Pterostilbene
SIGMA/P1499 - ≥97% (HPLC), solid
Synonym: Pterocarpus marsupium; 3,5-Dimethoxy-4′-hydroxystilbene; 4-[(1E)
CAS Number: 537-42-8
Empirical Formula (Hill Notation): C16H16O3
Molecular Weight: 256.30
MDL Number: MFCD00238710
Linear Formula: C16H16O3
Product Type: Chemical
| assay | ≥97% (HPLC) |
| form | solid |
| InChI | 1S/C16H16O3/c1-18-15-9-13 |
| InChI key | VLEUZFDZJKSGMX-ONEGZZNKSA |
| Quality Level | 100 ![]() |
| SMILES string | COc1cc(OC)cc(C=Cc2ccc(O |
| solubility | DMSO: >20 mg/mL |
| H2O: insoluble | |
| storage condition | protect from light |
| storage temp. | 2-8°C |
| Application: | Pterostilbene has been used: • to investigate its anti-oxidative stress activities and the involvement of the nuclear factor (erythroid-derived 2)-like 2 (Nrf2)-antioxidant response element (ARE) signaling pathway • to determine its effects on transcriptional activation of estrogen receptor-α (ERα) in hormone resistant breast cancer cells) • to study its effects on the cytotoxicity of 2-chloroethyl ethyl sulphide (CEES) in human epidermoid carcinoma cells (A-431) through MTT (3-[4,5-dimethylthiazol-2 |
| Biochem/physiol Actions: | Antioxidant, antiproliferative, apoptosis inducer, antihyperglycemic, antidiabetic. |
| Biochem/physiol Actions: | Pterostilbene exhibits antineoplastic properties in some of the malignancies, hence it is considered as an active anticancer agent. It has the ability to stimulate apoptosis and block the viability of cell in estrogen-receptor positiv |
| Disclaimer: | Air-sensitive |
| General description: | Pterostilbene (trans-3,5- |
| Packaging: | 10 mg in glass bottle |
| Symbol | ![]() GHS05,GHS09 |
| Signal word | Danger |
| Hazard statements | H318 - H411 |
| Precautionary statements | P273 - P280 - P305 + P351 + P338 + P310 |
| Hazard Codes | Xi,N |
| Risk Statements | 41-51/53 |
| Safety Statements | 26-39-61 |
| RIDADR | UN 3077 9 / PGIII |
| WGK Germany | WGK 3 |
| Purity | ≥97% (HPLC) |
| Storage Temp. | 2-8°C |
| UNSPSC | 12352200 |



