e.g. piperazine-2,5-diones, A61K31/00; ergot alkaloids of the cyclic peptide type A61K31/48; containing macromolecular compounds having statistically distributed amino acid units A61K31/74; medicinal preparations containing antigens or antibodies A61K39/00; medicinal preparations characterised by the non-active ingredients, e.g. peptides as drug carriers, A61K47/00) · CPC title
Sugars, nucleosides, nucleotides or nucleic acids · CPC title
Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title
for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics · CPC title
the organic macromolecular compound being a polyoxyalkylene oligomer, polymer or dendrimer, e.g. PEG, PPG, PEO or polyglycerol · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.