dmea-pnu159682

MPB-VC-PAB-DMEA-PNU159682 is a thiol-reactive Drug-linker. PNU159682 is a DNA topoisomerase II (Topo II) inhibitor, which is commonly used in the synthesis of antibody-drug conjugates (ADCs).

MC-VC-PAB-DMEA-PNU159682 is a thiol-reactive Drug-linker. PNU159682 is a DNA topoisomerase II (Topo II) inhibitor, which is commonly used in the synthesis of antibody-drug conjugates (ADCs).

DBCO-PEG4-DMEA-PNU159682 is a click-reactive Drug-linker that contains a DBCO group and can undergo strain-promoted acetylene-nitridation cycloaddition reaction (SPAAC) with molecules containing Azide groups. PNU159682 is a DNA topoisomerase II (Topo II) inhibitor with excellent cytotoxicity. DBCO-PEG4-DMEA-PNU159682 can be used in the synthesis of antibody-drug conjugates (ADC).

DBCO-PEG4-GGFG-DMEA-PNU159682 is a click-reactive Drug-linker that contains a DBCO group and can undergo strain-promoted acetylene-nitride cycloaddition reaction (SPAAC) with molecules containing Azide groups. PNU159682 is a DNA topoisomerase II (Topo II) inhibitor. DBCO-PEG4-GGFG-DMEA-PNU159682 can be used in the synthesis of antibody-drug conjugates (ADC).

NH2-VC-PAB-DMEA-PNU159682 is a transpeptidase reaction-type Drug-linker with an innovative highly stable and degradable linker. PNU159682 is a DNA topoisomerase II (Topo II) inhibitor with excellent cytotoxicity, which can be used in the synthesis of antibody-drug conjugates (ADCs).

NH2-PEG3-DMEA-PNU159682 is a transpeptidase reaction-type Drug-linker with an innovative highly stable and degradable linker. PNU159682 is a DNA topoisomerase II (Topo II) inhibitor with excellent cytotoxicity, which can be used in the synthesis of antibody-drug conjugates (ADCs).

VA-PAB-DMEA-PNU159682 is a transpeptidase reaction-type Drug-linker with an innovative highly stable and degradable linker. PNU159682 is a DNA topoisomerase II (Topo II) inhibitor with excellent cytotoxicity and can be used in the synthesis of antibody-drug conjugates (ADCs).

Compound I.47 (vc-PAB-DMEA-PNU159682) is utilized in the synthesis of ADC molecules using a Sulfomaleimide-based linker. This compound demonstrates good serum stability [1].

C-lock-G5-DUO-5 is a Drug-linker. DUO-5 is a microtubule inhibitor, a novel toxin molecule with anti-cancer activity. It is connected to C-lock-G5 through a stable covalent irreversible linkage, re-introducing covalent bonding, achieving better stability and improved PK characteristics.

DMEA-PNU-159682 (molecule D12) is an ADC cytotoxin molecule that includes neomycin (MMDX) metabolites from liver microsomes and the effective ADC cytotoxin PNU-159682.

DBCO-PEG4-VC-PAB-DMEA-PNU-159682, a drug-linker conjugate for antibody-drug conjugates (ADC), comprises the ADC linker DBCO-PEG4-VC-PAB and the potent ADC cytotoxin DMEA-PNU-159682, which includes metabolites of nemorubicin (MMDX) from liver microsomes and the ADC cytotoxin PNU-159682[1].

Mal-PEG4-VC-PAB-DMEA-PNU-159682 is a drug-linker conjugate designed for antibody-drug conjugate (ADC) therapy. It combines the ADC linker, Mal-PEG4-VC-PAB, with the potent ADC cytotoxin, DMEA-PNU-159682. The cytotoxin, DMEA-PNU-159682, is derived from metabolites of nemorubicin (MMDX) found in liver microsomes, as well as the ADC cytotoxin PNU-159682 [1].

Mal-Phe-C4-VC-PAB-DMEA-PNU-159682 is a drug-linker conjugate utilized in antibody-drug conjugate (ADC) therapy. It comprises the ADC linker Mal-Phe-C4-VC-PAB and the potent ADC cytotoxin DMEA-PNU-159682, which encompasses metabolites of nemorubicin (MMDX) derived from liver microsomes, as well as the ADC cytotoxin PNU-159682 [1].