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SP-96

Katalog-Nr.GC61287 Copy One-Click Copy Product Info

SP-96 ist ein hochpotenter, selektiver und nicht ATP-kompetitiver Aurora B (IC50=0,316 nM)-Inhibitor und zeigt eine >2000-fache SelektivitÄt gegenÜber FLT3 und KIT. SP-96 zeigt eine selektive Wachstumshemmung im NCI60-Screening, einschließlich MDA-MD-468 (GI50 = 107 nM). SP-96 kann fÜr die Erforschung von dreifach negativem Brustkrebs (TNBC) verwendet werden.

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SP-96 Chemische Struktur

Cas No.: 2682114-54-9

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10mM (in 1mL DMSO)
180,00 $
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1mg
82,00 $
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5mg
180,00 $
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10mg
288,00 $
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25mg
486,00 $
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Sample solution is provided at 25 µL, 10mM.



Description of SP-96

SP-96 is a highly potent, selective and non-ATP-competitive Aurora B (IC50=0.316 nM) inhibitor and shows >2000 fold selectivity against FLT3 and KIT. SP-96 shows selective growth inhibition in NCI60 screening, incluing MDA-MD-468 (GI50=107 nM). SP-96 can be used for the research of triple negative breast cancer (TNBC)[1].

SP-96 is a highly potent, selective and non-ATP-competitive Aurora B (IC50=0.316 nM) inhibitor and shows >2000 fold selectivity against FLT3 (IC50=1475.6 nM) and KIT (IC50=1307.6 nM)[1].SP-96 (0-1 µM; 24 hours) is not promiscuous, rather selective for a few cell lines, it inhibits MDA-MB-468, CCRF-CEM, COLO 205 and A498 cell growth with GI50 values of 107 nM,47.4 nM, 50.3 nM and 53.2 nM, respectively[1].SP-96 (63.2 nM) inhibits Aurora B activity in H460 cells by the characteristics of increased DNA content, and it increases cell volume with enormous nucleus[1].SP-96 (0-2 µM) inhibits Aurora B enzymatic activity with an IC50 of 0.316 nM and inhibits Aurora A with observed IC50 value of 18.975 nM. SP-146 shows >2000 fold selectivity against FLT3 (IC50=1475.6 nM) and KIT (IC50=1307.6 nM). Meanwhile, it exhibits inhibitory effects on other receptor tyrosine kinases (RTKs) namely EGFR, RET and HER2 with IC50 value ≥2 µM[1]. Cell Viability Assay[1] Cell Line: MDA-MB-468, CCRF-CEM, COLO 205 and A498 cell

[1]. Naga Rajiv Lakkaniga,et al. Discovery of SP-96, the first non-ATP-competitive Aurora Kinase B inhibitor, for reduced myelosuppression.Eur J Med Chem. 2020 Jul 12;203:112589.

Chemical Properties of SP-96

Cas No. 2682114-54-9 SDF
Canonical SMILES O=C(NC1=CC=CC(NC2=C3C=CC(C4=CN(C)N=C4)=CC3=NC=N2)=C1)NC5=CC=CC(F)=C5
Formula C25H20FN7O M.Wt 453.47
Löslichkeit 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.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of SP-96

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1 mg 5 mg 10 mg
1 mM 2.2052 mL 11.0261 mL 22.0522 mL
5 mM 441 μL 2.2052 mL 4.4104 mL
10 mM 220.5 μL 1.1026 mL 2.2052 mL
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

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Average Rating: 5 ★★★★★ (Based on Reviews and 39 reference(s) in Google Scholar.)

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