DBCO-C4-Val-Cit-PABC-PNP

DBCO-C4-Val-Cit-PABC-PNP Catalog number: BADC-01342

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Category
ADCs Linker
Product Name
DBCO-C4-Val-Cit-PABC-PNP
Catalog Number
BADC-01342
Molecular Formula
C46H49N7O10
Molecular Weight
859.94
DBCO-C4-Val-Cit-PABC-PNP

Ordering Information

Catalog Number Size Price Quantity
BADC-01342 -- $--
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Synonyms
N-[6-(11,12-Didehydrodibenzo[b,f]azocin-5(6H)-yl)-6-oxohexanoyl]-L-valyl-N5-carbamoyl-N-[4-({[(4-nitrophenoxy)carbonyl]oxy}methyl)phenyl]-L-ornithinamide; L-Ornithinamide, N-[6-(11,12-didehydrodibenz[b,f]azocin-5(6H)-yl)-1,6-dioxohexyl]-L-valyl-N5-(aminocarbonyl)-N-[4-[[[(4-nitrophenoxy)carbonyl]oxy]methyl]phenyl]-
InChI
InChI=1S/C46H49N7O10/c1-30(2)42(51-40(54)15-7-8-16-41(55)52-28-34-12-4-3-10-32(34)19-20-33-11-5-6-14-39(33)52)44(57)50-38(13-9-27-48-45(47)58)43(56)49-35-21-17-31(18-22-35)29-62-46(59)63-37-25-23-36(24-26-37)53(60)61/h3-6,10-12,14,17-18,21-26,30,38,42H,7-9,13,15-16,27-29H2,1-2H3,(H,49,56)(H,50,57)(H,51,54)(H3,47,48,58)/t38-,42-/m0/s1
InChIKey
RJGJTFMRBABKDS-PIFUBOJPSA-N
Density
1.4±0.1 g/cm3
Appearance
Light Yellow Solid
Purity
≥95%
Storage
Store at -20°C
Boiling Point
1165.5±65.0°C at 760 mmHg

DBCO-C4-Val-Cit-PABC-PNP, a versatile chemical reagent, plays a pivotal role in targeted drug delivery and bioconjugation. Here are four key applications of this compound:

Antibody-Drug Conjugates (ADCs): At the forefront of cancer therapy, DBCO-C4-Val-Cit-PABC-PNP is extensively utilized in crafting antibody-drug conjugates. By linking a cytotoxic drug to an antibody through this versatile linker, targeted delivery to cancer cells is accomplished. This strategy not only amplifies therapeutic effectiveness but also mitigates harm to normal tissues, marking a breakthrough in precision medicine.

Click Chemistry: In the realm of bioorthogonal chemistry, this reagent shines in facilitating stable covalent bonds between biomolecules. Its strain-promoted alkyne-azide cycloaddition (SPAAC) capability enables specific and efficient linking without the need for a catalyst. This feature proves invaluable in labeling biomolecules for imaging or functional investigations, opening new avenues for innovative research in molecular biology.

Controlled Drug Release: Engineered for precision, DBCO-C4-Val-Cit-PABC-PNP responds to specific enzymes like cathepsin B, prevalent in tumor microenvironments. This unique attribute allows for the precise release of therapeutic agents directly at the designated target site, curtailing systemic side effects and optimizing drug efficacy. Such tailored drug delivery heralds a paradigm shift in cancer treatment.

Protein Modification: In the realm of protein engineering and biotechnology, this reagent serves as a cornerstone for protein modification with minimal perturbation to their native function. By conjugating therapeutic moieties or other functional groups to proteins, novel functionalities can be conferred, paving the way for advanced biopharmaceuticals and diagnostic tools. This innovative application underscores the transformative potential of DBCO-C4-Val-Cit-PABC-PNP in shaping the future of biotechnology.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Historical Records: DBCO-C4-Val-Cit-PABC-PNP
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