(-)-TEPHROSIN

(-)-TEPHROSIN Basic information
Product Name:(-)-TEPHROSIN
Synonyms:13,13a-Dihydro-7a-hydroxy-9,10-dimethoxy-3,3-dimethyl-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one;Hydroxydeguelin;Isotephrosin;Deguelinol I;Tephrosin (synthetic);3H-Bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7- (7aH)-one,13,13a-dihydro-7a-hydroxy-9,10- dimethoxy-3,3-dimethyl-,(7aR,13aR)-;Tephrosin >=95% (LC/MS-ELSD);(-)-TEPHROSIN USP/EP/BP
CAS:76-80-2
MF:C23H22O7
MW:410.42
EINECS:
Product Categories:Miscellaneous Natural Products
Mol File:76-80-2.mol
(-)-TEPHROSIN Structure
(-)-TEPHROSIN Chemical Properties
Melting point 198° (218-220°)
Boiling point 450.42°C (rough estimate)
density 1.2284 (rough estimate)
refractive index 1.5300 (estimate)
storage temp. -20°C
solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form Cryst.
pka10.47±0.40(Predicted)
Safety Information
Hazard Codes N
Risk Statements 50
Safety Statements 61
RIDADR UN 3077 9 / PGIII
WGK Germany 3
MSDS Information
(-)-TEPHROSIN Usage And Synthesis
UsesTephrosin as a natural rotenoid obtained from Tephrosia vogelii and displays anticancer activity.
DefinitionChEBI: A member of the class of rotenones that is 13,13a-dihydro-3H-chromeno[3,4-b]pyrano[2,3-h]chromen-7(7aH)-one substituted with geminal methyl groups at position 3, hydroxy group at position 7a a d methoxy groups at positions 9 and 10 (the 7aR,13aR stereoisomer). It is isolated from the leaves and twigs of Antheroporum pierrei and exhibits antineoplastic and pesticidal activities.
targetROS | PARP | Autophagy | HSP (e.g. HSP90) | EGFR | Akt | ERK | Caspase | AMPK | mTOR
(-)-TEPHROSIN Preparation Products And Raw materials
2-(3,4-Dihydroxyphenyl)-8-(2-O-beta-L-galactopyranosyl-beta-D-glucopyranosyl)-5,7-dihydroxy-4H-1-Benzopyran-4-one Hydroxyecdysone HYDROXOCOBALAMIN (4E,6E)-1,7-Diphenyl-4,6-heptadien-3-one Artemether beta-Sitosterol hydroxygenkwanin alpha-Terpineol beta-Eudesmol MOSLOFLAVONE alpha-Cyperone

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