H6N
Protocatechuic aldehyde
Created: | 2018-11-18 |
Last modified: | 2024-09-27 |
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Chemical Details | |
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Formal Charge | 0 |
Atom Count | 16 |
Chiral Atom Count | 0 |
Bond Count | 16 |
Aromatic Bond Count | 6 |
Chemical Component Summary | |
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Name | Protocatechuic aldehyde |
Systematic Name (OpenEye OEToolkits) | 3,4-bis(oxidanyl)benzaldehyde |
Formula | C7 H6 O3 |
Molecular Weight | 138.121 |
Type | NON-POLYMER |
Chemical Descriptors | |||
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Type | Program | Version | Descriptor |
SMILES | CACTVS | 3.385 | Oc1ccc(C=O)cc1O |
SMILES | OpenEye OEToolkits | 2.0.6 | c1cc(c(cc1C=O)O)O |
Canonical SMILES | CACTVS | 3.385 | Oc1ccc(C=O)cc1O |
Canonical SMILES | OpenEye OEToolkits | 2.0.6 | c1cc(c(cc1C=O)O)O |
InChI | InChI | 1.03 | InChI=1S/C7H6O3/c8-4-5-1-2-6(9)7(10)3-5/h1-4,9-10H |
InChIKey | InChI | 1.03 | IBGBGRVKPALMCQ-UHFFFAOYSA-N |
Drug Info: DrugBank
DrugBank ID | DB11268 |
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Name | Protocatechualdehyde |
Groups | experimental |
Description | Also known as protocatechuic aldehyde, protocatechualdehyde is a naturally-occuring phenolic aldehyde that is found in barley, green cavendish bananas, grapevine leaves and root of the herb S. miltiorrhiza [A27224]. Protocatechualdehyde possesses antiproliferative and pro-apoptotic properties against human breast cancer cells and colorectal cancer cells by reducing the expression of pro-oncogenes β-catenin and cyclin D1. |
Synonyms |
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Brand Names | O Hui White Extreme Cellight |
Categories |
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CAS number | 139-85-5 |
Related Resource References
Resource Name | Reference |
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PubChem | 8768 |
ChEMBL | CHEMBL222021 |
ChEBI | CHEBI:50205 |
CCDC/CSD | MASBUD, AWIVAG |
COD | 7213183 |