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Details

Stereochemistry ACHIRAL
Molecular Formula C21H24N4O2.ClH
Molecular Weight 400.902
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PELANSERIN HYDROCHLORIDE

SMILES

Cl.O=C1NC2=C(C=CC=C2)C(=O)N1CCCN3CCN(CC3)C4=CC=CC=C4

InChI

InChIKey=SXZRLCAHCIRKJU-UHFFFAOYSA-N
InChI=1S/C21H24N4O2.ClH/c26-20-18-9-4-5-10-19(18)22-21(27)25(20)12-6-11-23-13-15-24(16-14-23)17-7-2-1-3-8-17;/h1-5,7-10H,6,11-16H2,(H,22,27);1H

HIDE SMILES / InChI

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

Molecular Formula C21H24N4O2
Molecular Weight 364.4409
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Pelanserin is an antagonist of the serotonin 5-HT2 receptor and blocks alpha 1-adrenoceptor. Experiments on dogs have revealed that pelanserin showed adequate pharmacokinetic and pharmacodynamics profiles as an antihypertensive agent that is why the drug possessed potential therapeutic usefulness in the treatment of hypertension. Pelanserin was undergoing phase II clinical trials by Cinvestav in Mexico; however, these studied were discontinued.

Approval Year

PubMed

PubMed

TitleDatePubMed
Carbopol 934-Sodium Alginate-Gelatin Mucoadhesive Ondansetron Tablets for Buccal Delivery: Effect of pH Modifiers.
2010-07
Influence of Organic Acids on Diltiazem HCl Release Kinetics from Hydroxypropyl Methyl Cellulose Matrix Tablets.
2010-07
Alkylation of 2,4-(1H,3H)-quinazolinediones with dialkyl carbonates under microwave irradiations.
2009-05-20
Mechanism of the antihypertensive effect of TR2515, a potent serotonin antagonist.
1984
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:58:49 GMT 2025
Edited
by admin
on Mon Mar 31 17:58:49 GMT 2025
Record UNII
4J8I18ZP0A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PELANSERIN HYDROCHLORIDE
USAN  
USAN  
Official Name English
TR-2515
Preferred Name English
PELANSERIN HYDROCHLORIDE [USAN]
Common Name English
PELANSERIN HCL
Common Name English
3-[3-(4-Phenyl-1-piperazinyl)propyl]-2,4(1H,3H)-quinazolinedione monohydrochloride
Systematic Name English
2,4(1H,3H)-QUINAZOLINEDIONE, 3-(3-(4-PHENYL-1-PIPERAZINYL)PROPYL)-, MONOHYDROCHLORIDE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C66885
Created by admin on Mon Mar 31 17:58:49 GMT 2025 , Edited by admin on Mon Mar 31 17:58:49 GMT 2025
Code System Code Type Description
FDA UNII
4J8I18ZP0A
Created by admin on Mon Mar 31 17:58:49 GMT 2025 , Edited by admin on Mon Mar 31 17:58:49 GMT 2025
PRIMARY
USAN
Y-63
Created by admin on Mon Mar 31 17:58:49 GMT 2025 , Edited by admin on Mon Mar 31 17:58:49 GMT 2025
PRIMARY
NCI_THESAURUS
C76966
Created by admin on Mon Mar 31 17:58:49 GMT 2025 , Edited by admin on Mon Mar 31 17:58:49 GMT 2025
PRIMARY
EPA CompTox
DTXSID00195546
Created by admin on Mon Mar 31 17:58:49 GMT 2025 , Edited by admin on Mon Mar 31 17:58:49 GMT 2025
PRIMARY
CAS
42877-18-9
Created by admin on Mon Mar 31 17:58:49 GMT 2025 , Edited by admin on Mon Mar 31 17:58:49 GMT 2025
PRIMARY
PUBCHEM
65436
Created by admin on Mon Mar 31 17:58:49 GMT 2025 , Edited by admin on Mon Mar 31 17:58:49 GMT 2025
PRIMARY
ChEMBL
CHEMBL2110706
Created by admin on Mon Mar 31 17:58:49 GMT 2025 , Edited by admin on Mon Mar 31 17:58:49 GMT 2025
PRIMARY
SMS_ID
300000055573
Created by admin on Mon Mar 31 17:58:49 GMT 2025 , Edited by admin on Mon Mar 31 17:58:49 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY