Details
Stereochemistry | ACHIRAL |
Molecular Formula | C22H23F2NO2.ClH |
Molecular Weight | 407.881 |
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)C(=O)C3=CC=C(F)C=C3
InChI
InChIKey=BUPKTBMYUMORNV-UHFFFAOYSA-N
InChI=1S/C22H23F2NO2.ClH/c23-19-7-3-16(4-8-19)21(26)2-1-13-25-14-11-18(12-15-25)22(27)17-5-9-20(24)10-6-17;/h3-10,18H,1-2,11-15H2;1H
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 | C22H23F2NO2 |
Molecular Weight | 371.4203 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
CNS Activity
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL2093870 Sources: https://www.ncbi.nlm.nih.gov/pubmed/1479590 |
4.3 nM [Ki] | ||
Target ID: CHEMBL2096905 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Lenperone Approved UseTreatment of acute schizophrenia |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/561037
50 hospitalized schizophrenic patients were treated 20-30 days with Lenperone. The therapeutic effective dose was 30-50 mg/day. The highest daily dosage was 90 mg.
Route of Administration:
Oral
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 05:12:45 GMT 2023
by
admin
on
Sat Dec 16 05:12:45 GMT 2023
|
Record UNII |
96Q0TL6O3G
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Systematic Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C28197
Created by
admin on Sat Dec 16 05:12:45 GMT 2023 , Edited by admin on Sat Dec 16 05:12:45 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
100000086665
Created by
admin on Sat Dec 16 05:12:45 GMT 2023 , Edited by admin on Sat Dec 16 05:12:45 GMT 2023
|
PRIMARY | |||
|
96Q0TL6O3G
Created by
admin on Sat Dec 16 05:12:45 GMT 2023 , Edited by admin on Sat Dec 16 05:12:45 GMT 2023
|
PRIMARY | |||
|
C100204
Created by
admin on Sat Dec 16 05:12:45 GMT 2023 , Edited by admin on Sat Dec 16 05:12:45 GMT 2023
|
PRIMARY | |||
|
SUB02889MIG
Created by
admin on Sat Dec 16 05:12:45 GMT 2023 , Edited by admin on Sat Dec 16 05:12:45 GMT 2023
|
PRIMARY | |||
|
32592
Created by
admin on Sat Dec 16 05:12:45 GMT 2023 , Edited by admin on Sat Dec 16 05:12:45 GMT 2023
|
PRIMARY | |||
|
303301
Created by
admin on Sat Dec 16 05:12:45 GMT 2023 , Edited by admin on Sat Dec 16 05:12:45 GMT 2023
|
PRIMARY | |||
|
DTXSID20947620
Created by
admin on Sat Dec 16 05:12:45 GMT 2023 , Edited by admin on Sat Dec 16 05:12:45 GMT 2023
|
PRIMARY | |||
|
24677-86-9
Created by
admin on Sat Dec 16 05:12:45 GMT 2023 , Edited by admin on Sat Dec 16 05:12:45 GMT 2023
|
PRIMARY | |||
|
C77573
Created by
admin on Sat Dec 16 05:12:45 GMT 2023 , Edited by admin on Sat Dec 16 05:12:45 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
PARENT -> SALT/SOLVATE |
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |