Details
Stereochemistry | RACEMIC |
Molecular Formula | C10H13NO4 |
Molecular Weight | 211.2145 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(N)(CC1=CC(O)=C(O)C=C1)C(O)=O
InChI
InChIKey=CJCSPKMFHVPWAR-UHFFFAOYSA-N
InChI=1S/C10H13NO4/c1-10(11,9(14)15)5-6-2-3-7(12)8(13)4-6/h2-4,12-13H,5,11H2,1H3,(H,14,15)
Molecular Formula | C10H13NO4 |
Molecular Weight | 211.2145 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Methyldopa is an aromatic-amino-acid decarboxylase inhibitor in animals and in man. Methyldopa is a medication that has been used to treat high blood pressure since the 1960s. Methyldopa is indicated in the treatment of moderate to severe hypertension, including that complicated by renal disease. Only methyldopa, the L-isomer of alpha-methyldopa, has the ability to inhibit dopa decarboxylase and to deplete animal tissues of norepinephrine. D-isomer is relatively inactive. In man the antihypertensive activity appears to be due solely to the L-isomer, which became generally known
as methyldopa (Aldomet). About twice the dose of the racemate (Methyldopa anhydrous, (±)-; DL-alpha-methyldopa) is required for equal antihypertensive effect. Racemic alpha-methyldopa was shown to be much less effective or ineffective for the treatment of hypertension. The comparative study of the hypotensive effect of L-alpha-methyl-dopa (L-isomer) versus the racemic form was performed. The short-term hypotensive effects of the racemic form and the L-isomer of alpha-methyl-dopa were compared in 13 hospitalized patients with arterial hypertension. After a placebo period the active preparations in a fixed dose of 1.5 g daily were administered for three-day periods separated by a second placebo period of three days, the sequence of the active
drugs being alternated. Both substances were shown to exert
significant hypotensive effects. The L-isomer produced significant blood-pressure reductions irrespective of whether or not it was given first, whereas the racemic form was effective only when given first. The blood-pressure levels obtained with the L-isomer were throughout lower than those with the racemic form. Methyldopa is a centrally acting antihypertensive agent. It is metabolized to alpha-methylnorepinephrine in the brain, and this compound is thought to activate central alpha-2 adrenergic receptors
CNS Activity
Curator's Comment: Methyldopa crosses the blood brain barrier. The transport of methyldopa into CNS is apparently an active process. Some effects, such as coma and mental depression, are due to the effects of methyldopa on the CNS.
Methyldopa produces a number of side effects due to alpha-2-adrenergic agonist effects.
Approval Year
Sample Use Guides
Adults
Hypertension
The usual starting oral dose is 250 mg of anhydrous
methyldopa two or three times daily for the first 48
hours. The daily dosage then may be increased or
decreased, at intervals of not less than two days, until
the desired response is obtained. To minimize sedation,
increase the dose in the evening.
No advantage is obtained at doses larger than 3 g daily.
The usual maintenance dosage is 500 mg to 2 g of
anhydrous methyldopa daily in two to four doses. In the
elderly, the usual dose is 125 mg twice daily, with a
maximum of 2 g/day.
A gradual hypotensive response occurs in most patients
in 12 to 24 hours.
Route of Administration:
Oral
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:52:42 GMT 2023
by
admin
on
Sat Dec 16 08:52:42 GMT 2023
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Record UNII |
33TD13T99R
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Record Status |
Validated (UNII)
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Record Version |
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WHO-ATC |
C02AB02
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WHO-VATC |
QC02AB02
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33TD13T99R
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CHEMBL718
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alpha-Methyldopa
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DTXSID60970356
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55-40-3
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m7397
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200-232-4
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4138
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