| Identification | Back Directory | [Name]
L-Ornithinamide, N-[25-(9H-fluoren-9-yl)-1,23-dioxo-4,7,10,13,16,19,24-heptaoxa-22-azapentacos-1-yl]-L-valyl-N5-(aminocarbonyl)-N-[4-(hydroxymethyl)phenyl]- | [CAS]
2055024-57-0 | [Synonyms]
Fmoc-PEG6-Val-Cit-PAB-OH
FmocNH-PEG6-C2-Val-Cit-PAB-OH
L-Ornithinamide, N-[25-(9H-fluoren-9-yl)-1,23-dioxo-4,7,10,13,16,19,24-heptaoxa-22-azapentacos-1-yl]-L-valyl-N5-(aminocarbonyl)-N-[4-(hydroxymethyl)phenyl]- | [Molecular Formula]
C48H68N6O13 | [MOL File]
2055024-57-0.mol | [Molecular Weight]
937.09 |
| Hazard Information | Back Directory | [Uses]
Fmoc-PEG6-Val-Cit-PAB-OH is an enzyme-cleavable ADC linker featuring a Boc-protected amine, a hydrophilic PEG spacer, and a Val-Cit-PAB dipeptide. The benzylic alcohol on the PAB can be used to attach with reactive groups such as PNP for conjugation with drug payloads. The Fmoc protecting group may be removed with piperidine to reveal a primary amine which may be used in coupling reactions to form amides. The Val-Cit-PAB is cleaved by cellular proteases for efficient release of payloads to the cell. |
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