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D-Alaninamide, L-tyrosyl-N-[1-[(carboxyacetyl)amino]-2-phenylethyl]-, (S)is a complex chemical compound that is a derivative of alaninamide and L-tyrosine. It is composed of an alaninamide molecule attached to a tyrosine molecule through a carboxyacetyl group, resulting in a unique structure and properties. This chemical compound has potential applications in pharmaceuticals and biotechnology, as it may have biological activity and be used in drug development. Its intricate structure and composition make it an interesting target for further research and potential uses in various fields.

95617-70-2

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95617-70-2 Usage

Uses

Used in Pharmaceutical Industry:
D-Alaninamide, L-tyrosyl-N-[1-[(carboxyacetyl)amino]-2-phenylethyl]-, (S)is used as a potential drug candidate for the development of new medications due to its unique structure and potential biological activity.
Used in Biotechnology Industry:
D-Alaninamide, L-tyrosyl-N-[1-[(carboxyacetyl)amino]-2-phenylethyl]-, (S)is used as a research target for understanding its properties and exploring its potential applications in various biotechnological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 95617-70-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,6,1 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 95617-70:
(7*9)+(6*5)+(5*6)+(4*1)+(3*7)+(2*7)+(1*0)=162
162 % 10 = 2
So 95617-70-2 is a valid CAS Registry Number.

95617-70-2Downstream Products

95617-70-2Relevant academic research and scientific papers

Synthesis and Pharmacological Activity of Partially Modified Retro-Inverso Dermorphin Tetrapeptides

Salvadori, Severo,Marastoni, Mauro,Balboni, Gianfranco,Sarto, Gian Pietro,Tomatis, Roberto

, p. 769 - 774 (2007/10/02)

We studied the effect of partial retro-inverso modification of selected peptide bonds of N-terminal tetrapeptide analogues of dermorphin (H-Tyr-D-Ala-Phe-Gly-Tyr-Pro-Ser-NH2).Among the 14 compounds synthesized and tested for opioid activity, some tetrapeptides have the C-terminus carrying different amide moieties; retromodifications concern the Phe-Gly bond (Ia-f) and/or the C-terminal carboxamide function (IIIa-d, IIa-d).All pseudotetrapeptide derivatives showed opioid activity in vitro and in vivo.The most potent compounds (II) have a biological potency comparable with that of the original tetrapeptides in the guinea pig ileum preparation and in the mouse tail-flick test after intracerebral or subcutaneous administration.

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