(2E)-2,3-Diphenylacrylic acid

CAS: 91-48-5

Ref. 3D-FD133268

Produktinformation

• Name: (2E)-2,3-Diphenylacrylic acid
• Synonyme: benzeneacetic acid, alpha-(phenylmethylene)-, (2E)-2,3-diphenylprop-2-enoate, (2E)-2,3-diphenylprop-2-enoic acid, (2Z)-2,3-diphenylprop-2-enoate, (2Z)-2,3-diphenylprop-2-enoic acid, (E)-2,3-Diphenyl-2-propenoic acid, (E)-2,3-Diphenylacrylic acid, (E)-2,3-Diphenylpropenoic acid, (E)-α-(Phenylmethylene)benzeneacetic acid, (E)-α-Phenylcinnamic acid, (E)-α-Stilbenecarboxylic acid, (αE)-α-(Phenylmethylene)benzeneacetic acid, 2,3-Diphenylprop-2-Enoic Acid, Acrylic acid, 2,3-diphenyl-, (E)-, Acrylic acid, 2,3-diphenyl-, trans-, Benzeneacetic acid, α-(phenylmethylene)-, (E)-, Benzeneacetic acid, α-(phenylmethylene)-, (αE)-, Phenylcinnamicacid,98%, a-(Phenylmethylene)benzeneacetic acid, Pract., a-Phenyl-trans-cinnamic acid, Pract., trans-2,3-Diphenyl-2-propenoic acid, trans-2,3-Diphenylacrylic acid, trans-2,3-Diphenylpropenoic acid, trans-α-Phenylcinnamic acid

Beschreibung

(2E)-2,3-Diphenylacrylic acid is a stilbene derivative that has been shown to inhibit tyrosinase activity in vitro. The molecular modelling studies of the compound have revealed that it binds to the active site of the enzyme through hydrogen bonding interactions and competitively inhibits the substrate binding site. (2E)-2,3-Diphenylacrylic acid has also been shown to inhibit melanogenesis in vitro by inhibiting cinchonidine uptake. In addition, this molecule has been found to be an effective inhibitor of chloride uptake as well as having an effect on intermolecular hydrogen bonding.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 224.25 g/mol
• Formel: C₁₅H₁₂O₂
• Reinheit: Min. 95%
• InChl: InChI=1S/C15H12O2/c16-15(17)14(13-9-5-2-6-10-13)11-12-7-3-1-4-8-12/h1-11H,(H,16,17)/b14-11+
• InChI Key: InChIKey=BIDDLDNGQCUOJQ-SDNWHVSQSA-N
• SMILES: O=C(O)/C(=C/c1ccccc1)c1ccccc1