17136-28-6 Usage
General Description
H-BETA-ALA-PHE-OH is a chemical compound with the molecular formula C26H30N2O4. It is a peptide consisting of three amino acids: beta-alanine, alanine, and phenylalanine. H-BETA-ALA-PHE-OH has potential applications in the field of pharmaceuticals and biochemistry due to its ability to modulate biological processes and interact with specific cellular receptors. It may also have implications in the development of new drugs and therapies for various medical conditions. Additionally, H-BETA-ALA-PHE-OH has the potential to be used as a research tool in studies related to protein structure and function, as well as in the synthesis of other bioactive compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 17136-28-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,3 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17136-28:
(7*1)+(6*7)+(5*1)+(4*3)+(3*6)+(2*2)+(1*8)=96
96 % 10 = 6
So 17136-28-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H16N2O3/c13-7-6-11(15)14-10(12(16)17)8-9-4-2-1-3-5-9/h1-5,10H,6-8,13H2,(H,14,15)(H,16,17)
17136-28-6Relevant articles and documents
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.
