Dioscin
Based on 11 publication(s) in Google Scholar
Dioscin (CCRIS 4123; Collettiside III) is a natural plant-derived steroidal saponin that has good anti-cancer activity against a variety of cancer cells. Dioscin causes DNA damage and induces apoptosis in HeLa and SiHa cells. Dioscin regulates ROS-mediated DNA damage and mitochondrial signaling pathways, exerting anticancer activity.
Nur für Forschungszwecke. Wir verkaufen nicht an Patienten.
- Reinheit: 99.95%
- CAS. Nr.: 19057-60-4
- Formel: C45H72O16
- Molecular Weight:869.04
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Speicherung:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 2 years , -20°C, 1 year
Publications Citing Use of MedChemExpress (MCE) Dioscin
More- J Pharm Anal. 2025 Nov 11.
- Br J Pharmacol. 2021 Sep;178(18):3648-3666. [Abstract]
- Antioxidants (Basel). 2024 May 29;13(6):667. [Abstract]
- Front Pharmacol. 2020 Jul 24;11:1099. [Abstract]
- Int Immunopharmacol. 2023 Apr:117:109839. [Abstract]
- Molecules. 2019 Jun 14;24(12):2222. [Abstract]
- Mol Med Rep. 2017 Oct;16(4):4922-4926. [Abstract]
- J Cancer. 2023 Jul 9;14(11):2027-2038. [Abstract]
- Med Chem Res. 2021 Mar 17.
- Folia Histochem Cytobiol. 2024;62(2):110-121. [Abstract]
- Chem Pharm Bull (Tokyo). 2020;68(8):717-725. [Abstract]
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RT-PCR
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WB
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Histological Imaging/Staining
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IP
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Flow Cytometry
Biologische Aktivität
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| A2780 | IC50 |
0.581 μM
Compound: Dioscin
|
Cytotoxicity against human A2780 cells by MTT assay
Cytotoxicity against human A2780 cells by MTT assay
|
[PMID: 21482468] |
| A2780 | IC50 |
0.87 μM
Compound: Dioscin
|
Cytotoxicity against human A2780 cells by MTT assay
Cytotoxicity against human A2780 cells by MTT assay
|
[PMID: 22429911] |
| A2780 | IC50 |
4.46 μM
Compound: Dioscin
|
Cytotoxicity against human A2780 cells after 72 hrs by MTT assay
Cytotoxicity against human A2780 cells after 72 hrs by MTT assay
|
[PMID: 19362474] |
| A549 | IC50 |
0.454 μM
Compound: Dioscin
|
Cytotoxicity against human A549 cells by MTT assay
Cytotoxicity against human A549 cells by MTT assay
|
[PMID: 21482468] |
| A549 | IC50 |
0.7 μM
Compound: Dioscin
|
Cytotoxicity against human A549 cells after 72 hrs by MTT assay
Cytotoxicity against human A549 cells after 72 hrs by MTT assay
|
[PMID: 19362474] |
| A549 | IC50 |
0.81 μM
Compound: Dioscin
|
Cytotoxicity against human A549 cells by MTT assay
Cytotoxicity against human A549 cells by MTT assay
|
[PMID: 22429911] |
| A549 | IC50 |
4.2 μM
Compound: dioscin
|
Cytotoxicity against human A549 cells by MTT assay
Cytotoxicity against human A549 cells by MTT assay
|
[PMID: 16905317] |
| BC1 cell line | IC50 |
3.8 μM
Compound: 2
|
Cytotoxicity against human BC1 cells after 72 hrs by SRB assay
Cytotoxicity against human BC1 cells after 72 hrs by SRB assay
|
[PMID: 12088425] |
| Bel-7402 | IC50 |
0.23 μM
Compound: Dioscin
|
Cytotoxicity against human Bel7402 cells after 72 hrs by MTT assay
Cytotoxicity against human Bel7402 cells after 72 hrs by MTT assay
|
[PMID: 19362474] |
| Bel-7402 | IC50 |
0.81 μM
Compound: Dioscin
|
Cytotoxicity against human Bel7402 cells by MTT assay
Cytotoxicity against human Bel7402 cells by MTT assay
|
[PMID: 22429911] |
| Bel-7402 | IC50 |
0.93 μM
Compound: Dioscin
|
Cytotoxicity against human Bel7402 cells by MTT assay
Cytotoxicity against human Bel7402 cells by MTT assay
|
[PMID: 21482468] |
| BGC-823 | IC50 |
0.268 μM
Compound: Dioscin
|
Cytotoxicity against human BGC823 cells by MTT assay
Cytotoxicity against human BGC823 cells by MTT assay
|
[PMID: 21482468] |
| BGC-823 | IC50 |
1.08 μM
Compound: Dioscin
|
Cytotoxicity against human BGC823 cells by MTT assay
Cytotoxicity against human BGC823 cells by MTT assay
|
[PMID: 22429911] |
| BGC-823 | IC50 |
2 μM
Compound: dioscin
|
Cytotoxicity against human BGC823 cells by MTT assay
Cytotoxicity against human BGC823 cells by MTT assay
|
[PMID: 16905317] |
| BXPC-3 | GI50 |
1.3 μg/mL
Compound: 4, dioscin
|
Growth inhibition of humanBxPC3 cells after 48 hrs
Growth inhibition of humanBxPC3 cells after 48 hrs
|
[PMID: 15921418] |
| BXPC-3 | IC50 |
0.7 μM
Compound: Dioscin
|
Cytotoxicity against human BxPC3 cells after 72 hrs by MTT assay
Cytotoxicity against human BxPC3 cells after 72 hrs by MTT assay
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[PMID: 19362474] |
| Capan-2 | IC50 |
0.05 μM
Compound: Dioscin
|
Cytotoxicity against human Capan2 cells after 72 hrs by MTT assay
Cytotoxicity against human Capan2 cells after 72 hrs by MTT assay
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[PMID: 19362474] |
| Col2 | IC50 |
2.8 μM
Compound: 2
|
Cytotoxicity against human Col2 cells after 72 hrs by SRB assay
Cytotoxicity against human Col2 cells after 72 hrs by SRB assay
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[PMID: 12088425] |
| DU-145 | GI50 |
>10 μg/mL
Compound: 4, dioscin
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Growth inhibition of human DU145 cells after 48 hrs
Growth inhibition of human DU145 cells after 48 hrs
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[PMID: 15921418] |
| HCT-8 | IC50 |
0.34 μM
Compound: Dioscin
|
Cytotoxicity against human HCT8 cells by MTT assay
Cytotoxicity against human HCT8 cells by MTT assay
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[PMID: 22429911] |
| HCT-8 | IC50 |
0.351 μM
Compound: Dioscin
|
Cytotoxicity against human HCT8 cells by MTT assay
Cytotoxicity against human HCT8 cells by MTT assay
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[PMID: 21482468] |
| HCT-8 | IC50 |
0.56 μM
Compound: Dioscin
|
Cytotoxicity against human HCT8 cells after 72 hrs by MTT assay
Cytotoxicity against human HCT8 cells after 72 hrs by MTT assay
|
[PMID: 19362474] |
| HeLa | IC50 |
0.5 μM
Compound: Dioscin
|
Cytotoxicity against human HeLa cells by MTT assay
Cytotoxicity against human HeLa cells by MTT assay
|
[PMID: 22429911] |
| HGC-27 | IC50 |
5.9 μM
Compound: dioscin
|
Cytotoxicity against human HGC27 cells by MTT assay
Cytotoxicity against human HGC27 cells by MTT assay
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[PMID: 16905317] |
| HL-60 | IC50 |
2 μM
Compound: 6
|
Cytotoxicity against human HL60 cells after 72 hrs by MTT assay
Cytotoxicity against human HL60 cells after 72 hrs by MTT assay
|
[PMID: 12828464] |
| HL-60 | IC50 |
3.8 μM
Compound: 1
|
Cytotoxicity against human HL60 cells assessed as cell viability after 72 hrs by MTT assay
Cytotoxicity against human HL60 cells assessed as cell viability after 72 hrs by MTT assay
|
[PMID: 22405922] |
| K562 | IC50 |
4.7 μM
Compound: 1
|
Cytotoxicity against human K562 cells assessed as cell viability after 48 hrs by MTT assay
Cytotoxicity against human K562 cells assessed as cell viability after 48 hrs by MTT assay
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[PMID: 23621869] |
| K562/Adr | IC50 |
3.3 μM
Compound: 1
|
Cytotoxicity against human K562/ADR cells assessed as cell viability after 48 hrs by MTT assay
Cytotoxicity against human K562/ADR cells assessed as cell viability after 48 hrs by MTT assay
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[PMID: 23621869] |
| KB | ED50 |
21 μM
Compound: 8
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Growth inhibition of human KB cells xenografted in ip dosed NCr nu/nu mouse administered once daily from day 3 to 6 after implantation measured on day 7 by MTT-based hollow-fiber test
Growth inhibition of human KB cells xenografted in ip dosed NCr nu/nu mouse administered once daily from day 3 to 6 after implantation measured on day 7 by MTT-based hollow-fiber test
|
[PMID: 19161316] |
| KB | IC50 |
0.53 μM
Compound: Dioscin
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Cytotoxicity against human KB cells by MTT assay
Cytotoxicity against human KB cells by MTT assay
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[PMID: 22429911] |
| KB | IC50 |
20.7 μM
Compound: 2
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Cytotoxicity against human KB cells after 72 hrs by SRB assay
Cytotoxicity against human KB cells after 72 hrs by SRB assay
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[PMID: 12088425] |
| KB-V1 | IC50 |
>23 μM
Compound: 2
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Cytotoxicity against human KBV1 cells after 72 hrs by SRB assay
Cytotoxicity against human KBV1 cells after 72 hrs by SRB assay
|
[PMID: 12088425] |
| KETR3 | IC50 |
0.447 μM
Compound: Dioscin
|
Cytotoxicity against human Ketr3 cells by MTT assay
Cytotoxicity against human Ketr3 cells by MTT assay
|
[PMID: 21482468] |
| KM-20L2 | GI50 |
1.3 μg/mL
Compound: 4, dioscin
|
Growth inhibition of human KM20L2 cells after 48 hrs
Growth inhibition of human KM20L2 cells after 48 hrs
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[PMID: 15921418] |
| LNCaP | ED50 |
1.7 μM
Compound: 8
|
Growth inhibition of human LNCAP cells xenografted in ip dosed NCr nu/nu mouse administered once daily from day 3 to 6 after implantation measured on day 7 by MTT-based hollow-fiber test
Growth inhibition of human LNCAP cells xenografted in ip dosed NCr nu/nu mouse administered once daily from day 3 to 6 after implantation measured on day 7 by MTT-based hollow-fiber test
|
[PMID: 19161316] |
| LNCaP | IC50 |
1.7 μM
Compound: 2
|
Cytotoxicity against human LNCAP cells after 72 hrs by SRB assay
Cytotoxicity against human LNCAP cells after 72 hrs by SRB assay
|
[PMID: 12088425] |
| Lu1 | ED50 |
1.2 μM
Compound: 8
|
Growth inhibition of human Lu1 cells xenografted in ip dosed NCr nu/nu mouse administered once daily from day 3 to 6 after implantation measured on day 7 by MTT-based hollow-fiber test
Growth inhibition of human Lu1 cells xenografted in ip dosed NCr nu/nu mouse administered once daily from day 3 to 6 after implantation measured on day 7 by MTT-based hollow-fiber test
|
[PMID: 19161316] |
| Lu1 | IC50 |
1.2 μM
Compound: 2
|
Cytotoxicity against human Lu1 cells after 72 hrs by SRB assay
Cytotoxicity against human Lu1 cells after 72 hrs by SRB assay
|
[PMID: 12088425] |
| MCF7 | GI50 |
0.68 μg/mL
Compound: 4, dioscin
|
Growth inhibition of human MCF7 cells after 48 hrs
Growth inhibition of human MCF7 cells after 48 hrs
|
[PMID: 15921418] |
| MCF7 | IC50 |
0.879 μM
Compound: Dioscin
|
Cytotoxicity against human MCF7 cells by MTT assay
Cytotoxicity against human MCF7 cells by MTT assay
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[PMID: 21482468] |
| MCF7 | IC50 |
1.03 μM
Compound: Dioscin
|
Cytotoxicity against human MCF7 cells after 72 hrs by MTT assay
Cytotoxicity against human MCF7 cells after 72 hrs by MTT assay
|
[PMID: 19362474] |
| MCF7 | IC50 |
22.4 μM
Compound: 2
|
Cytotoxicity against human MCF7 cells after 72 hrs by SRB assay
Cytotoxicity against human MCF7 cells after 72 hrs by SRB assay
|
[PMID: 12088425] |
| NCI-H460 | GI50 |
1.8 μg/mL
Compound: 4, dioscin
|
Growth inhibition of human NCI-H460 cells after 48 hrs
Growth inhibition of human NCI-H460 cells after 48 hrs
|
[PMID: 15921418] |
| NCI-H460 | IC50 |
4.56 μM
Compound: 12
|
Cytotoxicity against human NCI-H460 cells incubated for 24 hrs by MTT assay
Cytotoxicity against human NCI-H460 cells incubated for 24 hrs by MTT assay
|
[PMID: 28606759] |
| P388 | ED50 |
>10 μg/mL
Compound: 4, dioscin
|
Growth inhibition of mouse P388 cells after 48 hrs
Growth inhibition of mouse P388 cells after 48 hrs
|
[PMID: 15921418] |
| P388 | IC50 |
21.9 μM
Compound: 2
|
Cytotoxicity against mouse P388 cells after 72 hrs by SRB assay
Cytotoxicity against mouse P388 cells after 72 hrs by SRB assay
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[PMID: 12088425] |
| PANC-1 | IC50 |
0.81 μM
Compound: Dioscin
|
Cytotoxicity against human PANC1 cells after 72 hrs by MTT assay
Cytotoxicity against human PANC1 cells after 72 hrs by MTT assay
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[PMID: 19362474] |
| SF-268 | GI50 |
1.2 μg/mL
Compound: 4, dioscin
|
Growth inhibition of human SF268 cells after 48 hrs
Growth inhibition of human SF268 cells after 48 hrs
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[PMID: 15921418] |
| SK-MEL-2 | IC50 |
1.8 μM
Compound: 2
|
Cytotoxicity against human SK-MEL-2 cells after 72 hrs by SRB assay
Cytotoxicity against human SK-MEL-2 cells after 72 hrs by SRB assay
|
[PMID: 12088425] |
| SW1990 | IC50 |
0.5 μM
Compound: Dioscin
|
Cytotoxicity against human SW1990 cells after 72 hrs by MTT assay
Cytotoxicity against human SW1990 cells after 72 hrs by MTT assay
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[PMID: 19362474] |
| SW626 | IC50 |
3.1 μM
Compound: 2
|
Cytotoxicity against human SW626 cells after 72 hrs by SRB assay
Cytotoxicity against human SW626 cells after 72 hrs by SRB assay
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[PMID: 12088425] |
Dioscin (1.25-5 μg/mL; 6-24 h) increases intracellular calcium levels and induces apoptosis in HeLa and SiHa cells[4].
Dioscin (1.25-5 μg/mL; 6-24 h) Dioscin up-regulates the protein levels of Bak, Bax, Bid, p53, caspase-3, caspase-9, and down-regulates the proteins of Bcl-2 and Bcl-xl level[4].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Dioscin can reduce liver ischemia-reperfusion injury in rats by inhibiting oxidative-nitrative stress, inflammation and apoptosis[6].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS. Nr. 19057-60-4
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Appearance Solid
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Molecular Weight 869.04
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Formel C45H72O16
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Color White to off-white
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SMILES
O[C@@H]1[C@@H](O)[C@H](C)O[C@@]([H])(O[C@H]2[C@H](O)[C@@H](O[C@]3([H])O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)[C@@](O[C@@H]4CC5=CC[C@]([C@]([H])(C[C@@]6([H])[C@]7([H])[C@H](C)[C@]8(OC[C@H](C)CC8)O6)[C@]7(C)CC9)([H])[C@@]9([H])[C@@]5(C)CC4)([H])O[C@@H]2CO)[C@@H]1O
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Synonyms
Collettiside III; CCRIS 4123
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Structure Classification
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Initial Source
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Versand
Room temperature in continental US; may vary elsewhere.
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Speicherung
Powder -20°C 3 years 4°C 2 years In solvent -80°C 2 years -20°C 1 year
Publications (11)
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Journal Impact Factor
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Most Recent
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Dioscin purchased from MedChemExpress. Usage Cited in: J Pharm Anal. 2025 Nov 11.
Dioscin (200 nM, 24 h) alleviates gout by inhibiting hypoxia-inducible factor 1-alpha (HIF-1α) in CD4+ T cells. Quantitative PCR analysis revealing significantly elevated mRNA levels of HIF-1α after DIO treatment (n = 3).
Dioscin purchased from MedChemExpress. Usage Cited in: J Pharm Anal. 2025 Nov 11.
Dioscin (200 nM, 24 h) alleviates gout by inhibiting hypoxia-inducible factor 1-alpha (HIF-1α) in CD4+ T cells. Western blot analysis revealing significantly elevated protein levels of HIF-1α after DIO treatment (n = 3).
Dioscin purchased from MedChemExpress. Usage Cited in: J Pharm Anal. 2025 Nov 11.
Representative images and hematoxylin and eosin (H&E) analysis of footpads after IOX4 and Dioscin (20 mg/kg, intraperitoneal injection weekly over a six-week period) treatment (n = 3).
Dioscin purchased from MedChemExpress. Usage Cited in: J Pharm Anal. 2025 Nov 11.
Pull-down analysis between Dioscin (200 nM, 24 h) and HIF-1α in primary CD4+ T cells (n = 3).
Dioscin purchased from MedChemExpress. Usage Cited in: J Pharm Anal. 2025 Nov 11.
Dioscin (20 mg/kg, intraperitoneal injection weekly over a six-week period) reshapes CD4+ T cell differentiation via hypoxia-inducible factor 1-alpha (HIF-1α). T helper 17 (Th17) cell proportions in the blood, intestine, and spleen of DIO-treated urate oxidase (Uox)-knockout (KO) mice (n = 8).
Dioscin purchased from MedChemExpress. Usage Cited in: J Pharm Anal. 2025 Nov 11.
Dioscin (20 mg/kg, intraperitoneal injection weekly over a six-week period) reshapes CD4+ T cell differentiation via hypoxia-inducible factor 1-alpha (HIF-1α). Multiplex immunofluorescence staining of Th17 cells in the footpad of DIO-treated Uox-KO mice (n = 3): representative images and quantitative analysis of Th17 cell numbers.
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Br J Pharmacol
Cerebroprotection by dioscin after experimental subarachnoid haemorrhage via inhibiting NLRP3 inflammasome through SIRT1-dependent pathway. [Abstract]2021 Sep;178(18):3648-3666. PMID: 33904167 -
Antioxidants (Basel)
Pitavastatin Calcium Confers Fungicidal Properties to Fluconazole by Inhibiting Ubiquinone Biosynthesis and Generating Reactive Oxygen Species. [Abstract]2024 May 29;13(6):667. PMID: 38929106 -
Front Pharmacol
Dioscin Promotes Prostate Cancer Cell Apoptosis and Inhibits Cell Invasion by Increasing SHP1 Phosphorylation and Suppressing the Subsequent MAPK Signaling Pathway. [Abstract]2020 Jul 24;11:1099. PMID: 32792945 -
Int Immunopharmacol
Dioscin modulates macrophages polarization and MDSCs differentiation to inhibit tumorigenesis of colitis-associated colorectal cancer. [Abstract]2023 Apr:117:109839. PMID: 36809720
Dioscin purchased from MedChemExpress. Usage Cited in: Int Immunopharmacol. 2023 Apr:117:109839. [Abstract]
Dioscin-Medium group (5 mg/kg; p.o.; every-two days for 12 weeks) profoundly inhibits the phosphorylation of NF-ĸB in mice (Fig H and I). Dioscin-Low (Dio-L, 2.5 mg/kg), Dioscin-Medium (Dio-M, 5 mg/kg) and Dioscin-High (Dio-H, 10 mg/Kg).
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Molecules
Dioscin Inhibits the Invasion and Migration of Hepatocellular Carcinoma HepG2 Cells by Reversing TGF-β1-Induced Epithelial-Mesenchymal Transition. [Abstract]2019 Jun 14;24(12):2222. PMID: 31197076 -
Mol Med Rep
Dioscin enhances osteoblastic cell differentiation and proliferation by inhibiting cell autophagy via the ASPP2/NF-κβ pathway. [Abstract]2017 Oct;16(4):4922-4926. PMID: 28849197
Dioscin purchased from MedChemExpress. Usage Cited in: Mol Med Rep. 2017 Oct;16(4):4922-4926. [Abstract]
Dioscin concentrations of 0.5, 1, 5, 10 and 25 µg/mL promotes the expression of ALP and inhibits the expression of LC3B in MC3T3-E1 cells, in a concentration-dependent manner.
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J Cancer
Dioscin inhibiting EGFR-mediated Survivin expression promotes apoptosis in oral squamous cell carcinoma cells. [Abstract]2023 Jul 9;14(11):2027-2038. PMID: 37497406 -
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Folia Histochem Cytobiol
Dioscin attenuates lupus nephritis in NZB/W F1 mice by decreasing NF-κB activation and NLRP3 inflammasome. [Abstract]2024;62(2):110-121. PMID: 39042029 -
Chem Pharm Bull (Tokyo)
Dioscin Protects against Aβ1-42 Oligomers-Induced Neurotoxicity via the Function of SIRT3 and Autophagy. [Abstract]2020;68(8):717-725. PMID: 32741912
Lösungsmittel & Löslichkeit
DMSO : ≥ 100 mg/mL (115.07 mM; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
* "≥" means soluble, but saturation unknown.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)
Select the appropriate dissolution method based on your experimental animal and administration route.
- For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
- To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
- The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 2.25 mg/mL (2.59 mM); Clear solution
This protocol yields a clear solution of ≥ 2.25 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (22.5 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)
Solubility: ≥ 2.25 mg/mL (2.59 mM); Clear solution
This protocol yields a clear solution of ≥ 2.25 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (22.5 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
For the following dissolution methods, please prepare the working solution directly:
It is recommended to prepare fresh solutions and use them promptly within a short period of time.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Add each solvent one by one: 0.5% CMC-Na/saline water
Solubility: 5 mg/mL (5.75 mM); Suspended solution; Need ultrasonic
Please enter the basic information of animal experiments:
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-
-
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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
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%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
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%+
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+%Tween-80 + +
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%Saline +
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Working solution concentration: 0.22 mg/mL
Method for preparing stock solution: mg drug dissolved in μL DMSO. Stock solution concentration: mg/mL.
1. Take μL DMSO stock solution;
2. Add μL .
μL , mix evenly;
3. Then add μL Tween 80, mix evenly;
4. Then add μL
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Reinheit & Dokumentation
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Data Sheet (280 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Handling Instructions (2659 KB)
Verweise
[1]. Chen J, et al. Dioscin-induced apoptosis of human LNCaP prostate carcinoma cells through activation of caspase-3 and modulation of Bcl-2 protein family. J Huazhong Univ Sci Technolog Med Sci. 2014 Feb;34(1):125-30. [Content Brief]
[2]. Qu X, et al. Dioscin inhibits osteoclast differentiation and bone resorption though down-regulating the Akt signaling cascades. Biochem Biophys Res Commun. 2014 Jan 10;443(2):658-65. [Content Brief]
[3]. Qin J, et al. Dioscin prevents the mitochondrial apoptosis and attenuates oxidative stress in cardiac H9c2 cells. Drug Res (Stuttg). 2014 Jan;64(1):47-52. [Content Brief]
[4]. Zhao X, et al. Dioscin Induces Apoptosis in Human Cervical Carcinoma HeLa and SiHa Cells through ROS-Mediated DNA Damage and the Mitochondrial Signaling Pathway. Molecules. 2016 Jun 4;21(6):730. [Content Brief]
[5]. Xu T, et al. A 90-day subchronic toxicological assessment of dioscin, a natural steroid saponin, in Sprague-Dawley rats. Food Chem Toxicol. 2012 May;50(5):1279-87. [Content Brief]
[6]. Tao X, et al. Dioscin attenuates hepatic ischemia-reperfusion injury in rats through inhibition of oxidative-nitrative stress, inflammation and apoptosis. Transplantation. 2014 Sep 27;98(6):604-11. [Content Brief]
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 1.1507 mL | 5.7535 mL | 11.5070 mL | 28.7674 mL |
| 5 mM | 0.2301 mL | 1.1507 mL | 2.3014 mL | 5.7535 mL | |
| 10 mM | 0.1151 mL | 0.5753 mL | 1.1507 mL | 2.8767 mL | |
| 15 mM | 0.0767 mL | 0.3836 mL | 0.7671 mL | 1.9178 mL | |
| 20 mM | 0.0575 mL | 0.2877 mL | 0.5753 mL | 1.4384 mL | |
| 25 mM | 0.0460 mL | 0.2301 mL | 0.4603 mL | 1.1507 mL | |
| 30 mM | 0.0384 mL | 0.1918 mL | 0.3836 mL | 0.9589 mL | |
| 40 mM | 0.0288 mL | 0.1438 mL | 0.2877 mL | 0.7192 mL | |
| 50 mM | 0.0230 mL | 0.1151 mL | 0.2301 mL | 0.5753 mL | |
| 60 mM | 0.0192 mL | 0.0959 mL | 0.1918 mL | 0.4795 mL | |
| 80 mM | 0.0144 mL | 0.0719 mL | 0.1438 mL | 0.3596 mL | |
| 100 mM | 0.0115 mL | 0.0575 mL | 0.1151 mL | 0.2877 mL |