Flagranone C
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
| Category | Antibiotics |
| Catalog number | BBF-00934 |
| CAS | |
| Molecular Weight | 336.29 |
| Molecular Formula | C16H16O8 |
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Description
Flagranone C is a cyclohexenone oxide antibiotic produced by Duddingtonia flagrans.
Specification
| IUPAC Name | [6-[(E)-1-acetyloxy-3-methyl-4-oxobut-2-enyl]-2,5-dioxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl]methyl acetate |
| Canonical SMILES | CC(=CC(C12C(O1)C(=O)C(=CC2=O)COC(=O)C)OC(=O)C)C=O |
| InChI | InChI=1S/C16H16O8/c1-8(6-17)4-13(23-10(3)19)16-12(20)5-11(7-22-9(2)18)14(21)15(16)24-16/h4-6,13,15H,7H2,1-3H3/b8-4+ |
| InChI Key | HSTGWHJVZDXYFE-XBXARRHUSA-N |
Properties
| Appearance | Yellow Oil |
Reference Reading
1. Structures of flagranones A, B and C, cyclohexenoxide antibiotics from the nematode-trapping fungus Duddingtonia flagrans
M G Anderson, R W Rickards, E Lacey J Antibiot (Tokyo). 1999 Nov;52(11):1023-8. doi: 10.7164/antibiotics.52.1023.
Spectroscopic data define the structures of the flagranones A (2), B (3) and C (4) from the nematode-trapping fungus Duddingtonia flagrans. These antibiotics are structurally related to the farnesylated cyclohexenoxides of the oligosporon group recently isolated from the nematode-trapping fungus Arthrobotrys oligospora, and show similar antimicrobial activity.
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Bio Calculators
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O √ c22h30n40 ╳
