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Details

Stereochemistry ACHIRAL
Molecular Formula C23H25ClN4O4.ClH
Molecular Weight 493.383
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CAPESEROD HYDROCHLORIDE

SMILES

Cl.NC1=C2OCCOC2=C(C=C1Cl)C3=NN(C4CCN(CCC5=CC=CC=C5)CC4)C(=O)O3

InChI

InChIKey=LNNFXZHLRNQJIT-UHFFFAOYSA-N
InChI=1S/C23H25ClN4O4.ClH/c24-18-14-17(20-21(19(18)25)31-13-12-30-20)22-26-28(23(29)32-22)16-7-10-27(11-8-16)9-6-15-4-2-1-3-5-15;/h1-5,14,16H,6-13,25H2;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 C23H25ClN4O4
Molecular Weight 456.922
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Capeserod is benzodioxanoxadiazolone derivative patented by patented by pharmaceutical company Synthelabo S. A. as a novel 5-hydroxytryptamine4 receptor partial agonist with potent cognition-enhancing properties. In cells expressing the 5-HT4(b) and 5-HT4(e) splice variants, Capeserod acted as a partial agonist, stimulating cAMP prodn. with a maximal effect of 40 to 50% of serotonin. However, in the rat esophagus preparation, Capeserod acted as a 5-HT4 antagonist with a pKb of 8.81. In addition, Capeserod potently improved performance in several tests of learning and memory. In the object recognition task, it improved retention at 24 h when administered i.p. or p.o. (0.001-0.1 mg/kg). This effect was antagonized by the 5-HT4 antagonist SDZ 205,557, itself without effect, demonstrating that the promnesic effects of Capeserod are mediated by 5-HT4 agonism. Capeserod also reversed the cognitive deficits of aged rats in the linear maze task and the scopolamine-induced deficit of mice in the water maze task. Furthermore, the combined administration of an inactive dose of Capeserod with the cholinesterase inhibitor rivastigmine resulted in a significant promnesic effect, suggesting a synergistic interaction. Capeserod was devoid of unwanted cardiovascular, gastrointestinal, or central nervous system effects with doses up to more than 100-fold higher than those active in the cognitive tests. These results characterize Capeserod as a novel promnesic agent acting via 5-HT4 receptors, with an excellent preclinical profile.

Approval Year

PubMed

PubMed

TitleDatePubMed
The promnesic effect of G-protein-coupled 5-HT4 receptors activation is mediated by a potentiation of learning-induced spine growth in the mouse hippocampus.
2008 Sep
Antidepressant properties of the 5-HT4 receptor partial agonist, SL65.0155: behavioral and neurochemical studies in rats.
2009 Oct 1
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 13:38:26 GMT 2023
Edited
by admin
on Sat Dec 16 13:38:26 GMT 2023
Record UNII
5M8TM6AN9Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CAPESEROD HYDROCHLORIDE
Common Name English
SL-650155
Common Name English
1,3,4-OXADIAZOL-2(3H)-ONE, 5-(8-AMINO-7-CHLORO-2,3-DIHYDRO-1,4-BENZODIOXIN-5-YL)-3-(1-(2-PHENYLETHYL)-4-PIPERIDINYL)-, HYDROCHLORIDE (1:1)
Systematic Name English
Code System Code Type Description
FDA UNII
5M8TM6AN9Q
Created by admin on Sat Dec 16 13:38:26 GMT 2023 , Edited by admin on Sat Dec 16 13:38:26 GMT 2023
PRIMARY
EPA CompTox
DTXSID10430955
Created by admin on Sat Dec 16 13:38:26 GMT 2023 , Edited by admin on Sat Dec 16 13:38:26 GMT 2023
PRIMARY
CAS
191023-43-5
Created by admin on Sat Dec 16 13:38:26 GMT 2023 , Edited by admin on Sat Dec 16 13:38:26 GMT 2023
PRIMARY
PUBCHEM
9805718
Created by admin on Sat Dec 16 13:38:26 GMT 2023 , Edited by admin on Sat Dec 16 13:38:26 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE