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Details

Stereochemistry ACHIRAL
Molecular Formula C16H24N2O
Molecular Weight 260.3746
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ROPINIROLE

SMILES

CCCN(CCC)CCC1=CC=CC2=C1CC(=O)N2

InChI

InChIKey=UHSKFQJFRQCDBE-UHFFFAOYSA-N
InChI=1S/C16H24N2O/c1-3-9-18(10-4-2)11-8-13-6-5-7-15-14(13)12-16(19)17-15/h5-7H,3-4,8-12H2,1-2H3,(H,17,19)

HIDE SMILES / InChI
Molecular Formula C16H24N2O
Molecular Weight 260.3746
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Sat Dec 16 15:50:19 UTC 2023
Edited
by admin
on Sat Dec 16 15:50:19 UTC 2023
Record UNII
030PYR8953
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ROPINIROLE
INN   MI   USAN   VANDF   WHO-DD  
USAN   INN  
Official Name English
Ropinirole [WHO-DD]
Common Name English
ROPINIROLE [MI]
Common Name English
NARAPIN
Common Name English
SK&F 101468
Code English
ROPITOR
Brand Name English
ROPINIROLE [USAN]
Common Name English
NSC-758917
Code English
ROPINIROLE [VANDF]
Common Name English
ropinirole [INN]
Common Name English
SK&F-101468
Code English
Classification Tree Code System Code
NCI_THESAURUS C38149
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
NDF-RT N0000175768
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
LIVERTOX NBK548175
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
NDF-RT N0000000117
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
WHO-ATC N04BC04
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
WHO-VATC QN04BC04
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
Code System Code Type Description
EPA CompTox
DTXSID8045195
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY
WIKIPEDIA
ROPINIROLE
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY
LACTMED
Ropinirole
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY
CHEBI
8888
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY
NSC
758917
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY
USAN
TT-138
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY
PUBCHEM
5095
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY
FDA UNII
030PYR8953
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY
DRUG CENTRAL
2402
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY
INN
6436
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY
MERCK INDEX
m9658
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY Merck Index
EVMPD
SUB10380MIG
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY
RXCUI
72302
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY RxNorm
DRUG BANK
DB00268
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY
IUPHAR
7295
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY
ChEMBL
CHEMBL589
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY
NCI_THESAURUS
C61931
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY
MESH
C046649
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY
CAS
91374-21-9
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY
DAILYMED
030PYR8953
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY
HSDB
8252
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY
SMS_ID
100000084378
Created by admin on Sat Dec 16 15:50:20 UTC 2023 , Edited by admin on Sat Dec 16 15:50:20 UTC 2023
PRIMARY
Related Record Type Details
Structure of ROPINIROLE HYDROCHLORIDE
SALT/SOLVATE -> PARENT
D(2) DOPAMINE RECEPTOR
TARGET -> AGONIST
D(3) DOPAMINE RECEPTOR
TARGET -> AGONIST
PLASMA PROTEIN FRACTION (HUMAN)
BINDER->LIGAND
BINDING
Related Record Type Details
Structure of 4-[2-(Dipropylamino)ethyl]-1,3-dihydro-7-hydroxy-2H-indol-2-one
METABOLITE -> PARENT
Related Record Type Details
Structure of ROPINIROLE
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC
Volume of Distribution PHARMACOKINETIC
NIH
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