PAROXETINE

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C19H20FNO3
Molecular Weight	329.3654
Optical Activity	( - )
Defined Stereocenters	2 / 2
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of PAROXETINE

Structure Search

SMILES

FC1=CC=C(C=C1)[C@@H]2CCNC[C@H]2COC3=CC=C4OCOC4=C3

InChI

InChIKey=AHOUBRCZNHFOSL-YOEHRIQHSA-N

InChI=1S/C19H20FNO3/c20-15-3-1-13(2-4-15)17-7-8-21-10-14(17)11-22-16-5-6-18-19(9-16)24-12-23-18/h1-6,9,14,17,21H,7-8,10-12H2/t14-,17-/m0/s1

HIDE SMILES / InChI

Approval Year

Name

Type

Language

PAROXETINE

Official Name

English

PAROGEN

Common Name

English

(-)-TRANS-4-(P-FLUOROPHENYL)-3-((3,4-(METHYLENEDIOXY)PHENOXY)METHYL)PIPERIDINE

Common Name

English

paroxetine [INN]

Common Name

English

PIPERIDINE, 3-((1,3-BENZODIOXOL-5-YLOXY)METHYL)-4-(4-FLUOROPHENYL)-, (3S-TRANS)-

Systematic Name

English

PAROXETINE [VANDF]

Common Name

English

MOTIVAN

Common Name

English

FROSINOR

Common Name

English

(-)-(3S,4R)-4-(P-FLUOROPHENYL)-3-((3,4-METHYLENEDIOXY)PHENOXY)METHYL)PIPERIDINE

Common Name

English

(-)3S,4R-PAROXETINE

Common Name

English

BESITRAM

Common Name

English

ARKETIS

Common Name

English

(3S,4R)-3-((1,3-BENZODIOXOL-5-YLOXY)METHYL)-4-(4-FLUOROPHENYL)PIPERIDINE

Systematic Name

English

PAROXETINE [MART.]

Common Name

English

PAXPAR

Common Name

English

CASBOL

Common Name

English

DAPAROX

Common Name

English

FG-7051

Common Name

English

PAROXETINE [USAN]

Common Name

English

Paroxetine [WHO-DD]

Common Name

English

PAROXETINE [MI]

Common Name

English

XETANOR

Common Name

English

AROTIN

Common Name

English

BRL-29060

Code

English

Classification Tree Code System Code

LIVERTOX

NBK548306

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

NDF-RT

N0000000109

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

WHO-VATC

QN06AB05

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

NCI_THESAURUS

C94725

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

NCI_THESAURUS

C265

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

NDF-RT

N0000175696

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

WHO-ATC

N06AB05

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

Code System Code Type Description

WIKIPEDIA

PAROXETINE

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

EVMPD

SUB09631MIG

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

DAILYMED

41VRH5220H

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

FDA UNII

41VRH5220H

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

MERCK INDEX

m8418

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

Merck Index

IUPHAR

4790

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

ChEMBL

CHEMBL490

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

NCI_THESAURUS

C61879

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

LACTMED

Paroxetine

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

INN

4327

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

SMS_ID

100000091962

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

CHEBI

7936

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

DRUG BANK

DB00715

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

EPA CompTox

DTXSID3023425

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

CAS

61869-08-7

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

RXCUI

32937

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

RxNorm

PUBCHEM

43815

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

HSDB

7175

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

MESH

D017374

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

DRUG CENTRAL

2068

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

USAN

AA-62

Created by admin on Fri Dec 15 15:31:05 UTC 2023 , Edited by admin on Fri Dec 15 15:31:05 UTC 2023

PRIMARY

ACTIVE MOIETY


					41VRH5220H

METABOLITE INACTIVE (PARENT)


					Q8ZXG5RT43

PHENOL, 4-((4-(4-FLUOROPHENYL)-3-PIPERIDINYL)METHOXY)-2-METHOXY-, (3S-TRANS)-

METABOLITE INACTIVE (PARENT)


					C9948KW92X

4-(((3S,4R)-4-(4-FLUOROPHENYL)-3-PIPERIDINYL)METHOXY)-1,2-BENZENEDIOL

METABOLITE INACTIVE (PARENT)


					LEP9GA88HK

PHENOL, 5-((4-(4-FLUOROPHENYL)-3-PIPERIDINYL)METHOXY)-2-METHOXY-, (3S-TRANS)-

METABOLITE INACTIVE (PARENT)


					2CA3VJ3K3V

(3S,4R)-4-(4-FLUOROPHENYL)-3-PIPERIDINEMETHANOL

PARENT (SALT/SOLVATE)


					3I3T11UD2S

PAROXETINE HYDROCHLORIDE ANHYDROUS

SALT/SOLVATE (PARENT)


					M711N184JE

PAROXETINE MESYLATE

SALT/SOLVATE (PARENT)


					F726G2563Q

PAROXETINE MALEATE

SALT/SOLVATE (PARENT)


					YPO0NTK49O

PAROXETINE ACETATE

SALT/SOLVATE (PARENT)


					X2ELS050D8

PAROXETINE HYDROCHLORIDE