- Sedanolide
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- $32.00 / 1mg
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2026-01-05
- CAS:6415-59-4
- Min. Order:
- Purity: 99.82%
- Supply Ability: 10g
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| | SEDANOLIDE Basic information |
| Product Name: | SEDANOLIDE | | Synonyms: | SEDANOLIDE;3-BUTYL-3A,4,5,6-TETRAHYDRO-1(3H)-ISOBENZOFURANON;3-BUTYL-3A,4,5,6-TETRAHYDRO-1(3H)-ISOBENZOFURANONE;3-BUTYL-3ALPHA,4,5,6-TETRAHYDRO-1(3H)-ISOBENZOFURANONE;SEDANOLIDE FROM CELERY SEEDS OIL;fromceleryseedsoil;neocnidilide;SECO-ISOLARICIRESINOL DIGLUCOSIDE(SDG)(SH) | | CAS: | 6415-59-4 | | MF: | C12H18O2 | | MW: | 194.27 | | EINECS: | | | Product Categories: | Heterocycles | | Mol File: | 6415-59-4.mol |  |
| | SEDANOLIDE Chemical Properties |
| 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. | | color | White to off-white | | Odor | at 100.00 %. herbal celery | | Odor Type | herbal | | LogP | 2.756 (est) | | CAS DataBase Reference | 6415-59-4(CAS DataBase Reference) |
| | SEDANOLIDE Usage And Synthesis |
| Chemical Properties | White powder, soluble in organic solvents such as methanol, ethanol, and DMSO. It comes from the rhizome of Ligusticum chuanxiong Hort. | | 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]. | | in vivo | Sedanolide increases the activity of glutathione-S-transferase (GST) in the liver, small intestinal mucosa, and forestomach of A/J mice[1]. | | 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 |
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