
CAS 109770-86-7
:Formule :C22H28O7
InChI :InChI=1S/C22H28O7/c1-13-6-5-7-14(2)11-19(20-15(3)21(25)28-18(20)10-13)29-22(26)17(12-23)8-9-27-16(4)24/h7-8,10,18-20,23H,3,5-6,9,11-12H2,1-2,4H3/b13-10+,14-7+,17-8+/t18-,19-,20+/m1/s1
Code InChI :CUJJANFZVGSCSV-UHIMBCETSA-N
SMILES :C/C/1=C\[C@@H]2[C@@H]([C@@H](C/C(=C/CC1)/C)OC(=O)/C(=C/COC(=O)C)/CO)C(=C)C(=O)O2
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8 β-(4-Acetoxy-5-hydroxytigloyloxy)costunolide
CAS :8 beta-(4-Acetoxy-5-hydroxytigloyloxy)costunolide is a natural product for research related to life sciences.Formule :C22H28O7Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :404.4598β-(4-Acetoxy-5-hydroxytigloyloxy)costunolide
CAS :Formule :C22H28O7Degré de pureté :95%~99%Masse moléculaire :404.459[(3aR,4R,6Z,10Z,11aR)-6,10-Dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-4-acetyloxy-2-(hydroxyme thyl)but-2-enoate
CAS :[(3aR,4R,6Z,10Z,11aR)-6,10-Dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-4-acetyloxy-2-(hydroxyme thyl)but-2-enoate is a highly specialized sesquiterpene lactone. This compound is typically derived from certain plant species noted for their medicinal properties, particularly those belonging to the Asteraceae family. It functions by interacting with cellular pathways, often through the inhibition of specific enzymes or by modulating signaling pathways, leading to various biological effects such as anti-inflammatory and anticancer activities. Researchers are exploring the mechanism by which this compound exerts such effects, often focusing on its role in modulating oxidative stress and cellular apoptosis.Formule :C22H28O7Degré de pureté :Min. 95%Masse moléculaire :404.5 g/mol


