35446-34-5 Usage
Chemical class
Peptides
It belongs to the class of molecules known as peptides.
Structural components
Proline backbone, acetylamino group, phenylprop-2-enoyl group
The compound has a proline backbone with an additional acetylamino and phenylprop-2-enoyl group, giving it a unique structural profile.
Stereochemistry
(2E)-configuration
The compound has an (2E)-configuration, which refers to the geometry of the double bond in the molecule.
Functional profile
Potential biological activities
It may exhibit biological activities such as enzyme inhibition, receptor binding, or other pharmacological effects.
Field of interest
Drug development and pharmaceuticals
The compound is of interest in the field of drug development and pharmaceuticals due to its potential biological activities.
Research applications
Structure-activity relationships, molecular interactions
Its chemical structure and properties make it a valuable tool for studying structure-activity relationships and molecular interactions in biological systems.
Potential applications
Medicine and biotechnology
Further research and evaluation may reveal its potential applications in medicine and biotechnology.
Molecular weight
Approximately 323.37 g/mol
The molecular weight is an approximate value that indicates the mass of one mole of the compound.
Solubility
Soluble in polar solvents
The compound is likely to be soluble in polar solvents, such as water or methanol, due to the presence of polar functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 35446-34-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,4,4 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35446-34:
(7*3)+(6*5)+(5*4)+(4*4)+(3*6)+(2*3)+(1*4)=115
115 % 10 = 5
So 35446-34-5 is a valid CAS Registry Number.
35446-34-5Relevant academic research and scientific papers
Complexes of Ca2+ and Mg2+ with N-acetyl-α,β-dehydrodipeptides: The state in an alcoholic solution and its relationship with asymmetric induction upon diastereoselective hydrogenation
Lisichkina,Larina,Peregudov,Vasil'era,Belikov
, p. 895 - 898 (2007/10/03)
In an alcoholic solution, N-acetyl-α,β-dehydrodipeptides interact with Ca2+ and Mg2+ ions to form complex particles containing several dehydrodipeptide molecules per metal ion. The composition of these particles and steric interactions in them determine the acidity of the carboxyl groups and the degree of asymmetric induction upon diastereoselective hydrogenation.
