Fusarubin

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| ImageFile = Fusarubin.svg

| ImageSize = 200px

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| IUPACName = 3,5,10-trihydroxy-7-methoxy-3-methyl-1,4-dihydrobenzo[g]isochromene-6,9-dione

| OtherNames = Oxyjavanicin{{cite journal |title=Fusarubin |journal=Pubchem.ncbi.NLM.nih.gov |url=https://pubchem.ncbi.nlm.nih.gov/compound/Fusarubin |language=en}}

| Section1 = {{Chembox Identifiers

| CASNo = 1702-77-8

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| ChEBI =

| ChEMBL = 1224816

| ChemSpiderID = 66134

| EINECS =

| PubChem = 73421

| UNII = 7O2VQR7EHB

| StdInChI=1S/C15H14O7/c1-15(20)4-6-7(5-22-15)13(18)10-8(16)3-9(21-2)14(19)11(10)12(6)17/h3,17-18,20H,4-5H2,1-2H3

| StdInChIKey = FKJXMYJPOKQPSS-UHFFFAOYSA-N

| SMILES = CC1(CC2=C(CO1)C(=C3C(=O)C=C(C(=O)C3=C2O)OC)O)O

}}

| Section2 = {{Chembox Properties

| C=15 | H=14 | O=7

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Fusarubin is a naphthoquinone derived mycotoxin which is produced by the fungi Fusarium solani.{{cite book |last1=Bycroft |first1=Barrie W. |last2=Payne |first2=David J. |title=Dictionary of Antibiotics and Related Substances: with CD-ROM, Second Edition |date=9 August 2013 |publisher=CRC Press |isbn=978-1-4822-8215-3 |page=858 |language=en}}{{cite book |last1=Buckingham |first1=John |title=Dictionary of Organic Compounds |date=1987 |publisher=Taylor & Francis |isbn=978-0-412-17050-8 |page=345 |language=en}} Fusarubin has the molecular formula C15H14O7.

== References ==

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Further reading

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  • {{cite journal |last1=Pedersen |first1=Tobias Bruun |last2=Nielsen |first2=Mikkel Rank |last3=Kristensen |first3=Sebastian Birkedal |last4=Spedtsberg |first4=Eva Mie Lang |last5=Yasmine |first5=Wafaa |last6=Matthiesen |first6=Rikke |last7=Kaniki |first7=Samba Evelyne Kabemba |last8=Sørensen |first8=Trine |last9=Petersen |first9=Celine |last10=Muff |first10=Jens |last11=Sondergaard |first11=Teis Esben |last12=Nielsen |first12=Kåre Lehmann |last13=Wimmer |first13=Reinhard |last14=Sørensen |first14=Jens Laurids |title=Heterologous Expression of the Core Genes in the Complex Fusarubin Gene Cluster of Fusarium Solani |journal=International Journal of Molecular Sciences |date=14 October 2020 |volume=21 |issue=20 |pages=7601 |doi=10.3390/ijms21207601|pmid=33066643 |pmc=7589453 |doi-access=free }}

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Category:Mycotoxins

Category:1,4-Naphthoquinones

Category:Methoxy compounds

Category:Triols

Category:Benzoisochromenes

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