Liriodendrina - ≥85% , CAS No.573-44-4

CAS: 573-44-4 Cat. No.: L171049 Formula: C₃₄H₄₆O₁₈ Peso molecolare: 742.72

QUALITÀ & PUREZZA ≥85%

Synonyms

Eleutheroside E|Liriodendrin|Eleutheroside D|39432-56-9|573-44-4|Acanthoside D|2-[4-[6-[3,5-dimethoxy-4-[3,4,5-triidrossi-6-(idrossimetil)ossan-2-il]ossifenil]-1,3,3a,4,6,6a-esaidrofuro[3,4-c]furan-3-il]-2,6-dimetossifenossi]-6-(idrossimetil)ossan-3,4,

Storage

Conservare a -20°C

Shipped In

Cassetta del ghiaccio + cuscini per il ghiaccio

Panoramica

Descrizione del prodotto

Prodotto naturale derivato da fonte vegetale.

Specifiche

Sinonimi

Eleutheroside E | Liriodendrin | Eleutheroside D | 39432-56-9 | 573-44-4 | Acanthoside D | 2-[4-[6-[3,5-dimethoxy-4-[3,4,5-triidrossi-6-(idrossimetil)ossan-2-il]ossifenil]-1,3,3a,4,6,6a-esaidrofuro[3,4-c]furan-3-il]-2,6-dimetossifenossi]-6-(idrossimetil)ossan-3,4,

Specifiche e purezza

≥85%

Meccanismi biochimici e fisiologici

La liriodendrina ha dimostrato proprietà antinfiammatorie e antinocicettive; la somministrazione di liriodendrina ha causato una riduzione dell'edema acuto della zampa indotto dalla carragenina nei ratti.

Condizioni di conservazione di stoccaggio

Conservare a -20°C

Spedito in

Cassetta del ghiaccio + cuscini per il ghiaccio

Purezza

≥85%

Nomi e identificatori

Pubchem Sid

504757954

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504757954

Sorrisi canonici

COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC

IUPAC Name

2-[4-[6-[3,5-dimethoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

InChIKey

FFDULTAFAQRACT-UHFFFAOYSA-N

INCHI

1S/C34H46O18/c1-43-17-5-13(6-18(44-2)31(17)51-33-27(41)25(39)23(37)21(9-35)49-33)29-15-11-48-30(16(15)12-47-29)14-7-19(45-3)32(20(8-14)46-4)52-34-28(42)26(40)24(38)22(10-36)50-34/h5-8,15-16,21-30,33-42H,9-12H2,1-4H3

Isomeri SMILES

COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC

Peso molecolare

742.72

Reaxy-Rn

34681975

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=34681975&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lignans, neolignans and related compounds
    • Classe Lignan glycosides

• Kingdom: Organic compounds
• Superclass: Lignans, neolignans and related compounds
• Classe: Lignan glycosides
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Lignan glycosides
• Alternative Parents: Furofuran lignans Fatty acyl glycosides of mono- and disaccharides Phenolic glycosides Alkyl glycosides O-glycosyl compounds Dimethoxybenzenes Anisoles Furofurans Phenoxy compounds Alkyl aryl ethers Monosaccharides Oxanes Tetrahydrofurans Secondary alcohols Polyols Dialkyl ethers Acetals Oxacyclic compounds Hydrocarbon derivatives Primary alcohols
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Lignan glycoside - Furanoid lignan - Furofuran lignan skeleton - Phenolic glycoside - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - O-glycosyl compound - Glycosyl compound - M-dimethoxybenzene - Dimethoxybenzene - Phenol ether - Methoxybenzene - Furofuran - Anisole - Phenoxy compound - Alkyl aryl ether - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Monosaccharide - Oxane - Tetrahydrofuran - Secondary alcohol - Organoheterocyclic compound - Ether - Dialkyl ether - Acetal - Polyol - Oxacycle - Organic oxygen compound - Alcohol - Primary alcohol - Hydrocarbon derivative - Organooxygen compound - Aromatic heteropolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as lignan glycosides. These are aromatic polycyclic compounds containing a carbohydrate component glycosidically linked to a lignan moiety. They include 1-aryltetralin lactones.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Proprietà chimiche e fisiche

• Peso molecolare: 742.700 g/mol
• XLogP3: -1.400
• Hydrogen Bond Donor Count: 8
• Hydrogen Bond Acceptor Count: 18
• Rotatable Bond Count: 12
• Exact Mass: 742.268 Da
• Monoisotopic Mass: 742.268 Da
• Topological Polar Surface Area: 254.000 Ų
• Heavy Atom Count: 52
• Formal Charge: 0
• Complexity: 1010.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 14
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1