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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
Structure of METHYLDOPA ANHYDROUS, (±)-

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)

HIDE SMILES / InChI

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

PubMed

PubMed

TitleDatePubMed
L-alpha-methyl-dopa versus the racemic form--a comparative study of the hypotensive effect.
1966 Jun
[Dosage of racemic methyldopa (Hyperpax)].
1969 Dec 15
Reasons for failure of antihypertensive treatment.
1983 Jun 18

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 Sat Dec 16 08:52:42 GMT 2023
Edited
by admin
on Sat Dec 16 08:52:42 GMT 2023
Record UNII
33TD13T99R
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
METHYLDOPA ANHYDROUS, (±)-
Common Name English
(±)-METHYLDOPA
Systematic Name English
DL-.ALPHA.-METHYL-3-(3,4-DIHYDROXYPHENYL)ALANINE
Common Name English
DL-METHYLDOPA
Common Name English
METHYLDOPA DL-FORM [MI]
Common Name English
DL-.ALPHA.-METHYL DOPA
Common Name English
RACEMIC .ALPHA.-METHYLDOPA
Common Name English
METHYLDOPA (RACEMIC)
Common Name English
DL-2-METHYL-3-(3,4-DIHYDROXYPHENYL)ALANINE
Common Name English
(±)-.ALPHA.-METHYLDOPA
Common Name English
2-(3,4-DIHYDROXYBENZYL)-2-AMINOPROPANOIC ACID
Systematic Name English
TYROSINE, 3-HYDROXY-.ALPHA.-METHYL-
Systematic Name English
Classification Tree Code System Code
WHO-ATC C02AB02
Created by admin on Sat Dec 16 08:52:42 GMT 2023 , Edited by admin on Sat Dec 16 08:52:42 GMT 2023
WHO-VATC QC02AB02
Created by admin on Sat Dec 16 08:52:42 GMT 2023 , Edited by admin on Sat Dec 16 08:52:42 GMT 2023
Code System Code Type Description
FDA UNII
33TD13T99R
Created by admin on Sat Dec 16 08:52:42 GMT 2023 , Edited by admin on Sat Dec 16 08:52:42 GMT 2023
PRIMARY
ChEMBL
CHEMBL718
Created by admin on Sat Dec 16 08:52:42 GMT 2023 , Edited by admin on Sat Dec 16 08:52:42 GMT 2023
PRIMARY
WIKIPEDIA
alpha-Methyldopa
Created by admin on Sat Dec 16 08:52:42 GMT 2023 , Edited by admin on Sat Dec 16 08:52:42 GMT 2023
PRIMARY
EPA CompTox
DTXSID60970356
Created by admin on Sat Dec 16 08:52:42 GMT 2023 , Edited by admin on Sat Dec 16 08:52:42 GMT 2023
PRIMARY
CAS
55-40-3
Created by admin on Sat Dec 16 08:52:42 GMT 2023 , Edited by admin on Sat Dec 16 08:52:42 GMT 2023
PRIMARY
MERCK INDEX
m7397
Created by admin on Sat Dec 16 08:52:42 GMT 2023 , Edited by admin on Sat Dec 16 08:52:42 GMT 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
200-232-4
Created by admin on Sat Dec 16 08:52:42 GMT 2023 , Edited by admin on Sat Dec 16 08:52:42 GMT 2023
PRIMARY
PUBCHEM
4138
Created by admin on Sat Dec 16 08:52:42 GMT 2023 , Edited by admin on Sat Dec 16 08:52:42 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY