Penicillamine

Penicillamine
Systematic (IUPAC) name
(2S)-2-amino-3-methyl-3-sulfanyl-butanoic acid
Clinical data
Trade names Cuprimine
AHFS/Drugs.com monograph
Pregnancy cat. D (Aust.)
Legal status Prescription
Routes Oral
Pharmacokinetic data
Bioavailability Variable
Metabolism Hepatic
Half-life 1 hour
Excretion Renal
Identifiers
CAS number 52-67-5 Y
ATC code M01CC01
PubChem CID 5852
DrugBank APRD01171
ChemSpider 5643 Y
UNII GNN1DV99GX Y
KEGG D00496 Y
ChEBI CHEBI:7959 Y
ChEMBL CHEMBL1430 Y
Chemical data
Formula C5H11NO2S 
Mol. mass 149.212 g/mol
SMILES eMolecules & PubChem
 N(what is this?)  (verify)

Penicillamine is a pharmaceutical of the chelator class. It is sold under the trade names of Cuprimine and Depen. The pharmaceutical form is D-penicillamine, as L-penicillamine is toxic (it inhibits the action of pyridoxine). It is a metabolite of penicillin, although it has no antibiotic properties.

Contents

Uses

Penicillamine is used as a form of immunosuppression to treat rheumatoid arthritis. It works by reducing numbers of T-lymphocytes, inhibiting macrophage function, decreasing IL-1, decreasing rheumatoid factor, and preventing collagen from cross-linking.

It is used as a chelating agent:

Adverse effects

Adverse effects include:

History

Dr. John Walshe (1956) first described the use of penicillamine in Wilson's disease.[5] He had discovered the compound in the urine of patients (including himself) who had taken penicillin, and experimentally confirmed that it increased urinary copper excretion by chelation. He had initial difficulty convincing several world experts of the time (Drs Denny Brown and Cumings) of its efficacy, as they held that Wilson's disease was not primarily a problem of copper homeostasis but of amino acid metabolism, and that dimercaprol should be used as a chelator. Later studies confirmed both the copper-centered theory and the efficacy of D-penicillamine. Walshe also pioneered other chelators in Wilson's such as triethylene tetramine, 2HCl, and tetrathiomolybdate.[6]

References

  1. ^ Table 14-2 in: Mitchell, Richard Sheppard; Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson. Robbins Basic Pathology. Philadelphia: Saunders. ISBN 1-4160-2973-7.  8th edition.
  2. ^ Robbins and Cotran, Pathological Basis of Disease 8th Edition, Kumar et al
  3. ^ Bolognia, Jean; et al (2007). Dermatology. Philadelphia: Elsevier. ISBN 1416029990. 2nd edition.
  4. ^ Underwood, J. C. E. (2009). General and systemic Pathology. Elsevier Limited. ISBN 9780443068898. 
  5. ^ Walshe JM (January 1956). "Wilson's disease; new oral therapy". Lancet 267 (6906): 25–6. doi:10.1016/S0140-6736(56)91859-1. PMID 13279157. 
  6. ^ Walshe JM (August 2003). "The story of penicillamine: a difficult birth". Mov. Disord. 18 (8): 853–9. doi:10.1002/mds.10458. PMID 12889074. 

External links