CAS 487-36-5
:(+)-Pinoresinol
Descripción:
(+)-Pinoresinol es un lignano que ocurre de forma natural, un tipo de compuesto orgánico que forma parte de una clase más amplia de fitocompuestos. Se caracteriza por su naturaleza quiral, existiendo en una forma enantiomérica específica, lo que contribuye a su actividad biológica. La fórmula molecular de (+)-Pinoresinol típicamente incluye átomos de carbono, hidrógeno y oxígeno, reflejando su estructura como un compuesto fenólico. Esta sustancia es conocida por sus propiedades antioxidantes, que pueden ayudar a neutralizar los radicales libres, ofreciendo así potencialmente beneficios para la salud. Se encuentra en varias plantas, incluyendo ciertas semillas y frutas, y ha sido estudiada por sus posibles efectos terapéuticos, incluyendo actividades antiinflamatorias y anticancerígenas. Además, (+)-Pinoresinol puede desempeñar un papel en la medicina tradicional y es de interés en el campo de la química de productos naturales por sus posibles aplicaciones en farmacéuticos y nutracéuticos. Su número CAS, 487-36-5, es un identificador único que facilita la catalogación y el estudio de este compuesto en la literatura científica y bases de datos.
Fórmula:C20H22O6
InChI:InChI=1S/C20H22O6/c1-23-17-7-11(3-5-15(17)21)19-13-9-26-20(14(13)10-25-19)12-4-6-16(22)18(8-12)24-2/h3-8,13-14,19-22H,9-10H2,1-2H3/t13-,14-,19+,20+/m0/s1
Clave InChI:InChIKey=HGXBRUKMWQGOIE-AFHBHXEDSA-N
SMILES:O(C)C=1C=C([C@@H]2[C@@]3([C@@]([C@H](OC3)C4=CC(OC)=C(O)C=C4)(CO2)[H])[H])C=CC1O
Sinónimos:- (+)-Pinoresinol
- (+)-epi-Pinoresinol
- 1H,3H-Furo[3,4-c]furan, phenol deriv.
- 4,4'-(1R,3aR,4S,6aR)-tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diylbis(2-methoxyphenol)
- 4,4'-tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diylbis(2-methoxyphenol)
- 4,4′-[(1S,3aR,4S,6aR)-Tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diyl]bis[2-methoxyphenol]
- NSC 35444
- Phenol, 4,4′-(tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diyl)bis[2-methoxy-, [1S-(1α,3aα,4α,6aα)]-
- Phenol, 4,4′-(tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diyl)bis[2-methoxy-, stereoisomer
- d-Pinoresinol
- phenol, 4,4'-(tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diyl)bis[2-methoxy-
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Encontrado 13 productos.
(+)-Pinoresinol
CAS:Fórmula:C20H22O6Pureza:>98.0%(GC)Forma y color:White to Almost white powder to crystalinePeso molecular:358.39(+)-Pinoresinol
CAS:(+)-Pinoresinol analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.Fórmula:C20H22O6Pureza:(HPLC) ≥95%Forma y color:PowderPeso molecular:358.39Phenol,4,4'-[(1S,3aR,4R,6aS)-tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diyl]bis[2-methoxy-
CAS:Fórmula:C20H22O6Pureza:95%Forma y color:SolidPeso molecular:358.3851(+)-Pinoresinol
CAS:Fórmula:C20H22O6Pureza:(HPLC) ≥ 98.0%Forma y color:White to off-white powderPeso molecular:358.394,4'-((1S,3Ar,4S,6Ar)-Hexahydrofuro[3,4-C]Furan-1,4-Diyl)Bis(2-Methoxyphenol)
CAS:<p>4,4'-((1S,3Ar,4S,6Ar)-Hexahydrofuro[3,4-C]Furan-1,4-Diyl)Bis(2-Methoxyphenol)</p>Pureza:99%Peso molecular:358.39g/mol(+)-Pinoresinol
CAS:Pinoresinol , among plant lignans, has the strongest antiinflammatory properties by acting on the NF-κB signaling pathway in human intestinal Caco-2 cells.Fórmula:C20H22O6Pureza:95%~99%Forma y color:PowderPeso molecular:358.39Pinoresinol
CAS:<p>Pinoresinol ((+)-Pinoresinol) has antiinflammatory, hepatoprotective, and fungicidal activities, it can protect pial microcirculation from I-reperfusion injury</p>Fórmula:C20H22O6Pureza:98.67%Forma y color:SolidPeso molecular:358.39(+)-pinoresinol
CAS:Oxygen-heterocyclic compoundFórmula:C20H22O6Pureza:≥ 90.0 % (HPLC)Forma y color:PowderPeso molecular:358.39(+)-Pinoresinol (>80% ee)
CAS:<p>Applications (+)-Pinoresinol is a lignan found in olive oil and in other plants. This phenolic compound was reported to have antioxidant and anticancer potential.<br>References Owen, R., et al.: Eur. J. Cancer, 36, 1235 (2000); Owen, R., et al.: Food Chem. Toxicol., 38, 647 (2000);<br></p>Fórmula:C20H22O6Forma y color:NeatPeso molecular:358.38(+)-Pinoresinol
CAS:<p>(+)-Pinoresinol is a chiral lignan compound, which is primarily found in various plant sources such as flaxseed, sesame seeds, and olive oil. It plays a significant role in the plant's defense mechanisms by contributing to the formation of the plant cell wall and acting as an antioxidant.</p>Fórmula:C20H22O6Pureza:Min. 97 Area-%Forma y color:PowderPeso molecular:358.39 g/mol(+/-)-Pinoresinol
CAS:<p>(+/-)-Pinoresinol is a plant-derived lignan, which is primarily sourced from various plant species, including olives, sesame seeds, and other lignan-rich plants. As an emerging compound in the field of natural products, it is extracted through processes targeting its abundant presence in lignin-containing materials. The mode of action of (+/-)-Pinoresinol involves its participation in the antioxidant defense system, where it can effectively scavenge free radicals and modulate oxidative stress. This activity is mediated by its ability to influence cellular pathways associated with oxidative systems and signal transduction mechanisms.</p>Fórmula:C20H22O6Pureza:Min. 95%Forma y color:PowderPeso molecular:358.4 g/mol










