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ADC Related

Chemical Structure Cat. No. Product Name CAS No.
Rebeccamycin Chemical Structure
BCP41470 Rebeccamycin 93908-02-2
Rebeccamycin, an antitumor antibiotic, inhibits DNA topoisomerase I.
N-Succinimidyl 4-formylbenzoate Chemical Structure
BCP41302 N-Succinimidyl 4-formylbenzoate 60444-78-2
N-Succinimidyl 4-formylbenzoate is a useful protective group in antibody drug conjugates.
DSN28369 Chemical Structure
BCP41005 DSN28369 2413428-36-9
DSN28369 is a heterobifunctional linker, and useful to make antibody drug conjuate (ADC).
MP-PEG8-VA-PABC-PBD Dimer Chemical Structure
BCP40699 MP-PEG8-VA-PABC-PBD Dimer 1595275-62-9
Tesirine is a cathepsin B-cleavable valine-alanine pyrrolobenzodiazepine (PBD) dimer as antibody-drug conjugate (ADC) payload
Azido-PEG4-NHS Ester Chemical Structure
BCP40277 Azido-PEG4-NHS Ester 944251-24-5
NHS-PEG4-azide is a useful protective group in antibody drug conjugates.
N3-PEG3-C2-NHS ester Chemical Structure
BCP39814 N3-PEG3-C2-NHS ester 1245718-89-1
N3-PEG3-C2-NHS ester is a nonclaevable 3-unit PEG linker used in the synthesis of antibody-drug conjugates (ADCs).
N3-PEG2-C2-NHS ester Chemical Structure
BCP39813 N3-PEG2-C2-NHS ester 1312309-64-0
N3-PEG2-C2-NHS ester is a nonclaevable 2-unit PEG linker used in the synthesis of antibody-drug conjugates (ADCs).
Esperamicin A1 Chemical Structure
BCP39058 Esperamicin A1 99674-26-7
Esperamicin A1 is an enediyne antitumor antibiotics of bacterial origin; acts by binding to DNA and causes strand scission.
Duocarmycin MA Chemical Structure
BCP39048 Duocarmycin MA 1613286-57-9
Duocarmycin MA is an antibody drug conjugates (ADCs) toxin.
SuO-Val-Cit-PAB-MMAE Chemical Structure
BCP38506 SuO-Val-Cit-PAB-MMAE SVCPM
SuO-Val-Cit-PAB-MMAE is a drug-linker conjugate for ADC by using the anti-mitotic agent, monomethyl auristatin E (MMAE, a tubulin inhibitor), linked via the peptide SuO-Val-Cit-PAB.
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