Cinnamaldehyde

CAS: 104-55-2

Ref. TM-T4S1551

Produktinformation

• Name: Cinnamaldehyde
• Synonyme: Cinnamic Aldehyde, (2E)-3-phenylprop-2-enal, (2Z)-3-phenylprop-2-enal, 2-Phenylprop-2-Enal, 2-Propenal, 3-phenyl-, 3-Phenyl-2-propen-1-al, 3-Phenyl-2-propenal, 3-Phenyl-2-propenaldehyde, 3-Phenyl-2-propene-1-al, 3-Phenylacrolein, 3-Phenylacrylaldehyde, 3-Phenylprop-2-Enal, 3-Phenylpropenal, Abion CA, Benzylideneacetaldehyde, Cassia aldehyde, Cinamaldehido, Cinnacure, Cinnam Aldehyde, Cinnamal, Cinnamic aldehyde, Cinnamite, Cinnamyl Aldehyde, Natural Cinnamyl Aldehyde, Nsc 16935, Nsc 40346, Phenylacrolein, Xc 800, Zimtaldehyd, Zimtaldehyde, trans-3-Phenyl-2-propenal, trans-Cinnamaldehyde, β-Phenylacrolein
• CAS: 104-55-2

Beschreibung

1. Cinnamaldehyde (Cinnamic Aldehyde) has antipyretic activity. 2. Cinnamaldehyde is a sedative agent. 3. Cinnamaldehyde inhibits invasive capabilities of MDA-MB-435S cells was correlated with down-regulating the expression of miR-27a. 4. Cinnamaldehyde induces the generation of reactive oxygen species and exerts vasodilator and anticancer effects. 5. Cinnamaldehyde appears to be a promising candidate as an adjuvant in combination therapy with 5-fluorouracil (5-FU) and oxaliplatin (OXA), two chemotherapeutic agents used in CRC treatment. The possible mechanisms of its action may involve the regulation of drugmetabolizing genes. 6. Cinnamaldehyde plays a certain role in inhibiting the occurrence and progression of melanoma and its action mechanism may be manifested by inhibiting expression of VEGF and HIF-α, thus blood vessel simulation and formation of new blood vessels of melanoma cells, and growth of tumors accordingly.

• Marke: Targetmol

Chemische Eigenschaften

• Molekulargewicht: 132.16
• Formel: C₉H₈O
• Reinheit: 85%
• Farbe/Form: Yellowish Oily Liquid