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Z-L-Arg(NO2)-L-Pro-NHEt is a synthetic tripeptide composed of three amino acids: Z-L-arginine (with a nitro group), L-proline, and N-hydroxyethyl-L-proline. The "Z" group, or benzyloxycarbonyl, is a protecting group used in peptide synthesis to prevent unwanted side reactions. The nitro group (NO2) is attached to the arginine, which can affect the peptide's reactivity and properties. This specific sequence and structure of amino acids may have unique biological activities or be used as a building block in the synthesis of larger peptides or proteins. The nitro group on the arginine can also be significant in terms of the peptide's potential to act as a nitric oxide donor or to influence the peptide's stability and reactivity in biological systems.

51536-91-5

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51536-91-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51536-91-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,3 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51536-91:
(7*5)+(6*1)+(5*5)+(4*3)+(3*6)+(2*9)+(1*1)=115
115 % 10 = 5
So 51536-91-5 is a valid CAS Registry Number.

51536-91-5Relevant academic research and scientific papers

SYNTHESIS AND INVESTIGATION OF THE ANTITUMORAL ACTIVITY OF SHORTENED ANALOGS OF LULIBERIN

Semko, T. V.,Burov, S. V.,Veselkina, O. S.,Vlasov, G. P.

, p. 607 - 612 (2007/10/03)

With the aim of obtaining antitumoral drugs possessing a binary action mechanism, we have synthesized a series of shortened analogs of luliberin, including some containing a 1-carboxymethyl-5-fluorouracil residue.Their antitumoral and hormonal activities

SYNTHESIS OF BIOLOGICALLY ACTIVE ANALOGS OF LULIBERIN WITH SHORTENED AMINO ACID SEQUENCES

Burov, S. V.,Nikolaev, S. V.,Smironova, M. P.,Lupanova, G. E.,Bobrov, Yu. F.,et al.

, p. 732 - 737 (2007/10/02)

Two new analogs of the releasing factor of the luteinizing hormone with shortened amino acid sequences have been synthesized by the methods of classical peptide chemistry.The influence of the preparations on the action of chorionic gonadotropin and on the

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