Boc-Cys(Acm)-OH

CAS: 19746-37-3

Ref. 3D-FB36789

Produktinformation

• Name: Boc-Cys(Acm)-OH
• Synonyme: <span class="text-smallcaps">L</span>-Cysteine, S-[(acetylamino)methyl]-N-[(1,1-dimethylethoxy)carbonyl]-, Alanine, 3-[(acetamidomethyl)thio]-N-carboxy-, N-tert-butyl ester, <span class="text-smallcaps">L</span>-, N-T-boc-S-acetamidomethyl-L-cysteine, N-tert-Butoxycarbonyl-S-(acetamidomethyl)-<span class="text-smallcaps">L</span>-cysteine, S-[(Acetylamino)methyl]-N-[(1,1-dimethylethoxy)carbonyl]-<span class="text-smallcaps">L</span>-cysteine, S-[(acetylamino)methyl]-N-(tert-butoxycarbonyl)-D-cysteine, S-[(acetylamino)methyl]-N-(tert-butoxycarbonyl)-L-cysteine
• CAS: 19746-37-3

Beschreibung

Boc-Cys(Acm)-OH is an amide that is used in the preparation of trifluoroacetic acid and its derivatives. It has acidic properties and a diversity of chemical reactions, including receptor binding. Boc-Cys(Acm)-OH is synthesized by solid-phase synthesis from acyl chloride and Cys(Acm) in the presence of a base such as triethylamine or pyridine. The compound is characterized as having natriuretic, brain natriuretic peptide (BNP), inhibitory effects on cellular growth, and hydrogen fluoride scavenging activity. Boc-Cys(Acm)-OH also has anti-anorectic properties due to its disulfide bond, which prevents it from being hydrolyzed into two amino acids.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 292.35 g/mol
• Formel: C₁₁H₂₀N₂O₅S
• Reinheit: Min. 95%
• InChl: InChI=1S/C11H20N2O5S/c1-7(14)12-6-19-5-8(9(15)16)13-10(17)18-11(2,3)4/h8H,5-6H2,1-4H3,(H,12,14)(H,13,17)(H,15,16)/t8-/m0/s1
• InChI Key: InChIKey=HLCTYBOTPCIHTG-QMMMGPOBSA-N
• SMILES: CC(=O)NCSC[C@H](NC(=O)OC(C)(C)C)C(=O)O