DBCO-Val-Cit-PABC-PNP

DBCO-Val-Cit-PABC-PNP

• UNSPSC Description: DBCO-Val-Cit-PABC-PNP is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]. DBCO-Val-Cit-PABC-PNP is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.
• Target Antigen: ADC Linker
• Type: ADC Related
• Related Pathways: Antibody-drug Conjugate/ADC Related
• Field of Research: Cancer
• Assay Protocol: https://www.medchemexpress.com/dbco-val-cit-pabc-pnp.html
• Purity: 96.54
• Solubility: DMSO : 100 mg/mL (ultrasonic)
• Smiles: CC([C@@H](C(N[C@H](C(NC1=CC=C(C=C1)COC(OC2=CC=C(C=C2)[N+]([O-])=O)=O)=O)CCCNC(N)=O)=O)NC(CCCCC(N3CC4=C(C#CC5=C3C=CC=C5)C=CC=C4)=O)=O)C
• Molecular Weight: 859.92
• References & Citations: [1]Beck A, et al. Strategies and challenges for the next generation of antibody-drug conjugates. Nat Rev Drug Discov. 2017 May;16(5):315-337.
• Shipping Conditions: Blue Ice
• Storage Conditions: -20°C (Powder, sealed storage, away from moisture)
• Clinical Information: No Development Reported