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  • Drug-Linker Conjugates for ADC
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nemorubicin

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    7
    TargetMol | Inhibitors_Agonists
  • PROTAC Products
    3
    TargetMol | PROTAC
Nemorubicin
PNU-152243A, PNU 152243, Methoxymorpholinyldoxorubicin
T4469108852-90-0
Nemorubicin (PNU 152243) is a doxorubicin derivative that differs significantly from its parent drug in terms of spectrum of antitumor activity, metabolism and toxicity profile. The drug is active on tumors resistant to alkylating agents, topoisomerase II inhibitors and platinum derivatives.
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Nemorubicin HCL
T71467108943-08-4
Nemorubicin HCL is the salt form of Nemorubicin, also known as PNU152243A, a doxorubicin derivative that differs significantly from its parent drug in terms of spectrum of antitumor activity, metabolism and toxicity profile. The drug is active on tumors resistant to alkylating agents, topoisomerase II inhibitors and platinum derivatives. It works primarily through topoisomerase I inhibition. Of note, Nemorubicin is active in cells with upregulation of the nucleotide excision repair (NER) pathway, where current therapies fail. Nemorubicin is biotransformed in the liver into cytotoxic metabolites that may further contribute to render this drug highly active against primary liver tumors or liver metastases.
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1-2 weeks
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Mal-PEG4-VC-PAB-DMEA-PNU-159682
T182922259318-52-8
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].
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DBCO-PEG4-VC-PAB-DMEA-PNU-159682
T178022259318-56-2
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].
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DMEA-PNU-159682 dichloroacetate
T877161799421-49-0
Dichloroacetate DMEA-PNU-159682 (molecule D12) is a potent ADC cytotoxin that incorporates metabolites of nemorubicin (MMDX) derived from liver microsomes, and the powerful ADC cytotoxin, PNU-159682 [1] [2].
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Mal-Phe-C4-VC-PAB-DMEA-PNU-159682
T183022259318-54-0
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].
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IDP-73152
T714651091682-50-6
IDP-73152 is a peptide deformylase inhibitor.
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8-10 weeks
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