CHLORPHENIRAMINE

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C16H19ClN2
Molecular Weight	274.788
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of CHLORPHENIRAMINE

Structure Search

SMILES

CN(C)CCC(C1=CC=C(Cl)C=C1)C2=CC=CC=N2

InChI

InChIKey=SOYKEARSMXGVTM-UHFFFAOYSA-N

InChI=1S/C16H19ClN2/c1-19(2)12-10-15(16-5-3-4-11-18-16)13-6-8-14(17)9-7-13/h3-9,11,15H,10,12H2,1-2H3

HIDE SMILES / InChI

Molecular Formula	C16H19ClN2
Molecular Weight	274.788
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Approval Year

Substance Class	Chemical Created by `admin` on `Sat Dec 16 17:09:18 UTC 2023` Edited by `admin` on `Sat Dec 16 17:09:18 UTC 2023`
Record UNII	3U6IO1965U
Record Status	`Validated (UNII)`
Record Version

Download

Related Record	Type

Name

Type

Language

CHLORPHENIRAMINE

Common Name

English

CHLORPHENIRAMINE [VANDF]

Common Name

English

CHLORPHENIRAMINE [MI]

Common Name

English

CHLORPHENIRAMINE COMPONENT OF TUZISTRA

Brand Name

English

chlorphenamine [INN]

Common Name

English

Chlorphenamine [WHO-DD]

Common Name

English

CHLORPHENIRAMINE [HSDB]

Common Name

English

CLOFENIRAMINA

Brand Name

English

783AHI015X

Common Name

English

2-(P-CHLORO-.ALPHA.-(2-(DIMETHYLAMINO)ETHYL)BENZYL)PYRIDINE

Common Name

English

CHLORPHENAMINE

Official Name

English

TUZISTRA COMPONENET OF CHLORPHENIRAMINE

Brand Name

English

Classification Tree Code System Code

WHO-ATC

R06AB04

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

NDF-RT

N0000175587

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

NDF-RT

N0000000190

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

WHO-VATC

QR06AB04

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

LIVERTOX

195

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

WHO-ESSENTIAL MEDICINES LIST

03

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

WHO-ATC

R06AB54

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

NCI_THESAURUS

C29578

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

WHO-VATC

QR06AB54

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

Code System Code Type Description

DRUG CENTRAL

616

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

EPA CompTox

DTXSID0022804

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

NCI_THESAURUS

C61672

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

PUBCHEM

2725

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

RXCUI

2400

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

HSDB

3032

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

DRUG BANK

DB01114

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

ECHA (EC/EINECS)

205-054-0

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

LACTMED

Chlorpheniramine

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

CAS

132-22-9

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

DAILYMED

3U6IO1965U

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

INN

104

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

WIKIPEDIA

CHLORPHENAMINE

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

EVMPD

SUB06201MIG

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

MESH

D002744

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

SMS_ID

100000090540

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

MERCK INDEX

m3456

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

Merck Index

IUPHAR

6976

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

FDA UNII

3U6IO1965U

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

ChEMBL

CHEMBL505

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

CHEBI

52010

Created by admin on Sat Dec 16 17:09:20 UTC 2023 , Edited by admin on Sat Dec 16 17:09:20 UTC 2023

PRIMARY

Related Record Type Details


					V1Q0O9OJ9Z

CHLORPHENIRAMINE MALEATE

SALT/SOLVATE -> PARENT


					28XBT591QG

HISTAMINE H1 RECEPTOR

TARGET -> INHIBITOR


					3Q9Q0B929N

DEXCHLORPHENIRAMINE

ENANTIOMER -> RACEMATE


					5S6VUP419V

CHLORPHENIRAMINE HYDROCHLORIDE

SALT/SOLVATE -> PARENT


					6D53G0FD0Z

PLASMA PROTEIN FRACTION (HUMAN)

BINDER->LIGAND

Interaction Type:

BINDING

Amount:


					6NP3XSMIP3

MULTIDRUG AND TOXIN EXTRUSION PROTEIN 1

TRANSPORTER -> INHIBITOR

CHLORPHENIRAMINE POLISTIREX

SUB_CONCEPT->SUBSTANCE


					B46KUN2O9L

MATE-2

TRANSPORTER -> INHIBITOR


					EY9131E63D

CHLORPHENIRAMINE, (-)-

ENANTIOMER -> RACEMATE

Related Record Type Details


					0D64JQ680A

MONODESMETHYLCHLORPHENIRAMINE

METABOLITE -> PARENT


					WW1P1ER09X

DIDESMETHYLCHLORPHENIRAMINE

METABOLITE -> PARENT

Related Record Type Details


					IXA7C9ZN03

BROMPHENIRAMINE MALEATE

PARENT -> IMPURITY

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

USP

Amount:

Related Record Type Details


					3U6IO1965U

CHLORPHENIRAMINE

ACTIVE MOIETY