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Tomentosin

CAS No.
33649-15-9
Chemical Name:
Tomentosin
Synonyms
C09562;Tomentosin;Tomentosin (Parthenium);(3aα)-3-Methylene-6-(3-oxobutyl)-7β-methyl-3,3aα,4,7,8,8aα-hexahydro-2H-cyclohepta[b]furan-2-one;(3aR)-3,3aα,4,7,8,8aα-Hexahydro-7β-methyl-3-methylene-6-(3-oxobutyl)-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)-
CBNumber:
CB32159341
Molecular Formula:
C15H20O3
Molecular Weight:
248.32
MDL Number:
MOL File:
33649-15-9.mol
Last updated:2023-05-04 17:34:37

Tomentosin Properties

Melting point 121-122 °C(Solv: methanol (67-56-1))
Boiling point 416.2±45.0 °C(Predicted)
Density 1.08±0.1 g/cm3(Predicted)
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.

Tomentosin Chemical Properties,Uses,Production

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

Tomentosin Preparation Products And Raw materials

Raw materials

Preparation Products

Tomentosin Suppliers

Global( 4)Suppliers
Supplier Tel Email Country ProdList Advantage
Chengdu Caoyuankang Biological Technology Co., Ltd. 028-1343889 13438890071 3003796343@qq.com China 538 58
Naturewill Biotechnology Co., Ltd. 18113192475 18113192475 3157321941@qq.com China 5000 58
Nanjing Shizhou Biology Technology Co.,Ltd 025-85560043 15850508050 rose.shi@synzest.com China 6111 58

33649-15-9(Tomentosin)Related Search:

(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 Tomentosin Tomentosin (Parthenium) C09562 2H-Cyclohepta[b]furan-2-one, 3,3a,4,7,8,8a-hexahydro-7-methyl-3-methylene-6-(3-oxobutyl)-, (3aR,7S,8aR)- 33649-15-9