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Details

Stereochemistry ACHIRAL
Molecular Formula C16H20ClN3.ClH
Molecular Weight 326.264
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHLOROPYRAMINE HYDROCHLORIDE

SMILES

Cl.CN(C)CCN(CC1=CC=C(Cl)C=C1)C2=CC=CC=N2

InChI

InChIKey=VEYWWAGBHABATA-UHFFFAOYSA-N
InChI=1S/C16H20ClN3.ClH/c1-19(2)11-12-20(16-5-3-4-10-18-16)13-14-6-8-15(17)9-7-14;/h3-10H,11-13H2,1-2H3;1H

HIDE SMILES / InChI

Molecular Formula C16H20ClN3
Molecular Weight 289.803
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Chloropyramine is an antagonist of H1 histamine receptors. It is indicated for the treatment of various forms of allergic reactions. Chloropyramine is a drug capable of (1) inhibiting the biochemical function of VEGFR-3 and FAK, (2) inhibiting proliferation of a diverse set of cancer cell types in vitro, and (3) reducing tumor growth in vivo.

Originator

Curator's Comment: references retrieved from www.drugfuture.com/chemdata/chloropyramine.html # Wyeth Holdings Corp., Merck Sharp & Dohme Corp., Geigy

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
ALLERGOSAN

Approved Use

In the form of solution for injection, it is used in: acute allergic reactions related to urticaria treatment (due to foods, medicines, helminthes, etc.) and insect bite; in allergic reactions of general type (anaphylactic shock, serum disease, Quincke’s edema), when the product is used as a part of the complex therapy. In the form of tablets: for treatment of allergic rhinitis, conjunctivities, hay fever, drug and food allergy, allergic reactions after insect bite. In the form of ointment or cream it is used for treatment of allergic skin reactions.
PubMed

PubMed

TitleDatePubMed
Actions of endothelin and corticotropin releasing factor in the guinea-pig ileum: no evidence for an interaction with capsaicin-sensitive neurons.
2003 Aug
Severe anaphylactic reaction during the second infusion of infliximab in a patient with psoriatic arthritis.
2005 Sep-Oct
Characterization of histamine-induced relaxation in pre-contracted rat aorta.
2009 Apr
Small molecule chloropyramine hydrochloride (C4) targets the binding site of focal adhesion kinase and vascular endothelial growth factor receptor 3 and suppresses breast cancer growth in vivo.
2009 Aug 13
[Discriminant function analysis in the assessment of laboratory test data in the correction of traditional therapy for mild icteric form of viral hepatitis B in children with food allergy].
2010 Jun
Patents

Sample Use Guides

Composition: One ampoule of 2 ml contains 20 mg chloropyramine hydrochloride (10 mg/ml). One coated tablet contains 25 mg chloropyramine hydrochloride. 1 g of ointment (1%) contains 10 mg chloropyramine hydrochloride. 1 g of cream (1%) contains 10 mg chloropyramine hydrochloride. Dosage and administration: Parenteral administration: in severe allergic reactions 1-2 ampoules intramuscularly or intravenously. Oral administration: adults - 25 mg (1 tabl.) 3-4 times daily (up to 150 mg, if necessary); children over 5 years: 1 tablet, 2-3 times daily. External application: affected area should be treated once or several times a day by applying a thin layer of ointment or cream.
Route of Administration: Other
SKN-AS and SK-N-BE(2) neuroblastoma cells were treated with varying concentrations of chloropyramine hydrochloride (C4) for 24 h and cellular viability was measured. Both cell lines demonstrated a decrease in survival that was signifi-cant at 100 μM concentration. The calculated LC50 for C4 was similar in the two cell lines at 170 μM in the SK-N-AS cell line and 144 mM in the SK-N-BE(2) cell line.
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:41:09 GMT 2023
Edited
by admin
on Fri Dec 15 17:41:09 GMT 2023
Record UNII
FWA92Z14NN
Record Status Validated (UNII)
Record Version
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Name Type Language
CHLOROPYRAMINE HYDROCHLORIDE
MART.   MI   WHO-DD  
Systematic Name English
N-(4-CHLOROBENZYL)-N'N'-DIMETHYL-N-(2-PYRIDYL) ETHYLENEDIAMINE HYDROCHLORIDE
Common Name English
HALOPYRAMINE HYDROCHLORIDE
Common Name English
Chloropyramine hydrochloride [WHO-DD]
Common Name English
CHLOROPYRAMINE HCL
Common Name English
CHLOROPYRAMINE HYDROCHLORIDE [MI]
Common Name English
NSC-409949
Code English
CHLOROPYRAMINE HYDROCHLORIDE [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29578
Created by admin on Fri Dec 15 17:41:09 GMT 2023 , Edited by admin on Fri Dec 15 17:41:09 GMT 2023
Code System Code Type Description
ECHA (EC/EINECS)
228-216-2
Created by admin on Fri Dec 15 17:41:09 GMT 2023 , Edited by admin on Fri Dec 15 17:41:09 GMT 2023
PRIMARY
SMS_ID
100000085646
Created by admin on Fri Dec 15 17:41:09 GMT 2023 , Edited by admin on Fri Dec 15 17:41:09 GMT 2023
PRIMARY
CAS
6170-42-9
Created by admin on Fri Dec 15 17:41:09 GMT 2023 , Edited by admin on Fri Dec 15 17:41:09 GMT 2023
PRIMARY
NSC
409949
Created by admin on Fri Dec 15 17:41:09 GMT 2023 , Edited by admin on Fri Dec 15 17:41:09 GMT 2023
PRIMARY
DRUG BANK
DBSALT000909
Created by admin on Fri Dec 15 17:41:09 GMT 2023 , Edited by admin on Fri Dec 15 17:41:09 GMT 2023
PRIMARY
PUBCHEM
25294
Created by admin on Fri Dec 15 17:41:09 GMT 2023 , Edited by admin on Fri Dec 15 17:41:09 GMT 2023
PRIMARY
NCI_THESAURUS
C97693
Created by admin on Fri Dec 15 17:41:09 GMT 2023 , Edited by admin on Fri Dec 15 17:41:09 GMT 2023
PRIMARY
MESH
C004664
Created by admin on Fri Dec 15 17:41:09 GMT 2023 , Edited by admin on Fri Dec 15 17:41:09 GMT 2023
PRIMARY
EPA CompTox
DTXSID9048859
Created by admin on Fri Dec 15 17:41:09 GMT 2023 , Edited by admin on Fri Dec 15 17:41:09 GMT 2023
PRIMARY
FDA UNII
FWA92Z14NN
Created by admin on Fri Dec 15 17:41:09 GMT 2023 , Edited by admin on Fri Dec 15 17:41:09 GMT 2023
PRIMARY
EVMPD
SUB01233MIG
Created by admin on Fri Dec 15 17:41:09 GMT 2023 , Edited by admin on Fri Dec 15 17:41:09 GMT 2023
PRIMARY
MERCK INDEX
m3434
Created by admin on Fri Dec 15 17:41:09 GMT 2023 , Edited by admin on Fri Dec 15 17:41:09 GMT 2023
PRIMARY Merck Index
RXCUI
236457
Created by admin on Fri Dec 15 17:41:09 GMT 2023 , Edited by admin on Fri Dec 15 17:41:09 GMT 2023
PRIMARY RxNorm
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