Showing metabocard for GEODIN (MMDBc0017663)
Xenobiotic
| Record Information | |||||||||||||
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| Version | 2.0 | ||||||||||||
| Status | Detected and Quantified | ||||||||||||
| Creation Date | 2021-05-15 07:58:56 UTC | ||||||||||||
| Update Date | 2025-10-07 16:06:43 UTC | ||||||||||||
| Metabolite ID | MMDBc0017663 | ||||||||||||
| Metabolite Identification | |||||||||||||
| Common Name | GEODIN | ||||||||||||
| Description | GEODIN is a secondary metabolite belonging to the chemical class of anthraquinones, known for its diverse bioactivities. Chemically, GEODIN has a complex structure characterized by a fused ring system that is typical of anthraquinones, which contributes to its various biological functions. It is involved in several biosynthetic pathways, particularly in the production of other bioactive compounds. For instance, the geodin biosynthetic pathway includes key enzymes such as GedR and GedA, which play crucial roles in the accumulation of related metabolites like emodin (PMID:36328293 ). Research has shown that modifications to the 4-OH group of GEODIN can enhance its antibacterial and antifungal properties, leading to the development of novel ester derivatives with improved bioactivity (PMID:38462767 , PMID:37865972 ). Additionally, GEODIN and its derivatives have been linked to various health benefits, including cholesterol regulation and anti-inflammatory effects (PMID:38419626 ). Overall, GEODIN exemplifies the intricate relationship between chemical structure and biological activity, making it a significant compound in natural product chemistry. | ||||||||||||
| Structure |  | ||||||||||||
| Synonyms | Not Available | ||||||||||||
| Molecular Formula | C17H12Cl2O7 | ||||||||||||
| Average Mass | 399.18 | ||||||||||||
| Monoisotopic Mass | 397.9960081 | ||||||||||||
| IUPAC Name | Not Available | ||||||||||||
| Traditional Name | Not Available | ||||||||||||
| CAS Registry Number | Not Available | ||||||||||||
| SMILES | Not Available | ||||||||||||
| InChI Identifier | InChI=1S/C17H12Cl2O7/c1-6-11(18)13(21)10-14(12(6)19)26-17(15(10)22)8(16(23)25-3)4-7(20)5-9(17)24-2/h4-5,21H,1-3H3 | ||||||||||||
| InChI Key | LUBKKVGXMXTXOZ-UHFFFAOYSA-N | ||||||||||||
| Chemical Taxonomy | |||||||||||||
| Functional Ontology | |||||||||||||
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| Physical Properties | |||||||||||||
| State | Expected Solid | ||||||||||||
| 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 | Not Available | ||||||||||||
| PDB ID | Not Available | ||||||||||||
| ChEBI ID | Not Available | ||||||||||||
| Food Biomarker Ontology | Not Available | ||||||||||||
| CMMC Knowledgebase | Not Available | ||||||||||||
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