
CAS 193969-08-3
:Formule :C23H28O12
InChI :InChI=1S/C23H28O12/c1-31-15-7-10(2-3-13(15)25)21(30)33-9-11-6-14(26)12-4-5-32-22(17(11)12)35-23-20(29)19(28)18(27)16(8-24)34-23/h2-7,12,14,16-20,22-29H,8-9H2,1H3/t12-,14+,16+,17+,18+,19-,20+,22-,23-/m0/s1
Code InChI :VTYVNBXSLBXSGD-IFWLTBFJSA-N
SMILES :COC1=C(C=CC(=C1)C(=O)OCC2=C[C@H]([C@H]3[C@@H]2[C@@H](OC=C3)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)O
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5 produits trouvés.
10-O-Vanilloylaucubin
CAS :10-O-VanilloylaucubinFormule :C23H28O12Degré de pureté :≥95%Masse moléculaire :496.4610-O-Vanilloylaucubin
CAS :10-O-Vanilloylaucubin shows significant writhing inhibition following oral administration at doses of 25 mg/kg.suggests that it has analgesic effects.Formule :C23H28O12Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :496.4610-O-Vanilloylaucubin
CAS :Formule :C23H28O12Degré de pureté :95%~99%Couleur et forme :PowderMasse moléculaire :496.46510-o-Vanilloylaucubin
CAS :10-o-Vanilloylaucubin is a naturally occurring iridoid glycoside, which is a type of secondary metabolite primarily found in certain plant species. It is typically sourced from various members of the plant families Gentianaceae and Plantaginaceae. The compound exhibits a unique mode of action that involves modulating biological pathways associated with inflammation and cell proliferation. Its potential to interfere with these pathways positions it as a candidate for further research into anti-inflammatory and anti-cancer therapies.
Formule :C23H28O12Degré de pureté :Min. 95%Masse moléculaire :496.5 g/mol





