Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C17H16O7 |
| Molecular Weight | 332.3047 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)C1=C(C(=O)C2=C(O)C=C(C)C=C2O)C(OC)=CC(O)=C1
InChI
InChIKey=YJRLSCDUYLRBIZ-UHFFFAOYSA-N
InChI=1S/C17H16O7/c1-8-4-11(19)15(12(20)5-8)16(21)14-10(17(22)24-3)6-9(18)7-13(14)23-2/h4-7,18-20H,1-3H3
| Molecular Formula | C17H16O7 |
| Molecular Weight | 332.3047 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL379 Sources: https://www.ncbi.nlm.nih.gov/pubmed/24099774 |
24.4 µM [IC50] | ||
Target ID: GO:0043308 Sources: https://www.ncbi.nlm.nih.gov/pubmed/10450959 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:47:50 GMT 2025
by
admin
on
Mon Mar 31 21:47:50 GMT 2025
|
| Record UNII |
8NA53C271Z
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
8NA53C271Z
Created by
admin on Mon Mar 31 21:47:50 GMT 2025 , Edited by admin on Mon Mar 31 21:47:50 GMT 2025
|
PRIMARY | |||
|
77639
Created by
admin on Mon Mar 31 21:47:50 GMT 2025 , Edited by admin on Mon Mar 31 21:47:50 GMT 2025
|
PRIMARY | |||
|
519-57-3
Created by
admin on Mon Mar 31 21:47:50 GMT 2025 , Edited by admin on Mon Mar 31 21:47:50 GMT 2025
|
PRIMARY | |||
|
DTXSID80199860
Created by
admin on Mon Mar 31 21:47:50 GMT 2025 , Edited by admin on Mon Mar 31 21:47:50 GMT 2025
|
PRIMARY | |||
|
16159
Created by
admin on Mon Mar 31 21:47:50 GMT 2025 , Edited by admin on Mon Mar 31 21:47:50 GMT 2025
|
PRIMARY | |||
|
160505
Created by
admin on Mon Mar 31 21:47:50 GMT 2025 , Edited by admin on Mon Mar 31 21:47:50 GMT 2025
|
PRIMARY |