(±)-Dihydroactinidiolide 7272 52)6)90-58-49(42(77)41(76)47(92-58)53(81)82)94-57-48(40(75)38(73)32(21-66)89-57)93-55-43(78)39(74)37(72)31(20-65)88-55/h11

52)6)90-58-49(42(77)41(76)47(92-58)53(81)82)94-57-48(40(75)38(73)32(21-66)89-57)93-55-43(78)39(74)37(72)31(20-65)88-55/h11

4)14-12-22(20)24

) reduces the expression of LPS-induced IκB mRNA

InChiKey: QTAOMKOIBXZKND-PPHPATTJSA-N

Formula: C21H33NO7

(±)-Dihydroactinidiolide 7272 52)6)90-58-49(42(77)41(76)47(92-58)53(81)82)94-57-48(40(75)38(73)32(21-66)89-57)93-55-43(78)39(74)37(72)31(20-65)88-55/h11() Dihydroactinidiolide, an important aroma compound of black tea and tobacco, has been isolated from several plants. () Dihydroactinidiolide can be formation from Carotene by the treatment of polyphenoloxidase, the lipoxygenase, and the xanthine oxidase. Product information CAS Number: 15356 74 8 Molecular Weight: 180. 24 Formula: C11H16O2 Chemical Name: 4,4,7a trimethyl 2,4,5,6,7,7a hexahydro 1 benzofuran 2 one Smiles: CC1(C)CCCC2(C)OC(=O)C=C12