Vibralactone K

Vibralactone K

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Vibralactone K
Category Others
Catalog number BBF-04386
CAS 1623786-66-2
Molecular Weight 210.27
Molecular Formula C12H18O3
Purity ≥98%

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Description

Vibralactone K is isolated from Boreostereum vibrans and has no cytotoxicity against five human cancer cell lines.

Specification

Synonyms 1H-Cyclopenta[c]furan-1-one, hexahydro-6-hydroxy-5-(3-methyl-2-buten-1-yl)-, (3aS,5S,6R,6aR)-
Storage Store at 2-8°C
IUPAC Name (3aR,4R,5S,6aS)-4-hydroxy-5-(3-methylbut-2-enyl)-1,3a,4,5,6,6a-hexahydrocyclopenta[c]furan-3-one
Canonical SMILES CC(=CCC1CC2COC(=O)C2C1O)C
InChI InChI=1S/C12H18O3/c1-7(2)3-4-8-5-9-6-15-12(14)10(9)11(8)13/h3,8-11,13H,4-6H2,1-2H3/t8-,9+,10+,11+/m0/s1
InChI Key SCJICIQXRZEFQL-LNFKQOIKSA-N

Properties

Appearance Oily Matter
Boiling Point 371.0±25.0°C at 760 mmHg
Density 1.1±0.1 g/cm3
Solubility Soluble in Methanol

Reference Reading

1. Three new vibralactone-related compounds from cultures of Basidiomycete Boreostereum vibrans
Gang-Qiang Wang, Kun Wei, Ling Zhang, Zheng-Hui Li, Qiu-An Wang, Ji-Kai Liu J Asian Nat Prod Res. 2014;16(5):447-52. doi: 10.1080/10286020.2014.901312. Epub 2014 Apr 1.
Three new compounds, named as vibralactones K-M (1-3), together with vibralactone (4) have been isolated from cultures of the Basidiomycete Boreostereum vibrans. Their structures were determined on the basis of spectroscopic evidences (1D and 2D NMR, HRMS, UV, and IR data), chemical methods and literature data. None of the compounds was cytotoxic against five human cancer cell lines and showed inhibitory activity on the pancreatic lipase.

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* 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

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Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
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