ADCs Cytotoxin with Linkers
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ADCs Cytotoxin with Linkers

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Catalog Product Name CAS Number
BADC-00755 DBCO-PEG4-VA-PBD
DBCO-PEG4-VA-PBD is a drug-linker conjugate for ADC by using PBD (Pyrrolobenzodiazepine dimers, a potent antitumor antibiotic), linked via DBCO-PEG4-VA. Inquiry
BADC-00756 DBCO-PEG4-vc-PAB-MMAF
DBCO-PEG4-vc-PAB-MMAF is a drug-linker conjugate for ADC by using Monomethylauristatin F (MMAF, a potent tubulin polymerization inhibitor), linked via DBCO-PEG4-vc-PAB. Inquiry
BADC-00757 DBCO-PEG4-vc-PAB-MMAD
DBCO-PEG4-vc-PAB-MMAD is a drug-linker conjugate for ADC by using Monomethyl Dolastatin 10 (MMAD, a potent tubulin inhibitor), linked via DBCO-PEG4-vc-PAB. Inquiry
BADC-00758 DBCO-PEG4-vc-PAB-Duocarmycin TM
DBCO-PEG4-vc-PAB-Duocarmycin TM is a drug-linker conjugate for ADC by using Duocarmycin TM (a potent antitumor antibiotic), linked via DBCO-PEG4-vc-PAB. Inquiry
BADC-00759 DBCO-PEG4-vc-PAB-(PEG2)-Duocarmycin TM
DBCO-PEG4-vc-PAB-(PEG2)-Duocarmycin TM is a drug-linker conjugate for ADC by using Duocarmycin TM (a potent antitumor antibiotic), linked via DBCO-PEG4-vc-PAB-(PEG2). Inquiry
BADC-00760 DBCO-PEG4-vc-PAB-Duocarmycin DM
DBCO-PEG4-vc-PAB-Duocarmycin DM is a drug-linker conjugate for ADC by using Duocarmycin DM (a potent antitumor antibiotic), linked via DBCO-PEG4-vc-PAB. Inquiry
BADC-00761 DBCO-PEG4-vc-PAB-(PEG2)-Duocarmycin DM
DBCO-PEG4-vc-PAB-(PEG2)-Duocarmycin DM is a drug-linker conjugate for ADC by using Duocarmycin DM (a potent antitumor antibiotic), linked via DBCO-PEG4-vc-PAB-(PEG2). Inquiry
BADC-00762 DBCO-PEG4-VC-PAB-DMEA-PNU159682 2259318-56-2
DBCO-PEG4-VC-PAB-DMEA-PNU159682 is a drug-linker conjugate for ADC by using PNU159682 (a potent DNA topoisomerase II inhibitor), linked via DBCO-PEG4-VC-PAB-DMEA. Inquiry
BADC-00763 DBCO-PEG4-DMEA-PNU159682
DBCO-PEG4-DMEA-PNU159682 is a drug-linker conjugate for ADC by using PNU159682 (a potent DNA topoisomerase II inhibitor), linked via DBCO-PEG4-DMEA. Inquiry
BADC-00764 DBCO-PEG4-GGFG-DX8951
DBCO-PEG4-GGFG-DX8951 is a drug-linker conjugate for ADC by using DX8951 (Synonyms: Exatecan, a DNA topoisomerase I inhibitor), linked via DBCO-PEG4-GGFG. Inquiry
BADC-00765 DBCO-PEG4-vc-PAB-Ahx-DM1
DBCO-PEG4-vc-PAB-Ahx-DM1 is a drug-linker conjugate for ADC by using DM1 (Maytansinoid DM1, a microtubulin inhibitor), linked via DBCO-PEG4-vc-PAB-Ahx. Inquiry
BADC-00766 DBCO-PEG8-VA-PAB-SG3199
DBCO-PEG8-VA-PAB-SG3199 is a drug-linker conjugate for ADC by using SG3199 (a PBD dimer,has a potently cytotoxic against cancer cell lines), linked via DBCO-PEG8-VA-PAB. Inquiry
BADC-00768 Gly3-MMAF
Gly3-MMAF is a drug-linker conjugate for ADC by using Monomethylauristatin F (MMAF,a potent tubulin polymerization inhibitor), linked via Gly3. Inquiry
BADC-00769 Gly5-Ahx-DM1
Gly5-Ahx-DM1 is a drug-linker conjugate for ADC by using DM1 (Maytansinoid DM1, a microtubulin inhibitor), linked via Gly5-Ahx. Inquiry
BADC-00770 PNU159682-EDA-Gly3
PNU159682-EDA-Gly3 is a drug-linker conjugate for ADC by using PNU159682 (a potent DNA topoisomerase II inhibitor), linked via EDA-Gly3. Inquiry
BADC-00847 CL2-SN-38 1036969-20-6
CL2-SN-38 is a cleavable linker-based antibody-drug conjugate (ADC) containing the topoisomerase I inhibitor SN-38 and a maleimidocaproyl linker. Inquiry
BADC-00848 MC-DM1 1375089-56-7
MC-DM1 is a drug-linker conjugate composed of a potent microtubule-disrupting agent DM1 and a linker MC to make antibody drug conjugate (ADC). Inquiry
BADC-00850 MC-VC-PABC-Aur0101 1438849-92-3
MC-VC-PABC-Aur0101 is a drug-linker conjugate for ADC with potent antitumor activity by using Aur0101 (an auristatin microtubule inhibitor), linked via the ADC linker MC-VC-PABC. Inquiry
BADC-00851 Tesirine 1595275-62-9
Tesirine (SG3249) is a drug-linker conjugates for ADC which is used in the treatment of several cancers. PBD Dimer is a DNA alkylating which inhibits DNA replication. Inquiry
BADC-00853 MC-VC-PABC-DNA31 1639352-03-6
MC-VC-PABC-DNA31 is a drug-linker conjugate for ADC with potent antitumor activity by using DNA31 (a potent RNA polymerase inhibitor), linked via the ADC linker MC-VC-PABC. Inquiry
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