Showing metabocard for Neosolaniol (MMDBc0060787)
Microbial
Record Information | |||||||||||||
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Version | 1.0 | ||||||||||||
Status | Detected and Quantified | ||||||||||||
Creation Date | 2025-10-02 23:08:29 UTC | ||||||||||||
Update Date | 2025-10-08 21:35:21 UTC | ||||||||||||
Metabolite ID | MMDBc0060787 | ||||||||||||
Metabolite Identification | |||||||||||||
Common Name | Neosolaniol | ||||||||||||
Description | Neosolaniol is a mycotoxin belonging to the chemical class of trichothecenes, which are characterized by their complex multi-ring structures. This compound is produced by various fungal species and has been identified in both in vitro and in vivo studies, highlighting its prevalence in contaminated environments (PMID:39453190 ). Neosolaniol is involved in metabolic pathways alongside other mycotoxins such as T-2 and HT-2 toxins, where it is often detected as a metabolite during the degradation processes (PMID:38790801 ). Research has shown that neosolaniol can be produced by specific fungal strains, indicating its biosynthetic pathways within certain fungal species (PMID:38549274 ). Furthermore, studies have demonstrated that neosolaniol can contribute to the toxicological effects of mycotoxin mixtures, as evidenced by increased Salmonella loads in experimental models when combined with other mycotoxins (PMID:37104905 ). The need for comprehensive monitoring of neosolaniol and other unregulated mycotoxins has been emphasized due to their potential health risks (PMID:39093417 ). Overall, neosolaniol's chemical structure and its involvement in various metabolic pathways underscore its significance in mycotoxin research and environmental safety. | ||||||||||||
Structure | |||||||||||||
Synonyms |
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Molecular Formula | C19H26O8 | ||||||||||||
Average Mass | 382.409 | ||||||||||||
Monoisotopic Mass | 382.162767797 | ||||||||||||
IUPAC Name | Not Available | ||||||||||||
Traditional Name | Not Available | ||||||||||||
CAS Registry Number | Not Available | ||||||||||||
SMILES | Not Available | ||||||||||||
InChI Identifier | Not Available | ||||||||||||
InChI Key | TVZHDVCTOCZDNE-WVJYZQHISA-N | ||||||||||||
Chemical Taxonomy | |||||||||||||
Description | Belongs to the class of organic compounds known as trichothecenes. These are sesquiterpene mycotoxins structurally characterized by the presence of an epoxide ring and a benzopyran derivative with a variant number of hydroxyl, acetyl, or other substituents. The most important structural features causing the biological activities of trichothecenes are the 12,13-epoxy ring, the presence of hydroxyl or acetyl groups at appropriate positions on the trichothecene nucleus and the structure and position of the side-chain. | ||||||||||||
Kingdom | Organic compounds | ||||||||||||
Super Class | Lipids and lipid-like molecules | ||||||||||||
Class | Prenol lipids | ||||||||||||
Sub Class | Sesquiterpenoids | ||||||||||||
Direct Parent | Trichothecenes | ||||||||||||
Alternative Parents | |||||||||||||
Substituents |
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Molecular Framework | Aliphatic heteropolycyclic compounds | ||||||||||||
External Descriptors | Not Available | ||||||||||||
Functional Ontology | |||||||||||||
Not Available | |||||||||||||
Physical Properties | |||||||||||||
State | Not Available | ||||||||||||
Predicted Properties | Not Available | ||||||||||||
Spectra | |||||||||||||
Not Available | |||||||||||||
Biological Properties | |||||||||||||
Cellular Locations | Not Available | ||||||||||||
Biospecimen Locations | Not Available | ||||||||||||
Tissue Locations | Not Available | ||||||||||||
Associated OMIM IDs | |||||||||||||
Human Proteins and Enzymes | |||||||||||||
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Human Pathways | |||||||||||||
Pathways |
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Microbial Pathways | |||||||||||||
Pathways | This table shows at most 5 pathways. For the full list of associated pathways: See All Associated Bacterial Pathways
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Metabolic Reactions | |||||||||||||
Reactions This table shows at most 20 reactions. For the full list of associated reactions: See All Associated Reactions
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Health Effects and Bioactivity | |||||||||||||
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Microbial Sources | |||||||||||||
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Other Exposures |
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Host Biospecimen and Location | |||||||||||||
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External Links | |||||||||||||
HMDB ID | Not Available | ||||||||||||
DrugBank ID | Not Available | ||||||||||||
Phenol Explorer Compound ID | Not Available | ||||||||||||
FooDB ID | Not Available | ||||||||||||
KNApSAcK ID | C00012613 | ||||||||||||
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 | 13818797 | ||||||||||||
PDB ID | Not Available | ||||||||||||
ChEBI ID | Not Available | ||||||||||||
Food Biomarker Ontology | Not Available | ||||||||||||
CMMC Knowledgebase | TVZHDVCTOCZDNE-WVJYZQHISA-N | ||||||||||||
References | |||||||||||||
Synthesis Reference | Not Available | ||||||||||||
General References |
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