Functionalizing reagents and their uses
Reagents and methods for functionalizing polypeptides with moieties (alkylene glycol) molecules and glycan groups are disclosed that are based on a functionalizing reagent which comprises a nitrogen containing heterocyclic aromatic ring having a vinyl substituent that is capable of reacting with one or more thiol groups that are naturally present, or have been introduced into, the polypeptide, for example by employing a thiol group of one or more cysteine residues. The functionalizing reagent is covalently linked to a poly(alkylene glycol) molecule, such as a polyethylene glycol (PEG) molecule, or a glycan group so that the reaction between the vinyl group and the thiol group in the polypeptide covalently links the polypeptide to the poly(alkylene glycol) molecule and/or the glycan group.
1. A compound represented by formula:
wherein:
X and Y are independently selected from CH or N;
wherein at least R 1 , and optionally R 2 , are covalently linked to a poly(alkylene glycol) molecule and/or a glycan group;
wherein
R 1 , and optionally R 2 , are independently selected from:
—(CH 2 ) n —Z—(CH 2 ) o —R, where Z is O, S or NH, n is 0 to 10, o is 0 to 10 and where R is a hydrogen, a poly(alkylene glycol) molecule or a glycan group, or
—C(O)—Z—(CH 2 ) o —R, Z is O, S or NH, o is 0 to 10 and where R is a hydrogen, a poly(alkylene glycol) molecule or a glycan group; or
—(CH 2 ) n —Z—C(O)—(CH 2 ) o —R, where Z is O, S or NH, n is 0 to 10, o is 0 to 10 and where R is a hydrogen, a poly(alkylene glycol) molecule or a glycan group; or
—Y—(CH 2 ) n —Z—C(O)—(CH 2 ) o —R, where Y is an aryl group, O, S or NH, Z is O or NH, n is 0 to 10, o is 0 to 10 and where R is a hydrogen, a poly(alkylene glycol) molecule or a glycan group; or
—Y—R, where Y is O or S, R is a hydrogen, a glycan, a poly(alkylene glycol) molecule, aryl or C 1-10 alkyl;
with the proviso that when R 2 is not linked to a poly(alkylene glycol) molecule or a glycan group, it may additionally be selected from hydrogen or an electron withdrawing group, such as halogen (F, Cl, or Br), —NO 2 , —CO 2 H, —CO 2 R 4 , COR 4 , —CHO, —CN, —CF 3 , —SO 2 NR 4 R 5 , alkyl or phenyl, where R 4 and R 5 are independently selected from hydrogen or C 1-10 alkyl;
or R 2 and R 3 together form a fused (hetero) aromatic ring substituent which may include, but is not limited to, an indole, indazole, benzimidazole, quinoline, isoquinoline, aziradine or a purine;
or R 3 is selected from hydrogen or a substituent selected from halo, hydroxy, ether, formyl, acyl, carboxy, ester, acyloxy, amido, acylamido, thioamido, tetrazolyl, amino, nitro, nitroso, azido, cyano isocyano, cyanato, isocyanato, thiocyano, isothiocyano, thioether, sulfonic acid, sulfonate, sulfone, sulfonyloxy, sulfinyloxy, sulfamino, sulfonamino, sulfinamino, sulfamyl, sulfonamido, C 1-7 alkyl.
2. The compound of claim 1 , wherein X and Y are both CH or one of X and Y is CH and the other is N.
3. The compound of claim 1 , wherein the poly(alkylene glycol) molecule is a polyethylene glycol.
4. The compound of claim 1 , wherein one of R 1 or R 2 comprises a poly(alkylene glycol) molecule or a glycan group.
5. The compound of claim 1 , wherein R 1 and R 2 comprise a poly(alkylene glycol) molecule and/or a glycan group.
6. The compound of claim 1 , wherein one of R 1 and R 2 comprises a poly(alkylene glycol) molecule and the other of R 1 and R 2 comprises a glycan group.
7. The compound claim 1 , wherein the R 1 and/or R 2 groups for linking the poly(alkylene glycol) molecule and/or the glycan group to the nitrogen containing heterocyclic aromatic ring are independently selected from —(CH 2 )n-Z—(CH 2 ) o —R or —C(O)—Z—(CH 2 ) o —R.
8. The compound of claim 1 , wherein in the R 1 and R 2 in said formula represent —(CH 2 ) n —Z—R or —C(O)—Z—R.
9. A conjugate formed by the reaction of a compound according to claim 1 and one or more thiol groups of a polypeptide.
10. A compound represented by one of the general formulae:
wherein:
at least R 1 , and optionally R 2 , are covalently linked to a poly(alkylene glycol) molecule and/or a glycan group;
and further wherein:
R 1 , and optionally R 2 , are independently selected from:
—(CH 2 ) n —Z—(CH 2 ) o —R, where Z is O, S or NH, n is 0 to 10, o is 0 to 10 and where R is a hydrogen, a poly(alkylene glycol) molecule or a glycan group, or
—C(O) n —Z—(CH 2 ) o —R, Z is O, S or NH, o is 0 to 10 and where R is a hydrogen, a poly(alkylene glycol) molecule or a glycan group, or
—(CH 2 ) n —Z—C(O)—(CH 2 ) o —R, where Z is O, S or NH, n is 0 to 10, o is 0 to 10 and where R is a hydrogen, a poly(alkylene glycol) molecule or a glycan group; or
—Y—(CH 2 ) n —Z—C(O)—(CH 2 ) o —R, where Y is an aryl group, O, S or NH, Z is O or NH, n is 0 to 10, o is 0 to 10 and where R is a hydrogen, a poly(alkylene glycol) molecule or a glycan group, or —Y—R, where Y is O or S, R is a hydrogen, a glycan, a poly(alkylene glycol) molecule, aryl or C 1-10 alkyl;
with the proviso that when R 2 is not linked to a poly(alkylene glycol) molecule or a glycan group, it may additionally be selected from hydrogen or an electron withdrawing group, such as halogen (F, Cl, or Br), —NO 2 , —CO 2 H, —CO 2 R 4 , COR 4 , —CHO, —CN, —CF 3 , —SO 2 NR 4 R 5 , alkyl or phenyl, where R 4 and R 5 are independently selected from hydrogen or C 1-10 alkyl.
11. A conjugate formed by the reaction of a compound according to claim 10 and one or more thiol groups of a polypeptide.