madopar

CAS No.
37270-69-2
Chemical Name:
madopar
Synonyms
madopar
CBNumber:
CB51397816
Molecular Formula:
C10H15N3O5.C9H11NO4
Molecular Weight:
454.433
MDL Number:
MOL File:
37270-69-2.mol

Pharmacokinetic data

Protein binding Benserazide: 0, Levodopa: 10-30%
Excreted unchanged in urine Benserazide: 0 (64 as metabs), Levodopa: <1%
Biological half-life Benserazide: 1.5 / Increased, Levodopa: 1.5 / Increased by 25%

madopar price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0028179 MADOPAR 95.00% 37270-69-2 5MG $495.98 2021-12-16 Buy
Product number Packaging Price Buy
API0028179 5MG $495.98 Buy

madopar Chemical Properties,Uses,Production

Drug interactions

Potentially hazardous interactions with other drugs
Anaesthetics: risk of arrhythmias with volatile liquid anaesthetics such as halothane
. Antidepressants: hypertensive crisis with MAOIs and linezolid (including moclobemide) - avoid for at least 2 weeks after stopping MAOI.
Bupropion: increased risk of side effects of levodopa
Ferrous sulphate: reduces AUC of levodopa by 30-50%, clinically significant in some but not all patients.

Metabolism

Levodopa is rapidly decarboxylated by the enzyme aromatic l-amino acid decarboxylase, mostly in the gut, liver, and kidney, to dopamine, which is metabolised in turn, principally to dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA). Other routes of metabolism include O-methylation, transamination, and oxidation, producing a variety of minor metabolites including noradrenaline and 3-O-methyldopa; the latter may accumulate in the CNS due to its relatively long half-life.
About 80% of an oral dose of levodopa is excreted in the urine within 24 hours, mainly as dihydroxyphenylacetic and homovanillic acids. Only small amounts of levodopa are excreted unchanged in the faeces. Benserazide is rapidly excreted in the urine in the form of metabolites, mostly within the first 6 hours; 85% of urinary excretion occurrs within 12 hours. It is mainly metabolised in the gut and appears to protect levodopa against decarboxylation primarily in the gut, but alsoin the rest of the body, mainly by way of its metabolite trihydroxybenzylhydrazine.

madopar Preparation Products And Raw materials

Raw materials

Preparation Products

madopar Suppliers

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madopar 37270-69-2