Cyclooctyne-O-amido-PEG4-VC-PAB-Gly-Gly-NH-O-CO-Exatecan

Catalog No.: A41450
Drug-Linker Conjugates for ADC
Cyclooctyne-O-amido-PEG4-VC-PAB-Gly-Gly-NH-O-CO-Exatecan is a specialized drug-linker conjugate designed for antibody-drug conjugate (ADC) applications. This compound features an Exatecan cytotoxin, which targets and inhibits DNA topoisomerase I, leading to apoptotic cell death in cancer cells. It is ideal for research in targeted cancer therapies, enhancing the effectiveness of ADCs while minimizing systemic toxicity.
Grouped product items
Size Price Stock Qty
1mg
$385.00
In stock
5mg
$985.00
In stock
Bulk Size
Bulk Discount
Free Delivery on orders over $500
Research use only. We do not sell to patients.

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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
Science VOLUME 369, ISSUE 6510 (2020)
Science VOLUME 356, ISSUE 6336 (2017)
Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
DescriptionCyclooctyne-O-amido-PEG4-VC-PAB-Gly-Gly-NH-O-CO-Exatecan is a specialized drug-linker conjugate designed for antibody-drug conjugate (ADC) applications. This compound features an Exatecan cytotoxin, which targets and inhibits DNA topoisomerase I, leading to apoptotic cell death in cancer cells. It is ideal for research in targeted cancer therapies, enhancing the effectiveness of ADCs while minimizing systemic toxicity.
Product Information
Catalog NumA41450
FormulaC69H90FN11O19
Molecular Weight1396.51
CAS Number2699066-62-9
SMILESO=C(COC1CCCCCC#C1)NCCOCCOCCOCCOCCC(N[C@@H](C(C)C)C(N[C@@H](CCCNC(N)=O)C(NC(C=C2)=CC=C2COC(NCC(NCOCC(N[C@@H]3C4=C5C(C(N6C5)=CC([C@](O)(C(OC7)=O)CC)=C7C6=O)=NC8=CC(F)=C(C)C(CC3)=C84)=O)=O)=O)=O)=O)=O
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