75176-09-9 Usage
Description
(2S,4R)-4-Methoxyproline is a chemical compound derived from the amino acid proline, featuring a specific stereochemistry with a 2S and 4R configuration. The "4-methoxy" in its name indicates the presence of a methoxy group attached to the fourth carbon atom of the proline molecule. This unique structure and its potential therapeutic properties make (2S,4R)-4-Methoxyproline a subject of interest for research in pharmaceuticals and drug development.
Uses
Used in Pharmaceutical Industry:
(2S,4R)-4-Methoxyproline is used as a pharmaceutical compound for its potential therapeutic properties. Its unique structure allows it to be a subject of interest for research and development in various scientific and medical fields, contributing to the advancement of drug discovery and treatment options.
Used in Drug Development:
(2S,4R)-4-Methoxyproline is utilized in drug development as a promising candidate for the creation of new medications. Its distinct stereochemistry and the presence of the methoxy group may offer novel mechanisms of action or improved pharmacological properties, making it valuable in the design and synthesis of innovative therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 75176-09-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,7 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75176-09:
(7*7)+(6*5)+(5*1)+(4*7)+(3*6)+(2*0)+(1*9)=139
139 % 10 = 9
So 75176-09-9 is a valid CAS Registry Number.
75176-09-9Relevant articles and documents
Effect of proline analogues on the conformation of elastin peptides
Pepe, Antonietta,Crudele, Maria Antonietta,Bochicchio, Brigida
, p. 1326 - 1335 (2013)
Three elastin model peptides containing the repetitive motif -VGVXGVG-, where X corresponds to (2S)-proline (Pro), (2S,4R)-4-hydroxy-proline (Hyp) and (2S,4R)-4-methoxy-proline (Mop), were synthesized in order to define the effect of the introduction of an electronegative group on the conformation and self-assembling properties of the peptides. Circular dichroism, NMR and FT-IR spectroscopies evidenced outstanding differences at molecular and supramolecular level. This work constitutes the basis for the proper design of elastin-inspired drugs with tailored conformational properties.
