54745-27-6 Usage
Uses
Given the provided materials, specific applications for H-PHE-BETA-ALA-OH are not detailed. However, based on the properties of its constituent amino acids, potential uses in various industries could be hypothesized as follows:
Used in Pharmaceutical Industry:
H-PHE-BETA-ALA-OH could be used as a therapeutic agent for conditions related to neurotransmitter production or muscle function, given the roles of phenylalanine in protein synthesis and neurotransmitter production, and beta-alanine as a precursor to carnosine, which is involved in muscle function and lactic acid buffering.
Used in Sports Nutrition Industry:
As a sports supplement, H-PHE-BETA-ALA-OH might be utilized to enhance muscle performance and reduce muscle fatigue, capitalizing on the muscle-buffering properties of carnosine derived from beta-alanine.
Used in Cosmetics Industry:
In the cosmetics sector, H-PHE-BETA-ALA-OH could be employed as an active ingredient for skin care products, potentially benefiting from the antioxidant properties of phenylalanine or the skin-conditioning effects of beta-alanine.
Check Digit Verification of cas no
The CAS Registry Mumber 54745-27-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,4 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54745-27:
(7*5)+(6*4)+(5*7)+(4*4)+(3*5)+(2*2)+(1*7)=136
136 % 10 = 6
So 54745-27-6 is a valid CAS Registry Number.
54745-27-6Relevant academic research and scientific papers
A new molecular scaffold for the formation of supramolecular peptide double helices: The crystallographic insight
Guha, Samit,Drew, Michael G. B.,Banerjee, Arindam
, p. 1347 - 1350 (2007/12/29)
A series of water-soluble synthetic dipeptides (1-3) with an N-terminally located β-alanine residue, β-alanyl-L-valine (1), β-alanyl-L- isoleucine (2), and β-alanyl-L-phenylalanine (3), form hydrogen-bonded supramolecular double helices with a pitch length of 1 nm, whereas the C-terminally positioned β-alanine containing dipeptide (4), L-phenylalanyl-β-alanine, does not form a supramolecular double helical structure. β-Ala-Xaa (Xaa = Val/lle/Phe) can be regarded as a new motif for the formation of supramolecular double helical structures in the solid state.
