Showing metabocard for Purpurogenolide E (MMDBc0021920)
Microbial
Record Information | |||||||||||||
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Version | 1.0 | ||||||||||||
Status | Detected and Quantified | ||||||||||||
Creation Date | 2021-05-15 12:04:38 UTC | ||||||||||||
Update Date | 2022-08-12 20:01:48 UTC | ||||||||||||
Metabolite ID | MMDBc0021920 | ||||||||||||
Metabolite Identification | |||||||||||||
Common Name | Purpurogenolide E | ||||||||||||
Description | CHEMBL3929442 belongs to the class of organic compounds known as furopyrans. These are organic polycyclic compounds containing a furan ring fused to a pyran ring. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds. Based on a literature review very few articles have been published on CHEMBL3929442. | ||||||||||||
Structure | |||||||||||||
Synonyms | Not Available | ||||||||||||
Molecular Formula | C24H28O8 | ||||||||||||
Average Mass | 444.48 | ||||||||||||
Monoisotopic Mass | 444.178417862 | ||||||||||||
IUPAC Name | Not Available | ||||||||||||
Traditional Name | Not Available | ||||||||||||
CAS Registry Number | Not Available | ||||||||||||
SMILES | Not Available | ||||||||||||
InChI Identifier | InChI=1S/C24H28O8/c1-10-19(28)17-18-20(30-10)31-21(29)23(18,4)8-14-12(9-25)11-6-16(27)32-22(2,3)13(11)7-15(26)24(14,17)5/h10,17-18,20,25H,6-9H2,1-5H3/t10-,17+,18-,20-,23-,24-/m1/s1 | ||||||||||||
InChI Key | JIEVZPUBUDASNE-YTHIZTJUSA-N | ||||||||||||
Chemical Taxonomy | |||||||||||||
Description | Belongs to the class of organic compounds known as furopyrans. These are organic polycyclic compounds containing a furan ring fused to a pyran ring. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds. | ||||||||||||
Kingdom | Organic compounds | ||||||||||||
Super Class | Organoheterocyclic compounds | ||||||||||||
Class | Furopyrans | ||||||||||||
Sub Class | Not Available | ||||||||||||
Direct Parent | Furopyrans | ||||||||||||
Alternative Parents | |||||||||||||
Substituents |
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Molecular Framework | Aliphatic heteropolycyclic compounds | ||||||||||||
External Descriptors | Not Available | ||||||||||||
Functional Ontology | |||||||||||||
Not Available | |||||||||||||
Physical Properties | |||||||||||||
State | Expected Solid | ||||||||||||
Predicted Properties | Not Available | ||||||||||||
Spectra | |||||||||||||
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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 | Not Available | ||||||||||||
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 | Not Available | ||||||||||||
Chemspider ID | 76768466 | ||||||||||||
KEGG Compound ID | Not Available | ||||||||||||
BioCyc ID | Not Available | ||||||||||||
BiGG ID | Not Available | ||||||||||||
Wikipedia Link | Not Available | ||||||||||||
METLIN ID | Not Available | ||||||||||||
PubChem Compound | 134139030 | ||||||||||||
PDB ID | Not Available | ||||||||||||
ChEBI ID | Not Available | ||||||||||||
Food Biomarker Ontology | Not Available | ||||||||||||
CMMC Knowledgebase | Not Available | ||||||||||||
General References | |||||||||||||