SN-38 [86639-52-3]

Référence M3016-50mg

Conditionnement : 50mg

Marque : AbMole Bioscience


All AbMole products are for research use only, cannot be used for human consumption.

SN-38 Structure
Synonym:

NK012; 7-ethyl-10-hydroxycamtothecin


Quality Control & Documentation
Biological Activity

SN-38 is an active metabolite of CPT-11, inhibits DNA topoisomerase I, DNA synthesis and causes frequent DNA single-strand breaks.

Product Citations
  • BMC Biol. 2021 May 20;19(1):108.

    Very long intergenic non-coding (vlinc) RNAs directly regulate multiple genes in cis and trans
    SN-38 purchased from AbMole

  • Nat Commun. 2019 Dec 20;10(1):5799.

    Novel approach reveals genomic landscapes of single-strand DNA breaks with nucleotide resolution in human cells.
    SN-38 purchased from AbMole

Customer Product Validations & Biological Datas
Source Customer experimental result (2018).
Method Cell viability assay
Cell Lines MDA-MB-231 cells
Concentrations 32nM
Incubation Time 4 days
Results MDA-MB-231 cells were treated with 32nM SN-38 for 4 days and then incubated for 4 days. Most of the MDA-MB-231 cells were transformed into senescent cells.
Source J Immunol Res (2018). Figure 1. SN-38
Method flow cytometry
Cell Lines NB cell lines
Concentrations 1 nM
Incubation Time 24 hours
Results Cisplatin at 2 μM, etoposide at 0.1 μM, irinotecan at 1 nM, and topotecan at 10nM induced apoptosis of all NB cell lines after 48 hours of treatment, with the exception of SK-N-AS treated with the first three drugs and SK-N-BE(2)c treated with all four drugs
Protocol (for reference only)
Cell Experiment
Cell lines A-172, U-87, and LA-567
Preparation method MTT assay
Concentrations 0 -1000 nM
Incubation time 48 h
Animal Experiment
Animal models Nontumor-bearing mice
Formulation dissolved in DMSO (1 mg/mL)
Dosages 1 mg/kg
Administration i.v.
Chemical Information
Molecular Weight 392.4
Formula C22H20N2O5
CAS Number 86639-52-3
Solubility (25°C) DMSO 21 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Stewart CF, et al. Cancer Chemother Pharmacol. Disposition of irinotecan and SN-38 following oral and intravenous irinotecan dosing in mice.

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