CAS 98665-11-3

Formule : C33H46O9

InChI : InChI=1S/C33H46O9/c1-16(12-19(35)13-17(2)29(40)41-9)20-14-24(38)33(8)25-21(36)15-22-30(4,5)23(37)10-11-31(22,6)26(25)27(39)28(32(20,33)7)42-18(3)34/h16-17,20,22-23,28,37H,10-15H2,1-9H3/t16-,17?,20-,22+,23+,28-,31+,32+,33+/m1/s1

Code InChI : KXYWXCIDKNDYTK-RRHNHSKDSA-N

SMILES : C[C@H](CC(=O)CC(C)C(=O)OC)[C@H]1CC(=O)[C@@]2([C@@]1([C@@H](C(=O)C3=C2C(=O)C[C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)OC(=O)C)C)C

Methyl ganoderate H

CAS : 98665-11-3

Methyl ganoderate H is a natural product for research related to life sciences. The catalog number is TN4545 and the CAS number is 98665-11-3.

Formule : C₃₃H₄₆O₉

Degré de pureté : 98%

Couleur et forme : Solid

Masse moléculaire : 586.7129

Ref: TM-TN4545

Methyl ganoderate H

CAS : 98665-11-3

Methyl ganoderate H is a natural triterpenoid compound, which is derived from the fruiting bodies of Ganoderma fungi. These fungi, commonly known as Reishi mushrooms, are well-regarded in traditional medicine for their rich bioactive profiles. The mode of action of Methyl ganoderate H involves modulating various biological pathways, possibly influencing cellular processes through its interaction with membrane lipids and proteins. This compound is renowned for its pharmacological potential, which includes antioxidant, anti-inflammatory, and anticancer effects due to its ability to scavenge free radicals and mitigate oxidative stress.

Formule : C₃₃H₄₆O₉

Degré de pureté : Min. 95%

Masse moléculaire : 586.70 g/mol

Ref: 3D-YDA66511