![]() Piceatannol structure
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Common Name | Piceatannol | ||
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CAS Number | 10083-24-6 | Molecular Weight | 244.243 | |
Density | 1.5±0.1 g/cm3 | Boiling Point | 507.3±38.0 °C at 760 mmHg | |
Molecular Formula | C14H12O4 | Melting Point | 223-227ºC | |
MSDS | Chinese USA | Flash Point | 252.2±21.4 °C |
Use of PiceatannolPiceatannol is a selective inhibitor of protein tyrosine kinase Syk. It could inhibit ICa,L, Ito, IKr, Ca2+ transients and Na+-Ca2+ exchange except IK1. Shows multiple biological activities such as anti-inflammatory, antiproliferative and immunomodulatory effects.In vitro: The treatment of human myeloid cells with piceatannol suppressed TNF-induced DNA binding activity of NF-κB. The effect of piceatannol was not restricted to myeloid cells, as TNF-induced NF-κB activation was also suppressed in lymphocyte and epithelial cells. Piceatannol also inhibited NF-κB activated by H2O2, PMA, LPS, okadaic acid, and ceramide. [1] |
Name | Piceatannol |
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Synonym | More Synonyms |
Description | Piceatannol is a selective inhibitor of protein tyrosine kinase Syk. It could inhibit ICa,L, Ito, IKr, Ca2+ transients and Na+-Ca2+ exchange except IK1. Shows multiple biological activities such as anti-inflammatory, antiproliferative and immunomodulatory effects.In vitro: The treatment of human myeloid cells with piceatannol suppressed TNF-induced DNA binding activity of NF-κB. The effect of piceatannol was not restricted to myeloid cells, as TNF-induced NF-κB activation was also suppressed in lymphocyte and epithelial cells. Piceatannol also inhibited NF-κB activated by H2O2, PMA, LPS, okadaic acid, and ceramide. [1] |
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Related Catalog | |
References |
Density | 1.5±0.1 g/cm3 |
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Boiling Point | 507.3±38.0 °C at 760 mmHg |
Melting Point | 223-227ºC |
Molecular Formula | C14H12O4 |
Molecular Weight | 244.243 |
Flash Point | 252.2±21.4 °C |
Exact Mass | 244.073563 |
PSA | 80.92000 |
LogP | 2.69 |
Vapour Pressure | 0.0±1.4 mmHg at 25°C |
Index of Refraction | 1.801 |
Storage condition | 2-8°C |
Water Solubility | H2O: 0.5 mg/mL |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Safety Phrases | 24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2907299090 |
HS Code | 2907299090 |
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Summary | 2907299090 polyphenols; phenol-alcohols。supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward)。VAT:17.0%。tax rebate rate:9.0%。MFN tariff:5.5%。general tariff:30.0% |
A unique mechanism of curcumin inhibition on F1 ATPase
Biochem. Biophys. Res. Commun. 452(4) , 940-4, (2014) • Polyphenols lowered the rotation rate of F1 ATPase by increasing catalytic dwell. • Curcumin showed different inhibitory mechanism from other polyphenols. • γ subunit carboxyl terminus is not requir... |
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Antibody-opsonized bacteria evoke an inflammatory dendritic cell phenotype and polyfunctional Th cells by cross-talk between TLRs and FcRs.
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TH2 cells and their cytokines regulate formation and function of lymphatic vessels.
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3,3',4'5-Tetrahydroxystilbene |
E-Piceatannol |
1,2-Benzenediol, 4-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]- |
3,3′,4,5′-Tetrahydroxy-trans-stilbene |
3,3',4,5'-Tetrahydroxy-trans-stilbene |
3,4,3',5'-Tetrahydroxy-trans-stilbene |
4-[(E)-2-(3,5-Dihydroxyphenyl)vinyl]benzene-1,2-diol |
3,5,3',4'-tetrahydroxystilbene |
4-[(E)-2-(3,5-Dihydroxyphenyl)vinyl]-1,2-benzenediol |
Piceatannol |
4-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]benzene-1,2-diol |
MFCD00221715 |
4-(2-(3,5-Dihydroxyphenyl)vinyl)-1,2-benzenediol |
(E)-4-[2-(3,5Dihydroxyphenyl)ethenyl]1,2-benzenediol |
(E)-4-(3,5-Dihydroxystyryl)benzene-1,2-diol |
5-[(E)-2-(3,4-Dihydroxyphenyl)vinyl]benzene-1,3-diol |
trans-3,3',4,5'-tetrahydroxystilbene |
3,3',4,5'-tetrahydroxystilbene |
Piceatannol, (E)- |