IP Library › Granted Patent US 7,807,678
Granted Patent B2
US 7,807,678 · App. 10/776,419 · Granted Oct 5, 2010

Peptidomimetics of biologically active metallopeptides

Assignee: Palatin Technologies, Inc.
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Quick Facts
Patent No.
US 7,807,678
App. No.
10/776,419
Granted
Oct 5, 2010
Kind
B2
Abstract

The invention relates to a method of deriving a peptidomimetic of a biologically active metallopeptide, wherein the peptidomimetic includes at least one non-peptide ring structure defining a template space superimposable on a corresponding defined template space of the metallopeptide, and where the peptidomimetic further includes at least two elements independently including an amino acid residue, amino acid side chain moiety or derivative thereof, the elements defining and occupying a similar descriptor space as corresponding elements of the metallopeptide. The invention further relates to peptidomimetics with a template space heterocyclic ring structure, including 5-, 6- and 8-membered and 5-5- and 6-5-bicyclic fused ring structure melanocortin receptor-specific peptidomimetics.

Claims (12)

1. A peptidomimetic of the formula:

wherein

X 1 is (CH 2 ) m ;

X 2 bearing the R 5 substituent is N and all other X 2 are CH 2 ;

R 5 is

R 6 is —(CH 2 ) 4 NH 2 , —(CH 2 ) 3 NHC(NH 2 )═NH, —(CH 2 ) 3 NHCOCH 3 , —(CH 2 ) 3 NHCOOCH 3 , —(CH 2 ) 2 NHC(NH 2 )═NH, —(CH 2 ) 2 NHCONH 2 , —(CH 2 ) 4 NHCOH, —(CH 2 ) 4 NHCOCH 3 , —(CH 2 ) 3 NHCONHCH 3 , —(CH 2 ) 3 NHSO 2 NH 2 , —(CH 2 ) 3 NHSO 2 CH 3 , —(CH 2 ) 3 NH 2 , —(CH 2 ) 2 CONH 2 , —(CH 2 ) 3 NH(C═NH)NHMe, —(CH 2 ) 3 NH(C═NH)NHEt, —(CH 2 ) 3 NH(C═NH)NHPr, —(CH 2 ) 3 NH(C═NH)NHPr-i, —(CH 2 ) 3 NH(C═NH)NH 2 , —(CH 2 ) 4 NHCONH 2 , —(CH 2 ) 4 NH(C═NH)NH 2 ,

R 7 is R 9 -R 8 -;

R 8 is an L- or D-configuration of Phe, Phe(2-Cl), Phe(4-Cl), Phe(2,4-diCl), Phe(3,4-diCl), Phe(4-NO 2 ), Phe(4-Me), Phe(4-Phenyl), HPhe, Phg, Trp, NaI 1, NaI 2, Bip, Dip, Bpa, Ser(Bzl), Lys(Z), Lys(Z-2′Br), Lys(Bz), Thr(Bz1), Cys(Bz1), Tyr(BzlCl 2 ), pF-Phe, Phe(4-Br), Phe(4-CF 3 ), Phe(3,4-diF), Phe(4-I) or Phe(3,4-di-OMe);

R 9 is optionally not present or is an L- or D-configuration of H is, Ser(Bzl), Tic, heptanoyl-Ser(Bzl), hexanoyl-Ser(Bzl), Hyp(Bzl), 4-phenylPro, 5-phenylPro, Tiq, Atc, Igl, Hyp(O-2-Naphthyl), Hyp(O-Phenyl), 2-Aic, Idc, 1-Aic, NH 2 (CH 2 ) 6 CO—, Benzyl, Beta-homoSer(Bz1), Ser(O-2-Naphthyl), Ser(O-Phenyl), Ser(O-4-Cl-Phenyl), Ser(O-2-Cl-Phenyl), Thr(Bzl), Tic, heptanoyl-Thr(Bzl), hexanoyl-Thr(Bzl), Beta-homoThr(Bzl), Thr(O-2-Naphthyl), Thr(O-Phenyl), Thr(O-4-Cl-Phenyl) or Thr(O-2-Cl-Phenyl);

n is 1; and

mist.

2. A pharmaceutical composition comprising the peptidomimetic of claim 1 and a pharmaceutically acceptable carrier.

Assignments (3)
TERMINATION OF CONFIRMATORY PATENT LICENSES Recorded Dec 23, 2009
From: PALATIN TECHNOLOGIES INC.
To: ASTRAZENECA AB
Reel/Frame 023699/0161 →
LICENSE Recorded Apr 2, 2009
From: PALATIN TECHNOLOGIES, INC.
To: ASTRAZENECA AB
Reel/Frame 022482/0408 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 9, 2004
From: SHARMA, SHUBH D.; SHI, YI-QUN; RAJPUROHIT, RAMESH; WU, ZHIJUN
To: PALATIN TECHNOLOGIES, INC.
Reel/Frame 014714/0361 →
Continuity (3)
Continuation PCTUS022557400 · Aug 12, 2002
Provisional Application 6031140400 · Aug 10, 2001
Related Publication 20040171520A1 · Sep 2, 2004