Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C22H26N2O3 |
| Molecular Weight | 366.4534 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C(CCCOC(CN2C=CN=C2)C3=CC=C(OC)C=C3)C=C1
InChI
InChIKey=HLMBXBGDBBCYII-UHFFFAOYSA-N
InChI=1S/C22H26N2O3/c1-25-20-9-5-18(6-10-20)4-3-15-27-22(16-24-14-13-23-17-24)19-7-11-21(26-2)12-8-19/h5-14,17,22H,3-4,15-16H2,1-2H3
| Molecular Formula | C22H26N2O3 |
| Molecular Weight | 366.4534 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: GO:0002115 Sources: https://www.ncbi.nlm.nih.gov/pubmed/16396967 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:53:22 GMT 2025
by
admin
on
Mon Mar 31 22:53:22 GMT 2025
|
| Record UNII |
I61V87164A
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
145122
Created by
admin on Mon Mar 31 22:53:22 GMT 2025 , Edited by admin on Mon Mar 31 22:53:22 GMT 2025
|
PRIMARY | |||
|
I61V87164A
Created by
admin on Mon Mar 31 22:53:22 GMT 2025 , Edited by admin on Mon Mar 31 22:53:22 GMT 2025
|
PRIMARY | |||
|
162849-90-3
Created by
admin on Mon Mar 31 22:53:22 GMT 2025 , Edited by admin on Mon Mar 31 22:53:22 GMT 2025
|
PRIMARY | |||
|
DTXSID401148768
Created by
admin on Mon Mar 31 22:53:22 GMT 2025 , Edited by admin on Mon Mar 31 22:53:22 GMT 2025
|
PRIMARY | |||
|
104956
Created by
admin on Mon Mar 31 22:53:22 GMT 2025 , Edited by admin on Mon Mar 31 22:53:22 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |