U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C16H19ClN2O
Molecular Weight 290.788
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARBINOXAMINE

SMILES

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

InChI

InChIKey=OJFSXZCBGQGRNV-UHFFFAOYSA-N
InChI=1S/C16H19ClN2O/c1-19(2)11-12-20-16(15-5-3-4-10-18-15)13-6-8-14(17)9-7-13/h3-10,16H,11-12H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C16H19ClN2O
Molecular Weight 290.788
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Description
Curator's Comment: description was created based on several sources, including: https://www.drugs.com/pro/carbinoxamine.html

Carbinoxamine is a histamine-H1 receptor blocking agent. It is an antihistamine with anticholinergic (drying) and sedative properties. Carbinoxamine appears to compete with histamine (type H1) for receptor sites on effector cells in the gastrointestinal tract, blood vessels and respiratory tract. Carbinoxamine is effective for the symptomatic treatment of seasonal and perennial allergic rhinitis; vasomotor rhinitis; allergic conjunctivitis due to inhalant allergens and foods; mild, uncomplicated allergic skin manifestations of urticaria and angioedema; dermatographism; as therapy for anaphylactic reactions adjunctive to epinephrine and other standard measures after the acute manifestations have been controlled. Most common adverse reactions are: sedation, sleepiness, dizziness, disturbed coordination, epigastric distress, and thickening of bronchial secretions. Avoid concomitant use of alcohol and CNS depressants (hypnotics sedatives, tranquilizers, etc.) due to additive adverse effects.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
2.3 nM [Ki]
Target ID: CHEMBL289
Sources: DOI: 10.14896/jssxmeeting.21.0.296.1
25.0 µM [Ki]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
CARBINOXAMINE MALEATE

Approved Use

Carbinoxamine maleate is effective for the symptomatic treatment of: Seasonal and perennial allergic rhinitis. Vasomotor rhinitis. Allergic conjunctivitis due to inhalant allergens and foods. Mild, uncomplicated allergic skin manifestations of urticaria and angioedema. Dermatographism. As therapy for anaphylactic reactions adjunctive to epinephrine and other standard measures after the acute manifestations have been controlled. Amelioration of the severity of allergic reactions to blood or plasma.

Launch Date

2003
Palliative
CARBINOXAMINE MALEATE

Approved Use

Carbinoxamine maleate is effective for the symptomatic treatment of: Seasonal and perennial allergic rhinitis. Vasomotor rhinitis. Allergic conjunctivitis due to inhalant allergens and foods. Mild, uncomplicated allergic skin manifestations of urticaria and angioedema. Dermatographism. As therapy for anaphylactic reactions adjunctive to epinephrine and other standard measures after the acute manifestations have been controlled. Amelioration of the severity of allergic reactions to blood or plasma.

Launch Date

2003
Palliative
CARBINOXAMINE MALEATE

Approved Use

Carbinoxamine maleate is effective for the symptomatic treatment of: Seasonal and perennial allergic rhinitis. Vasomotor rhinitis. Allergic conjunctivitis due to inhalant allergens and foods. Mild, uncomplicated allergic skin manifestations of urticaria and angioedema. Dermatographism. As therapy for anaphylactic reactions adjunctive to epinephrine and other standard measures after the acute manifestations have been controlled. Amelioration of the severity of allergic reactions to blood or plasma.

Launch Date

2003
Palliative
CARBINOXAMINE MALEATE

Approved Use

Carbinoxamine maleate is effective for the symptomatic treatment of: Seasonal and perennial allergic rhinitis. Vasomotor rhinitis. Allergic conjunctivitis due to inhalant allergens and foods. Mild, uncomplicated allergic skin manifestations of urticaria and angioedema. Dermatographism. As therapy for anaphylactic reactions adjunctive to epinephrine and other standard measures after the acute manifestations have been controlled. Amelioration of the severity of allergic reactions to blood or plasma.

Launch Date

2003
Palliative
CARBINOXAMINE MALEATE

Approved Use

Carbinoxamine maleate is effective for the symptomatic treatment of: Seasonal and perennial allergic rhinitis. Vasomotor rhinitis. Allergic conjunctivitis due to inhalant allergens and foods. Mild, uncomplicated allergic skin manifestations of urticaria and angioedema. Dermatographism. As therapy for anaphylactic reactions adjunctive to epinephrine and other standard measures after the acute manifestations have been controlled. Amelioration of the severity of allergic reactions to blood or plasma.

Launch Date

2003
Palliative
CARBINOXAMINE MALEATE

Approved Use

Carbinoxamine maleate is effective for the symptomatic treatment of: Seasonal and perennial allergic rhinitis. Vasomotor rhinitis. Allergic conjunctivitis due to inhalant allergens and foods. Mild, uncomplicated allergic skin manifestations of urticaria and angioedema. Dermatographism. As therapy for anaphylactic reactions adjunctive to epinephrine and other standard measures after the acute manifestations have been controlled. Amelioration of the severity of allergic reactions to blood or plasma.

Launch Date

2003
Palliative
CARBINOXAMINE MALEATE

Approved Use

Carbinoxamine maleate is effective for the symptomatic treatment of: Seasonal and perennial allergic rhinitis. Vasomotor rhinitis. Allergic conjunctivitis due to inhalant allergens and foods. Mild, uncomplicated allergic skin manifestations of urticaria and angioedema. Dermatographism. As therapy for anaphylactic reactions adjunctive to epinephrine and other standard measures after the acute manifestations have been controlled. Amelioration of the severity of allergic reactions to blood or plasma.

Launch Date

2003
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
16.9 ng/mL
8 mg single, oral
dose: 8 mg
route of administration: Oral
experiment type: SINGLE
co-administered: PHENYLPROPANOLAMINE
CARBINOXAMINE MALEATE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
4.5 ng/mL
4 mg single, oral
dose: 4 mg
route of administration: Oral
experiment type: SINGLE
co-administered: PHENYLEPHRINE
CARBINOXAMINE MALEATE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
13.5 ng/mL
4 mg 2 times / day multiple, oral
dose: 4 mg
route of administration: Oral
experiment type: MULTIPLE
co-administered: PHENYLEPHRINE
CARBINOXAMINE MALEATE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
14.5 h
8 mg single, oral
dose: 8 mg
route of administration: Oral
experiment type: SINGLE
co-administered: PHENYLPROPANOLAMINE
CARBINOXAMINE MALEATE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
30 h
4 mg single, oral
dose: 4 mg
route of administration: Oral
experiment type: SINGLE
co-administered: PHENYLEPHRINE
CARBINOXAMINE MALEATE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
22 h
4 mg 2 times / day multiple, oral
dose: 4 mg
route of administration: Oral
experiment type: MULTIPLE
co-administered: PHENYLEPHRINE
CARBINOXAMINE MALEATE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
Funbound

Funbound

ValueDoseCo-administeredAnalytePopulation
31%
unknown, unknown
CARBINOXAMINE MALEATE plasma
Homo sapiens
population: UNKNOWN
age: UNKNOWN
sex: UNKNOWN
food status: UNKNOWN
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 of a list of potentially inappropriate drugs for the korean elderly using the delphi method.
2010-12
4-(4-Chloro-phen-yl)-4-hy-droxy-piperidinium maleate maleic acid solvate.
2010-07-14
LC for analysis of two sustained-release mixtures containing cough cold suppressant drugs.
2010-07
[1,2]-Anionic rearrangement of 2-benzyloxypyridine and related pyridyl ethers.
2009-10-16
Discovery of novel and cardioselective diltiazem-like calcium channel blockers via virtual screening.
2008-09-25
Characterization of antihistamine-human serum protein interactions by capillary electrophoresis.
2007-04-20
Possible role of pseudoephedrine and other over-the-counter cold medications in the deaths of very young children.
2007-03
Mechanism of the condensation of homocysteine thiolactone with aldehydes.
2006-10-25
Spectrophotometric determination of carbinoxamine maleate in pharmaceutical formulations by ternary complex formation with Cu(II) and eosin.
2006-06-01
Over-the-counter cold medications-postmortem findings in infants and the relationship to cause of death.
2005-10
Simultaneous determination of ingredients in a cold medicine by cyclodextrin-modified microemulsion electrokinetic chromatography.
2005-03-09
Quantitation of antihistamines in pharmaceutical preparations by liquid chromatography with a micellar mobile phase of sodium dodecyl sulfate and pentanol.
2002-01-05
Cold-syrup induced movement disorder.
2001-06
Chromatographic analysis of phenethylamine-antihistamine combinations using C8, C18 or cyano columns and micellar sodium dodecyl sulfate-pentanol mixtures.
2001-04
[Serous otitis media. Comparative study of carbinoxamine- pseudoephedrine vs astemizole-pseudoephedrine].
1997-05-01
The need for rational therapeutics in the use of cough and cold medicine in infants.
1992-04
[Antimycobacterial antihistaminics].
1989-08
Clistin maleate; a clinical appraisal of a new antihistaminic.
1954-11
Patents

Sample Use Guides

Tablets: 1 or 2 tablets (4 to 8 mg) 3 to 4 times daily Oral Solution: 1 or 2 teaspoonfuls (4 to 8 mg) 3 to 4 times daily.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:59:37 GMT 2025
Edited
by admin
on Mon Mar 31 17:59:37 GMT 2025
Record UNII
982A7M02H5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CARBINOXAMINE
INN   MI   VANDF   WHO-DD  
INN  
Official Name English
CARBINOXAMINE [MI]
Preferred Name English
ETHANAMINE, 2-((4-CHLOROPHENYL)-2-PYRIDINYLMETHOXY)-N,N-DIMETHYL-
Systematic Name English
2-(P-CHLORO-.ALPHA.-(2-(DIMETHYLAMINO)ETHOXY)BENZYL)PYRIDINE
Common Name English
carbinoxamine [INN]
Common Name English
Carbinoxamine [WHO-DD]
Common Name English
CARBINOXAMINE [VANDF]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29578
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
WHO-ATC R06AA08
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
WHO-VATC QR06AA08
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
NDF-RT N0000175587
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
LIVERTOX NBK548003
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
Code System Code Type Description
DRUG BANK
DB00748
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
PRIMARY
EPA CompTox
DTXSID4022737
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
PRIMARY
FDA UNII
982A7M02H5
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
PRIMARY
CAS
486-16-8
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
PRIMARY
MERCK INDEX
m3070
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
PRIMARY Merck Index
LACTMED
Carbinoxamine
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-628-6
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
PRIMARY
MESH
C004649
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
PRIMARY
CHEBI
3398
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
PRIMARY
DRUG CENTRAL
499
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
PRIMARY
WIKIPEDIA
CARBINOXAMINE
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
PRIMARY
PUBCHEM
2564
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
PRIMARY
INN
359
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
PRIMARY
RXCUI
20220
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
PRIMARY RxNorm
DAILYMED
982A7M02H5
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
PRIMARY
SMS_ID
100000081340
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
PRIMARY
ChEMBL
CHEMBL864
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
PRIMARY
IUPHAR
7139
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
PRIMARY
NCI_THESAURUS
C65286
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
PRIMARY
EVMPD
SUB06128MIG
Created by admin on Mon Mar 31 17:59:37 GMT 2025 , Edited by admin on Mon Mar 31 17:59:37 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY