Acylated glucagon analogues

1. A compound having the formula:

R 1 —P 1 —P 2 —R 2

wherein

R 1 is H, C 1-4 alkyl, acetyl, formyl, benzoyl or trifluoroacetyl;

R 2 is OH or NH 2 ;

P 1 is a peptide having the sequence:

H-X2-X3-GTFTSDYSKYLDSΨAAHDFVEWLLSA

wherein:

X2 is selected from Aib, Ala, D-Ala, Ser, N-Me-Ser, Ac3c, Ac4c and Ac5c; and

X3 is selected from Gln and His;

P 2 is absent or is a sequence of 1-20 amino acid units independently selected from the group consisting of Ala, Leu, Ser, Thr, Tyr, Cys, Glu, Lys, Arg, Dbu, Dpr and Orn;

or a pharmaceutically acceptable salt thereof; and

ψ is a residue of Lys, Arg, Orn or Cys in which the side chain is conjugated to a substituent having the formula —Z 2 —Z 1 ;

—Z 1 is a fatty chain having a polar group at one end of the chain and connected via a bond to Z 2 at the end of the chain distal from the polar group, and

wherein —Z 1 is selected from carboxyphenoxynonanoyl, 13-carboxy-tridecanoyl, 15-carboxy-pentadecanoyl and 17-carboxy-heptadecanoyl-; and

—Z 2 — is a spacer selected from:

isoGlu, isoGlu-Peg3-Peg3, isoGlu-Peg4-Peg4, Peg3-Peg3-isoGlu, isoGlu-Gly-Ser-Gly-Ser-Gly-Gly (isoGlu-GSGSGG), and Ala-Ala-Peg3-Peg3 (AA-Peg3-Peg3);

or a pharmaceutically acceptable salt thereof.

2. A compound according to claim 1 wherein P 1 has the sequence:

H-Aib-QGTFTSDYSKYLDSΨAAHDFVEWLLSA.

3. A compound according to claim 2 which is:

H-H-Aib-QGTFTSDYSKYLDSΨAAHDFVEWLLSA-NH 2 .

4. A compound according to claim 1 wherein Z 1 —Z 2 is selected from:

(i) [17-Carboxy-heptadecanoyl]-isoGlu-Peg3-Peg3;

(ii) [17-Carboxy-heptadecanoyl]-isoGlu;

(iii) [13-Carboxy-tridecanoyl]-isoGlu-Peg3-Peg3;

(iv) [Carboxyphenoxynonanoyl]-isoGlu-Peg3-Peg3;

(v) [13-Carboxy-tridecanoyl]-isoGlu-Peg4-Peg4;

(vi) [17-Carboxy-heptadecanoyI]-Peg3-Peg3-isoGlu;

(vii) [17-Carboxy-heptadecanoyl]-isoGlu-GSGSGG; and

(viii) [17-Carboxy-heptadecanoyl]-AA-Peg3-Peg3.

5. A compound according to claim 1 wherein P1 has the sequence: H-Aib-QGTFTSDYSKYLDS-K([15-carboxy-pentadecanoyl]-isoGlu)-AAHDFVEWLLSA.

6. A compound according to claim 5 which is: H-H-Aib-QGTFTSDYSKYLDS-K([15-carboxy-pentadecanoyl]-isoGlu)-AAHDFVEWLLSA-NH 2 .

7. A compound according to claim 1 wherein Z 2 —Z 1 is [17-carboxy-heptadecanoyl]-isoGlu-Peg3-Peg3 or [17-carboxy-heptadecanoyl]-isoGlu-GSGSGG.

8. A composition comprising a compound according to claim 1 in admixture with a carrier.

9. A composition according to claim 8 wherein the composition is a pharmaceutical composition, and the carrier is a pharmaceutically acceptable carrier.

10. A method of preventing weight gain or promoting weight loss in an individual in need thereof, said method comprising administering to the individual a compound of claim 1 .

11. A method of lowering circulating LDL levels, and/or increasing HDL/LDL ratio in an individual in need thereof, said method comprising administering to the individual a compound of claim 1 .

12. A method of treating a condition caused or characterised by excess body weight, said method comprising administering to the individual a compound of claim 1 .

13. A method of preventing or treating obesity, morbid obesity, morbid obesity prior to surgery, obesity linked inflammation, obesity linked gallbladder disease, obesity induced sleep apnea, diabetes, metabolic syndrome, hypertension, atherogenic dyslipidemia, atherosclerosis, arteriosclerosis, coronary heart disease, peripheral artery disease, stroke, or microvascular disease, said method comprising administering to the individual a compound of claim 1 .

14. A method of preventing weight gain or promoting weight loss in an individual in need thereof; lowering circulating LDL levels, and/or increasing HDL/LDL ratio in an individual in need thereof; treating a condition caused or characterised by excess body weight; or preventing or treating obesity, morbid obesity, morbid obesity prior to surgery, obesity linked inflammation, obesity linked gallbladder disease, obesity induced sleep apnea, diabetes, metabolic syndrome, hypertension, atherogenic dyslipidemia, atherosclerosis, arteriosclerosis, coronary heart disease, peripheral artery disease, stroke, or microvascular disease, said method comprising administering to the individual a compound of claim 1 as part of a combination therapy together with an agent for treatment of diabetes, obesity, dyslipidemia or hypertension.

15. The method of claim 14 , wherein the agent for treatment of diabetes is selected from the group consisting of a biguanide (e.g. metformin), a sulfonylurea, a meglitinide or glinide (e.g. nateglinide), a DPP-IV inhibitor, an SGLT2 inhibitor, a glitazone, a different GLP-1 agonist, an insulin, and an insulin analogue.

16. The method of claim 14 , wherein the agent for treatment of obesity is selected from the group consisting of a glucagon-like peptide receptor 1 agonist, a peptide YY receptor agonist or analogue thereof, a cannabinoid receptor 1 antagonist, a lipase inhibitor, a melanocortin receptor 4 agonist, a melanin concentrating hormone receptor 1 antagonist, phentermine, a combination of norepinephrine/dopamine reuptake inhibitor and opioid receptor antagonist (e.g. a combination of phentermine and topiramate), a combination of bupropion and naltrexone, and a serotonergic agent.

17. The method of claim 14 , wherein the agent for treatment of hypertension is selected from the group consisting of an angiotensin-converting enzyme inhibitor, an angiotensin II receptor blocker, a diuretic, a beta-blocker, and a calcium channel blocker.

18. The method of claim 14 , wherein the agent for treatment of dyslipidemia is selected from the group consisting of a statin, a fibrate, a niacin, and a cholesterol absorption inhibitor.

19. A therapeutic kit comprising a compound according to claim 1 optionally in admixture with a carrier.

20. A method of producing a compound according to claim 1 , the method comprising expressing a precursor peptide sequence from a nucleic acid construct that encodes the precursor peptide, recovering the expression product, and modifying the precursor peptide to yield a compound according to claim 1 .

21. A method according to claim 20 comprising modifying the precursor peptide to introduce the substituent at residue ψ.