Peptide pharmaceuticals for insulin resistance
AssigneeMederis Diabetes LLC
InventorJohn J. Nestor
Life of this patent
Estimating the term…
Abstract
Described herein are methods of syntheses and therapeutic uses of covalently modified peptides and/or proteins. The covalently modified peptides and/or proteins allow for improved pharmaceutical properties of peptide and protein-based therapeutics.
Claims40
A peptide product comprising a surfactant X, covalently attached to a peptide, the peptide comprising a linker amino acid U and at least one other amino acid:
- wherein the surfactant X is a group of Formula I:
- wherein:
- R1a is independently, at each occurrence, a bond, H, a substituted or unsubstituted C1-C30 alkyl group, a substituted or unsubstituted alkoxyaryl group, a substituted or unsubstituted aralkyl group, or a steroid nucleus containing moiety;
- R1b, R1c, and R1d are each, independently at each occurrence, a bond, H, a substituted or unsubstituted C1-C30 alkyl group, a substituted or unsubstituted alkoxyaryl group, or a substituted or unsubstituted aralkyl group;
- W1 is independently, at each occurrence, —CH2—, —CH2—O—, —(C═O), —(C═O)—O—, —(C═O)—NH—, —(C═S)—, —(C═S)—NH—, or —CH2—S—;
- W2 is —O—, —CH2— or —S—;
- R2 is independently, at each occurrence, a bond to U, H, a substituted or unsubstituted C1-C30 alkyl group, a substituted or unsubstituted alkoxyaryl group, or a substituted or unsubstituted aralkyl group, —NH2, —SH, C2-C4-alkene, C2-C4-alkyne, —NH(C═O)—CH2—Br, —(CH2)m-maleimide, or —N3;
- n is 1, 2 or 3;
- and
- m is 1-10;
- the peptide is selected from Formula II:
- (SEQ. ID. NO. 1)
- aa1-aa2-aa3-aa4-aa5-aa6-aa7-aa8-aa9-aa10-aa11-aa12-
- aa13-aa14-aa15-aa16-aa17-aa18-aa19-aa20-aa21-aa22-
- aa23-aa24-aa25-aa26-aa27-aa28-aa29-aa30-aa31-aa32-
- aa33-aa34-aa35-aa36-aa37-Z Formula II
- wherein:
- Z is OH, or —NH—R3, wherein R3 is H, or C1-C12 substituted or unsubstituted alkyl, or a PEG chain of less than 10 Da;
- aa1 is His, N—Ac-His, pGlu-His, or N—R3-His;
- aa2 is Ser, Ala, Gly, Aib, Ac4c, or Ac5c;
- aa3 is Gln, or Cit;
- aa4 is Gly, or D-Ala;
- aa5 is Thr, or Ser;
- aa6 is Phe, Trp, F2Phe, Me2Phe, or Nal2;
- aa7 is Thr, or Ser;
- aa8 is Ser, or Asp;
- aa9 is Asp, or Glu;
- aa10 is Tyr, Leu, Met, Nal2, Bip, or Bip2EtMeO;
- aa11 is Ser, Asn, or U;
- aa12 is Lys, Glu, Ser, Arg, or U;
- aa13 is absent or Tyr, Gln, Cit, or U;
- aa14 is absent or Leu, Met, Nle, or U;
- aa15 is absent or Asp, Glu, or U;
- aa16 is absent or Ser, Gly, Glu, Aib, Ac5c, Lys, Arg, or U;
- aa17 is absent or Arg, hArg, Gln, Glu, Cit, Aib, Ac4c, Ac5c, or U;
- aa18 is absent or Arg, hArg, Ala, Aib, Ac4c, Ac5c, or U;
- aa19 is absent or Ala, Val, Aib, Ac4c, Ac5c, or U;
- aa20 is absent or Gln, Lys, Arg, Cit, Glu, Aib, Ac4c, Ac5c, or U;
- aa21 is absent or Asp, Glu, Leu, Aib, Ac4c, Ac5c, or U;
- aa22 is absent or Phe, Trp, Nal2, Aib, Ac4c, Ac5c, or U
- aa23 is absent or Val, Ile, Aib, Ac4c, Ac5c, or U;
- aa24 is absent or Gln, Ala, Glu, Cit, or U;
- aa25 is absent or Trp, Nal2, or U;
- aa26 is absent or Leu, or U;
- aa27 is absent or Met, Val, Nle, Lys, or U;
- aa28 is absent or Asn, Lys, or U;
- aa29 is absent or Thr, Gly, Aib, Ac4c, Ac5c, or U;
- aa30 is absent or Lys, Aib, Ac4c, Ac5c, or U;
- aa31 is absent or Arg, Aib, Ac4c, Ac5c, or U;
- aa32 is absent or Asn, Aib, Ac4c, Ac5c, or U;
- aa33 is absent or Arg, Aib, Ac4c, Ac5c, or U;
- aa34 is absent or Asn, Aib, Ac4c, Ac5c, or U;
- aa35 is absent or Asn, Aib, Ac4c, Ac5c, or U;
- aa36 is absent or Ile, Aib, Ac4c, Ac5C, or U;
- aa36 is absent or Ala, Aib, Ac4c, Ac5C, or U;
- aa37 absent or U;
- U is a natural or unnatural amino acid comprising a functional group used for covalent attachment to the surfactant X;
- wherein any two of aa1-aa37 are optionally cyclized through their side chains to form a lactam linkage;
- and
- provided that one, or at least one of aa11-aa37 is the linker amino acid U covalently attached to X.
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Dependencies are inferred from the claim text.