General
Preferred name
TRIHEXYPHENIDYL
Synonyms
TRIHEXYPHENIDYL HYDROCHLORIDE ()
1-Piperidinepropanol, alpha-cyclohexyl-alpha-phenyl-, hydrochloride, mixt. with n-methyl-n-(2-phenylethyl)benzeneethanamine hydrochloride ()
Benzhexol hydrochloride ()
Artane hydrochloride ()
Tremin ()
Triesifenidile ()
Artane ()
Trihexyphenidyl HCl ()
Benzhexol ()
(S)-Trihexyphenidyl ()
(R)-Trihexyphenidyl ()
DL-trihexyphenidyl hydrochloride ()
Trihexyphenidyl-D,L Hydrochloride ()
Trihexyphenidyl hydrochloride ()
Benzhexol hydrochloride, Artane hydrochloride ()
Trihexylphenedyl ()
Cyclodolum ()
Parcopane ()
Agitane ()
NSC-757357 ()
Aparkane ()
Trihexyphenidyli hydrochloridum ()
Triphedinon ()
Broflex ()
Cyclodol ()
Bentex ()
Sedrina ()
Romparkin ()
Apo-trihex ()
NSC-12268 ()
Trihexyphenidyl (hydrochloride) ()
P&D ID
PD010217
CAS
52-49-3
58947-95-8
144-11-6
Tags
natural product
drug
available
Approved by
FDA
First approval
1949
Drug Status
approved
Drug indication
Antiparkinsonian
Obesity
Parkinson disease
Anticholinergic
Dystonia
Max Phase
Phase 4
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 Trihexyphenidyl is an antispasmodic, antimuscarinic drug.
Marketed formulations may contain trihexyphenidyl hydrochloride (PubChem CID 66007). (GtoPdb)
TOXICITY Symptoms of overdose include mydriasis, dryness of mucous membranes, red face, atonic states of bowels and bladder, and hyperthermia in high doses. Trihexyphenidyl causes agitation, confusion, and hallucinations due to its effects on the central nervous system. Untreated overdose may result in death, especially in children. Respiratory depression and cardiac arrest may be seen as premortal signs.
DESCRIPTION Muscarinic acetylcholine receptor antagonist; centrally acting anticholinergic (LOPAC library)
DESCRIPTION Trihexyphenidyl is a Mucarinic Cholinergic receptor antagonist using for the treatment of Parkinson's disease. It also has a direct antispasmodic action on smooth muscle. (BOC Sciences Bioactive Compounds)
Cell lines
0
Organisms
1
Compound Sets
26
BOC Sciences Bioactive Compounds
Cayman Chemical Bioactives
CeMM library of unique drugs (CLOUD)
ChEMBL Approved Drugs
DrugBank
DrugBank Approved Drugs
DrugCentral
DrugCentral Approved Drugs
DrugMAP
DrugMAP Approved Drugs
DrugMatrix
Enamine BioReference Compounds
Guide to Pharmacology
JUMP-Target 1 Compound Set
LOPAC library
LSP-MoA library (Laboratory of Systems Pharmacology)
NCATS Inxight Approved Drugs
NIH Clinical Collections (NCC)
NPC Screening Collection
Prestwick Chemical Library
ReFrame library
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
The Spectrum Collection
External IDs
54
Properties
(calculated by RDKit )
Molecular Weight
301.24
Hydrogen Bond Acceptors
2
Hydrogen Bond Donors
1
Rotatable Bonds
5
Ring Count
3
Aromatic Ring Count
1
cLogP
4.33
TPSA
23.47
Fraction CSP3
0.7
Chiral centers
1.0
Largest ring
6.0
QED
0.87
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Target
Muscarinic acetylcholine receptor M1
AChR
mAChR
CHRM3
Selectivity
Muscarinic
MOA
muscarinic acetylcholine receptor antagonist
Pathway
Neuroscience
Therapeutic Class
Antiparkinson Agents
Solubility
Soluble in DMSO
Source data