BIPERIDEN HYDROCHLORIDE

Details

Stereochemistry	UNKNOWN
Molecular Formula	C21H29NO.ClH
Molecular Weight	347.922
Optical Activity	UNSPECIFIED
Defined Stereocenters	0 / 4
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

Cl.OC(CCN1CCCCC1)(C2CC3CC2C=C3)C4=CC=CC=C4

InChI

InChIKey=RDNLAULGBSQZMP-UHFFFAOYSA-N

InChI=1S/C21H29NO.ClH/c23-21(19-7-3-1-4-8-19,11-14-22-12-5-2-6-13-22)20-16-17-9-10-18(20)15-17;/h1,3-4,7-10,17-18,20,23H,2,5-6,11-16H2;1H

HIDE SMILES / InChI

Molecular Formula	ClH
Molecular Weight	36.461
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Molecular Formula	C21H29NO
Molecular Weight	311.4611
Charge	0
Count

Stereochemistry	MIXED
Additional Stereochemistry	No
Defined Stereocenters	0 / 4
E/Z Centers	0
Optical Activity	UNSPECIFIED

Description
Sources: https://mri.cts-mrp.eu/Human/Downloads/AT_H_0521_002_FinalSPC.pdf
Curator's Comment: description was created based on several sources, including https://www.tga.gov.au/alert/akineton-biperiden-hydrochloride-2-mg-tablets https://www.drugs.com/pro/akineton.html

Biperiden, sold under the brandname Akineton was used as an adjunct in the therapy of all forms of parkinsonism (postencephalitic, arteriosclerotic and idiopathic). Was also useful in the control of extrapyramidal disorders due to central nervous system drugs such as phenothiazines and other groups of psychotropics. Biperiden is a weak peripheral anticholinergic agent. It has, therefore, some antisecretory, antispasmodic and mydriatic effects. In addition, biperiden possesses nicotinolytic activity. Parkinsonism is thought to result from an imbalance between the excitatory (cholinergic) and inhibitory (dopaminergic) systems in the corpus striatum. The mechanism of action of centrally active anticholinergic drugs such as biperiden is considered to relate to competitive antagonism of acetylcholine at cholinergic receptors in the corpus striatum, which then restores the balance. Atropine-like side effects such as dry mouth; blurred vision; drowsiness; euphoria or disorientation; urinary retention; postural hypotension; constipation; agitation; disturbed behavior may been seen. Only limited pharmacokinetic studies of biperiden in humans are available.

CNS Activity

Originator

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
Muscarinic acetylcholine receptor M1 168 Target ID: CHEMBL216 Sources: https://www.ncbi.nlm.nih.gov/pubmed/9798802	Antagonist 2849

Conditions

Condition	Modality	Highest Phase	Product
Postencephalitic parkinsonism 7 Sources: https://mri.cts-mrp.eu/Human/Downloads/AT_H_0521_002_FinalSPC.pdf https://www.ncbi.nlm.nih.gov/pubmed/14393477 http://www.clinicaladvisor.com/akineton/drug/3903/	Palliative	Approved 8583	AKINETON Approved Use For use as an adjunct in the therapy of all forms of parkinsonism (postencephalitic, arteriosclerotic and idiopathic). Useful in the control of extrapyramidal disorders due to central nervous system drugs such as phenothiazines and other groups of psychotropics. Launch Date 1959
Idiopathic Parkinson's disease 19 Sources: https://mri.cts-mrp.eu/Human/Downloads/AT_H_0521_002_FinalSPC.pdf http://www.clinicaladvisor.com/akineton/drug/3903/	Palliative	Approved 8583	AKINETON Approved Use For use as an adjunct in the therapy of all forms of parkinsonism (postencephalitic, arteriosclerotic and idiopathic). Useful in the control of extrapyramidal disorders due to central nervous system drugs such as phenothiazines and other groups of psychotropics. Launch Date 1959
Arteriosclerotic parkinsonism 5 Sources: https://mri.cts-mrp.eu/Human/Downloads/AT_H_0521_002_FinalSPC.pdf http://www.clinicaladvisor.com/akineton/drug/3903/	Palliative	Approved 8583	AKINETON Approved Use For use as an adjunct in the therapy of all forms of parkinsonism (postencephalitic, arteriosclerotic and idiopathic). Useful in the control of extrapyramidal disorders due to central nervous system drugs such as phenothiazines and other groups of psychotropics. Launch Date 1959

C_max

Value	Dose	Co-administered	Analyte	Population
13.5 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/3709619/	4 mg single, intravenous dose: 4 mg route of administration: Intravenous experiment type: SINGLE co-administered:		BIPERIDEN plasma	Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED

AUC

Value	Dose	Co-administered	Analyte	Population
62.8 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/3709619/	4 mg single, intravenous dose: 4 mg route of administration: Intravenous experiment type: SINGLE co-administered:		BIPERIDEN plasma	Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED

T_1/2

Value	Dose	Co-administered	Analyte	Population
24.3 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/3709619/	4 mg single, intravenous dose: 4 mg route of administration: Intravenous experiment type: SINGLE co-administered:		BIPERIDEN plasma	Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED

Doses

Dose	Population	Adverse events
600 mg 1 times / day single, oral Overdose Dose: 600 mg, 1 times / day Route: oral Route: single Dose: 600 mg, 1 times / day Sources: https://link.springer.com/article/10.2165/00128415-201013120-00042	unhealthy, 35 Health Status: unhealthy Age Group: 35 Sex: F Sources: https://link.springer.com/article/10.2165/00128415-201013120-00042	Other AEs: Hallucinations, Coma... Other AEs: Hallucinations Coma Sources: https://link.springer.com/article/10.2165/00128415-201013120-00042
4 mg 3 times / day multiple, oral Highest studied dose Dose: 4 mg, 3 times / day Route: oral Route: multiple Dose: 4 mg, 3 times / day Sources: https://pubmed.ncbi.nlm.nih.gov/8570773/	unhealthy, 44 (29-55) Health Status: unhealthy Age Group: 44 (29-55) Sex: M+F Sources: https://pubmed.ncbi.nlm.nih.gov/8570773/	Sources: https://pubmed.ncbi.nlm.nih.gov/8570773/

AEs

AE	Significance	Dose	Population
Coma		600 mg 1 times / day single, oral Overdose Dose: 600 mg, 1 times / day Route: oral Route: single Dose: 600 mg, 1 times / day Sources: https://link.springer.com/article/10.2165/00128415-201013120-00042	unhealthy, 35 Health Status: unhealthy Age Group: 35 Sex: F Sources: https://link.springer.com/article/10.2165/00128415-201013120-00042
Hallucinations		600 mg 1 times / day single, oral Overdose Dose: 600 mg, 1 times / day Route: oral Route: single Dose: 600 mg, 1 times / day Sources: https://link.springer.com/article/10.2165/00128415-201013120-00042	unhealthy, 35 Health Status: unhealthy Age Group: 35 Sex: F Sources: https://link.springer.com/article/10.2165/00128415-201013120-00042

Overview

CYP3A4	CYP2C9	CYP2D6	hERG
inhibitor 2252 activator 150 substrate 1946		inhibitor 2507 substrate 1388

OverviewOther

Other Inhibitor	Other Substrate	Other Inducer
P-gp 1741	P-gp 2052 CYP1A2 1197

Drug as perpetrator

Target	Modality	Activity
P-gp 1932	inhibitor 4027 Sources: https://www.ebi.ac.uk/chembl/g/#browse/activities/full_state/eyJsaXN0Ijp7InNldHRpbmdzX3BhdGgiOiJFU19JTkRFWEVTX05PX01BSU5fU0VBUkNILkFDVElWSVRZIiwiY3VzdG9tX3F1ZXJ5IjoidGFyZ2V0X2NoZW1ibF9pZDpDSEVNQkw0MzAyIiwidXNlX2N1c3RvbV9xdWVyeSI6dHJ1ZSwic2VhcmNoX3Rlcm0iOiIiLCJ0ZXh0X2ZpbHRlciI6IkNIRU1CTDExMDEifX0%3D	no
CYP3A4 2633	activator 342 Sources: https://link.springer.com/article/10.1007%2Fs002280050455	weak [Activation 0.1 uM]
CYP3A4 2633	inhibitor 4027 Sources: https://link.springer.com/article/10.1007%2Fs002280050455	yes [Inhibition 100 uM]
CYP2D6 2546	inhibitor 4027 Sources: https://go.drugbank.com/drugs/DB00810, https://link.springer.com/article/10.1007%2Fs002280050322, https://bioinformatics.charite.de/transformer/index.php?site=fullinfo&cname=000514658	yes [Ki 0.45 uM]

Drug as victim

Target	Modality	Activity
P-gp 2052	substrate 4014 Sources: https://pubmed.ncbi.nlm.nih.gov/22554863/, https://www.ebi.ac.uk/chembl/g/#browse/activities/full_state/eyJsaXN0Ijp7InNldHRpbmdzX3BhdGgiOiJFU19JTkRFWEVTX05PX01BSU5fU0VBUkNILkFDVElWSVRZIiwiY3VzdG9tX3F1ZXJ5IjoidGFyZ2V0X2NoZW1ibF9pZDpDSEVNQkw0MzAyIiwidXNlX2N1c3RvbV9xdWVyeSI6dHJ1ZSwic2VhcmNoX3Rlcm0iOiIiLCJ0ZXh0X2ZpbHRlciI6IkNIRU1CTDExMDEifX0%3D	no
CYP2D6 1388	substrate 4014 Sources: https://pubmed.ncbi.nlm.nih.gov/9342584/, https://www.tandfonline.com/doi/abs/10.1080/03602530903118729	yes [Km 37 uM]
CYP1A2 1197	substrate 4014 Sources: https://www.tandfonline.com/doi/abs/10.1080/03602530903118729	yes
CYP3A4 1946	substrate 4014 Sources: https://www.tandfonline.com/doi/abs/10.1080/03602530903118729	yes

Sourcing

Vendor/Aggregator	ID	URL
001 Chemical	DY445564	https://www.001chemical.com/chem/514-65-8
Ambinter	Amb10843814	http://www.ambinter.com/reference/10843814
BioCrick	BCC4274	http://www.biocrick.com/Biperiden-BCC4274.html
BLD Pharm	BD116739	http://www.bldpharm.com/products/514-65-8.html
Chem Scene	CS-1797	http://www.chemscene.com/514-65-8.html
ChemMol	49427588	http://www.chemmol.com/chemmol/49427588.html
Chemspace	CSSB00020627468	https://chem-space.com/CSSB00020627468
CSNpharm	CSN10453	https://www.csnpharm.com/products/biperiden.html
DC Chemicals	DC23078	http://www.dcchemicals.com/product_show-DC23078.html
eNovation Chemicals	D383306	http://www.enovationchem.com/productDetails.asp?productID=D383306
Lab Network	LN01267554	https://labnetwork.com/frontend-app/p/#!/moleculedetails/LN01267554
MedChem Express	HY-13204A	https://www.medchemexpress.com/Biperiden.html
Molcore	MC445564	https://www.molcore.com/product/514-65-8
MuseChem	I003854	https://www.musechem.com/product/I003854.html
Parchem	28356	http://www.parchem.com/chemical-supplier-distributor/Biperiden-018356.aspx
Smolecule	S521354	http://www.smolecule.com/products/s521354
THE BioTek	bt-262503	https://www.thebiotek.com/product/inhibitors/bt-262503
Vesino Industrial Co Ltd	VA10409	http://www.vsnchem.com/goto/product/23881/
Vitas-M Laboratory	STL582281	http://www.request.vitasmlab.biz/index.php?option=com_search_stk&Itemid=22&stk=STL582281&?utm_source=pubchem&utm_medium=p_search_link&utm_campaign=pubchem_search&utm_content=pubchem_slink
Yuhao Chemical	HL1932	http://www.chemyuhao.com/514-65-8.html

PubMed

Title	Date	PubMed
Simultaneous prescribing of atypical antipsychotics, conventional antipsychotics and anticholinergics-a European study.	2007-06	17333501
Acute dystonia after injection of pegylated interferon alpha-2b.	2007-04-15	17279542
Acute dystonia resulting from abrupt bupropion discontinuation.	2007-04-13	17218049
Early onset of treatment effects with oral risperidone.	2007-01-19	17239237
Neuroleptic malignant syndrome induced by ziprasidone on the second day of treatment.	2007	17366349
[The prevalence and pharmacological cost of Parkinson's disease in Spain].	2006-11-30	17133323
Kinetic and molecular evidences that human cardiac muscle express non-M2 muscarinic receptor subtypes that are able to interact themselves.	2006-11	16965921
[Therapy of postoperative nausea and vomiting in ENT--tardive dyskinesia as an adverse effect of metoclopramid--a case report].	2006-11	16586284
Biperiden-induced delirium model in rats: a behavioral and electroencephalographic study.	2006-10-18	16938281
Modification of practice-dependent plasticity in human motor cortex by neuromodulators.	2006-08	16221926
Antipsychotics-induced hypersensitivity of visual perception.	2006-07	16860706
Association between two distinct executive tasks in schizophrenia: a functional transcranial Doppler sonography study.	2006-05-24	16723019
Acute dystonic reaction to metoclopramide in patients carrying homozygous cytochrome P450 2D6 genetic polymorphisms.	2006-05	16702617
Acute dystonia with low-dosage aripiprazole in Tourette's disorder.	2006-04	16569800
Sudden akathisia after a ziprasidone dose reduction.	2006-03	16513883
Application of a generic physiologically based pharmacokinetic model to the estimation of xenobiotic levels in human plasma.	2006-01	16221756
Pharmacological modulation of cholinergic brain activity and its reflection in special EEG frequency ranges from various brain areas in the freely moving rat (Tele-Stereo-EEG).	2005-12	16009538
Clozapine improves working memory updating in schizophrenia.	2005-12	15905072
Evaluation of the clinical efficacy of risperidone for untreated and treated cases of schizophrenia from various aspects.	2005-10	16194258
Measurement of anticholinergic effects of psychotropic drugs in humans.	2005-09	16189744
Modulation of memory and visuospatial processes by biperiden and rivastigmine in elderly healthy subjects.	2005-09	16041534
Scopolamine-induced convulsions in fasted mice after food intake: effects of glucose intake, antimuscarinic activity and anticonvulsant drugs.	2005-09	15919102
Neuropsychological measures of attention and memory function in schizophrenia: relationships with symptom dimensions and serum monoamine activity.	2005-08-09	16091141
Anaphylactic reaction and unrelated, subsequent, known side effects during therapy with thiethylperazine.	2005-08	16101941
Administration of haloperidol with biperiden reduces mRNAs related to the ubiquitin-proteasome system in mice.	2005-06-15	15803500
Possible malignant neuroleptic syndrome that associated with hypothyroidism.	2005-06	15927337
Alterations in behavioral responses to a cholinergic agonist in post-pubertal rats with neonatal ventral hippocampal lesions: relationship to changes in muscarinic receptor levels.	2005-06	15637638
The effects of amisulpride on five dimensions of psychopathology in patients with schizophrenia: a prospective open-label study.	2005-05-03	15869707
Role of nitric oxide on motor behavior.	2005-03	16047547
Beneficial antipsychotic effects of allopurinol as add-on therapy for schizophrenia: a double blind, randomized and placebo controlled trial.	2005-02	15694232
Major depressive disorder with psychotic features induced by interferon-alpha treatment for hepatitis C in a polydrug abuser.	2005-01	15671136
Tardive nocturnal akathisia due to clozapine treatment.	2005	16240977
Antiparkinsonian-like effects of Plumbago scandens on tremorine-induced tremors methodology.	2004-12	15582683
Ecstasy and acute dystonia.	2004-11	15390124
Development of a screening method for the most commonly abused anticholinergic drugs in Jordan; trihexyphenidyl, procyclidine and biperiden.	2004-10	15363448
Reversible orofacial dyskinesia after ofloxacin treatment.	2004-06	15197723
Use of polypharmacotherapy in pregnancy: a prospective outcome in a case.	2004-05	15093969
Comparisons of psychotropic drug prescribing patterns in acute psychiatric wards across Europe.	2004-03	14747883
Effects of discontinuation of long-term anticholinergic treatment in elderly schizophrenia patients.	2004-01	15101567
Anticholinergic drugs--functional antidotes for the treatment of tabun intoxication.	2004	15168875
Motor disturbances in mice with deficiency of the sodium channel gene Scn8a show features of human dystonia.	2003-12	14769375
[Acute dystonic reaction due to quinine].	2003-12	14697088
[Utility of quetiapine in tardive dyskinesia].	2003-11-26	14639511
Influences of an anticholinergic antiparkinsonian drug, parkinsonism, and psychotic symptoms on cardiac autonomic function in schizophrenia.	2003-10	14520119
In vitro drug-drug interactions with perospirone and concomitantly administered drugs in human liver microsomes.	2003-09-25	14503667
A CYP2D6 phenotype-genotype mismatch in Japanese psychiatric patients.	2003-09	14571354
Adjunctive estrogen treatment in women with chronic schizophrenia: a double-blind, randomized, and placebo-controlled trial.	2003-09	14499318
A comparison of the neuroprotective efficacy of pharmacological pretreatment and antidotal treatment in soman-poisoned rats.	2003	14677718
Use of pimozide in the Pisa syndrome.	1992-08	1322069
Antagonism by antimuscarinic and neuroleptic compounds at the five cloned human muscarinic cholinergic receptors expressed in Chinese hamster ovary cells.	1992-02	1346637

Patents

Sample Use Guides

In Vivo Use Guide

Parkinsonism: Dosage should be individualized. Begin with 1/2 a tablet twice daily, and gradually increase to 1 tablet, 3-4 times daily.

Route of Administration: Oral

In Vitro Use Guide

(+)-Biperiden had its highest affinity to M1-receptors (pA2 = 9.07), had low affinity to cardiac M2 alpha-receptors (pA2 = 7.25) and intermediate affinity to ileal M2 beta-receptors (pA2 = 8.27). The ability of (+)-biperiden to discriminate between ileal M2 beta- and cardiac M2 alpha-receptors (factor = 10) was similar to that of 4-diphenylacetoxy-N-methylpiperidine methiodide (4-DAMP, factor = 9). In contrast, (-)-biperiden displayed low but nearly undistinguishable affinity for all muscarinic receptor subtypes studied (pA2 = 5.59 +/- 6.38). (+)-Biperiden discriminated strongly between M1- and cardiac M2 alpha-receptors (factor 66), thus being even more selective than pirenzepine (factor 28) which makes it one of the most M1-/cardiac M2 alpha-selective antimuscarinic drugs now available.

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:06:45 GMT 2025` Edited by `admin` on `Mon Mar 31 18:06:45 GMT 2025`
Record UNII	K35N76CUHF
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

BIPERIDEN HYDROCHLORIDE

Common Name

English

AKINETON

Preferred Name

English

NSC-170950

Code

English

BIPERIDEN HYDROCHLORIDE [ORANGE BOOK]

Common Name

English

NSC-84989

Code

English

BIPERIDEN HYDROCHLORIDE [WHO-IP]

Common Name

English

BIPERIDEN HYDROCHLORIDE [EP MONOGRAPH]

Common Name

English

AKINOPHYL

Brand Name

English

BIPERIDEN HYDROCHLORIDE [MI]

Common Name

English

BIPERIDEN HYDROCHLORIDE [JAN]

Common Name

English

BIPERIDEN HYDROCHLORIDE [USP IMPURITY]

Common Name

English

TASMOLIN

Common Name

English

Biperiden hydrochloride [WHO-DD]

Common Name

English

BIPERIDEN HCL

Common Name

English

BIPERIDEN HYDROCHLORIDE [MART.]

Common Name

English

1-PIPERIDINEPROPANOL, .ALPHA.-BICYCLO(2.2.1)HEPT-5-EN-2-YL-.ALPHA.-PHENYL-, HYDROCHLORIDE

Systematic Name

English

BIPERIDENI HYDROCHLORIDUM [WHO-IP LATIN]

Common Name

English

?-5-Norbornen-2-yl-?-phenyl-1-piperidinepropanol hydrochloride

Systematic Name

English

BIPERIDEN HYDROCHLORIDE [VANDF]

Common Name

English

Classification Tree Code System Code

NCI_THESAURUS

C38149