
CAS 145163-97-9
:Fórmula:C29H48O2
InChI:InChI=1S/C29H48O2/c1-7-20(18(2)3)9-8-19(4)23-10-11-24-27-25(13-15-29(23,24)6)28(5)14-12-22(30)16-21(28)17-26(27)31/h17-20,22-25,27,30H,7-16H2,1-6H3/t19-,20+,22+,23-,24+,25+,27+,28+,29-/m1/s1
Clave InChI:ICFXJOAKQGDRCT-HPYBIPJLSA-N
SMILES:CC[C@@H](CC[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2C(=O)C=C4[C@@]3(CC[C@@H](C4)O)C)C)C(C)C
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(3β,24S)-3-Hydroxystigmast-5-en-7-one
CAS:(3β,24S)-3-Hydroxystigmast-5-en-7-one (Compound 31), isolated from Lindera akoensis, exhibits anti-inflammatory activity [1].Fórmula:C29H48O2Forma y color:SolidPeso molecular:428.69023Beta-Hydroxyporiferast-5-en-7-one
CAS:Producto controlado3Beta-Hydroxyporiferast-5-en-7-one is a sterol derivative, which is a phytosterol found in various plant sources. Its presence is particularly noted in dietary plants, where sterols function as essential membrane components. The compound is produced through biochemical transformations of naturally occurring phytosterols within plant biosynthesis pathways.Fórmula:C29H48O2Pureza:Min. 95%Peso molecular:428.7 g/mol


