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Details

Stereochemistry RACEMIC
Molecular Formula C21H27NO3S2.ClH.H2O
Molecular Weight 460.05
Optical Activity ( + / - )
Defined Stereocenters 0 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MAZATICOL HYDROCHLORIDE MONOHYDRATE

SMILES

O.Cl.CN1C2CCC(C)(C)C1CC(C2)OC(=O)C(O)(C3=CC=CS3)C4=CC=CS4

InChI

InChIKey=ISDSJXYEVLNWPV-UHFFFAOYSA-N
InChI=1S/C21H27NO3S2.ClH.H2O/c1-20(2)9-8-14-12-15(13-16(20)22(14)3)25-19(23)21(24,17-6-4-10-26-17)18-7-5-11-27-18;;/h4-7,10-11,14-16,24H,8-9,12-13H2,1-3H3;1H;1H2

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including, https://www.ncbi.nlm.nih.gov/pubmed/5000167, https://medical.mt-pharma.co.jp/di/file/dc/pnt.htm

Mazaticol is an anti-acetylcholine agent used in Japan for the treatment of Parkinson's syndrome.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
PENTONA

Approved Use

Parkinson's syndrome due to psychotropic drug administration
Doses

Doses

DosePopulationAdverse events​
8 mg single, oral
Studied dose
Dose: 8 mg
Route: oral
Route: single
Dose: 8 mg
Sources:
healthy, ADULT
Health Status: healthy
Age Group: ADULT
Sex: M
Food Status: UNKNOWN
Sources:
Other AEs: uditory hallucination, Delirium...
Other AEs:
uditory hallucination (83.3%)
Delirium
Sources:
AEs

AEs

AESignificanceDosePopulation
Delirium
8 mg single, oral
Studied dose
Dose: 8 mg
Route: oral
Route: single
Dose: 8 mg
Sources:
healthy, ADULT
Health Status: healthy
Age Group: ADULT
Sex: M
Food Status: UNKNOWN
Sources:
uditory hallucination 83.3%
8 mg single, oral
Studied dose
Dose: 8 mg
Route: oral
Route: single
Dose: 8 mg
Sources:
healthy, ADULT
Health Status: healthy
Age Group: ADULT
Sex: M
Food Status: UNKNOWN
Sources:
PubMed

PubMed

TitleDatePubMed
Population pharmacokinetics of haloperidol using routine clinical pharmacokinetic data in Japanese patients.
2002
Effects of anticholinergic antiparkinsonian drugs on binding of muscarinic receptor subtypes in rat brain.
1990-09
Computerized EEG study on drug-induced extrapyramidalism in schizophrenic patients.
1982
Metabolic fate of 6,6,9-trimethyl-9-azabicyclo(3,3,1)non-3 -yl , -di(2-thienyl)glycolate hydrochloride monohydrate (PG-501).
1972-08
[Absorption, distribution and excretion of 14 C-labelled 6,6,9-trimethyl-9-azabicyclo(3,3,1)non-3 -yl a,a-di(2-thienyl)glycolate hydrochloride monohydrate (PG-501)].
1972-08
[Pharmacological properties of 6,6,9-trimethyl-9-azabicyclo (3,3,1)non-3 beta-yl-alpha, alpha-di(2-thienyl) glycolate hydrochloride monohydrate (PG-501), a new anti-parkinsonian agent].
1971-07
Pharmacology of a new anti-parkinsonian drug: KAO-264.
1971-04

Sample Use Guides

1 tablet (4 mg) is administered orally three times a day. In case of taking Pentona 1%, 0.4 g should be administered the same way.
Route of Administration: Oral
In Vitro Use Guide
Curator's Comment: the full-text can be found here: https://www.jstage.jst.go.jp/article/fpj1944/67/4/67_4_387/_pdf
Anti-acetylcholine activity of mazaticol on he isolated guinea-pig ileum preparation was studied in vitro. ED50 value was 6.4*10(-9) g/ml.
Name Type Language
MAZATICOL HYDROCHLORIDE MONOHYDRATE
Common Name English
MAZATICOL HYDROCHLORIDE HYDRATE
JAN  
Preferred Name English
2-THIOPHENEACETIC ACID, .ALPHA.-HYDROXY-.ALPHA.-2-THIENYL-, 6,6,9-TRIMETHYL-9-AZABICYCLO(3.3.1)NON-3-YL ESTER, HYDROCHLORIDE, MONOHYDRATE, EXO-
Common Name English
MAZATICOL HYDROCHLORIDE HYDRATE [JAN]
Common Name English
Code System Code Type Description
PUBCHEM
11954326
Created by admin on Mon Mar 31 21:24:22 GMT 2025 , Edited by admin on Mon Mar 31 21:24:22 GMT 2025
PRIMARY
CAS
65104-02-1
Created by admin on Mon Mar 31 21:24:22 GMT 2025 , Edited by admin on Mon Mar 31 21:24:22 GMT 2025
PRIMARY
FDA UNII
T64234598Y
Created by admin on Mon Mar 31 21:24:22 GMT 2025 , Edited by admin on Mon Mar 31 21:24:22 GMT 2025
PRIMARY