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Details

Stereochemistry ACHIRAL
Molecular Formula C20H25NO
Molecular Weight 295.4186
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Pridinol

SMILES

OC(CCN1CCCCC1)(C2=CC=CC=C2)C3=CC=CC=C3

InChI

InChIKey=RQXCLMGKHJWMOA-UHFFFAOYSA-N
InChI=1S/C20H25NO/c22-20(18-10-4-1-5-11-18,19-12-6-2-7-13-19)14-17-21-15-8-3-9-16-21/h1-2,4-7,10-13,22H,3,8-9,14-17H2

HIDE SMILES / InChI
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
31.04 ng/mL
3 mg single, oral
dose: 3 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PRIDINOL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
197.11 ng × h/mL
3 mg single, oral
dose: 3 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PRIDINOL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
18 h
3 mg single, oral
dose: 3 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PRIDINOL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
Funbound

Funbound

ValueDoseCo-administeredAnalytePopulation
68.67%
PRIDINOL serum
Homo sapiens
Doses

Doses

DosePopulationAdverse events​
3 mg single, oral
Recommended
Dose: 3 mg
Route: oral
Route: single
Dose: 3 mg
Sources:
healthy, ADULT
Health Status: healthy
Age Group: ADULT
Sex: M+F
Food Status: FASTED
Sources:
PubMed

PubMed

TitleDatePubMed
Profiling of a prescription drug library for potential renal drug-drug interactions mediated by the organic cation transporter 2.
2011-07-14
Development and validation of a dissolution test for meloxicam and pridinol mesylate from combined tablet formulation.
2010-03
Development and validation of an HPLC method for the determination of process-related impurities in pridinol mesylate, employing experimental designs.
2009-11-10
Validated stability-indicating HPLC method for the determination of pridinol mesylate. Kinetics study of its degradation in acid medium.
2008-12-01
Method development and validation for the simultaneous determination of meloxicam and pridinol mesylate using RP-HPLC and its application in drug formulations.
2008-01-22
Suicide by multidrug ingestion: hypothesis on the role played by the self-administration of activated charcoal.
2007-03
Drug-human serum albumin binding studied by capillary electrophoresis with electrochemiluminescence detection.
2004-10
Effect of muscle relaxants on experimental jaw-muscle pain and jaw-stretch reflexes: a double-blind and placebo-controlled trial.
2003
Patents

Sample Use Guides

In Vivo Use Guide
Oral Muscle spasms Adult: As mesilate: Usual initial: 2-8 mg tid; Maintenance: 4-8 mg daily.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Name Type Language
C-238
Preferred Name English
Pridinol
HSDB   INN   MI   WHO-DD  
INN  
Official Name English
1,1-Diphenyl-3-(1-piperidyl)-1-propanol
Systematic Name English
Pridinol [HSDB]
Common Name English
1-Piperidinepropanol, ?,?-diphenyl-
Systematic Name English
Pridinol [WHO-DD]
Common Name English
3-(N-Piperidyl)-1,1-diphenyl-1-propanol
Systematic Name English
NSC-23016
Code English
Pridinol [MI]
Common Name English
Pridinol [INN]
Common Name English
Classification Tree Code System Code
WHO-VATC QM03BX03
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
WHO-ATC M03BX03
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
NCI_THESAURUS C29710
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
Code System Code Type Description
NCI_THESAURUS
C73319
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
PRIMARY
INN
1320
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
PRIMARY
PUBCHEM
4904
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
PRIMARY
CAS
511-45-5
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
PRIMARY
NSC
23016
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
PRIMARY
RXCUI
34479
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
PRIMARY RxNorm
ECHA (EC/EINECS)
208-128-0
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
PRIMARY
ChEMBL
CHEMBL404215
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
PRIMARY
FDA UNII
9E75Q6SUUB
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
PRIMARY
SMS_ID
100000081633
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
PRIMARY
MERCK INDEX
m9129
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
PRIMARY Merck Index
CHEBI
75247
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
PRIMARY
WIKIPEDIA
PRIDINOL
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
PRIMARY
MESH
C009185
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
PRIMARY
EPA CompTox
DTXSID0045090
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
PRIMARY
DRUG CENTRAL
2263
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
PRIMARY
EVMPD
SUB10037MIG
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
PRIMARY
DRUG BANK
DB13642
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
PRIMARY
HSDB
2684
Created by admin on Mon Mar 31 18:21:16 GMT 2025 , Edited by admin on Mon Mar 31 18:21:16 GMT 2025
PRIMARY