NZ583844A - Maytansinoid conjugates linked via a non-cleavable linker - Google Patents
Maytansinoid conjugates linked via a non-cleavable linkerInfo
- Publication number
- NZ583844A NZ583844A NZ583844A NZ58384404A NZ583844A NZ 583844 A NZ583844 A NZ 583844A NZ 583844 A NZ583844 A NZ 583844A NZ 58384404 A NZ58384404 A NZ 58384404A NZ 583844 A NZ583844 A NZ 583844A
- Authority
- NZ
- New Zealand
- Prior art keywords
- antibody
- ester
- cell
- maytansinoid
- dml
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 claims abstract description 13
- -1 sulfosuccinimidyl esters Chemical class 0.000 claims description 54
- 150000002148 esters Chemical class 0.000 claims description 41
- 125000004432 carbon atom Chemical group C* 0.000 claims description 24
- 229910052717 sulfur Inorganic materials 0.000 claims description 15
- 125000003342 alkenyl group Chemical group 0.000 claims description 11
- 125000003118 aryl group Chemical group 0.000 claims description 11
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 125000005842 heteroatom Chemical group 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 125000000304 alkynyl group Chemical group 0.000 claims description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 4
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 229940127089 cytotoxic agent Drugs 0.000 abstract description 4
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- 231100000599 cytotoxic agent Toxicity 0.000 abstract description 4
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- 125000005647 linker group Chemical group 0.000 description 110
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- 238000000034 method Methods 0.000 description 47
- JJAHTWIKCUJRDK-UHFFFAOYSA-N succinimidyl 4-(N-maleimidomethyl)cyclohexane-1-carboxylate Chemical compound C1CC(CN2C(C=CC2=O)=O)CCC1C(=O)ON1C(=O)CCC1=O JJAHTWIKCUJRDK-UHFFFAOYSA-N 0.000 description 36
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- 230000000694 effects Effects 0.000 description 28
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- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 26
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- WKPWGQKGSOKKOO-RSFHAFMBSA-N maytansine Chemical compound CO[C@@H]([C@@]1(O)C[C@](OC(=O)N1)([C@H]([C@@H]1O[C@@]1(C)[C@@H](OC(=O)[C@H](C)N(C)C(C)=O)CC(=O)N1C)C)[H])\C=C\C=C(C)\CC2=CC(OC)=C(Cl)C1=C2 WKPWGQKGSOKKOO-RSFHAFMBSA-N 0.000 description 12
- KIUMMUBSPKGMOY-UHFFFAOYSA-N 3,3'-Dithiobis(6-nitrobenzoic acid) Chemical compound C1=C([N+]([O-])=O)C(C(=O)O)=CC(SSC=2C=C(C(=CC=2)[N+]([O-])=O)C(O)=O)=C1 KIUMMUBSPKGMOY-UHFFFAOYSA-N 0.000 description 11
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- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 8
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- C07K16/3076—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells against structure-related tumour-associated moieties
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