US2003083236A1PendingUtilityA1
Myelopeptides and their therapeutic use
Priority: Jan 7, 1997Filed: Oct 22, 2002Published: May 1, 2003
Est. expiryJan 7, 2017(expired)· nominal 20-yr term from priority
A61P 31/12C07K 5/1019C07K 7/06A61P 31/04A61P 37/04A61K 38/00Y02A50/30
33
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Claims
Abstract
The present invention pertains to peptides comprising 4 to 10 amino acids including X 1 -Pro, Pro-X 2 or X 1 -Pro-X 2 , wherein X 1 and X 2 are independently selected from Lys, Arg, His, Asp, Glu, Asn and Gln, and the other amino acids are independently selected from Gly, Ala, Val, Leu, Ile, Nle, Nva, Pro, Phe, Tyr, Trp, Cys, Met, Ser and Thr. Such peptides, including LVCYPQ, FRPRIMTP, VVYPD and VDPP, are obtainable from porcine bone marrow cell culture, and have immunostimulating and anti-viral properties.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . A peptide comprising 4 to 10 amino acids including X 1 -Pro, Pro-X 2 or X 1 -Pro-X 2 , wherein X 1 and X 2 are independently selected from Lys, Arg, His, Asp, Glu, Asn and Gln, and the other amino acids are independently selected from Gly, Ala, Val, Leu, Ile, Nle, Nva, Pro, Phe, Tyr, Trp, Cys, Met, Ser and Thr.
2 . The peptide according to claim 1 , which comprises predominantly other amino acids as defined in claim 1 .
3 . The peptide according to claim 1 , wherein the N-terminal comprises 1, 2, 3 or 4 amino acids independently selected from Gly, Ala, Val, Leu, Ile, Nle, Nva, Phe, Tyr, Trp, Cys and Met.
4 . The peptide according to claim 1 , including Pro-X 2 .
5 . The peptide according to claim 1 , wherein X 2 is a terminal amino acid.
6 . The peptide according to claim 1 , including X 1 -Pro.
7 . The peptide according to claim 6 , including Z-X 1 -Pro, wherein Z is terminal and one of the other amino acids.
8 . The peptide according to claim 1 , which is or comprises LVCYPQ (SEQ ID NO. 3).
9 . The peptide according to claim 1 , which is or comprises FRPRIMTP (SEQ ID NO. 4).
10 . The peptide according to claim 1 , which is or comprises VVYPD (SEQ ID NO. 5).
11 . The peptide according to claim 1 , which is or comprises VDPP (SEQ ID NO. 6).
12 . The peptide according to claim 1 , free from other components of bone marrow.
13 . The peptide according to claim 1 , in a pharmaceutically acceptable carrier or diluent.
14 . The peptide according to claim 2 , wherein the N-terminal comprises 1, 2, 3 or 4 amino acids independently selected from Gly, Ala, Val, Leu, Ile, Nle, Nva, Phe, Tyr, Trp, Cys and Met.
15 . A method for the treatment or prophylaxis of a viral or bacterial infection, or a disease requiring immunostimulation, in a patient, said method comprising administering an effective amount of a peptide of claim 1 to the patient.Join the waitlist — get patent alerts
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