Inflammasome activation in myelodysplastic syndromes
US-2018050011-A1 · Feb 22, 2018 · US
US12077608B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12077608-B2 |
| Application number | US-201917268818-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 15, 2019 |
| Priority date | Aug 16, 2018 |
| Publication date | Sep 3, 2024 |
| Grant date | Sep 3, 2024 |
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.
Peptides useful as inflammasome inhibitors are disclosed and can comprise an H2 helix of a pyrin domain, wherein at least two non-consecutive amino acids of the H2 helix are covalently linked. Methods of treating a subject with a disease comprising administering to the subject the disclosed peptides are also disclosed. Further, disclosed herein are methods of inhibiting binding between a first polypeptide comprising a pyrin domain and a second polypeptide comprising a pyrin domain, the method comprising contacting either the first polypeptide or the second polypeptide with the disclosed peptides.
Opening claim text (preview).
What is claimed is: 1. A peptide comprising a H2 helix of a pyrin domain; wherein the peptide consists of only one pyrin domain helical structure; wherein the peptide is 15 amino acids or less; and wherein at least two non-consecutive amino acids of the H2 helix are covalently linked. 2. The peptide of claim 1 , wherein the peptide comprises fSAH-POP1-1 (SEQ ID NO: 1), fSAH-POP1-3 (SEQ ID NO: 3), fSAH-POP1-4 (SEQ ID NO: 4), fSAH-POP1-5 (SEQ ID NO: 5), fSAH-POP1-6 (SEQ ID NO: 6), fSAH-POP1-7 (SEQ ID NO: 7), fSAH-POP1-8 (SEQ ID NO: 8), fSAH-POP1-9 (SEQ ID NO: 9), fSAH-POP1-10 (SEQ ID NO: 10), fSAH-POP1-11 (SEQ ID NO: 11), fSAH-POP1-12 (SEQ ID NO: 12), fSAH-POP1-13 (SEQ ID NO: 13), fSAH-POP1-14 (SEQ ID NO: 14), fSAH-POP1-15 (SEQ ID NO: 15), fSAH-POP1-16 (SEQ ID NO: 16), fSAH-POP1-17 (SEQ ID NO: 17), fSAH-POP1-18 (SEQ ID NO: 18), fSAH-POP1-19 (SEQ ID NO: 19), fSAH-POP1-20 (SEQ ID NO: 20), fSAH-POP1-21 (SEQ ID NO: 21), fSAH-POP1-22 (SEQ ID NO: 22), fSAH-POP1-23 (SEQ ID NO: 23), fSAH-POP1-24 (SEQ ID NO: 24), fSAH-POP1-25 (SEQ ID NO: 25), fSAH-POP1-26 (SEQ ID NO: 26), fSAH-POP1-27 (SEQ ID NO: 27), fSAH-POP1-28 (SEQ ID NO: 28), fSAH-POP1-29 (SEQ ID NO: 29), fSAH-POP1-30 (SEQ ID NO: 30), fSAH-POP1-31 (SEQ ID NO: 31), SAH-POP1-1 (SEQ ID NO: 32), SAH-POP1-2 (SEQ ID NO: 33), SAH-POP1-3 (SEQ ID NO: 34), SAH-POP1-4 (SEQ ID NO: 35), SAH-POP1-5 (SEQ ID NO: 36), SAH-POP1-6 (SEQ ID NO: 37), SAH-POP1-7 (SEQ ID NO: 38), SAH-POP1-8 (SEQ ID NO: 39), SAH-POP1-17 (SEQ ID NO: 44), and/or SAH-POP1-18 (SEQ ID NO: 45).
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
from mammals · CPC title
specific for leukemia · CPC title
having 12 to 20 amino acids (gastrins C07K14/595; somatostatins C07K14/655; melanotropins C07K14/68) · CPC title
Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.