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Details

Stereochemistry ABSOLUTE
Molecular Formula C15H20Cl2N2O3
Molecular Weight 346.238
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RACLOPRIDE C-11

SMILES

CCN1CCC[C@H]1CNC(=O)C2=C(O[11CH3])C(Cl)=CC(Cl)=C2O

InChI

InChIKey=WAOQONBSWFLFPE-TXWZUYSVSA-N
InChI=1S/C15H20Cl2N2O3/c1-3-19-6-4-5-9(19)8-18-15(21)12-13(20)10(16)7-11(17)14(12)22-2/h7,9,20H,3-6,8H2,1-2H3,(H,18,21)/t9-/m0/s1/i2-1

HIDE SMILES / InChI

Molecular Formula C15H20Cl2N2O3
Molecular Weight 346.238
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 16:15:27 UTC 2023
Edited
by admin
on Fri Dec 15 16:15:27 UTC 2023
Record UNII
GE077RPG04
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RACLOPRIDE C-11
Common Name English
RACLOPRIDE C 11 [USAN]
Common Name English
[11C]-RACLOPRIDE
Common Name English
(S)-3,5-DICHLORO-N-((1-ETHYL-2-PYRROLIDINYL)METHYL)-6-HYDROXY-(.ALPHA.-(SUP 11)C)-O-ANISAMIDE
Common Name English
RACLOPRIDE C 11 [USP IMPURITY]
Common Name English
RACLOPRIDE C 11
USAN   USP  
USAN  
Official Name English
BENZAMIDE, 3,5-DICHLORO-N-((1-ETHYL-2-PYRROLIDINYL)METHYL)-2-HYDROXY-6-(METHOXY-(SUP 11)C)-, (S)-
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C2124
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C152140
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
PRIMARY
FDA UNII
GE077RPG04
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
PRIMARY
USAN
II-84
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
PRIMARY
ChEMBL
CHEMBL8809
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
PRIMARY
CAS
97849-54-2
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
PRIMARY
PUBCHEM
10958914
Created by admin on Fri Dec 15 16:15:27 UTC 2023 , Edited by admin on Fri Dec 15 16:15:27 UTC 2023
PRIMARY
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Co-incubation with a D2L-dopamine receptor sub-saturating concentration of raclopride produced an apparent decrease in the equilibrium dissociation constant of the radioligand (i.e. KD = 6.0 nm vs. 1.9 nm
NON-COMPETITIVE
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ACTIVE MOIETY