CAS 177931-17-8
:sauchinone
Description:
Sauchinone is a naturally occurring chemical compound classified as a sesquiterpene, primarily derived from the plant species *Saururus cernuus*, commonly known as lizard tail. It is characterized by its complex bicyclic structure, which contributes to its unique chemical properties. Sauchinone exhibits a range of biological activities, including anti-inflammatory, antioxidant, and potential anticancer effects, making it a subject of interest in pharmacological research. The compound is typically found in the form of a colorless to pale yellow liquid and has a distinctive odor. Its solubility varies, being more soluble in organic solvents than in water. The molecular formula of sauchinone reflects its composition of carbon, hydrogen, and oxygen atoms, which is typical for sesquiterpenes. Due to its bioactive properties, sauchinone is being explored for various therapeutic applications, although further studies are needed to fully understand its mechanisms of action and potential uses in medicine.
Formula: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
InChI key: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]
Synonyms:- (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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Found 7 products.
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).Formula:C20H20O6Purity:95%~99%Molecular weight:356.374Sauchinone
CAS:Sauchinone: Treats infections, prevents liver fibrosis, reduces oxidative stress, and protects skin and vascular cells.Formula:C20H20O6Purity:>99.99%Color and Shape:SolidMolecular weight:356.37Sauchinone
CAS:Oxygen-heterocyclic compoundFormula:C20H20O6Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight: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>Formula:C20H20O6Purity:Min. 95%Color and Shape:PowderMolecular weight:356.37 g/mol






