IP Library Granted Patent US 8,034,900
Granted Patent B2
US 8,034,900 · App. 10/541,078 · Granted Oct 11, 2011

Water-soluble thioester and selenoester compounds and methods for making and using the same

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Quick Facts
Patent No.
US 8,034,900
App. No.
10/541,078
Granted
Oct 11, 2011
Kind
B2
Abstract

Water-soluble thioester and selenoester compounds, their generators, as well as methods for making and using the same, are provided. The subject thioester and selenoester compounds are characterized by including an amino acid synthon having a C-terminal group bonded to a water-soluble polymer through a thioester or selenoester linkage. Solid phase resins and protocols for generating the subject compounds are also provided. The subject water soluble thioester and selenoester compounds and generators find use in a variety of different applications, including thioester or selenoester mediated chemical ligation reactions.

Claims (54)

1. A water-soluble thioester or selenoester compound of the formula:

wherein Y is selected from the group consisting of: an amino acid, a peptide, and a polypeptide;

X is sulfur or selenium;

n 1 and n 2 are each from 0 to 2, and n 3 is from 0 to 100;

R and R 1 are individually selected from the group consisting of: hydrogen, a side chain of an amino acid, a branched alkane, a cycloalkane, an alkyl-substituted aryl or heteroaryl group, and combinations thereof;

R 7 and R 8 are each, individually, selected from hydrogen, substituted and unsubstituted linear or branched chain alkyl, aryl, heteroaryl and benzyl;

U is a linker or spacer and may be present or absent and, when present, consists of a linear or branched chain alkyl or heteroalkyl group of up to 18 carbon atoms;

Polymer is a water-soluble polymer of a formula selected from the group consisting of: —[C(O)-φ-C(O)—NH-ψ-NH]n 5 and —[NH-ψ-NH—C(O)-φ-C(O)]n 5 , where n 5 is an integer from 2 to 100, and

φ and ψ are divalent radicals that may be the same or different and are selected from the group consisting of —((CH 2 )n 6 -(CH 2 CH 2 O)n 7 -(CH 2 )n 6 -)- and —((CH 2 )n 6 -(O—CH 2 —CH 2 )n 7 -(CH 2 )n 6 -)-, where n 6 is an integer from 1 to 6 and n 7 is an integer from 2-50, and where φ can also be —(CH 2 —CH 2 )— and ψ can also be —(CH 2 —(CH 2 —CH 2 —O) 3 —CH 2 —CH 2 —CH 2 )— or —(CH 2 —CH 2 —CH 2 —(O—CH 2 —CH 2 ) 3 —CH 2 )—.

2. The thioester or selenoester compound according to claim 1 wherein Y is a peptide or polypeptide.

3. The thioester or selenoester compound according to claim 2 wherein said peptide or polypeptide comprises protected amino acids.

4. The thioester or selenoester compound according to claim 2 wherein said Y contains an N-terminal amino acid containing a group that supports chemical ligation.

5. The thioester or selenoester compound according to claim 1 wherein

R 3 comprises a group of the formula —C(R 7 )(R 8 )-U-Polymer, where

R 7 and R 8 are each individually selected from the group consisting of: hydrogen or linear, branched, substituted, or unsubstituted alkyl, aryl, heteroaryl, and benzyl, and

U is selected from the group consisting of alkyl, aryl, heteroalkyl, heteroaryl, alkoxy, of up to 18 carbon atoms, and

Polymer is selected from the group consisting of: —[C(O)-φ-C(O)—NH-ψ-NH]n 5 and —[NH-ψ-NH—C(O)-φ-C(O)]n 5 , where n 5 is an integer from 1 to 100, and φ and ψ are divalent radicals selected from the group consisting of —((CH 2 )n 6 -(CH 2 CH 2 O)n 7 -(CH 2 )n 6 -)- and —((CH 2 )n 6 -(O—CH 2 —CH 2 )n 7 -(CH 2 )n 6 -)-, where n 6 is an integer from 1 to 6 and n 7 is an integer from 2-50.

6. The thioester or selenoester compound of claim 1 wherein Polymer comprises a divalent radical of having the structure:

where n 5 is an integer of from 2 to 12.

7. The thioester or selenoester compound of claim 5 wherein

φ is —(CH 2 —CH 2 )— and ψ is —(CH 2 —(CH 2 —CH 2 —O) 3 —CH 2 —CH 2 —CH 2 )— or —(CH 2 —CH 2 —CH 2 —(O—CH 2 —CH 2 ) 3 —CH 2 )—.

8. The thioester or selenoester compound of claim 1 wherein R is a group of the structure —C(R 4 )(R 5 )(R 6 ),

where R 4 , R 5 , and R 6 each individually are selected from the group consisting of: hydrogen, linear, branched, substituted or unsubstituted alkyl, aryl, heteroaryl, and benzyl.

9. The thioester or selenoester compound of claim 5 wherein

Y is a peptide or polypeptide;

X is sulfur;

n 1 and n 2 are 0;

R 7 and R 8 are each individually selected from the group consisting of: hydrogen, —CH 3 , and —CH(CH 3 ) 2 .

10. The thioester or selenoester compound of claim 9 wherein:

n 5 is from 2 to 50, n 6 is from 1 to 3, n 7 is from 2 to 5; and

φ is —(CH 2 —CH 2 )— and ψ is —(CH 2 —(CH 2 —CH 2 —O) 3 —CH 2 —CH 2 —CH 2 )— or —(CH 2 —CH 2 —CH 2 —(O—CH 2 —CH) 3 —CH 2 )—.

11. The thioester or selenoester compound of claim 1 wherein Y comprises an N-terminal group that supports chemical ligation.

12. The thioester or selenoester compound of claim 11 wherein the N-terminal group comprises cysteine or selenocysteine.

13. The thioester or selenoester compound of claim 12 wherein the cysteine or selenocysteine is protected.

14. A method of cleaving a thioester or selenoester compound from a solid support, said method comprising:

providing a thioester or selenoester generator having the formula:

wherein PG is a protecting group that may be present or absent,

Y is an amino acid, a peptide, or a polypeptide and may be present or absent, and when Y is absent PG is an amino protecting group that may be present or absent;

R and R 1 are individually selected from the group consisting of: hydrogen, a side chain of an amino acid, a branched alkane, a cycloalkane, an alkyl-substituted aryl or heteroaryl group, and combinations thereof;

R 3 is a group compatible with a thioester or selenoester and comprises a water-soluble polymer of a formula selected from the group consisting of: —[C(O)-φ-C(O)—NH-ψ-NH]n 5 and —[NH-ψ-NH—C(O)-φ-C(O)]n 5 , where n 5 is an integer from 2 to 100, and φ and ψ are divalent radicals that may be the same or different and are selected from the group consisting of —((CH 2 )n 6 -(CH 2 CH 2 O)n 7 -(CH 2 )n 6 -)- and —((CH 2 )n 6 -(O—CH 2 —CH 2 )n 7 -(CH 2 )n 6 -)-, where n 6 is an integer from 1 to 6 and n 7 is an integer from 2-50;

X is sulfur or selenium;

n 1 and n 2 each are from 0 to 2; n 3 is from 0 to 100;

each L 1 , L 2 and L 3 is a linker cleavable under non-nucleophilic conditions wherein only one of L 1 , L 2 , and L 3 is present;

Support is a solid phase, matrix or surface; and

(b) cleaving said linker under non-nucleophilic conditions to generate a thioester or selenoester compound comprising the formula:

15. A thioester or selenoester generator comprising a composition having the formula:

wherein PG is a protecting group that may be present or absent,

Y is an amino acid, a peptide, or a polypeptide and may be present or absent, and when Y is absent PG is an amino protecting group that may be present or absent;

R and R 1 are individually selected from the group consisting of: hydrogen, a side chain of an amino acid, a branched alkane, a cycloalkane, an alkyl-substituted aryl or heteroaryl group, and combinations thereof;

R 3 is a group compatible with a thioester or selenoester and comprises a water-soluble polymer of a formula selected from the group consisting of: —[C(O)-φ-C(O)—NH-ψ-NH]n 5 and —[NH-ψ-NH—C(O)-φ-C(O)]n 5 , where n 5 is an integer from 2 to 100, and φ and ψ are divalent radicals that may be the same or different and are selected from the group consisting of —((CH 2 )n 6 -(CH 2 CH 2 O)n 7 -(CH 2 )n 6 -)- and —((CH 2 )n 6 -(O—CH 2 —CH 2 )n 7 -(CH 2 )n 6 -)-, where n 6 is an integer from 1 to 6 and n 7 is an integer from 2-50;

X is sulfur or selenium;

n 1 and n 2 each are from 0 to 2; n 3 is from 0 to 100;

each L 1 , L 2 and L 3 is a linker cleavable under non-nucleophilic conditions wherein only one of L 1 , L 2 , and L 3 is present;

Support is a solid phase, matrix or surface.

Assignments (3)
AMYLIN PHARMACEUTICALS, LLC ASSIGNS AN EQUAL AND UNDIVIDED ONE-HALF OF ITS ENTIRE RIGHT, TITLE AND INTEREST TO ASTRAZENECA PHARMACEUTICALS LP Recorded Oct 26, 2012
From: AMYLIN PHARMACEUTICALS, LLC
To: ASTRAZENECA PHARMACEUTICALS LP
Reel/Frame 029195/0555 →
CHANGE OF NAME Recorded Oct 25, 2012
From: AMYLIN PHARMACEUTICALS, INC.
To: AMYLIN PHARMACEUTICALS, LLC
Reel/Frame 029198/0340 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 20, 2006
From: GRYPHON THERAPEUTICS, INC.
To: AMYLIN PHARMACEUTICALS, INC.
Reel/Frame 017042/0398 →