Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C11H14O5 |
| Molecular Weight | 226.2259 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCOC(=O)C1=CC(O)=C(O)C(O)=C1
InChI
InChIKey=XOPOEBVTQYAOSV-UHFFFAOYSA-N
InChI=1S/C11H14O5/c1-2-3-4-16-11(15)7-5-8(12)10(14)9(13)6-7/h5-6,12-14H,2-4H2,1H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Comparative cytotoxicity of alkyl gallates on mouse tumor cell lines and isolated rat hepatocytes. | 2007 Apr |
|
| Anti-HSV-1 and anti-HIV-1 activity of gallic acid and pentyl gallate. | 2008 Aug |
|
| An ellagitannin, n-butyl gallate, two aryltetralin lignans, and an unprecedented diterpene ester from Pelargonium reniforme. | 2008 Feb |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
14128
Created by
admin on Fri Dec 15 15:13:18 GMT 2023 , Edited by admin on Fri Dec 15 15:13:18 GMT 2023
|
PRIMARY | |||
|
33956
Created by
admin on Fri Dec 15 15:13:18 GMT 2023 , Edited by admin on Fri Dec 15 15:13:18 GMT 2023
|
PRIMARY | |||
|
1083-41-6
Created by
admin on Fri Dec 15 15:13:18 GMT 2023 , Edited by admin on Fri Dec 15 15:13:18 GMT 2023
|
PRIMARY | |||
|
214-107-7
Created by
admin on Fri Dec 15 15:13:18 GMT 2023 , Edited by admin on Fri Dec 15 15:13:18 GMT 2023
|
PRIMARY | |||
|
67HZ41U710
Created by
admin on Fri Dec 15 15:13:18 GMT 2023 , Edited by admin on Fri Dec 15 15:13:18 GMT 2023
|
PRIMARY | |||
|
DTXSID40148490
Created by
admin on Fri Dec 15 15:13:18 GMT 2023 , Edited by admin on Fri Dec 15 15:13:18 GMT 2023
|
PRIMARY |
SUBSTANCE RECORD
