DBCO-PEG8-VKG-CPT2
Based on 1 publication(s) in Google Scholar
DBCO-PEG8-VKG-CPT2 is a drug-linker conjugate for ADC. DBCO-PEG8-VKG-CPT2 consists of a topoisomerase 1 inhibitor (7-MAD-MDCPT) (HY-132162) and a stable and cleavable linker (DBCO-PEG8-VKG) (HY-175426). DBCO-PEG8-VKG-CPT2 can be used for synthesis of ADCs.
For research use only. We do not sell to patients.
- Formula: C73H93N9O20
- Molecular Weight:1416.57
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
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Biological Activity
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Chemical Information
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Publications Citing Use of MedChemExpress (MCE) DBCO-PEG8-VKG-CPT2
MoreAll Drug-Linker Conjugates for ADC Isoforms
MoreAll Topoisomerase Isoforms
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Biological Activity
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Topoisomerase I |
Chemical Information
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Molecular Weight 1416.57
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Formula C73H93N9O20
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SMILES
O=C(NCCOCCOCCOCCOCCOCCOCCOCCOCCC(N[C@@H](C(C)C)C(N[C@H](C(NCC(NCC1=C(C(C2=CC([C@@](CC)3O)=C4COC3=O)=NC5=CC6=C(C=C15)OCO6)CN2C4=O)=O)=O)CCCCN)=O)=O)CCC(N7C8=C(C#CC9=C(C7)C=CC=C9)C=CC=C8)=O
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Publications (1)
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Journal Impact Factor
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Most Recent
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
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