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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

Molecular Formula C20H25NO
Molecular Weight 295.4186
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

PubMed

PubMed

TitleDatePubMed
Drug-human serum albumin binding studied by capillary electrophoresis with electrochemiluminescence detection.
2004 Oct
Validated stability-indicating HPLC method for the determination of pridinol mesylate. Kinetics study of its degradation in acid medium.
2008 Dec 1
Development and validation of an HPLC method for the determination of process-related impurities in pridinol mesylate, employing experimental designs.
2009 Nov 10
Development and validation of a dissolution test for meloxicam and pridinol mesylate from combined tablet formulation.
2010 Mar
Profiling of a prescription drug library for potential renal drug-drug interactions mediated by the organic cation transporter 2.
2011 Jul 14
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
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:11:24 GMT 2023
Edited
by admin
on Fri Dec 15 16:11:24 GMT 2023
Record UNII
9E75Q6SUUB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PRIDINOL
HSDB   INN   MI   WHO-DD  
INN  
Official Name English
PRIDINOL [HSDB]
Common Name English
C-238
Code English
Pridinol [WHO-DD]
Common 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 Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
WHO-ATC M03BX03
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
NCI_THESAURUS C29710
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C73319
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
PRIMARY
INN
1320
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
PRIMARY
PUBCHEM
4904
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
PRIMARY
CAS
511-45-5
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
PRIMARY
NSC
23016
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
PRIMARY
RXCUI
34479
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
PRIMARY RxNorm
ECHA (EC/EINECS)
208-128-0
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
PRIMARY
ChEMBL
CHEMBL404215
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
PRIMARY
FDA UNII
9E75Q6SUUB
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
PRIMARY
SMS_ID
100000081633
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
PRIMARY
MERCK INDEX
m9129
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
PRIMARY Merck Index
CHEBI
75247
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
PRIMARY
WIKIPEDIA
PRIDINOL
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
PRIMARY
MESH
C009185
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
PRIMARY
EPA CompTox
DTXSID0045090
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
PRIMARY
DRUG CENTRAL
2263
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
PRIMARY
EVMPD
SUB10037MIG
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
PRIMARY
DRUG BANK
DB13642
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
PRIMARY
HSDB
2684
Created by admin on Fri Dec 15 16:11:24 GMT 2023 , Edited by admin on Fri Dec 15 16:11:24 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY