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Details

Stereochemistry ACHIRAL
Molecular Formula C18H26ClN3O3
Molecular Weight 367.87
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PRUCALOPRIDE

SMILES

COCCCN1CCC(CC1)NC(=O)C2=C3OCCC3=C(N)C(Cl)=C2

InChI

InChIKey=ZPMNHBXQOOVQJL-UHFFFAOYSA-N
InChI=1S/C18H26ClN3O3/c1-24-9-2-6-22-7-3-12(4-8-22)21-18(23)14-11-15(19)16(20)13-5-10-25-17(13)14/h11-12H,2-10,20H2,1H3,(H,21,23)

HIDE SMILES / InChI

Molecular Formula C18H26ClN3O3
Molecular Weight 367.87
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:38:52 UTC 2023
Edited
by admin
on Fri Dec 15 16:38:52 UTC 2023
Record UNII
0A09IUW5TP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PRUCALOPRIDE
EMA EPAR   INN   MART.   MI   USAN   WHO-DD  
INN   USAN  
Official Name English
R-093877
Code English
PRUCALOPRIDE [EMA EPAR]
Common Name English
PRUCALOPRIDE [MI]
Common Name English
R093877
Common Name English
PRUCALOPRIDE [USAN]
Common Name English
4-Amino-5-chloro-2,3-dihydro-N-[1-(3-methoxypropyl)-4-piperidyl]-7-benzofurancarboxamide
Systematic Name English
Prucalopride [WHO-DD]
Common Name English
PRUCALOPRIDE [MART.]
Common Name English
prucalopride [INN]
Common Name English
Classification Tree Code System Code
WHO-ATC A03AE04
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
NCI_THESAURUS C47794
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
WHO-ATC A06AX05
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
WHO-VATC QA06AX05
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
Code System Code Type Description
FDA UNII
0A09IUW5TP
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
PRIMARY
INN
7702
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
PRIMARY
RXCUI
2107310
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
PRIMARY
SMS_ID
100000080862
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
PRIMARY
DAILYMED
0A09IUW5TP
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
PRIMARY
EVMPD
SUB10155MIG
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
PRIMARY
NCI_THESAURUS
C74386
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
PRIMARY
MESH
C406662
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
PRIMARY
DRUG CENTRAL
3502
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
PRIMARY
EPA CompTox
DTXSID5057670
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
PRIMARY
LACTMED
Prucalopride
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
PRIMARY
ChEMBL
CHEMBL117287
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
PRIMARY
IUPHAR
243
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
PRIMARY
DRUG BANK
DB06480
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
PRIMARY
WIKIPEDIA
PRUCALOPRIDE
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
PRIMARY
USAN
YY-100
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
PRIMARY
MERCK INDEX
m9285
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
PRIMARY Merck Index
CAS
179474-81-8
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
PRIMARY
PUBCHEM
3052762
Created by admin on Fri Dec 15 16:38:52 UTC 2023 , Edited by admin on Fri Dec 15 16:38:52 UTC 2023
PRIMARY
Related Record Type Details
TRANSPORTER -> SUBSTRATE
EXCRETED UNCHANGED
URINE
TRANSPORTER -> SUBSTRATE
METABOLIC ENZYME -> SUBSTRATE
BINDER->LIGAND
BINDING
CUMULATIVE EXCRETION
FECAL
EXCRETED UNCHANGED
URINE
SALT/SOLVATE -> PARENT
TARGET -> AGONIST
Interaction with the 5-HT4 receptor leads to the elevation of cyclic adenosine monophosphate (cAMP) levels in HEK293 cells
EC50
CUMULATIVE EXCRETION
URINE
BINDER->LIGAND
In human plasma, the binding of R093877 increased at higher pH values. In the pH-range 7.1 to 7.7, the percentage bound increased from 23.3% to 35.5%
BINDING
SALT/SOLVATE -> PARENT
Related Record Type Details
METABOLITE -> PARENT
Seven metabolites were recovered in urine and feces, with the most abundant metabolite R107504 (O-desmethyl prucalopride acid) accounting for 3.2% and 3.1% of the dose in urine and feces, respectively.
FECAL; URINE
Related Record Type Details
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Volume of Distribution PHARMACOKINETIC
Tmax PHARMACOKINETIC ROUTE OF ADMINISTRATION
PHARMACOKINETIC
Biological Half-life PHARMACOKINETIC DOSE
PHARMACOKINETIC
ROUTE OF ADMINISTRATION
PHARMACOKINETIC
BREAST MILK/PLASMA RATIO PHARMACOKINETIC COMMENTS
PHARMACOKINETIC