Details
Stereochemistry | ACHIRAL |
Molecular Formula | C22H24FN3OS.ClH |
Molecular Weight | 433.97 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.FC1=CC=C(C=C1)C(=O)CCCN2CCC(CC2)N3C(=S)NC4=C3C=CC=C4
InChI
InChIKey=VUGXUHIAJYYOSP-UHFFFAOYSA-N
InChI=1S/C22H24FN3OS.ClH/c23-17-9-7-16(8-10-17)21(27)6-3-13-25-14-11-18(12-15-25)26-20-5-2-1-4-19(20)24-22(26)28;/h1-2,4-5,7-10,18H,3,6,11-15H2,(H,24,28);1H
DescriptionSources: http://www.ncbi.nlm.nih.gov/pubmed/10215017Curator's Comment: description was created based on several sources, including:
https://medical.mt-pharma.co.jp/di/file/dc/tol_f.htm
https://www.medicallibrary-dsc.info/di/tolopelon_tablets_3mg/pdf/if_tp_tab_1301_09.pdf
Sources: http://www.ncbi.nlm.nih.gov/pubmed/10215017
Curator's Comment: description was created based on several sources, including:
https://medical.mt-pharma.co.jp/di/file/dc/tol_f.htm
https://www.medicallibrary-dsc.info/di/tolopelon_tablets_3mg/pdf/if_tp_tab_1301_09.pdf
Timiperone is a neuroleptic agent that was developed in Japan. Timiperone has a potent antipsychotic activity, which is comparable to other butyrophenones such as haloperidol (HAL). Timiperone has a five-eight-times higher affinity to dopamine receptors and a 15-times higher affinity to serotonin receptors than those of HAL. Clinical trials have suggested that TIM has a specific action against negative symptoms such as lack of initiative or blunted affect as well as positive symptoms such as delusions and hallucinations in schizophrenics.
CNS Activity
Originator
Sources: https://www.google.ch/patents/US3963727
Curator's Comment: Timiperone was created in 1973 by Daiichi Pharmaceutical Co., Ltd. (currently: Daiichi Sankyo Co., Ltd.).
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Effect of hyperprolactinemia induced by pituitary grafts or castration on porphyrin content of the mouse Harderian gland. | 2001 Aug |
|
Atypical properties of several classes of antipsychotic drugs on the basis of differential induction of Fos-like immunoreactivity in the rat brain. | 2004 Nov 26 |
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Systematic Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
65053-29-4
Created by
admin on Fri Dec 15 16:52:39 GMT 2023 , Edited by admin on Fri Dec 15 16:52:39 GMT 2023
|
NON-SPECIFIC STOICHIOMETRY | |||
|
62621-49-2
Created by
admin on Fri Dec 15 16:52:39 GMT 2023 , Edited by admin on Fri Dec 15 16:52:39 GMT 2023
|
PRIMARY | |||
|
15571090
Created by
admin on Fri Dec 15 16:52:39 GMT 2023 , Edited by admin on Fri Dec 15 16:52:39 GMT 2023
|
PRIMARY | |||
|
605T96VHKF
Created by
admin on Fri Dec 15 16:52:39 GMT 2023 , Edited by admin on Fri Dec 15 16:52:39 GMT 2023
|
PRIMARY |
ACTIVE MOIETY
SUBSTANCE RECORD