Hydroxytyrosol acetate g-Phe amide Smiles: CC1(C)[C@@H]2CC(=O)C3=C(C(=O)[C@@H](OC(C)=O)[C@]4(C)[C@H](CC(=O)[C@]43C)[C@H](C)CC(=O)CC(C)C(O)=O)[C@@]2(C)CCC1=O

Smiles: CC1(C)[C@@H]2CC(=O)C3=C(C(=O)[C@@H](OC(C)=O)[C@]4(C)[C@H](CC(=O)[C@]43C)[C@H](C)CC(=O)CC(C)C(O)=O)[C@@]2(C)CCC1=O

Once absorbed

SU3327 also inhibits protein-protein interactions between JNK and JNK Interacting Protein (JIP) with an IC50 of 239 nM

9)10/h14-17H

Hydroxytyrosol acetate g-Phe amide Smiles: CC1(C)[C@@H]2CC(=O)C3=C(C(=O)[C@@H](OC(C)=O)[C@]4(C)[C@H](CC(=O)[C@]43C)[C@H](C)CC(=O)CC(C)C(O)=O)[C@@]2(C)CCC1=OHydroxytyrosol acetate is found in the olive oil with an antioxidant activity. Hydroxytyrosol acetate had a weaker DPPH radical scavenging activity than hydroxytyrosol. Product information CAS Number: 69039 02 7 Molecular Weight: 196. 20 Formula: C10H12O4 Chemical Name: 2 (3,4 dihydroxyphenyl)ethyl acetate Smiles: CC(=O)OCCC1=CC(O)=C(O)C=C1 InChiKey: FGJGLFPNIZXRLV UHFFFAOYSA N InChi: InChI=1S C10H12O4 c1 7(11)14 5 4 8 2 3 9(12)10(13)6 8 h2 3,6,12