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Details

Stereochemistry ABSOLUTE
Molecular Formula C10H14N2O4
Molecular Weight 226.2292
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARBIDOPA ANHYDROUS

SMILES

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

InChI

InChIKey=TZFNLOMSOLWIDK-JTQLQIEISA-N
InChI=1S/C10H14N2O4/c1-10(12-11,9(15)16)5-6-2-3-7(13)8(14)4-6/h2-4,12-14H,5,11H2,1H3,(H,15,16)/t10-/m0/s1

HIDE SMILES / InChI

Molecular Formula C10H14N2O4
Molecular Weight 226.2292
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 15:23:25 UTC 2023
Edited
by admin
on Fri Dec 15 15:23:25 UTC 2023
Record UNII
KR87B45RGH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CARBIDOPA ANHYDROUS
Common Name English
carbidopa [INN]
Common Name English
Carbidopa [WHO-DD]
Common Name English
CARBIDOPA, L- ANHYDROUS
Common Name English
BENZENEPROPANOIC ACID, .ALPHA.-HYDRAZINO-3,4-DIHYDROXY-.ALPHA.-METHYL-, (S)-
Common Name English
CARBIDOPA ANHYDROUS [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C38149
Created by admin on Fri Dec 15 15:23:25 UTC 2023 , Edited by admin on Fri Dec 15 15:23:25 UTC 2023
NCI_THESAURUS C66884
Created by admin on Fri Dec 15 15:23:25 UTC 2023 , Edited by admin on Fri Dec 15 15:23:25 UTC 2023
Code System Code Type Description
RXCUI
1545982
Created by admin on Fri Dec 15 15:23:25 UTC 2023 , Edited by admin on Fri Dec 15 15:23:25 UTC 2023
PRIMARY RxNorm
DRUG BANK
DB00190
Created by admin on Fri Dec 15 15:23:25 UTC 2023 , Edited by admin on Fri Dec 15 15:23:25 UTC 2023
PRIMARY
CAS
28860-95-9
Created by admin on Fri Dec 15 15:23:25 UTC 2023 , Edited by admin on Fri Dec 15 15:23:25 UTC 2023
PRIMARY
DAILYMED
KR87B45RGH
Created by admin on Fri Dec 15 15:23:25 UTC 2023 , Edited by admin on Fri Dec 15 15:23:25 UTC 2023
PRIMARY
PUBCHEM
34359
Created by admin on Fri Dec 15 15:23:25 UTC 2023 , Edited by admin on Fri Dec 15 15:23:25 UTC 2023
PRIMARY
ECHA (EC/EINECS)
249-271-9
Created by admin on Fri Dec 15 15:23:25 UTC 2023 , Edited by admin on Fri Dec 15 15:23:25 UTC 2023
PRIMARY
INN
3258
Created by admin on Fri Dec 15 15:23:25 UTC 2023 , Edited by admin on Fri Dec 15 15:23:25 UTC 2023
PRIMARY
EVMPD
SUB06126MIG
Created by admin on Fri Dec 15 15:23:25 UTC 2023 , Edited by admin on Fri Dec 15 15:23:25 UTC 2023
PRIMARY
NCI_THESAURUS
C61803
Created by admin on Fri Dec 15 15:23:25 UTC 2023 , Edited by admin on Fri Dec 15 15:23:25 UTC 2023
PRIMARY
EVMPD
SUB22639
Created by admin on Fri Dec 15 15:23:25 UTC 2023 , Edited by admin on Fri Dec 15 15:23:25 UTC 2023
PRIMARY
EPA CompTox
DTXSID4022735
Created by admin on Fri Dec 15 15:23:25 UTC 2023 , Edited by admin on Fri Dec 15 15:23:25 UTC 2023
PRIMARY
MERCK INDEX
m3068
Created by admin on Fri Dec 15 15:23:25 UTC 2023 , Edited by admin on Fri Dec 15 15:23:25 UTC 2023
PRIMARY
FDA UNII
KR87B45RGH
Created by admin on Fri Dec 15 15:23:25 UTC 2023 , Edited by admin on Fri Dec 15 15:23:25 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
TARGET -> INHIBITOR
Inhibits peripheral metabolism of levodopa.
SOLVATE->ANHYDROUS
Related Record Type Details
PARENT -> METABOLITE
URINE
METABOLITE -> PARENT
URINE
METABOLITE -> PARENT
URINE
Related Record Type Details
ACTIVE MOIETY