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Boc-L-Sec(Mob)-OPfp
Nom chimique: N-alpha-tert-Butoxycarbonyl-4-methoxybenzyl-L-selenocysteine pentafluorophenyl ester // Synonymes: Boc-L-Sec(pMeOBzl)-OPfp, Boc-Sec(MBzl)-OPfp, Boc-L-Sec(Pmb)-OPfp, Boc-Sec(Mob)-OPfp, Boc-L-4-methoxybenzyl selenocysteine petafluorophenyl ester, 2,3,4,5,6-pentafluorophenyl(2R)-2-{[(tert-butoxy)car bonyl]amino}-3-{[(4-methoxyphenyl)methyl]selanyl}p
- n° Art.:BAA4830
- n° CAS:1257525-48-6
- Formule:C22H22F5NO5Se
- Storage temperature:-20°C
- Masse moléculaire:554,38 g/mol
- Pureté:min. 98%
- Pureté Énantiomérique:min. 99,7%
from 192,00 €
description
Isomeric purity >99.9%. Building block for the introduction of selenocysteine by SPPS in the terminal position. Due to difficult coupling of Boc-Sec(Mob), this is an alternative building block for introduction of Sec residue into peptides.
Peptides containing selenocysteine can be cleaved from the resin with simultaneous side-chain deprotection by treatment with 5% (v/v) water, 95% (v/v) trifluoroacetic acid (TFA), 0.4 M 2,2’-dithiobis(5-nitropyridine) (DTNP) for 7 min at 60 °C or 2 h at RT.
references
Reference:
Selenoglutaredoxin as a Glutathione Peroxidase Mimic; G. Casi, G. Roelfes, D. Hilvert; ChemBioChem 2008; 9(10): 1623-1631. https://doi.org/10.1002/cbic.200700745.
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