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Details

Stereochemistry ABSOLUTE
Molecular Formula C13H20N2O2
Molecular Weight 236.3101
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEVODROPROPIZINE

SMILES

OC[C@@H](O)CN1CCN(CC1)C2=CC=CC=C2

InChI

InChIKey=PTVWPYVOOKLBCG-ZDUSSCGKSA-N
InChI=1S/C13H20N2O2/c16-11-13(17)10-14-6-8-15(9-7-14)12-4-2-1-3-5-12/h1-5,13,16-17H,6-11H2/t13-/m0/s1

HIDE SMILES / InChI
Molecular Formula C13H20N2O2
Molecular Weight 236.3101
Charge 0
Count
Stereochemistry ABSOLUTE
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 Fri Dec 15 16:15:13 UTC 2023
Edited
by admin
on Fri Dec 15 16:15:13 UTC 2023
Record UNII
3O31P6T4G3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEVODROPROPIZINE
EP   INN   MART.   WHO-DD  
INN  
Official Name English
(2S)-3-(4-PHENYL-1-PIPERAZINYL)-1,2-PROPANEDIOL
Systematic Name English
RAPITUX
Brand Name English
DANKA
Brand Name English
LEVODROPROPIZINE [MART.]
Common Name English
LEVODROPROPIZINE [EP MONOGRAPH]
Common Name English
1,2-PROPANEDIOL, 3-(4-PHENYL-1-PIPERAZINYL)-, (S)-
Systematic Name English
DROPROPIZINE, (S)-
Common Name English
LEVOPRONT
Brand Name English
(-)-(S)-3-(4-PHENYL-1-PIPERAZINYL)-1,2-PROPANEDIOL
Systematic Name English
Levodropropizine [WHO-DD]
Common Name English
1,2-PROPANEDIOL, 3-(4-PHENYL-1-PIPERAZINYL)-, (2S)-
Systematic Name English
LEVOTUSS
Brand Name English
(-)-DROPROPIZINE
Common Name English
LVDP
Common Name English
L-DROPROPIZINE
Common Name English
levodropropizine [INN]
Common Name English
DROPROPIZINE S-FORM [MI]
Common Name English
(S)-(-)-DROPROPIZINE
Common Name English
DIPROPIZINE, (S)-ISOMER
Common Name English
Classification Tree Code System Code
WHO-VATC QR05DB27
Created by admin on Fri Dec 15 16:15:13 UTC 2023 , Edited by admin on Fri Dec 15 16:15:13 UTC 2023
WHO-ATC R05DB27
Created by admin on Fri Dec 15 16:15:13 UTC 2023 , Edited by admin on Fri Dec 15 16:15:13 UTC 2023
NCI_THESAURUS C66917
Created by admin on Fri Dec 15 16:15:13 UTC 2023 , Edited by admin on Fri Dec 15 16:15:13 UTC 2023
Code System Code Type Description
CAS
99291-25-5
Created by admin on Fri Dec 15 16:15:13 UTC 2023 , Edited by admin on Fri Dec 15 16:15:13 UTC 2023
PRIMARY
RXCUI
52014
Created by admin on Fri Dec 15 16:15:13 UTC 2023 , Edited by admin on Fri Dec 15 16:15:13 UTC 2023
PRIMARY RxNorm
ChEMBL
CHEMBL1288810
Created by admin on Fri Dec 15 16:15:13 UTC 2023 , Edited by admin on Fri Dec 15 16:15:13 UTC 2023
PRIMARY
EVMPD
SUB12105MIG
Created by admin on Fri Dec 15 16:15:13 UTC 2023 , Edited by admin on Fri Dec 15 16:15:13 UTC 2023
PRIMARY
DRUG BANK
DB12472
Created by admin on Fri Dec 15 16:15:13 UTC 2023 , Edited by admin on Fri Dec 15 16:15:13 UTC 2023
PRIMARY
MERCK INDEX
m4770
Created by admin on Fri Dec 15 16:15:13 UTC 2023 , Edited by admin on Fri Dec 15 16:15:13 UTC 2023
PRIMARY Merck Index
PUBCHEM
65859
Created by admin on Fri Dec 15 16:15:13 UTC 2023 , Edited by admin on Fri Dec 15 16:15:13 UTC 2023
PRIMARY
SMS_ID
100000092264
Created by admin on Fri Dec 15 16:15:13 UTC 2023 , Edited by admin on Fri Dec 15 16:15:13 UTC 2023
PRIMARY
NCI_THESAURUS
C81593
Created by admin on Fri Dec 15 16:15:13 UTC 2023 , Edited by admin on Fri Dec 15 16:15:13 UTC 2023
PRIMARY
MESH
C035916
Created by admin on Fri Dec 15 16:15:13 UTC 2023 , Edited by admin on Fri Dec 15 16:15:13 UTC 2023
PRIMARY
FDA UNII
3O31P6T4G3
Created by admin on Fri Dec 15 16:15:13 UTC 2023 , Edited by admin on Fri Dec 15 16:15:13 UTC 2023
PRIMARY
EPA CompTox
DTXSID8023210
Created by admin on Fri Dec 15 16:15:13 UTC 2023 , Edited by admin on Fri Dec 15 16:15:13 UTC 2023
PRIMARY
CHEBI
82722
Created by admin on Fri Dec 15 16:15:13 UTC 2023 , Edited by admin on Fri Dec 15 16:15:13 UTC 2023
PRIMARY
INN
6200
Created by admin on Fri Dec 15 16:15:13 UTC 2023 , Edited by admin on Fri Dec 15 16:15:13 UTC 2023
PRIMARY
WIKIPEDIA
LEVODROPROPIZINE
Created by admin on Fri Dec 15 16:15:13 UTC 2023 , Edited by admin on Fri Dec 15 16:15:13 UTC 2023
PRIMARY
DRUG CENTRAL
1568
Created by admin on Fri Dec 15 16:15:13 UTC 2023 , Edited by admin on Fri Dec 15 16:15:13 UTC 2023
PRIMARY
Related Record Type Details
Structure of DROPROPIZINE
RACEMATE -> ENANTIOMER
Related Record Type Details
Structure of DROPROPIZINE, (R)-
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of 1-PHENYLPIPERAZINE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of GLYCIDOL
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (GC)
EP
Related Record Type Details
Structure of LEVODROPROPIZINE
ACTIVE MOIETY
NIH
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