Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C23H25N3O2.C4H4O4 |
| Molecular Weight | 491.5357 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)\C=C/C(O)=O.O=C1CC2=C(N1)C=C3ON=C(CCC4CCN(CC5=CC=CC=C5)CC4)C3=C2
InChI
InChIKey=CTYSKGVFLJLGGX-BTJKTKAUSA-N
InChI=1S/C23H25N3O2.C4H4O4/c27-23-13-18-12-19-20(25-28-22(19)14-21(18)24-23)7-6-16-8-10-26(11-9-16)15-17-4-2-1-3-5-17;5-3(6)1-2-4(7)8/h1-5,12,14,16H,6-11,13,15H2,(H,24,27);1-2H,(H,5,6)(H,7,8)/b;2-1-
| Molecular Formula | C4H4O4 |
| Molecular Weight | 116.0722 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
| Molecular Formula | C23H25N3O2 |
| Molecular Weight | 375.4635 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Icopezil (previously known as CP-118,954) was developed as a selective acetylcholinesterase inhibitor for the treatment of cognitive disorders. Phase II trials of icopezil were underway in Japan and in the USA for the treatment of patients with Alzheimer's disease. However, Pfizer has discontinued these studies.
Originator
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis and evaluation of radioiodine-labelled CP-118,954 for the in-vivo imaging of acetylcholinesterase. | 2007-07 |
|
| Synthesis and evaluation of 2-[18F]fluoro-CP-118,954 for the in vivo mapping of acetylcholinesterase. | 2005-02 |
|
| Synthesis and evaluation of 5,7-dihydro-3-[2-[1-(4-[18F]-fluorobenzyl)-4-piperidinyl]ethyl]-6H-pyrrolo[3,2-f]-1,2-benzisoxazol-6-one for in vivo mapping of acetylcholinesterase. | 2004-06 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:04:58 GMT 2025
by
admin
on
Mon Mar 31 18:04:58 GMT 2025
|
| Record UNII |
1P15W0SPEN
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C47792
Created by
admin on Mon Mar 31 18:04:58 GMT 2025 , Edited by admin on Mon Mar 31 18:04:58 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
C99559
Created by
admin on Mon Mar 31 18:04:58 GMT 2025 , Edited by admin on Mon Mar 31 18:04:58 GMT 2025
|
PRIMARY | |||
|
CHEMBL359570
Created by
admin on Mon Mar 31 18:04:58 GMT 2025 , Edited by admin on Mon Mar 31 18:04:58 GMT 2025
|
PRIMARY | |||
|
1P15W0SPEN
Created by
admin on Mon Mar 31 18:04:58 GMT 2025 , Edited by admin on Mon Mar 31 18:04:58 GMT 2025
|
PRIMARY | |||
|
HH-14
Created by
admin on Mon Mar 31 18:04:58 GMT 2025 , Edited by admin on Mon Mar 31 18:04:58 GMT 2025
|
PRIMARY | |||
|
135462830
Created by
admin on Mon Mar 31 18:04:58 GMT 2025 , Edited by admin on Mon Mar 31 18:04:58 GMT 2025
|
PRIMARY | |||
|
300000055143
Created by
admin on Mon Mar 31 18:04:58 GMT 2025 , Edited by admin on Mon Mar 31 18:04:58 GMT 2025
|
PRIMARY | |||
|
145815-98-1
Created by
admin on Mon Mar 31 18:04:58 GMT 2025 , Edited by admin on Mon Mar 31 18:04:58 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
PARENT -> SALT/SOLVATE | |||
|
|
PARENT -> SALT/SOLVATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |