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Details

Stereochemistry ACHIRAL
Molecular Formula C19H19NS
Molecular Weight 293.426
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PIMETHIXENE

SMILES

CN1CCC(CC1)=C2C3=C(SC4=C2C=CC=C4)C=CC=C3

InChI

InChIKey=NZLVRVYNQYGMAB-UHFFFAOYSA-N
InChI=1S/C19H19NS/c1-20-12-10-14(11-13-20)19-15-6-2-4-8-17(15)21-18-9-5-3-7-16(18)19/h2-9H,10-13H2,1H3

HIDE SMILES / InChI

Molecular Formula C19H19NS
Molecular Weight 293.426
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Pimethixene is an antihistamine exerting sedative and antitussive properties. Pimethixene displayed high affinity to serotonin 5-HT2A and 2B, histamine H1 and muscarinic acetylcholine M2 receptors. Oral pimethixene used to calm dry cough and irritation coughs in children.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
10.14 null [pKi]
9.38 null [pKi]
10.22 null [pKi]
10.44 null [pKi]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
CALMIXENE

Approved Use

It is recommended to calm dry cough and irritation coughs in children older than 2 years, especially when they occur in the evening or at night
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
[ANTIANAPHYLACTIC PROPERTIES OF 9-(N-METHYL-4'-PIPERIDYLIDENE) THIOXANTHENE (BP 400) AND LYSOZYME, COMPARED TO THOSE OF PREDNISONE].
1963
BP 400 IN BRONCHIAL ASTHMA.
1963
[Clinical trials of a new antiallergic substance, 9-(N-methyl-4-piperidylidene)-thioxasthene (BP 400)].
1963 Mar 16
[PRELIMINARY FINDINGS ON THE USE OF 9-(METHYL-4'-PIPERIDYLIDENE)-THIOXANTHENE (BP 400) IN THE TREATMENT OF OBSTRUCTIVE RESPIRATORY INSUFFICIENCY].
1963 Oct
[Clinical experience with the application of pimethixene in the premedication of children].
1967 Sep
[On the pharmacology of 9,10-dihydro-10-(1-methyl-4-piperidylidene)-9-anthrol (WA 335), a histamine and serotonin antagonist (author's transl)].
1975 Nov
[New treatment of hyperkinesis in the child: pimethixene].
1978 Jul 15
LuxR-dependent quorum sensing: computer aided discovery of new inhibitors structurally unrelated to N-acylhomoserine lactones.
2010 Aug 1
BF-1--a novel selective 5-HT2B receptor antagonist blocking neurogenic dural plasma protein extravasation in guinea pigs.
2015 Mar 15
Patents

Sample Use Guides

Children from 24 to 30 months: 2 to 3 dosing cups (graduation at 5 ml) distributed over the day, Children from 30 months to 5 years: 3 to 4 dosing cups (graduation at 5 ml) distributed over the day, Children from 5 to 15 years: 5 to 6 dosing cups (graduation at 5 ml) distributed over the day. The strongest dose will be kept for the evening due to the possibility of drowsiness related with this medicine
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:56:15 GMT 2023
Edited
by admin
on Sat Dec 16 17:56:15 GMT 2023
Record UNII
T46J20J26F
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PIMETHIXENE
INN   MART.   WHO-DD  
INN  
Official Name English
pimethixene [INN]
Common Name English
CALMIXENE
Brand Name English
PIMETHIXENE [MART.]
Common Name English
Pimethixene [WHO-DD]
Common Name English
1-METHYL-4-(THIOXANTHEN-9-YLIDENE)PIPERIDINE
Systematic Name English
NSC-757828
Code English
BP-400
Code English
PIMETIXENE
Common Name English
BP 400
Code English
Classification Tree Code System Code
WHO-VATC QR06AX23
Created by admin on Sat Dec 16 17:56:15 GMT 2023 , Edited by admin on Sat Dec 16 17:56:15 GMT 2023
NCI_THESAURUS C29578
Created by admin on Sat Dec 16 17:56:15 GMT 2023 , Edited by admin on Sat Dec 16 17:56:15 GMT 2023
WHO-ATC R06AX23
Created by admin on Sat Dec 16 17:56:15 GMT 2023 , Edited by admin on Sat Dec 16 17:56:15 GMT 2023
Code System Code Type Description
CAS
314-03-4
Created by admin on Sat Dec 16 17:56:15 GMT 2023 , Edited by admin on Sat Dec 16 17:56:15 GMT 2023
PRIMARY
FDA UNII
T46J20J26F
Created by admin on Sat Dec 16 17:56:15 GMT 2023 , Edited by admin on Sat Dec 16 17:56:15 GMT 2023
PRIMARY
WIKIPEDIA
PIMETHIXENE
Created by admin on Sat Dec 16 17:56:15 GMT 2023 , Edited by admin on Sat Dec 16 17:56:15 GMT 2023
PRIMARY
DRUG BANK
DB13292
Created by admin on Sat Dec 16 17:56:15 GMT 2023 , Edited by admin on Sat Dec 16 17:56:15 GMT 2023
PRIMARY
EVMPD
SUB09840MIG
Created by admin on Sat Dec 16 17:56:15 GMT 2023 , Edited by admin on Sat Dec 16 17:56:15 GMT 2023
PRIMARY
INN
1739
Created by admin on Sat Dec 16 17:56:15 GMT 2023 , Edited by admin on Sat Dec 16 17:56:15 GMT 2023
PRIMARY
PUBCHEM
4822
Created by admin on Sat Dec 16 17:56:15 GMT 2023 , Edited by admin on Sat Dec 16 17:56:15 GMT 2023
PRIMARY
ChEMBL
CHEMBL152408
Created by admin on Sat Dec 16 17:56:15 GMT 2023 , Edited by admin on Sat Dec 16 17:56:15 GMT 2023
PRIMARY
SMS_ID
100000081932
Created by admin on Sat Dec 16 17:56:15 GMT 2023 , Edited by admin on Sat Dec 16 17:56:15 GMT 2023
PRIMARY
ECHA (EC/EINECS)
206-240-4
Created by admin on Sat Dec 16 17:56:15 GMT 2023 , Edited by admin on Sat Dec 16 17:56:15 GMT 2023
PRIMARY
DRUG CENTRAL
2169
Created by admin on Sat Dec 16 17:56:15 GMT 2023 , Edited by admin on Sat Dec 16 17:56:15 GMT 2023
PRIMARY
EPA CompTox
DTXSID0048476
Created by admin on Sat Dec 16 17:56:15 GMT 2023 , Edited by admin on Sat Dec 16 17:56:15 GMT 2023
PRIMARY
NCI_THESAURUS
C82276
Created by admin on Sat Dec 16 17:56:15 GMT 2023 , Edited by admin on Sat Dec 16 17:56:15 GMT 2023
PRIMARY
RXCUI
33712
Created by admin on Sat Dec 16 17:56:15 GMT 2023 , Edited by admin on Sat Dec 16 17:56:15 GMT 2023
PRIMARY RxNorm
NSC
757828
Created by admin on Sat Dec 16 17:56:15 GMT 2023 , Edited by admin on Sat Dec 16 17:56:15 GMT 2023
PRIMARY
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