LEVOCETIRIZINE

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

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C21H25ClN2O3
Molecular Weight	388.888
Optical Activity	UNSPECIFIED
Defined Stereocenters	1 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of LEVOCETIRIZINE

Structure Search

SMILES

OC(=O)COCCN1CCN(CC1)[C@H](C2=CC=CC=C2)C3=CC=C(Cl)C=C3

InChI

InChIKey=ZKLPARSLTMPFCP-OAQYLSRUSA-N

InChI=1S/C21H25ClN2O3/c22-19-8-6-18(7-9-19)21(17-4-2-1-3-5-17)24-12-10-23(11-13-24)14-15-27-16-20(25)26/h1-9,21H,10-16H2,(H,25,26)/t21-/m1/s1

HIDE SMILES / InChI

Approval Year

Name

Type

Language

LEVOCETIRIZINE

Official Name

English

(R)-CETIRIZINE

Common Name

English

CETIRIZINE (R)-FORM

Common Name

English

XAZAL

Brand Name

English

CETIRIZINE, (R)-

Common Name

English

Levocetirizine [WHO-DD]

Common Name

English

LEVOCETIRIZINE [VANDF]

Common Name

English

LEVOCETIRIZINE [USAN]

Common Name

English

(-)-CETIRIZINE

Common Name

English

ACETIC ACID, (2-(4-((R)-(4-CHLOROPHENYL)PHENYLMETHYL)-1-PIPERAZINYL)ETHOXY)-

Common Name

English

LEVOCETIRIZINE [MART.]

Common Name

English

CETIRIZINE (R)-FORM [MI]

Common Name

English

ACETIC ACID, (2-(4-((R)-(4-CHLOROPHENYL)PHENYLMETHYL)-1-PIPERAZINYL)ETHOXY)

Common Name

English

CETIRIZINE, (-)-

Common Name

English

levocetirizine [INN]

Common Name

English

(2-{4-[(R)-(4-Chlorophenyl)phenylmethyl]piperazin-1-yl}ethoxy)acetic acid

Systematic Name

English

Classification Tree Code System Code

WHO-ATC

R06AE09

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

WHO-VATC

QR06AE09

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

NCI_THESAURUS

C29578

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

NDF-RT

N0000175587

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

NDF-RT

N0000000190

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

LIVERTOX

551

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

Code System Code Type Description

SMS_ID

100000092505

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

PRIMARY

LACTMED

Levocetirizine

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

PRIMARY

RXCUI

356887

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

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RxNorm

CAS

130018-77-8

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

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INN

7700

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

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DAILYMED

6U5EA9RT2O

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

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WIKIPEDIA

LEVOCETIRIZINE

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

PRIMARY

NCI_THESAURUS

C66008

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

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ChEMBL

CHEMBL1201191

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

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DRUG BANK

DB06282

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

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USAN

TT-54

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

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EVMPD

SUB08467MIG

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

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FDA UNII

6U5EA9RT2O

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

PRIMARY

MESH

C472067

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

PRIMARY

MERCK INDEX

m3291

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

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Merck Index

IUPHAR

1214

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

PRIMARY

PUBCHEM

1549000

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

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EPA CompTox

DTXSID60156294

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

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DRUG CENTRAL

1566

Created by admin on Fri Dec 15 15:35:23 UTC 2023 , Edited by admin on Fri Dec 15 15:35:23 UTC 2023

PRIMARY

ACTIVE MOIETY


					6U5EA9RT2O

METABOLITE (PARENT)


					7J723YZJ8Q

4-((4-CHLOROPHENYL)-HYDROXYMETHYL)PHENOL

METABOLITE (PARENT)


					3937I0I7JC

LEVOCETIRIZINE N-OXIDE

METABOLITE (PARENT)


					32M769OW96

LEVOCETIRIZINE-TAURINE CONJUGATE

METABOLITE (PARENT)


					1ZMS7XQY28

N-ACETYL-S-(((R)-4-CHLOROPHENYL)(4-HYDROXYPHENYL)METHYL)-L-CYSTEINE