| Identification | Back Directory | [Name]
Fmoc-Val-Ala-pAB-PNP | [CAS]
1394238-92-6 | [Synonyms]
Fmoc-Val-Ala-pAB-PNP
Fmoc-Val-Ala-pAB-PNP USP/EP/BP
L-Alaninamide, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-valyl-N-[4-[[[(4-nitrophenoxy)carbonyl]oxy]methyl]phenyl]- | [Molecular Formula]
C37H36N4O9 | [MDL Number]
MFCD28557283 | [MOL File]
1394238-92-6.mol | [Molecular Weight]
680.7 |
| Questions And Answer | Back Directory | [Uses]
Fmoc-Val-Ala-PAB-PNP is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | [In vitro]
ADCs are comprised of an antibody to which is attached an ADC cytotoxin through an ADC linker. MCE has not independently confirmed the accuracy of these methods. They are for reference only. | [Storage]
Please store the product under the recommended conditions in the Certificate of Analysis. |
| Chemical Properties | Back Directory | [Boiling point ]
931.4±65.0 °C(Predicted) | [density ]
1.322±0.06 g/cm3(Predicted) | [form ]
Solid | [pka]
10.63±0.46(Predicted) | [color ]
White to light yellow |
| Hazard Information | Back Directory | [Description]
Fmoc-Val-Ala-PAB-PNP can be used to design cleavable ADC linkers. The Val-Ala, as shown in the ACD Zynlonta, is effectively cleaved by lysosomal proteolytic enzymes while being highly stable in human plasma. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. |
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