Vanillin acetate 14129 Smiles: C[C@@H]1[C@H]2[C@@H](OC=C([C@H]2C[C@@H]1O)C(O)=O)O[C@@H]1O[C@H](CO[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@H](O)[C@H]1O

Smiles: C[C@@H]1[C@H]2[C@@H](OC=C([C@H]2C[C@@H]1O)C(O)=O)O[C@@H]1O[C@H](CO[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@H](O)[C@H]1O

ICG001 have been shown to selectively inhibit colon carcinoma cell lines (SW480 and HCT-116 cells) but not normal colonic epithelial cells (CCD-841Co)

Compounds from Caesalpinia sappan with anti-inflammatory properties in macrophages and chondrocytes

Synthesis and Sensory Characteristics of Kokumi γ-[Glu]n-Phe in the Presence of Glutamine and Phenylalanine: Glutaminase from Bacillus amyloliquefaciens or Aspergillus oryzae as the Catalyst

50(6):572-9

Vanillin acetate 14129 Smiles: C[C@@H]1[C@H]2[C@@H](OC=C([C@H]2C[C@@H]1O)C(O)=O)O[C@@H]1O[C@H](CO[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](O)[C@H](O)[C@H]1OVanillin acetate is easily synthesized from vanillin by treatment with acetic anhydride. Product information CAS Number: 881 68 5 Molecular Weight: 194. 18 Formula: C10H10O4 Chemical Name: 4 formyl 2 methoxyphenyl acetate Smiles: CC(=O)OC1=CC=C(C=O)C=C1OC InChiKey: PZSJOBKRSVRODF UHFFFAOYSA N InChi: InChI=1S C10H10O4 c1 7(12)14 9 4 3 8(6 11)5 10(9)13 2 h3 6H,1 2H3 Technical Data Appearance: Solid Power Purity: 98% (or refer to the Certificate of