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Size | Price | Stock |
---|---|---|
5mg | $65 | 3-6 Days |
10mg | $95 | 3-6 Days |
25mg | $135 | 3-6 Days |
50mg | $235 | 3-6 Days |
100mg | $419 | 3-6 Days |
250mg | $680 | 3-6 Days |
500mg | $1150 | 3-6 Days |
Cat #: V3274 CAS #: 1796596-46-7 (NSC23005 sodium); 6314-70-1 (NSC23005 free acid) Purity ≥ 98%
Description: NSC23005 sodium is a novel and potent p18 inhibitor with ED50 of 5.21 nM in promoting Hematopoietic stem cells (HSCs) expansion in both murine and human models. Hematopoietic stem cells have emerged as promising therapeutic cell sources for high-risk hematological malignancies and immune disorders. However, their clinical use is limited by the inability to expand these cells ex vivo. Therefore, there is an urgent need to identify specific targets and effective probes that can expand HSCs. NSC23005 sodium represents novel chemical agents for murine and human HSCs ex vivo expansion and also can be used as valuable chemical probes for further HSC biology research towards promising utility for therapeutic purposes.
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Molecular Weight (MW) | 305.32 |
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Molecular Formula | C13H16NNaO4S |
CAS No. | 1796596-46-7 (NSC23005 sodium); 6314-70-1 (NSC23005 free acid) |
Storage | -20℃ for 3 years in powder form |
-80℃ for 2 years in solvent | |
Solubility In Vitro | DMSO: 6.5 mg/mL |
Water: | |
Ethanol: | |
SMILES Code | O=C([O-])C1=CC=C(S(=O)(NC2CCCCC2)=O)C=C1.[Na+] |
Synonyms | NSC23005; NSC-23005; NSC 23005; p18SMI-40; NSC23005 sodium |
Protocol | In Vitro | In vitro activity: NSC23005 sodium is a novel and potent p18 inhibitor with ED50 of 5.21 nM in promoting Hematopoietic stem cells (HSCs) expansion in both murine and human models. Hematopoietic stem cells have emerged as promising therapeutic cell sources for high-risk hematological malignancies and immune disorders. However, their clinical use is limited by the inability to expand these cells ex vivo. Therefore, there is an urgent need to identify specific targets and effective probes that can expand HSCs. NSC23005 sodium represents novel chemical agents for murine and human HSCs ex vivo expansion and also can be used as valuable chemical probes for further HSC biology research towards promising utility for therapeutic purposes. NSC23005 sodium is a novel class of INK4C (p18INK4C or p18) small molecule inhibitor (p18SMIs), which is initially found by in silico 3D screening. NSC23005 sodium shows the most potent bioactivity in hematopoietic stem cells (HSCs) expansion (ED50=5.21 nM). Notably, NSC23005 sodium does not show significant cytotoxicity toward 32D cells or HSCs, nor does it augment leukemia cell proliferation. NSC23005 sodium (ED50=5.21 nM), shows no activity in promoting the proliferation of leukemia cells. Kinase Assay: rior to culture, cKit-enriched BM cells (1 × 106/mL) were labeled with 5- (and 6-) carboxy-fluorescein diacetatesuccinimidylester (CFSE) dye (3 μM, Molecular Probes) in PBS supplemented with 0.1% bovine serum albumin. Labeling was performed in the dark at 37 °C for 10 min. Labeling was stopped by the addition of 5 volumes of ice cold PBS. 4 days after culture with cytokine plus compound, labeled cells were harvested and stained with the antibody cocktail for lineage markers, Sca-1, CD48, and CD150. During cell division, CFSE is distributed equally between daughter cells so that the generation of cells could be reflected by the content of CFSE and measured by the intensity of fluorescence. The CyAnsystem (DakoCytomation) was used for data acquisition. The data was analyzed using cells/Proliferation module of FlowJo software (Treestar, Inc.), which would fit a curve of the input data, automatically generate peaks standing for subpopulations with different fluorescence intensity and calculate the percentage of each peak and divided statistics results. Cell Assay: c-Kit enriched bone marrow (BM) cells are cultured for 5 days with cytokine combination plus NSC23005 sodium or DMSO. As positive controls, primary uncultured bone marrow cells are treated by ultraviolet radiation (UV) for 10 minutes prior to the staining process for apoptosis analysis. Apoptosis and cell death are measured by AnnexinV and DAPI staining in the Annexin V-FITC Apoptosis Detection Kit. Apoptosis is measured on an FACS analyzer. The data is analyzed using FlowJo software. |
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In Vivo | Mice (6–8 weeks old) were purchased from Jackson laboratory (Bar Harbor, ME) and housed in specific pathogen-free rooms within the animal-care facilities of the University of Pittsburgh Cancer Institute. All procedures of the mouse work were approved by the Institutional Animal Care and Use Committee at the University of Pittsburgh. HSCs expansion medium consists of BIT9500 (Stem Cell Technologies) supplemented with 50 ng/mL recombinant mouse (rm) SCF, 20 ng/mL FMS-like tyrosine kinase 3 ligand (Flt3L) and 10 ng/mL thrombopoietin (Tpo) (all from PeproTech, Inc.). p18SMI compounds were added where indicated. Bone marrow cells were harvested from C57BL/6 mice and made into a single-cell suspension. After immunomagnetic c-Kit enrichment (cKit-conjugated microbeads [MiltenyiBiotec, Bergisch-Gladbach]), cells were washed and resuspended in HSCs expansion medium. After culture, total nucleated cell counts were obtained, and a fraction of mononuclear cells (MNCs) or whole bone marrow cells were stained for flow cytometry analysis. Frequency of each cell population was determined by independently analyzing more than 5 × 105 cells per sample in triplicate. | |
Animal model | Mice (6–8 weeks old) |
Solvent volume to be added | Mass (the weight of a compound) | |||
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Mother liquor concentration | 1mg | 5mg | 10mg | 20mg |
1mM | 3.2753 mL | 16.3763 mL | 32.7525 mL | 65.5050 mL |
5mM | 0.6551 mL | 3.2753 mL | 6.5505 mL | 13.1010 mL |
10mM | 0.3275 mL | 1.6376 mL | 3.2753 mL | 6.5505 mL |
20mM | 0.1638 mL | 0.8188 mL | 1.6376 mL | 3.2753 mL |
This equation is commonly abbreviated as: C1 V1 = C2 V2
- (1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
- (2) Be sure to add the solvent(s) in order.