SEDANOLIDE
- Product Name
- SEDANOLIDE
- CAS No.
- 6415-59-4
- Chemical Name
- SEDANOLIDE
- Synonyms
- SEDANOLIDE;neocnidilide;Neocindilide;cis-Sedanolide;trans-Sedanolide;fromceleryseedsoil;(3S)-3aβ,4,5,6-Tetrahyd;SEDANOLIDE FROM CELERY SEEDS OIL;SECO-ISOLARICIRESINOL DIGLUCOSIDE(SDG)(SH);3-BUTYL-3A,4,5,6-TETRAHYDRO-1(3H)-ISOBENZOFURANON
- CBNumber
- CB5675984
- Molecular Formula
- C12H18O2
- Formula Weight
- 194.27
- MOL File
- 6415-59-4.mol
SEDANOLIDE Property
- Melting point:
- 30～31℃
- Boiling point:
- 342.0±11.0 °C(Predicted)
- Density
- 1.03
- storage temp.
- Store at -20°C, protect from light
- solubility
- insoluble in H2O; ≥52.8 mg/mL in EtOH; ≥6.65 mg/mL in DMSO
- form
- White to off-white solid.
- Odor
- at 100.00 %. herbal celery
- Odor Type
- herbal
- LogP
- 2.756 (est)
- CAS DataBase Reference
- 6415-59-4(CAS DataBase Reference)
N-Bromosuccinimide Price
- Product number
- 17166
- Product name
- Sedanolide
- Purity
- ≥95%
- Packaging
- 50mg
- Price
- $89
- Updated
- 2024/03/01
- Product number
- 17166
- Product name
- Sedanolide
- Purity
- ≥95%
- Packaging
- 100mg
- Price
- $151
- Updated
- 2024/03/01
- Product number
- 17166
- Product name
- Sedanolide
- Purity
- ≥95%
- Packaging
- 500mg
- Price
- $622
- Updated
- 2024/03/01
- Product number
- 361887
- Product name
- Trans-Sedanolide
- Packaging
- 10mg
- Price
- $632
- Updated
- 2021/12/16
- Product number
- S241500
- Product name
- Sedanolide
- Packaging
- 50mg
- Price
- $70
- Updated
- 2021/12/16
SEDANOLIDE Chemical Properties,Usage,Production
Uses
Sedanolide is a natural phthalide isolates from seed oil of Umbelliferae family. It induces the expression of glutathione S-transferase and reduces chemical induced carcinogenesis in mice.
Definition
ChEBI: Sedanolide is a member of 2-benzofurans.
Biological Activity
sedanolide is a natural compound produced in edible umbelliferous plants, such as celery seed oil [1].in hepg2 and caco-2 cells, treatment with sedanolide (7-500 μm) for 24h showed no effect on cell viability. in hepg2 cells cultured in sedanolide-free medium, sedanolide (500 μm) treatment for 72h decreased cell viability. pretreatment with sedanolide (100 μm) for 24 h and exposement to either h2o2 or tbooh did not exhibit statistically significant difference in viability from controls. in hepg2 following 24-h incubation with 500 μm sedanolide, a significant increase in dna strand breaks was observed. sedanolide did not modulate h2o2- and tbooh-induced dna damage. sedanolide was relatively nontoxic to cells in culture [1]. sedanolide (sn) possesses antioxidant effects. in human liver cancer (j5) cells, treatment with sedanolide suppressed j5 cell viability by inducing autophagy. sedanolide decreased protein expression levels of phosphoinositide 3-kinase (pi3k)-i, mammalian target of rapamycin (mtor) and akt and increased pi3k-iii, lc3-ii and beclin-1 protein levels. sedanolide increased the cytosolic phosphorylation of inhibitor of kappa b (iκb) and nuclear p65 and the dna-binding activity of nf-κb. sedanolide induced j5 cell autophagy by regulating pi3k, p53 and nf-κb autophagy-associated signaling pathways in j5 cells [2]. sedanolide (100 μg/ml) inhibited cyclooxygenases-1 and -2 at 250 pg/ml and blocked topoisomerase-i and-ii activity [3].
References
[1] woods j a, jewell c, o'brien n m. sedanolide, a natural phthalide from celery seed oil: effect on hydrogen peroxide and tert-butyl hydroperoxide-induced toxicity in hepg2 and caco-2 human cell lines[j]. in vitro & molecular toxicology: a journal of basic and applied research, 2001, 14(3): 233-240.
[2] hsieh s l, chen c t, wang j j, et al. sedanolide induces autophagy through the pi3k, p53 and nf-κb signaling pathways in human liver cancer cells[j]. international journal of oncology, 2015, 47(6): 2240-2246
[3] momin r a, nair m g. antioxidant, cyclooxygenase and topoisomerase inhibitory compounds from apium graveolens linn. seeds[j]. phytomedicine, 2002, 9(4): 312-318.
SEDANOLIDE Preparation Products And Raw materials
Raw materials
Preparation Products
SEDANOLIDE Suppliers
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