SN50 |
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Catalog No.GC31642
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SN50, el péptido inhibidor permeable a las células NF-κB.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 213546-53-3
Sample solution is provided at 25 µL, 10mM.
SN50, el péptido inhibidor permeable a las células NF-κB. Está compuesto por la región hidrofílica del péptido de señal del factor de crecimiento de fibroblastos de Kaposi como un motivo de translocación de membrana y una secuencia de localización nucelar derivada de la subunidad p50 de NF-κB[1].
SN50(20 µg/ml; 12 hs) podría inducir la diferenciación de la microglía en tipo M2 a través de la vía NF-κB. La microglía inducida por SN50 puede proteger a las neuronas de lesiones hipóxicas[2]. SN50 (25 µg/ml; 24 hs) podría inducir una diferenciación robusta de los GSCs, y las células pierden la motilidad neuroglobular, la invasividad y la insensibilidad al tratamiento tumorigenicidad de las células madre tumorales[4].
SN50(100µl,10,30,60µg/ml; i.p.;1h) atenuó la hipercoagulación alveolar y la inhibición de la fibrinólisis en el ARDS a través de la inhibición de la translocación NF-κB p65 [5]. SN50(1µM) protegió contra lesiones pulmonares inducidas por LPS en un pulmón de rata aislado al inhibir la translocación nuclear de NF-κB[6]. SN50 tópico (10µM; 12 días) supriomió la activación del factor nuclear-κB en las células locales y redujo la incidencia de defectos epiteliales/ulceración en ratones C57BL/6 que curan las córneas[7].
References:
[1]. Lin YZ, Yao SY,et al. Inhibition of nuclear translocation of transcription factor NF kappa B by a synthetic peptide containing a cell membrane-permeable motif and nuclear localization sequence. J Biol Chem. 1995;270(24):14255-8.
[2]. Chian CF, Chiang CH, et,al. Inhibitor of nuclear factor-κB, SN50, attenuates lipopolysaccharide-induced lung injury in an isolated and perfused rat lung model. Transl Res. 2014 Mar;163(3):211-20. doi: 10.1016/j.trsl.2013.10.002. Epub 2013 Oct 12. PMID: 24646628.
[3]. Zhang L, Ren X, et,al. The NFκB inhibitor, SN50, induces differentiation of glioma stem cells and suppresses their oncogenic phenotype. Cancer Biol Ther. 2014 May;15(5):602-11. doi: 10.4161/cbt.28158. Epub 2014 Feb 20. PMID: 24557012; PMCID: PMC4026083.
[4]. Zhao K, Zhu BS, et,al. SN50 enhances the effects of LY294002 on cell death induction in gastric cancer cell line SGC7901. Arch Med Sci. 2013 Dec 30;9(6):990-8. doi: 10.5114/aoms.2013.39790. Epub 2013 Dec 26. PMID: 24482641; PMCID: PMC3902720.
[5]. Wu Y, Wang Y, et,al.SN50 attenuates alveolar hypercoagulation and fibrinolysis inhibition in acute respiratory distress syndrome mice through inhibiting NF-κB p65 translocation. Respir Res. 2020 May 27;21(1):130. doi: 10.1186/s12931-020-01372-6. PMID: 32460750; PMCID: PMC7251840.
[6]. Chian CF, Chiang CH, et,al. Inhibitor of nuclear factor-κB, SN50, attenuates lipopolysaccharide-induced lung injury in an isolated and perfused rat lung model. Transl Res. 2014 Mar;163(3):211-20. doi: 10.1016/j.trsl.2013.10.002. Epub 2013 Oct 12. PMID: 24646628.
[7]. Saika S, Miyamoto T, et,al. Therapeutic effect of topical administration of SN50, an inhibitor of nuclear factor-kappaB, in treatment of corneal alkali burns in mice. Am J Pathol. 2005 May;166(5):1393-403. doi: 10.1016/s0002-9440(10)62357-7. PMID: 15855640; PMCID: PMC1606394.
| Experimentos celulares [1]: | |
Líneas celulares | Células similares al tronco del glioma GSC11 y GSC23 |
Método de preparación | Las células se cultivaron en un medio que contenía 2% de B-27, 20 ng/mLde EGF y 20 ng/mL de β-FGF en presencia o ausencia de SN50 (25 µg/mL) durante veinticuatro horas. |
Condiciones de reacción | 25 µg/ml; 24 horas |
Áreas de aplicación | SN50 puede inducir la diferenciación de GSC. |
| Experimentos con animales [2]: | |
Modelos animales | Ratones Balb/c macho (8-12 semanas) |
Método de preparación | Los ratones fueron hechos por inhalación de 50 µl de lipopolisacárido (LPS) (4 mg/ml). A los ratones se les inyectó intraperitonealmente diferentes dos de SN50 1 h antes de la inhalación de LPS. |
Forma de dosificación | 100µl,10,30,60µg/ml; i.p.;1h |
Áreas de aplicación | SN50 inhibió las expresiones de TF y PAI-1 en mRNA y en niveles de proteínas en ratones con síndrome de dificultad respiratoria aguda (ARDS) inducido por LPS. |
References: | |
| Cas No. | 213546-53-3 | SDF | |
| Canonical SMILES | Ala-Ala-Val-Ala-Leu-Leu-Pro-Ala-Val-Leu-Leu-Ala-Leu-Leu-Ala-Pro-Val-Gln-Arg-Lys-Arg-Gln-Lys-Leu-Met-Pro | ||
| Formula | C129H230N36O29S | M.Wt | 2781.5 |
| Solubility | Water : ≥ 50 mg/mL (17.98 mM) | Storage | Store at -20°C |
| General tips | Please select the appropriate solvent to prepare the stock solution according to the
solubility of the product in different solvents; once the solution is prepared, please store it in
separate packages to avoid product failure caused by repeated freezing and thawing.Storage method
and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored
at -20°C, please use it within 1 month. To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time. |
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| Shipping Condition | Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request. | ||
| Prepare stock solution | |||
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1 mg | 5 mg | 10 mg |
| 1 mM | 359.5 μL | 1.7976 mL | 3.5952 mL |
| 5 mM | 71.9 μL | 359.5 μL | 719 μL |
| 10 mM | 36 μL | 179.8 μL | 359.5 μL |
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Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
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3. All of the above co-solvents are available for purchase on the GlpBio website.
Quality Control & SDS
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- Purity: >98.00% Appearance: A solid
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Average Rating: 5 (Based on Reviews and 19 reference(s) in Google Scholar.)















