CAS 177931-17-8
:sauchinone
Description :
sauchinone est un composé chimique naturellement présent, classé comme un sesquiterpène, dérivé principalement de l'espèce végétale *Saururus cernuus*, communément appelée queue de lézard. Il se caractérise par sa structure bicyclique complexe, qui contribue à ses propriétés chimiques uniques. sauchinone présente une gamme d'activités biologiques, y compris des effets anti-inflammatoires, antioxydants et des effets anticancéreux potentiels, ce qui en fait un sujet d'intérêt dans la recherche pharmacologique. Le composé se trouve généralement sous forme de liquide incolore à jaune pâle et a une odeur distinctive. Sa solubilité varie, étant plus soluble dans les solvants organiques que dans l'eau. La formule moléculaire de sauchinone reflète sa composition en atomes de carbone, d'hydrogène et d'oxygène, typique des sesquiterpènes. En raison de ses propriétés bioactives, sauchinone est exploré pour diverses applications thérapeutiques, bien que d'autres études soient nécessaires pour comprendre pleinement ses mécanismes d'action et ses utilisations potentielles en médecine.
Formule :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
Code 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]
Synonymes :- (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)
Trier par
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7 produits concernés.
Sauchinone
CAS :Formule :C20H20O6Degré de pureté :97%Couleur et forme :SolidMasse moléculaire :356.3692Sauchinone
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).Formule :C20H20O6Degré de pureté :95%~99%Masse moléculaire :356.374Sauchinone
CAS :Sauchinone: Treats infections, prevents liver fibrosis, reduces oxidative stress, and protects skin and vascular cells.Formule :C20H20O6Degré de pureté :>99.99%Couleur et forme :SolidMasse moléculaire :356.37Sauchinone
CAS :Oxygen-heterocyclic compoundFormule :C20H20O6Degré de pureté :≥ 95.0 % (HPLC)Couleur et forme :PowderMasse moléculaire :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>Formule :C20H20O6Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :356.37 g/mol






