General
Preferred name
ZACOPRIDE
Synonyms
ZACOPRIDE HYDROCHLORIDE ()
Zacopride HCl ()
AHR-11190-B ()
(R)-ZACOPRIDE ()
ZACOPRIDE,R ()
ZACOPRIDE,S ()
Zacopride (hydrochloride) ()
P&D ID
PD014511
CAS
101303-98-4
99617-34-2
90182-92-6
Tags
drug candidate
natural product
available
Drug indication
Anti-Emetic
Stimulant (peristaltic)
Structure
Probe scores
P&D probe-likeness score
[[ v.score ]]%
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
DESCRIPTION KV11.1 (hERG) channel blocker; inhibits rapid delayed rectifier K+ current (IKr) (Tocris Bioactive Compound Library)
DESCRIPTION Highly potent 5-HT3 receptor antagonist. Also 5-HT4 agonist (Tocriscreen Plus)
DESCRIPTION Highly potent 5-HT3 receptor antagonist. Also 5-HT4 agonist (Tocriscreen Total)
DESCRIPTION Zacopride hydrochloride is a highly potent 5-HT3 receptor antagonist (Ki = 0.38 nM) and 5-HT4 receptor agonist (Ki = 373 nM). Zacopride hydrochloride acts as an antiemetic and anxiolytic following systemic administration in vivo. (BOC Sciences Bioactive Compounds)
Compound Sets
13
BOC Sciences Bioactive Compounds
DrugMatrix
Guide to Pharmacology
MedChem Express Bioactive Compound Library
NIH Clinical Collections (NCC)
NPC Screening Collection
ReFrame library
TargetMol Bioactive Compound Library
Tocris Bioactive Compound Library
Tocriscreen Plus
Tocriscreen Total
External IDs
42
Properties
(calculated by RDKit )
Molecular Weight
309.12
Hydrogen Bond Acceptors
4
Hydrogen Bond Donors
2
Rotatable Bonds
3
Ring Count
4
Aromatic Ring Count
1
cLogP
1.75
TPSA
67.59
Fraction CSP3
0.53
Chiral centers
1.0
Largest ring
6.0
QED
0.83
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Target Type
Ion Channels
Pathway
GPCR/G protein
Membrane Transporter/Ion Channel
Neuroscience
Neuronal Signaling
Target
5-HT3 antagonist
5-HT4 agonist
IK1/Kir2.1 agonist
Primary Target
5-HT3 Receptors
MOA
Antagonist
5-HT Receptor
Potassium Channel
Source data