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Catalog Number:
15965
CAS Number:
1049753-34-5
( S -γ-(2-Tienilmetil)-L-prolina·HCl
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$120.88 /25 mg
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Product Information

(S)-g-(2-Thienylmethyl)-L-proline·HCl is a hydrochloride salt of a proline derivative that exhibits unique properties beneficial for various applications in pharmaceutical and biochemical research. This compound is recognized for its potential role as a building block in the synthesis of bioactive molecules, particularly in the development of novel pharmaceuticals targeting neurological and metabolic disorders. Its thienylmethyl group enhances its interaction with biological systems, making it a valuable candidate for drug design and development.

Researchers and industry professionals can leverage (S)-g-(2-Thienylmethyl)-L-proline·HCl in the synthesis of peptides and other complex organic molecules, facilitating advancements in medicinal chemistry. Its specific stereochemistry contributes to its efficacy and selectivity in biological applications, setting it apart from similar compounds. This compound's versatility and potential for innovation make it an essential addition to any researcher's toolkit, particularly in fields focused on drug discovery and development.

CAS Number
1049753-34-5
Molecular Formula
C10H13NO2S · HCl
Molecular Weight
247.74
MDL Number
MFCD06796830
PubChem ID
53398307
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
1049753-34-5
Molecular Formula
C10H13NO2S · HCl
Molecular Weight
247.74
MDL Number
MFCD06796830
PubChem ID
53398307
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-g-(2-Thienylmethyl)-L-proline·HCl is widely utilized in research focused on

  • Pharmaceutical Development: This compound serves as a building block in the synthesis of novel pharmaceuticals, particularly in the development of drugs targeting neurological disorders due to its unique structural properties.
  • Biochemical Research: It is used in studies related to amino acid metabolism and protein synthesis, helping researchers understand the role of proline derivatives in biological systems.
  • Drug Formulation: The hydrochloride form enhances solubility, making it suitable for formulating oral medications, which improves bioavailability in therapeutic applications.
  • Material Science: This compound can be incorporated into polymers to create materials with specific mechanical properties, beneficial for applications in coatings and adhesives.
  • Analytical Chemistry: It is utilized as a reference standard in chromatography, aiding in the accurate quantification of similar compounds in complex mixtures.

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