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Benzyloxycarbonyl-L-glutamin-cyanmethylester, also known as Z-Gln-CH2CN, is a chemical compound that serves as a protected amino acid derivative. It is a key component in peptide synthesis, where it is used to protect the side chain of glutamine (Gln) during the formation of peptide bonds. The benzyloxycarbonyl (Z) group is a temporary protecting group that shields the amino group of glutamine, preventing unwanted side reactions. The cyanomethyl ester (CH2CN) group is another protecting group that masks the carboxylic acid group of glutamine, allowing for controlled peptide bond formation. Benzyloxycarbonyl-L-glutamin-cyanmethylester is crucial in the synthesis of peptides and proteins, as it enables the stepwise assembly of amino acids into longer chains while maintaining the desired sequence and protecting the reactive groups from unwanted reactions.

4840-35-1

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4840-35-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4840-35-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,4 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4840-35:
(6*4)+(5*8)+(4*4)+(3*0)+(2*3)+(1*5)=91
91 % 10 = 1
So 4840-35-1 is a valid CAS Registry Number.

4840-35-1Relevant academic research and scientific papers

Antineoplastic agents. 2. Structure-activity studies on N-protected vinyl, 1,2-dibromoethyl, and cyanomethyl esters of several amino acids

Loeffler,Sajadi,Hall

, p. 1584 - 1588 (2007/10/08)

Previously reported work on N-protected activated esters of phenylalanine has been extended to include N-protected vinyl, dibromoethyl, and cyanomethyl esters of several other amino acids. These compounds have been synthesized and evaluated in Ehrlich ascites carcinoma, Walker 256 carcinosarcoma, and P388 lymphocytic leukemia tests. Among compounds tested were derivatives of tyrosine, tryptophan, glycine, leucine, proline, aspartic acid, glutamic acid, 4-aminobutyric acid, and 6-aminocaproic acid. Compounds of greatest potential interest from this study are N-carbobenzoxyglycine 1,2-dibromoethyl ester and N-carbobenzoxy-L-leucine 1,2-dibromoethyl ester. Both compounds were highly active in Ehrlich ascites test systems (33 mg/kg/day). The glycine derivative was also active in the Walker 256 test (2.5 mg/kg/day). Values for LD50's in mice were 148 mg/kg (0.37 mmol/kg) and 225 mg/kg (0.50 mmol/kg) for glycine and leucine derivatives, respectively; therefore, these compounds do not appear to be toxic at effective dose levels.

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