CAS 177931-17-8
:sauchinona
Descripción:
sauchinona es un compuesto químico que ocurre de forma natural y se clasifica como un sesquiterpeno, derivado principalmente de la especie vegetal *Saururus cernuus*, comúnmente conocida como cola de lagarto. Se caracteriza por su compleja estructura bicíclica, que contribuye a sus propiedades químicas únicas. sauchinona exhibe una variedad de actividades biológicas, incluyendo efectos antiinflamatorios, antioxidantes y potenciales efectos anticancerígenos, lo que lo convierte en un tema de interés en la investigación farmacológica. El compuesto se encuentra típicamente en forma de un líquido incoloro a amarillo pálido y tiene un olor distintivo. Su solubilidad varía, siendo más soluble en disolventes orgánicos que en agua. La fórmula molecular de sauchinona refleja su composición de átomos de carbono, hidrógeno y oxígeno, que es típica de los sesquiterpenos. Debido a sus propiedades bioactivas, sauchinona está siendo explorado para diversas aplicaciones terapéuticas, aunque se necesitan más estudios para comprender completamente sus mecanismos de acción y posibles usos en medicina.
Fórmula:C20H20O6
InChI:InChI=1/C20H20O6/c1-9-3-11-13(21)5-17-20(25-8-24-17)19(11)18(10(9)2)12-4-15-16(23-7-22-15)6-14(12)26-20/h4-6,9-11,18-19H,3,7-8H2,1-2H3/t9-,10+,11+,18+,19+,20+/m1/s1
Clave InChI:InChIKey=GMTJIWUFFXGFHH-WPAOEJHSSA-N
SMILES:C[C@@H]1[C@@]2([C@]3([C@]4(C(=CC(=O)[C@@]3(C[C@H]1C)[H])OCO4)OC=5C2=CC6=C(C5)OCO6)[H])[H]
Sinónimos:- (5aR,7R,8S,8aR,14aS,14bR)-5a,6,7,8,8a,14b-Hexahydro-7,8-dimethyl-5H-benzo[kl]bis[1,3]dioxolo[4,5-b:4′,5′-g]xanthen-5-one
- (5aR,7R,8S,8aR,14aS,14bR)-7,8-dimethyl-5a,6,7,8,8a,14b-hexahydro-5H-benzo[kl]bis[1,3]dioxolo[4,5-b:4',5'-g]xanthen-5-one
- 5H-Benzo[kl]bis[1,3]dioxolo[4,5-b:4′,5′-g]xanthen-5-one, 5a,6,7,8,8a,14b-hexahydro-7,8-dimethyl-, (5aR,7R,8S,8aR,14aS,14bR)-
- 5H-Benzo[kl]bis[1,3]dioxolo[4,5-b:4′,5′-g]xanthen-5-one, 5a,6,7,8,8a,14b-hexahydro-7,8-dimethyl-, (5aα,7α,8β,8aβ,14aS*,14bβ)-
- 5H-benzo[kl][1,3]dioxolo[4,5-b]-1,3-dioxolo[4,5-g]xanthen-5-one, 5a,6,7,8,8a,14b-hexahydro-7,8-dimethyl-, (5aR,7R,8S,8aR,14aS,14bR)-
- Sauchinone
- (5aα,7α,8β,8aβ,14aS*,14bβ)-5a,6,7,8,8a,14b-Hexahydro-7,8-dimethyl-5H-benzo[kl]bis[1,3]dioxolo[4,5-b:4′,5′-g]xanthen-5-one
- 5H-Benzo[kl]bis[1,3]dioxolo[4,5-b:4',5'-g]xanthen-5-one, 5a,6,7,8,8a,14b-hexahydro-7,8-dimethyl-, (5aR,7R,8S,8aR,14aS,14bR)-
- Sauchinone, 98%, from Saururus chinensis (Lour. ) Baill
- Sauchinone >=98% (HPLC)
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Encontrado 7 productos.
Sauchinone
CAS:Sauchinone possesses diverse pharmacological properties, such as hepatoprotective, neuroprotective, anti-inflammatory and anti-tumor effects. Sauchinone protects skin keratinocytes through inhibition of extracellular signal-regulated kinase, c-Jun N-terminal kinase, and p38 MAPK signaling via upregulation of oxidative defense enzymes. Sauchinone can be used for the prevention of functional β-cell damage, it prevents cytokine-induced NO production, iNOS expression,JAK/STAT activation,and NF-κB activation and inhibition of glucose-stimulated insulin secretion (GSIS).Fórmula:C20H20O6Pureza:95%~99%Peso molecular:356.374Sauchinone
CAS:Sauchinone: Treats infections, prevents liver fibrosis, reduces oxidative stress, and protects skin and vascular cells.Fórmula:C20H20O6Pureza:>99.99%Forma y color:SolidPeso molecular:356.37Sauchinone
CAS:Oxygen-heterocyclic compoundFórmula:C20H20O6Pureza:≥ 95.0 % (HPLC)Forma y color:PowderPeso molecular:356.37Sauchinone
CAS:<p>Sauchinone is a natural compound that has shown to be effective in the treatment of bowel disease. This compound is an inhibitor of the toll-like receptor (TLR) and has shown to reduce inflammation and oxidative injury. Sauchinone has been found to increase the production of growth factor-β1, which may be useful for treating injuries such as burns or wounds. The matrix effect of sauchinone on cell culture was investigated using dextran sulfate, which is known to induce apoptosis in cells. Chromatographic analysis showed that sauchinone inhibited DNA binding activity and had an effect on dna binding activity. Molecular docking analysis showed that sauchinone binds with TLR4 and inhibits its signaling pathway, preventing aberrant reactions from occurring. Sauchinone also inhibits NF-κB activation by inhibiting nuclear translocation, thus suppressing inflammatory response.</p>Fórmula:C20H20O6Pureza:Min. 95%Forma y color:PowderPeso molecular:356.37 g/mol






