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QuickView for penicillamine (compound)


PubChem
Name: Penicillamine
PubChem Compound ID: 4727
Description: 3-Mercapto-D-valine. The most characteristic degradation product of the penicillin antibiotics. It is used as an antirheumatic and as a chelating agent in Wilson's disease.
Molecular formula: C5H11NO2S
Molecular weight: 149.212 g/mol
Synonyms:
nsc241261; NSC81988; 52-66-4; EINECS 200-147-2; 25526-04-9; Penicillamine; DL-.beta.-Mercaptovaline; AIDS-166472; D,L-Penicillamine; 1113-41-3.
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DrugBank
Identification
Name: Penicillamine
Name (isomeric): DB00859
Drug Type: small molecule
Description: 3-Mercapto-D-valine. The most characteristic degradation product of the penicillin antibiotics. It is used as an antirheumatic and as a chelating agent in Wilson's disease.
Synonyms:
Penicillamina [DCIT]; Dimethylcysteine; Penicillaminum [INN-Latin]; L-Penicillamine; Penicilamina [INN-Spanish]; D-Penicyllamine; beta-Thiovaline; Penicillamin; D-Penicillamine; Penicilllamine.
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Brand: Cuprimine, Mercaptovaline, Depamine, Trolovol, Kuprenil, Pendramine, Artamine, Cuprenil, Mercaptyl, Perdolat, Depen, Metalcaptase, Sufirtan, Cupripen, Distamine
Category: Chelating Agents, Antirheumatic Agents, Antidotes
CAS number: 52-67-5
Pharmacology
Indication: For treatment of Wilson's disease, cystinuria and active rheumatoid arthritis.
Pharmacology:
Penicillamine is a chelating agent used in the treatment of Wilson's disease. It is also used to reduce cystine excretion in cystinuria and to treat patients with severe, active rheumatoid arthritis unresponsive to conventional therapy. Penicillamine is used as a form of immunosuppression to treat rheumatoid arthritis. It works by reducing numbers ...
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Mechanism of Action:
Penicillamine is a chelating agent recommended for the removal of excess copper in patients with Wilson's disease. From in vitro studies which indicate that one atom of copper combines with two molecules of penicillamine. Penicillamine also reduces excess cystine excretion in cystinuria. This is done, at least in part, by disulfide interchange betw...
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Absorption: rapidly but incompletely
Protein binding: >80% (bound to plasma proteins)
Biotransformation: Hepatic
Route of elimination: Excretion is mainly renal, mainly as disulfides.
Half Life: 1 hour
Affected organisms: Humans and other mammals
Interactions
Food interaction:
Drink liberally.
Food reduces availability, take on an empty stomach.
Drug interaction:
Iron DextranThe multivalent agent decreases the effect of penicillamine
DigoxinPenicillamine decreases the effect of digoxin

Targets


Transporters