Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C22H28FNO3 |
| Molecular Weight | 373.461 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C(OC)C(=CC=C1)[C@H](O)C2CCN(CCC3=CC=C(F)C=C3)CC2
InChI
InChIKey=HXTGXYRHXAGCFP-OAQYLSRUSA-N
InChI=1S/C22H28FNO3/c1-26-20-5-3-4-19(22(20)27-2)21(25)17-11-14-24(15-12-17)13-10-16-6-8-18(23)9-7-16/h3-9,17,21,25H,10-15H2,1-2H3/t21-/m1/s1
| Molecular Formula | C22H28FNO3 |
| Molecular Weight | 373.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Volinanserin (MDL-100,907) is a highly selective 5-HT2A receptor antagonist. It is widely used in
scientific research to investigate the function of the 5-HT2A receptor. Volinanserin is also being trialed as a
potential antipsychotic, antidepressant and treatment for insomnia. Volinanserin (M-100907) was in
phase III trials for chronic schizophrenia. In August 1999, development was discontinued for acute
schizophrenia (schizoaffective disorder) on the basis of poor results. M-100907 is also active in animal
models involving blockade of NMDA glutamatergic channel receptors, an effect known to resemble some
behavioral symptoms of schizophrenia in man. M-100907 is also claimed in other patents for the
treatment of thromboembolic disorders, for the treatment of various developmental neurological
disorders such as autism and attention deficit hyperactivity disorder.
Originator
Approval Year
Funbound
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
3% |
5.01 μg/kg/min single, intravenous dose: 5.01 μg/kg/min route of administration: Intravenous experiment type: SINGLE co-administered: |
VOLINANSERIN plasma | Rattus norvegicus population: HEALTHY age: ADOLESCENT sex: FEMALE / MALE food status: UNKNOWN |
PubMed
| Title | Date | PubMed |
|---|---|---|
| 5-HT(2A) inverse-agonists for the treatment of insomnia. | 2008 |
|
| Effects of the serotonin 5-HT2A and 5-HT2C receptor ligands on the discriminative stimulus effects of nicotine in rats. | 2007-10-01 |
|
| Pharmacological characterisation of the agonist radioligand binding site of 5-HT(2A), 5-HT(2B) and 5-HT(2C) receptors. | 2004-08 |
|
| Regulation of septo-hippocampal activity by 5-hydroxytryptamine(2C) receptors. | 2003-08 |
|
| Evaluation of the ocular hypotensive response of serotonin 5-HT1A and 5-HT2 receptor ligands in conscious ocular hypertensive cynomolgus monkeys. | 2003-07 |
|
| Multiple conformations of native and recombinant human 5-hydroxytryptamine(2a) receptors are labeled by agonists and discriminated by antagonists. | 2001-10 |
|
| Attenuation of haloperidol-induced catalepsy by a 5-HT2C receptor antagonist. | 1999-02 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/10928313
Schizophrenia treatment: an oral dose of 20 mg per day ensures adequate 5HT(2A) receptor occupancy for clinical proof of concept.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/16154561
The selective 5-HT(2A) receptor antagonist Volinanserin (0.05 uM), strongly enhanced the reversal of amphetamine-induced inhibition by (-)sulpiride in A10, but its effectiveness was much smaller in A9 dopamine neurons in in rat midbrain slices.
| Substance Class |
Chemical
Created
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admin
on
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Mon Mar 31 18:43:41 GMT 2025
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EW71EE171J
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Validated (UNII)
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C66885
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5311271
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Volinanserin
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CHEMBL74355
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