CAS 487-36-5
:(+)-Pinoresinol
Description:
(+)-Pinoresinol is a naturally occurring lignan, a type of organic compound that is part of a larger class of phytochemicals. It is characterized by its chiral nature, existing in a specific enantiomeric form, which contributes to its biological activity. The molecular formula of (+)-Pinoresinol typically includes carbon, hydrogen, and oxygen atoms, reflecting its structure as a phenolic compound. This substance is known for its antioxidant properties, which can help in neutralizing free radicals, thereby potentially offering health benefits. It is found in various plants, including certain seeds and fruits, and has been studied for its potential therapeutic effects, including anti-inflammatory and anticancer activities. Additionally, (+)-Pinoresinol may play a role in traditional medicine and is of interest in the field of natural product chemistry for its potential applications in pharmaceuticals and nutraceuticals. Its CAS number, 487-36-5, is a unique identifier that facilitates the cataloging and study of this compound in scientific literature and databases.
Formula: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
InChI key: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
Synonyms:- (+)-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-
- See more synonyms
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Found 13 products.
(+)-Pinoresinol
CAS:Formula:C20H22O6Purity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalineMolecular weight:358.39(+)-Pinoresinol
CAS:(+)-Pinoresinol analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.Formula:C20H22O6Purity:(HPLC) ≥95%Color and Shape:PowderMolecular weight:358.39Phenol,4,4'-[(1S,3aR,4R,6aS)-tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diyl]bis[2-methoxy-
CAS:Formula:C20H22O6Purity:95%Color and Shape:SolidMolecular weight:358.3851(+)-Pinoresinol
CAS:Formula:C20H22O6Purity:(HPLC) ≥ 98.0%Color and Shape:White to off-white powderMolecular weight: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>Purity:99%Molecular weight: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.Formula:C20H22O6Purity:95%~99%Color and Shape:PowderMolecular weight:358.39Pinoresinol
CAS:<p>Pinoresinol ((+)-Pinoresinol) has antiinflammatory, hepatoprotective, and fungicidal activities, it can protect pial microcirculation from I-reperfusion injury</p>Formula:C20H22O6Purity:98.67%Color and Shape:SolidMolecular weight:358.39(+)-pinoresinol
CAS:Oxygen-heterocyclic compoundFormula:C20H22O6Purity:≥ 90.0 % (HPLC)Color and Shape:PowderMolecular weight: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>Formula:C20H22O6Color and Shape:NeatMolecular weight: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>Formula:C20H22O6Purity:Min. 97 Area-%Color and Shape:PowderMolecular weight: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>Formula:C20H22O6Purity:Min. 95%Color and Shape:PowderMolecular weight:358.4 g/mol










