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Details

Stereochemistry ABSOLUTE
Molecular Formula C10H13NO4
Molecular Weight 211.2145
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METHYLDOPA ANHYDROUS

SMILES

C[C@](N)(CC1=CC(O)=C(O)C=C1)C(O)=O

InChI

InChIKey=CJCSPKMFHVPWAR-JTQLQIEISA-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)/t10-/m0/s1

HIDE SMILES / InChI

Molecular Formula C10H13NO4
Molecular Weight 211.2145
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:57:41 UTC 2023
Edited
by admin
on Fri Dec 15 15:57:41 UTC 2023
Record UNII
M4R0H12F6M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
METHYLDOPA ANHYDROUS
Common Name English
J9.247I
Code English
ANHYDROUS METHYLDOPA
MART.  
Common Name English
(-)-.ALPHA.-METHYLDOPA
Common Name English
L-.ALPHA.-METHYL-3-(3,4)-DIHYDROXYPHENYLALANINE
Common Name English
L-TYROSINE, 3-HYDROXY-.ALPHA.-METHYL-
Systematic Name English
METHYLDOPA (LEVOROTATORY)
Common Name English
BAYER-1440L
Code English
(-)-METHYLDOPA
Systematic Name English
ANHYDROUS METHYLDOPA [MART.]
Common Name English
(-)-.ALPHA.-METHYL-3,4-DIHYDROXYPHENYLALANINE
Systematic Name English
L-.ALPHA.-METHYLDOPA
Common Name English
(2S)-2-AMINO-3-(3,4-DIHYDROXYPHENYL)-2-METHYLPROPANOIC ACID
Systematic Name English
.ALPHA.-METHYL-L-DOPA
Brand Name English
L-3-(3,4-DIHYDROXYPHENYL)-2-METHYLALANINE
Common Name English
Methyldopa [WHO-DD]
Common Name English
METHYL DOPA
Systematic Name English
methyldopa [INN]
Common Name English
METHYLDOPA [MI]
Common Name English
LEDERDOPA
Brand Name English
CARBIDOPA IMPURITY A [EP IMPURITY]
Common Name English
METHYLDOPA [HSDB]
Common Name English
NSC-169916
Code English
METHYLDOPA, ANHYDROUS
Common Name English
.ALPHA.-METHYL-L-3,4-DIHYDROXYPHENYLALANINE
Common Name English
(S)-(-)-.ALPHA.-METHYLDOPA
Common Name English
Classification Tree Code System Code
WHO-ATC C02AB01
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
NDF-RT N0000175554
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
WHO-ATC C02LB01
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
NDF-RT N0000009918
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
WHO-ATC C02AB
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
Code System Code Type Description
PUBCHEM
38853
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
PRIMARY
ECHA (EC/EINECS)
209-089-2
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
PRIMARY
RXCUI
1545996
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
PRIMARY RxNorm
EVMPD
SUB08867MIG
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
PRIMARY
INN
1110
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
PRIMARY
DAILYMED
M4R0H12F6M
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
PRIMARY
HSDB
218
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
PRIMARY
EPA CompTox
DTXSID5023295
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
PRIMARY
NCI_THESAURUS
C175729
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
PRIMARY
EVMPD
SUB26433
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
PRIMARY
MERCK INDEX
m7397
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
PRIMARY Merck Index
CAS
555-30-6
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
PRIMARY
FDA UNII
M4R0H12F6M
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
PRIMARY
DRUG BANK
DB00968
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
PRIMARY
NSC
169916
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
PRIMARY
WIKIPEDIA
METHYLDOPA
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
PRIMARY
CHEBI
61058
Created by admin on Fri Dec 15 15:57:41 UTC 2023 , Edited by admin on Fri Dec 15 15:57:41 UTC 2023
PRIMARY
Related Record Type Details
SOLVATE->ANHYDROUS
TARGET -> INHIBITOR
SALT/SOLVATE -> PARENT
SUBSTANCE->BASIS OF STRENGTH
Related Record Type Details
METABOLITE -> PARENT
ACTIVE IN RATS
METABOLITE -> PARENT
URINE
PARENT -> METABOLITE
URINE
METABOLITE -> PARENT
URINE
METABOLITE -> PARENT
METABOLITE -> PARENT
URINE
METABOLITE -> PARENT
Approximately 70 percent of the drug which is absorbed is excreted in the urine as methyldopa and its mono-0-sulfate conjugate
MAJOR
PLASMA; URINE
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
ACTIVE MOIETY