Kaji-ichigoside F1 d hydrochloride Smiles: CC(=O)[C@@]1(O)CC[C@H]2[C@@H]3C[C@H](C)C4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C

Smiles: CC(=O)[C@@]1(O)CC[C@H]2[C@@H]3C[C@H](C)C4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C

eprodisate competitively binds to the glycosaminoglycan binding sites on serum amyloid A (SAA)

AS2444697 (0

In Mice with experimental autoimmune encephalomyelitis

Kaji-ichigoside F1 d hydrochloride Smiles: CC(=O)[C@@]1(O)CC[C@H]2[C@@H]3C[C@H](C)C4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12CKaji ichigoside F1 is isolated from S. cuneata with hemolytic and in vitro antiviral activity. Product information CAS Number: 95298 47 8 Molecular Weight: 650. 84 Formula: C36H58O10 Chemical Name: (2S,3R,4S,5S,6R) 3,4,5 trihydroxy 6 (hydroxymethyl)oxan 2 yl (1R,2R,4aS,6aS,6bR,8aR,10S,11R,12aR,12bR,14bS) 1,10,11 trihydroxy 1,2,6a,6b,9,9,12a heptamethyl 1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b icosahydropicene 4a carboxylate Smiles: