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Z-β-Ala-Arg(NO2)-OBzl is a synthetic peptide compound consisting of four amino acids: Z (benzyloxycarbonyl), β-alanine, arginine with a nitro group (Arg(NO2)), and benzyloxycarbonyl (OBzl). Z-β-Ala-Arg(NO2)-OBzl is often used in chemical research and drug development due to its unique structure and properties. The Z group is a protecting group that shields the carboxylic acid group, while the OBzl group protects the amino group. The β-alanine and Arg(NO2) residues contribute to the peptide's overall structure and potential biological activity. Z-β-Ala-Arg(NO2)-OBzl is a versatile molecule that can be used as a building block for the synthesis of more complex peptides or as a probe to study protein-protein interactions and enzymatic activities.

97488-05-6

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97488-05-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97488-05-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,4,8 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 97488-05:
(7*9)+(6*7)+(5*4)+(4*8)+(3*8)+(2*0)+(1*5)=186
186 % 10 = 6
So 97488-05-6 is a valid CAS Registry Number.

97488-05-6Downstream Products

97488-05-6Relevant academic research and scientific papers

Tuftsin Analogues: Synthesis, Structure-Function Relationships, and Implications for Specificity of Tuftsin's Bioactivity

Dagan, Shlomo,Gottlieb, Philip,Tzehoval, Esther,Feldman, Michael,Fridkin, Mati,et al.

, p. 1961 - 1968 (1986)

Thirteen analogues of the natural macrophage activator peptide tuftsin, ten of which are novel, were synthesized with the aim of exploring the relation between their biological potency and their capacity to attach specifically to cellular tuftsin's recept

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