Heterocyclic self-immolative linkers and conjugates
View Patent ↗The present invention provides heterocyclic linker compounds useful for linking drug moieties to ligands. The compounds also include drug-ligand conjugates comprising a ligand capable of targeting a selected cell population, and a drug connected to the ligand by a heterocyclic linker moiety. The linker moiety comprises a peptide sequence that is a substrate for an intracellular enzyme, for example a cathepsin, that cleaves the peptide at an amide bond. The peptide further contains a self-immolating moiety which connects the drug and the protein peptide sequence. Upon cleavage of the peptide sequence by an intracellular enzyme the self-immolating moiety cleaves itself from the drug moiety such that the drug moiety is in an underivatized and active form.
1. A drug-ligand conjugate compound comprising a cell-specific ligand and a drug moiety conjugated by a linker wherein said linker comprises a heterocyclic self-immolative moiety of Formula I
where the wavy lines indicate the covalent attachment sites to the cell-specific ligand and the drug moiety, and wherein:
U is O, S or NR 6 ;
Q is CR 4 or N;
T is NH, NR 6 , O or S pending from said drug moiety;
R 1 , R 2 , R 3 and R 4 are independently selected from H, F, Cl, Br, I, OH, —N(R 5 ) 2 , —N(R 5 ) 3 + , C 1 -C 8 alkylhalide, carboxylate, sulfate, sulfamate, sulfonate, —SO 2 R 5 , —S(═O)R 5 , —SR 5 , —SO 2 N(R 5 ) 2 , —C(═O)R 5 , —CO 2 R 5 , —C(═O)N(R 5 ) 2 , —CN, —N 3 , —NO 2 , C 1 -C 8 alkoxy, C 1 -C 8 halosubstituted alkyl, polyethyleneoxy, phosphonate, phosphate, C 1 -C 8 alkyl, C 1 -C 8 substituted alkyl, C 2 -C 8 alkenyl, C 2 -C 8 substituted alkenyl, C 2 -C 8 alkynyl, C 2 -C 8 substituted alkynyl, C 6 -C 20 aryl, C 6 -C 20 substituted aryl, C 1 -C 20 heterocycle, and C 1 -C 20 substituted heterocycle; or when taken together, R 2 and R 3 form a carbonyl (═O), or spiro carbocyclic ring of 3 to 7 carbon atoms; and
R 5 and R 6 are independently selected from H, C 1 -C 8 alkyl, C 1 -C 8 substituted alkyl, C 2 -C 8 alkenyl, C 2 -C 8 substituted alkenyl, C 2 -C 8 alkynyl, C 2 -C 8 substituted alkynyl, C 6 -C 20 aryl, C 6 -C 20 substituted aryl, C 1 -C 20 heterocycle, and C 1 -C 20 substituted heterocycle;
where C 1 -C 8 substituted alkyl, C 2 -C 8 substituted alkenyl, C 2 -C 8 substituted alkynyl, C 6 -C 20 substituted aryl, and C 2 -C 20 substituted heterocycle are independently substituted with one or more substituents selected from F, Cl, Br, I, OH, —N(R 5 ) 2 , —N(R 5 ) 3 + , C 1 -C 8 alkylhalide, carboxylate, sulfate, sulfamate, sulfonate, C 1 -C 8 alkylsulfonate, C 1 -C 8 alkylamino, 4-dialkylaminopyridinium, C 1 -C 8 alkylhydroxyl, C 1 -C 8 alkylthiol, —SO 2 R 5 , —S(═O)R 5 , —SR 5 , —SO 2 N(R 5 ) 2 , —C(═O)R 5 , —CO 2 R 5 , —C(═O)N(R 5 ) 2 , —CN, —N 3 , —NO 2 , C 1 -C 8 alkoxy, C 1 C 8 trifluoroalkyl, C 1 -C 8 alkyl, C 3 -C 12 carbocycle, C 6 -C 20 aryl, C 2 -C 20 heterocycle, polyethyleneoxy, phosphonate, and phosphate.
2. The drug-ligand conjugate compound of claim 1 having Formula IV:
L-[A n -Z m -X-D] p IV
wherein
L is a cell-specific ligand;
A is a Spacer unit;
Z is an Amino Acid;
X is a heterocyclic self-immolative moiety of Formula I;
D is a drug moiety;
m is independently 1, 2, 3, 4, 5 or 6;
n is 0 or 1; and
p is 1, 2, 3, 4, 5, 6, 7 or 8.
3. The drug-ligand conjugate compound of claim 2 , wherein and Q is N; and U is S.
4. The drug-ligand conjugate compound of claim 2 , wherein Q is CH; and U is O.
5. The drug-ligand conjugate compound of claim 2 , wherein R 1 is CF 3 .
6. The drug-ligand conjugate compound of claim 2 , wherein R 1 is H.
7. The drug-ligand conjugate compound of claim 2 , wherein T is N or NH.
8. The drug-ligand conjugate compound of claim 2 wherein m is 1, and Z is selected from alanine, 2-amino-2-cyclohexylacetic acid, 2-amino-2-phenylacetic acid, arginine, asparagine, aspartic acid, cysteine, glutamine, glutamic acid, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, valine, γ-aminobutyric acid, α,α-dimethyl γ-aminobutyric acid, β,β-dimethyl γ-aminobutyric acid, ornithine, citrulline; and protected forms thereof.
9. The drug-ligand conjugate compound of claim 2 , wherein m is 2, and Z m is a dipeptide selected from glycine-glycine, alanine-phenylalanine, phenylalanine-lysine, valine-citrulline and valine-lysine.
10. The drug-ligand conjugate compound of claim 2 , wherein m is 3, and Z m is a tripeptide selected from glycine-glycine-glycine, glycine-alanine-phenylalanine, glycine-phenylalanine-lysine, glycine-valine-citrulline and glycine-valine-lysine.
11. The drug-ligand conjugate compound of claim 2 , wherein n is 1, and A is attached to a Cys residue of L which is a protein, peptide or antibody.
12. The drug-ligand conjugate compound of claim 2 , wherein n is 1, and A has the structure:
where the wavy lines indicate the covalent attachment sites to a sulfur atom of L and to Z m , and wherein R 17 is selected from (CH 2 ) r , C 3 -C 8 carbocyclyl, O(CH 2 ) r , arylene, (CH 2 ) r -arylene, -arylene-(CH 2 ) r —,(CH 2 ) r —(C 3 -C 8 carbocyclyl), (C 3 -C 8 carbocyclyl)-(CH 2 ) r , C 3 -C 8 heterocyclyl, (CH 2 ) r —(C 3 -C 8 heterocyclyl), —(C 3 -C 8 heterocyclyl)-(CH 2 ) r —, —(CH 2 ) r C(O)NR b (CH 2 ) r ,—, —(CH 2 CH 2 O) r —, —(CH 2 CH 2 O) r —CH 2 —, —(CH 2 ) r C(O)NR b (CH 2 CH 2 O) r —, —(CH 2 ) r C(O)NR b (CH 2 CH 2 O) r —CH 2 —, —(CH 2 CH 2 O) r C(O)NR b (CH 2 CH 2 O) r —, —(CH 2 CH 2 O) r C(O)NR b (CH 2 CH 2 O) r —CH 2 —, and —(CH 2 CH 2 O) r C(O)NR b (CH 2 ) r —; where r is independently an integer ranging from 1-10.
13. The drug-ligand conjugate compound of claim 12 wherein R 17 is selected from (CH 2 ) 5 , (CH 2 ) 2 , (CH 2 CH 2 O) 2 CH 2 , and CH 2 CH 2 C(O)NH(CH 2 CH 2 O) 2 CH 2 .
14. The drug-ligand conjugate compound of claim 2 , wherein n is 1, and A is selected from 4-(N-succinimidomethyl)cyclohexane-1-carbonyl, m-succinimidobenzoyl, 4-(p-succinimidophenyl)butyryl, 4-(2-acetamido)benzoyl, 3-thiopropionyl, 4-(1-thioethyl)-benzoyl, and 6-(3-thiopropionylamido)-hexanoyl.
15. The drug-ligand conjugate compound of claim 2 , wherein D is an auristatin drug moiety.
16. The drug-ligand conjugate compound of claim 2 , wherein D is a drug moiety selected from N8-acetyl spermidine, actinomycin, 9-amino camptothecin, aminopterin, anguidine, anthracycline, bleomycin, butyric acid, calicheamicin, camptothecin, camptothecin, 1-(2chloroethyl)-1,2-dimethanesulfonyl hydrazide, cis-platin, daunorubicin, diacetoxypentyldoxorubicin, 1,8-dihydroxy-bicyclo[7.3.1]trideca-4,9-diene-2,6-diyne-13-one, doxorubicin, esperamicin, etoposide, maytansine, maytansinol, 6-mercaptopurine, methotrexate, mitomycin-C, mitomycin-A, morpholino-doxorubicin, retinoic acid, tallysomycin, taxol, vinblastine, and vincristine; and salt forms thereof.
17. The drug-ligand conjugate of claim 2 wherein L is an antibody which binds to one or more tumor-associated antigens or cell-surface receptors selected from the group consisting of BMPR1B, E16, STEAP1, 0772P, MPF, Napi3b, Sema 5b, PSCA hlg, ETBR, MSG783, STEAP2, TrpM4, CRIPTO, CD21, CD79b, FcRH2, HER2, NCA, MDP, IL20Rα, Brevican, Ephb2R, ASLG659, PSCA, GEDA , BAFF-R, CD22, CD79a, CXCR5, HLA-DOB, P2X5, CD72, LY64, FCRH1, IRTA2.
18. The drug-ligand conjugate compound of claim 2 , wherein L is a ligand selected from the group consisting of bombesin, EDG, transferrin, gastrin, gastrin-releasing peptide, platelet-derived growth factor, IL-2, IL-6, TFG-alpha, TFG-beta, VGF, insulin and insulin-like growth factors I and II.
19. The drug-ligand conjugate compound of claim 17 , wherein said antigen is HER2.