Record Information |
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Version |
1.0 |
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Update Date |
1/22/2018 11:54:54 AM |
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Metabolite ID | PAMDB100062 |
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Identification |
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Name: |
asphodelin A |
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Description: | A hydroxycoumarin that is 4,7-dihydroxy-2H-chromen-2-one substituted by a 2,4-dihydroxyphenyl group at position 3. It is isolated from the roots of Asphodelus microcarpus and exhibits antimicrobial activity against bacteria like Staphyloc |
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Structure |
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Synonyms: | - 3-(2',4'-dihydroxyphenyl)-4,7-dihydroxy-2H-1-benzopyran-2-one
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Chemical Formula: |
C15H10O6 |
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Average Molecular Weight: |
286.2363 |
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Monoisotopic Molecular
Weight: |
286.048 |
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InChI Key: |
OZOZCKVLUMXFGS-UHFFFAOYSA-N |
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InChI: | InChI=1S/C15H10O6/c16-7-1-3-9(11(18)5-7)13-14(19)10-4-2-8(17)6-12(10)21-15(13)20/h1-6,16-19H |
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CAS
number: |
Not Available |
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IUPAC Name: | 3-(2,4-dihydroxyphenyl)-4,7-dihydroxy-2H-chromen-2-one |
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Traditional IUPAC Name: |
Not Available |
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SMILES: | Oc1ccc(c(O)c1)-c1c(O)c2ccc(O)cc2oc1=O |
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Chemical Taxonomy |
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Taxonomy Description | This compound belongs to the class of organic compounds known as hydroxyisoflavonoids. These are organic compounds containing an isoflavonoid skeleton carrying one or more hydroxyl groups. |
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Kingdom |
Organic compounds |
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Super Class | Phenylpropanoids and polyketides |
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Class |
Isoflavonoids |
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Sub Class | Hydroxyisoflavonoids |
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Direct Parent |
Hydroxyisoflavonoids |
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Alternative Parents |
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Substituents |
- Hydroxyisoflavonoid
- Isoflav-3-enone skeleton
- 4-hydroxycoumarin
- 7-hydroxycoumarin
- Hydroxycoumarin
- Coumarin
- Benzopyran
- 1-benzopyran
- Resorcinol
- 1-hydroxy-2-unsubstituted benzenoid
- 1-hydroxy-4-unsubstituted benzenoid
- Pyranone
- Phenol
- Benzenoid
- Pyran
- Monocyclic benzene moiety
- Vinylogous acid
- Heteroaromatic compound
- Lactone
- Oxacycle
- Organoheterocyclic compound
- Hydrocarbon derivative
- Organic oxide
- Organic oxygen compound
- Organooxygen compound
- Aromatic heteropolycyclic compound
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Molecular Framework |
Aromatic heteropolycyclic compounds |
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External Descriptors |
- polyphenol, hydroxycoumarin (CHEBI:65453)
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Physical Properties |
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State: |
Not Available |
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Charge: | 0 |
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Melting point: |
Not Available |
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Experimental Properties: |
Not Available |
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Predicted Properties |
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Biological Properties |
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Cellular Locations: |
Not Available |
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Reactions: | |
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Pathways: |
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Spectra |
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Spectra: |
Not Available |
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References |
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References: |
- El-Seedi HR. Antimicrobial arylcoumarins from Asphodelus microcarpus. J Nat
Prod. 2007 Jan;70(1):118-20. Pubmed: 17253862
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Synthesis Reference: |
Not Available |
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Material Safety Data Sheet (MSDS) |
Not Available |
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Links |
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External Links: |
Not Available |
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