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Details

Stereochemistry ABSOLUTE
Molecular Formula C7H15NO3
Molecular Weight 161.1989
Optical Activity ( - )
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEVOCARNITINE

SMILES

C[N+](C)(C)C[C@H](O)CC([O-])=O

InChI

InChIKey=PHIQHXFUZVPYII-ZCFIWIBFSA-N
InChI=1S/C7H15NO3/c1-8(2,3)5-6(9)4-7(10)11/h6,9H,4-5H2,1-3H3/t6-/m1/s1

HIDE SMILES / InChI
Molecular Formula C7H15NO3
Molecular Weight 161.1989
Charge 0
Count
Stereochemistry EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Sat Dec 16 15:52:46 UTC 2023
Edited
by admin
on Sat Dec 16 15:52:46 UTC 2023
Record UNII
0G389FZZ9M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEVOCARNITINE
EP   HSDB   INN   JAN   MART.   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD  
INN   USAN  
Official Name English
L-CARNITINE
FCC   VANDF  
Systematic Name English
LEVOCARNITINE [HSDB]
Common Name English
LEVOCARNITINE [USAN]
Common Name English
LEVOCARNITINE [MART.]
Common Name English
(3R)-3-HYDROXY-4-(TRIMETHYLAMMONIO)BUTANOATE
Systematic Name English
LEVOCARNITINE [VANDF]
Common Name English
CARNITINE, L-
Systematic Name English
LEVOCARNITINE [USP-RS]
Common Name English
CARNITOR
Brand Name English
levocarnitine [INN]
Common Name English
Levocarnitine [WHO-DD]
Common Name English
NSC-759132
Code English
LEVOCARNITINE [ORANGE BOOK]
Common Name English
LEVOCARNITINE [JAN]
Common Name English
1-PROPANAMINIUM, 3-CARBOXY-2-HYDROXY-N,N,N-TRIMETHYL-, HYDROXIDE, INNER SALT, (R)-
Common Name English
CARNITINE, (-)-
Systematic Name English
L-CARNITINE [VANDF]
Common Name English
L-CARNITINE [FCC]
Common Name English
CARNITINE [MI]
Common Name English
LEVOCARNITINE [EP MONOGRAPH]
Common Name English
(L-3-CARBOXY-2-HYDROXYPROPYL)TRIMETHYLAMMONIUM HYDROXIDE, INNER SALT
Common Name English
LEVOCARNITINE [USP MONOGRAPH]
Common Name English
Classification Tree Code System Code
NDF-RT N0000006688
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
FDA ORPHAN DRUG 76393
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
FDA ORPHAN DRUG 32488
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
NDF-RT N0000006688
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
FDA ORPHAN DRUG 17386
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
DSLD 255 (Number of products:1503)
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
FDA ORPHAN DRUG 1584
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
FDA ORPHAN DRUG 27888
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
FDA ORPHAN DRUG 103897
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
WHO-ATC A16AA01
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
NDF-RT N0000006688
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
WHO-VATC QA16AA51
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
NDF-RT N0000175903
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
FDA ORPHAN DRUG 1384
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
WHO-VATC QA16AA01
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
Code System Code Type Description
USAN
X-14
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY
NCI_THESAURUS
C26657
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY
INN
6098
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY
LACTMED
Levocarnitine
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY
GRAS Notification (GRN No.)
362
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY
FDA UNII
0G389FZZ9M
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY
ECHA (EC/EINECS)
208-768-0
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY
DRUG CENTRAL
513
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY
EVMPD
SUB08466MIG
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY
MERCK INDEX
m3119
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY Merck Index
CAS
541-15-1
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY
ChEMBL
CHEMBL1149
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY
CHEBI
16347
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY
SMS_ID
100000090324
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY
RS_ITEM_NUM
1359903
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY
NCI_THESAURUS
C1505
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
CONCEPT Dietary Supplement
NSC
759132
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY
DAILYMED
0G389FZZ9M
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY
RXCUI
42955
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY RxNorm
EPA CompTox
DTXSID4023208
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY
HSDB
7588
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY
PUBCHEM
10917
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY
DRUG BANK
DB00583
Created by admin on Sat Dec 16 15:52:48 UTC 2023 , Edited by admin on Sat Dec 16 15:52:48 UTC 2023
PRIMARY
Related Record Type Details
Structure of LEVOCARNITINE FUMARATE
PARENT -> SALT/SOLVATE
Structure of DL-CARNITINE
RACEMATE -> ENANTIOMER
OCTN-2
TRANSPORTER -> SUBSTRATE
Km
Structure of LEVOCARNITINE HYDROCHLORIDE
SALT/SOLVATE -> PARENT
Structure of LEVOCARNITINE TARTRATE
SALT/SOLVATE -> PARENT
Related Record Type Details
Structure of TRIMETHYLLLYSINE
PARENT -> METABOLITE
Structure of TRIMETHYLAMINE OXIDE
METABOLITE -> PARENT
Structure of Pivaloylcarnitine
METABOLITE INACTIVE -> PARENT
Excreted in kidneys. Responsible for the depletion carnitine.
Related Record Type Details
Structure of CAMPHORIC ACID
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of (3-CARBAMOYLALLYL)TRIMETHYLAMMONIUM
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of CROTONOBETAINE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of L-CARNITINAMIDE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
Structure of LEVOCARNITINE
ACTIVE MOIETY
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