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Monobenzyloxycarbonyl-L-cystine (MBC-L-cystine) is a chemical compound derived from the amino acid L-cystine, which is a dimeric form of cysteine. MBC-L-cystine is formed by attaching a benzyloxycarbonyl (Cbz) protecting group to the amino group of L-cystine. This modification is commonly used in peptide synthesis to protect the thiol group of cysteine, preventing unwanted side reactions and ensuring the correct formation of disulfide bonds during peptide assembly. The Cbz group can be removed under mild acidic conditions, allowing for the subsequent steps in peptide synthesis. MBC-L-cystine plays a crucial role in the synthesis of peptides and proteins containing cysteine residues, as it helps maintain the integrity of the peptide chain and facilitates the formation of the desired disulfide bond patterns.

6304-83-2

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6304-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6304-83-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6304-83:
(6*6)+(5*3)+(4*0)+(3*4)+(2*8)+(1*3)=82
82 % 10 = 2
So 6304-83-2 is a valid CAS Registry Number.

6304-83-2Relevant academic research and scientific papers

Protein folding: The synthesis and conformational studies on cystinyl- cystinyl-cystine [-CSSCCSSCCSSC-] a novel cross linking motif

Ranganathan, Subramania,Tamilarasu, Natarajan,Roy, Raja

, p. 9823 - 9834 (2007/10/03)

The cysteine capped, ends protected cross linked motifs 6 and 7, arising from pairs of proximally placed cysteines wherein within a 22 atom framework are inscribed 3 disulphide bridges and 2 peptide linkage, have been prepared and their conformations derived by detailed 1H NMR studies and molecular modeling protocols, where excellent agreement was seen. Both compounds 6 and 7 possess a C2 symmetric hydrogen bonded pair involving the peptide NH and the CO of the proximate N-protecting group (Boc or Z). The nature of the latter profoundly influences the conformation. Thus, in 6 where the unit is Boc a bend conformation was promoted by hydrophobic interactions; alternatively in 7 with a Z-protecting group the conformation was linear. Compounds 6 and 7 have much promise in diverse aspects of protein design.

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