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ADC Related

Chemical Structure Cat. No. Product Name CAS No.
Boc-Val-Cit-OH Chemical Structure
BCP36570 Boc-Val-Cit-OH 870487-08-4
Boc-Val-Cit-OH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
Vc-seco-duba Chemical Structure
BCP36557 Vc-seco-duba 1345681-58-4
Vc-seco-DUBA is a drug-linker conjugate for ADC with potent antitumor activity by using DUBA (DNA alkylating agent), linked via the ADC linker Vc-seco.
SPDB-DM4 Chemical Structure
BCP36463 SPDB-DM4 1626359-62-3
SPDB-DM4 is a drug-linker conjugate for ADC by using the maytansinebased payload (DM4, a tubulin inhibitor) via a SPDB linker, exhibiting potent anti-tumor activity.
N-Me-L-Ala-maytansinol Chemical Structure
BCP36454 N-Me-L-Ala-maytansinol 77668-69-0
N-Me-L-Ala-maytansinol is a hydrophobic, cell permeable payload used for making antibody-drug conjugate (ADC).
N-Me-D-Ala-maytansinol Chemical Structure
BCP36456 N-Me-D-Ala-maytansinol 77714-98-8
DBCO-C6-acid Chemical Structure
BCP36341 DBCO-C6-acid 1425485-72-8
DBCO-C6-acid is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). DBCO-C6-acid can be used in the synthesis of carmaphycin analogues.
Deruxtecan analog Chemical Structure
BCP36306 Deruxtecan analog 1599440-13-7
Deruxtecan is an ADC drug-linker conjugate composed of a derivative of DX-8951 (DXd) and a maleimide-GGFG peptide linker, used for synthesizing DS-8201 and U3-1402.
Vipivotide tetraxetan Linker Chemical Structure
BCP35796 Vipivotide tetraxetan Linker 1703768-74-4
Vipivotide tetraxetan Linker is a nonclaevable peptide linker for synthesis of Vipivotide tetraxetan (PSMA-617). Vipivotide tetraxetan (PSMA-617) is a ligand used to synthesize 177Lu-PSMA-617, which is a radioactive molecule for the treatment of prostate cancer.
Vipivotide tetraxetan Chemical Structure
BCP35795 Vipivotide tetraxetan 1702967-37-0
Vipivotide tetraxetan is a high potent prostate-specific membrane antigen (PSMA) inhibitor, with a Ki of 0.37 nM.
SMCC Chemical Structure
BCP35089 SMCC 71875-81-5
SMCC is a useful protective group in antibody drug conjugates.
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