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Catalog Number:
14299
CAS Number:
1330286-48-0
S-Acetamidomethyl-L- penicillamine hydrochloride
Purity:
≥ 98% (TLC)
Synonym(s):
L-Pen(Acm)-OH·HCl, S-Acetamidomethyl-β,β-Dimethyl-L-Cys-OH·HCl, H-Pen(Acm)-OH·HCl
Documents
$74.81 /250MG
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Product Information

(S)-Acetamidomethyl-L-penicillamine hydrochloride is a versatile compound recognized for its significant role in medicinal chemistry and pharmaceutical applications. This chiral molecule, a derivative of penicillamine, is primarily utilized in the treatment of conditions such as Wilson's disease and cystinuria, where it acts as a chelating agent to bind excess copper and cystine, facilitating their excretion from the body. Its unique structure enhances its bioavailability and efficacy, making it a preferred choice among healthcare professionals for managing these conditions.

In addition to its therapeutic uses, (S)-Acetamidomethyl-L-penicillamine hydrochloride is also valuable in research settings, particularly in studies focused on metal ion interactions and drug development. Its ability to form stable complexes with various metal ions opens avenues for exploring new treatments and understanding biochemical pathways. Researchers appreciate its relatively low toxicity and favorable pharmacokinetic profile, which further supports its application in both clinical and laboratory environments.

Synonyms
L-Pen(Acm)-OH·HCl, S-Acetamidomethyl-β,β-Dimethyl-L-Cys-OH·HCl, H-Pen(Acm)-OH·HCl
CAS Number
1330286-48-0
Purity
≥ 98% (TLC)
Molecular Formula
C8H16N2O3S·HCl
Molecular Weight
256.9
MDL Number
MFCD08458518
PubChem ID
138114174
Conditions
Store at 0-8°C
General Information
Synonyms
L-Pen(Acm)-OH·HCl, S-Acetamidomethyl-β,β-Dimethyl-L-Cys-OH·HCl, H-Pen(Acm)-OH·HCl
CAS Number
1330286-48-0
Purity
≥ 98% (TLC)
Molecular Formula
C8H16N2O3S·HCl
Molecular Weight
256.9
MDL Number
MFCD08458518
PubChem ID
138114174
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-Acetamidomethyl-L-penicillamine hydrochloride is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is used in the synthesis of novel drugs, particularly in the treatment of conditions like Wilson's disease, where it helps in copper chelation.
  • Biochemical Research: It serves as a valuable tool in studying enzyme inhibition and protein interactions, aiding researchers in understanding complex biological processes.
  • Analytical Chemistry: The compound is employed in various analytical techniques, including chromatography, to separate and identify other chemical substances effectively.
  • Material Science: It is utilized in the development of new materials with specific properties, particularly in the field of polymers and coatings.
  • Clinical Research: The compound is investigated for its potential therapeutic effects, contributing to clinical trials aimed at improving treatment protocols for related diseases.

Citations