Boc-L-Sec(Mob)-OH

Hazmat

Chemical name: N-alpha-t-Butyloxycarbonyl-Se-(4-methoxybenzyl)-L-selenocysteine // Synonyms: Boc-Sec(PMB)-OH, Boc-Sec(pMeOBzl)-OH, (R)-2-(t-butoxycarbonylamino)-3-(4-methoxybenzylselanyl)propanoic acid, Boc-Sec(Mob)-OH

  • Product code:BAA3760
  • CAS No.:959415-39-5
  • Formula:C16H23NO5Se
  • Molecular weight:388.32 g/mol
  • Purity :min. 98%
  • Enantiomeric Purity:min. 99,9%

from $135.00

Grouped product items
Qty Packing unit Price SKU Availability
100 mg
$135.00
BAA3760.0100
<10 business days
250 mg
$225.00
BAA3760.0250
<10 business days
500 mg
$405.00
BAA3760.0500
<10 business days
1 g
$630.00
BAA3760.1000
<10 business days
5 g
$2,250.00
BAA3760.5000
<10 business days
Safety Data Sheets
description

Selenocysteine (Sec) is a natural amino acid and this building block can be used to incorporate it into a peptide sequence. Sec has also been used successfully for native chemical ligation (NCL), as selenium shows higher nucleophilicity than sulfur. Acylation with an amino acid will result in a selenium ester as intermediate. After SeàN acyl shift the thermodynamically more stable amid will result forming a natural amide bond. Deselenification can be carried out with reductive agents yielding alanine at this position in the peptide sequence.

references

Selenopeptide chemistry; Markus Muttenthaler, Paul F. Alewood; J. Pept. Sci. 2008; 14(12): 1223-1239. DOI: org/10.1002/psc.1075

Rapid Additive-Free Selenocystine−Selenoester Peptide Ligation; Nicholas J. Mitchell, Lara R. Malins, Xuyu Liu, Robert E. Thompson, Bun Chan, Leo Radom, and Richard J. Payne; J. Am. Chem. Soc. 2015; 137: 14011−14014. DOI: 10.1021/jacs.5b07237

Oxidative Deselenization of Selenocysteine: Applications for Programmed Ligation at Serine; Lara R. Malins, Nicholas J. Mitchell, Sheena McGowan, and Richard J. Payne; Angew. Chem. Int. Ed. 2015; 54: 12716 -12721. DOI: 10.1002/anie.201504639

Selenopeptide chemistry; Markus Muttenthaler, Paul F. Alewood; J. Pept. Sci. 2008; 14(12): 1223-1239. DOI: org/10.1002/psc.1075

Synthesis of selenocysteine peptides and their oxidation to diselenide‐bridged compounds; Dörthe Besse, Luis Moroder; J. Peptide Sci. 1997; 3(6): 442-453. DOI: org/10.1002/(SICI)1099-1387(199711)3:6<442::AID-PSC122>3.0.CO;2-2

Synthetic study on selenocystine containing peptides; Takaki Koide, Hiromi Itoh, Akira Otaka, , Hiroyuki Yasui, Masataka Kuroda, Nobuyoshi Esaki, Kenji Soda, Nobutaka Fujii; Chem. Pharm. Bull. 1993; 41(3): 502-506. DOI: org/10.1248/cpb.41.502

Syntheses and Biological Activities of Selenium Analogs of α-Rat Atrial Natriuretic Peptide; Takaki Koide, Hiromi Itoh, Akira Otaka, Mayumi Furuya, Yasuo Kitajima, Nobutaka Fujii; Chem. Pharm. Bull. 1993; 41(9): 1596-1600 . DOI: org/10.1248/cpb.41.1596


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