Showing metabocard for (2R,3R)-dihydroflavonol (MMDBc0057140)
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| Version | 2.0 | ||||||||||||
| Status | Detected and Quantified | ||||||||||||
| Creation Date | 2022-11-09 19:13:06 UTC | ||||||||||||
| Update Date | 2025-10-07 16:09:51 UTC | ||||||||||||
| Metabolite ID | MMDBc0057140 | ||||||||||||
| Metabolite Identification | |||||||||||||
| Common Name | (2R,3R)-dihydroflavonol | ||||||||||||
| Description | (2R,3R)-dihydroflavonol is a flavonoid, a class of polyphenolic compounds characterized by a common chemical structure consisting of two aromatic rings connected by a three-carbon bridge. This compound features a specific stereochemistry at the 2 and 3 positions, which is crucial for its biological activity. In terms of its chemical structure, (2R,3R)-dihydroflavonol possesses hydroxyl groups that contribute to its reactivity and potential interactions with various biological targets. It has been identified in studies evaluating its antimicrobial properties, where it exhibited significant inhibitory activity against certain strains, with a minimum inhibitory concentration (MIC) of 7.8 μg/mL reported for a derivative compound (2",2"-dimethylpyran-(5",6":7,8)-5,2'-dihydroxy-4'-methoxy-(2R,3R)-dihydroflavonol) (PMID:24956381 ). This suggests that (2R,3R)-dihydroflavonol may be involved in pathways related to antimicrobial defense, potentially influencing the biosynthesis of secondary metabolites that confer resistance to pathogens. Overall, its structural attributes and biological interactions position (2R,3R)-dihydroflavonol as a significant compound within the flavonoid class. | ||||||||||||
| Structure |  | ||||||||||||
| Synonyms | Not Available | ||||||||||||
| Molecular Formula | C15H12O3 | ||||||||||||
| Average Mass | 240.258 | ||||||||||||
| Monoisotopic Mass | 240.078644246 | ||||||||||||
| IUPAC Name | Not Available | ||||||||||||
| Traditional Name | Not Available | ||||||||||||
| CAS Registry Number | Not Available | ||||||||||||
| SMILES | Not Available | ||||||||||||
| InChI Identifier | Not Available | ||||||||||||
| InChI Key | YEDFEBOUHSBQBT-LSDHHAIUSA-N | ||||||||||||
| Chemical Taxonomy | |||||||||||||
| Description | Belongs to the class of organic compounds known as flavanonols. Flavanonols are compounds containing a flavan-3-one moiety, with a structure characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a hydroxyl group and a ketone at the carbon C2 and C3, respectively. | ||||||||||||
| Kingdom | Organic compounds | ||||||||||||
| Super Class | Phenylpropanoids and polyketides | ||||||||||||
| Class | Flavonoids | ||||||||||||
| Sub Class | Flavans | ||||||||||||
| Direct Parent | Flavanonols | ||||||||||||
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| Molecular Framework | Aromatic heteropolycyclic compounds | ||||||||||||
| External Descriptors | Not Available | ||||||||||||
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| State | Not Available | ||||||||||||
| Predicted Properties | Not Available | ||||||||||||
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| Cellular Locations | Not Available | ||||||||||||
| Biospecimen Locations | Not Available | ||||||||||||
| Tissue Locations | Not Available | ||||||||||||
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| Pathways | Not Available | ||||||||||||
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Reactions This table shows at most 20 reactions. For the full list of associated reactions: See All Associated Reactions
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| HMDB ID | Not Available | ||||||||||||
| DrugBank ID | Not Available | ||||||||||||
| Phenol Explorer Compound ID | Not Available | ||||||||||||
| FooDB ID | Not Available | ||||||||||||
| KNApSAcK ID | Not Available | ||||||||||||
| Chemspider ID | Not Available | ||||||||||||
| KEGG Compound ID | Not Available | ||||||||||||
| BioCyc ID | Not Available | ||||||||||||
| BiGG ID | Not Available | ||||||||||||
| Wikipedia Link | Not Available | ||||||||||||
| METLIN ID | Not Available | ||||||||||||
| PubChem Compound | 736738 | ||||||||||||
| PDB ID | Not Available | ||||||||||||
| ChEBI ID | Not Available | ||||||||||||
| Food Biomarker Ontology | Not Available | ||||||||||||
| CMMC Knowledgebase | Not Available | ||||||||||||
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