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33649-15-9

33649-15-9 Structure

33649-15-9 Structure
IdentificationBack Directory
[Name]

Tomentosin
[CAS]

33649-15-9
[Synonyms]

C09562
Tomentosin
Tomentosin (Parthenium)
(3aR)-3,3aα,4,7,8,8aα-Hexahydro-7β-methyl-3-methylene-6-(3-oxobutyl)-2H-cyclohepta[b]furan-2-one
(3aα)-3-Methylene-6-(3-oxobutyl)-7β-methyl-3,3aα,4,7,8,8aα-hexahydro-2H-cyclohepta[b]furan-2-one
2H-Cyclohepta[b]furan-2-one, 3,3a,4,7,8,8a-hexahydro-7-methyl-3-methylene-6-(3-oxobutyl)-, (3aR,7S,8aR)-
[Molecular Formula]

C15H20O3
[MOL File]

33649-15-9.mol
[Molecular Weight]

248.32
Chemical PropertiesBack Directory
[storage temp. ]

-20°C
[solubility ]

Soluble in DMSO (50 mg/ml)
[form ]

oil
[color ]

Yellow
[Stability:]

Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 2 month.
Hazard InformationBack Directory
[Description]

Extracts of Inula which contain tomentosin (33649-15-9) have been used for centuries in traditional medicine for the treatment of inflammation.1 It suppresses the production of inflammatory mediators in RAW264.7 cells by inhibiting NFkB activation.2 It induces telomere shortening and caspase-dependent apoptosis in cervical cancer cells3 and induces apoptosis in human osteosarcoma MG-63 cells4. It causes G2/M arrest and apoptosis in human melanoma cell lines.5
[Definition]

ChEBI: Tomentosin is a sesquiterpene lactone.
[References]

Lu et al. (2012), Inula japonica extract inhibits mast cell-mediated allergic reaction and mast cell activation; Ethnopharmacol. 143 151 Park et al. (2014), Suppressive effect of tomentosin on the production of inflammatory mediators in RAW264.7 cells; Biol. Pharm. Bull., 37 1177 Merghoub et al. (2017), Tomentosin Induces Telomere Shortening and Caspase-Dependent Apoptosis in Cervical Cancer Cells; J. Cell Biochem., 118 1689 Lee et al. (2019), Tomentosin Displays Anti-Carcinogenic Effect in Human Osteosarcoma MG-63 Cells via the Induction of Intracellular Reactive Oxygen Species; Int. J. Mol. Sci., 20(6) 1508 Rozenblat et al. (2008), Induction of G2/M arrest and apoptosis by sesquiterpene lactones in human melanoma cell lines; Biochem. Pharmacol., 75 369
33649-15-9 suppliers list
Company Name: Chengdu Caoyuankang Biological Technology Co., Ltd.  
Tel: 13438898246 13438890025
Website: www.caoyuankang.cn
Company Name: Naturewill Biotechnology Co., Ltd.  
Tel: 18113192475 18113192475
Website: www.chemicalbook.com/supplier/24868677/
Company Name: Nanjing Shizhou Biology Technology Co.,Ltd  
Tel: 025-85560043 15850508050
Website: https://www.synzest.com
Company Name: TargetMol Chemicals Inc.  
Tel: 15002134094
Website: https://www.targetmol.cn/
Company Name: Focus Biomolecules  
Tel: 855-362-8721
Website: www.focusbiomolecules.com
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