Fmoc-3VVD-OH
Fmoc-3VVD-OH Basic information
- Product Name:
- Fmoc-3VVD-OH
- Synonyms:
-
- (5S,9S,11S,12R)-11-((S)-sec-butyl)-1-(9H-fluoren-9-yl)-5,9-diisopropyl-12-Methoxy-4,10-diMethyl-3,6,8-trioxo-2-oxa-4,7,10-triazatetradecan-14-oic acid
- Fmoc-3AA-orl
- FMOC-3AA-OH
- Fmoc-3vvd-OH
- Tripeptide (MMAE-3)
- Fmoc-Meval-val-dolaisoleucine-OH
- (5S,8S,11S,12R)-11-((S)-sec-butyl)-1-(9H-fluoren-9-yl)-5,8-diisopropyl-12-methoxy-4,10-dimethyl-3,6,9-trioxo-2-oxa-4,7,10-triazatetradecan-14-oic acid
- L-Valinamide, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-valyl-N-[(1S,2S)-1-[(1R)-2-carboxy-1-methoxyethyl]-2-methylbutyl]-N-methyl-
- CAS:
- 863971-44-2
- MF:
- C36H51N3O7
- MW:
- 637.81
- Product Categories:
-
- ADCs Linkers
- ADCs
- ADC LINKER
- Mol File:
- 863971-44-2.mol
Fmoc-3VVD-OH Chemical Properties
- Boiling point:
- 793.0±60.0 °C(Predicted)
- Density
- 1.144±0.06 g/cm3(Predicted)
- solubility
- DMSO: ≥ 37 mg/mL (58.01 mM)
- pka
- 4.08±0.10(Predicted)
- form
- Solid
- color
- White to off-white
- Water Solubility
- Water: < 0.1 mg/mL (insoluble)
- InChIKey
- JDMOCVJBADMSJP-FCUBIXSHSA-N
- SMILES
- C(NC(=O)[C@H](C(C)C)N(C(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O)C)(=O)[C@H](C(C)C)N([C@H]([C@H](OC)CC(O)=O)[C@@H](C)CC)C
Fmoc-3VVD-OH Usage And Synthesis
Description
Fmoc-3vvd-OH, chemically known as (5S,9S,11S,12R)-11-((S)-sec-butyl)-1-(9H-fluoren-9-yl)-5,9-diisopropyl-12-methoxy-4,10-dimethyl-3,6,8-trioxo-2-oxa-4,7,10-triazatetradecan-14-oic acid, is an antibody-drug conjugate (ADC) linker. Fmoc-3vvd-OH is also an intermediate in the synthesis of MMAE. The Fmoc protecting group can be removed with a base (usually piperidine) to reveal the methylated N-terminus of the peptide.
Uses
Fmoc-3VVD-OH is a cleavable ADC linker for antibody-drug conjugate (ADC) synthesis.
Biological Activity
Fmoc-3VVD-OH is a non-cleavable ADC linker for 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.
in vivo
ADCs consist of antibodies linked to ADC cytotoxins through ADC linkers.
target
Cleavable
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