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Tirbanibulin

🥰Excellent
Catalog No. T6345Cas No. 897016-82-9
Alias KX2-391, KX-01

Tirbanibulin (KX2-391) is a highly selective Src kinase inhibitor that has demonstrated efficacy in pre-Clinicalal animal models of colon, pancreatic, prostate and breast cancer. It is a substrate-targeted kinase inhibitor. KX2-391, belongs to an emerging new family of targeted cancer treatments called protein kinase inhibitors.

Tirbanibulin

Tirbanibulin

🥰Excellent
Purity: 99.67%
Catalog No. T6345Alias KX2-391, KX-01Cas No. 897016-82-9
Tirbanibulin (KX2-391) is a highly selective Src kinase inhibitor that has demonstrated efficacy in pre-Clinicalal animal models of colon, pancreatic, prostate and breast cancer. It is a substrate-targeted kinase inhibitor. KX2-391, belongs to an emerging new family of targeted cancer treatments called protein kinase inhibitors.
Pack SizePriceAvailabilityQuantity
2 mg$35In Stock
5 mg$57In Stock
10 mg$70In Stock
25 mg$143In Stock
50 mg$279In Stock
100 mg$483In Stock
1 mL x 10 mM (in DMSO)$63In Stock
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Purity:99.67%
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Product Introduction

Bioactivity
Description
Tirbanibulin (KX2-391) is a highly selective Src kinase inhibitor that has demonstrated efficacy in pre-Clinicalal animal models of colon, pancreatic, prostate and breast cancer. It is a substrate-targeted kinase inhibitor. KX2-391, belongs to an emerging new family of targeted cancer treatments called protein kinase inhibitors.
Targets&IC50
Src (HuH-7):9 nM(GI50), Src (HepG2):60 nM(GI50), Src (Hep3B):26 nM(GI50), Src (PLC/PRF/5):13 nM(GI50)
In vitro
KX2-391, a Src inhibitor targeting the Src substrate pocket, demonstrates steep dose-response curves against Huh7 (GI50 = 9 nM), PLC/PRF/5 (GI50 = 13 nM), Hep3B (GI50 = 26 nM), and HepG2 (GI50 = 60 nM), four hepatic cell cancer (HCC) cell lines. It also inhibits leukemia cells resistant to current drugs, including those with the T3151 mutation. In engineered Src-driven cell growth assays with NIH3T3/c-Src527F and SYF/c-Src527F cells, KX2-391 shows GI50 values of 23 nM and 39 nM, respectively. [1][2]
In vivo
In pre-Clinicalal animal models of cancer, orally administered KX2-391 is shown to inhibit primary tumor growth and to suppress metastasis. [2]
Cell Research
Liver cell lines including Huh7, PLC/PRF/5, Hep3B, and HepG2 (NutriCyte, Buffalo, NY) are routinely cultured and maintained in basal medium containing 2% fetal bovine serum (FBS) at 37 °C and 5% CO2. Cells are seeded at 4.0 × 103/190 μL and 8.0 × 103/190 μL per well of 96-well plate in basal medium containing 1.5% FBS. These are cultured overnight at 37 °C and 5% CO2 prior to the addition of KX2-391, at concentrations ranging from 6,564 to 0.012 nM in triplicates. Treated cells are incubated for 3 days. Ten microliters of 3-(4,5-dimethylthiazol- 2-yl)-2,5-diphenyltetrazolium bromide (MTT) solution (5 mg/mL) is then added to each well on day 3 and cells incubated for 4 hours. The formazan product is dissolved with 10% SDS in dilute HCl. Optical density at 570 nm is measured by using BioTek Synergy HT multiplatform microplate reader. For comparison of activity and potency, parallel experiments are performed using KX2-391. Growth inhibition curves, 50% inhibition concentration (GI50), and 80% inhibition concentration (GI80) are determined using GraphPad Prism 5 statistical software. Data are normalized to represent percentage of maximum response as well as reported in optical density at wavelength of 570 nm (OD570) signal format.</ (Only for Reference)
AliasKX2-391, KX-01
Chemical Properties
Molecular Weight431.53
FormulaC26H29N3O3
Cas No.897016-82-9
SmilesO=C(Cc1ccc(cn1)-c1ccc(OCCN2CCOCC2)cc1)NCc1ccccc1
Relative Density.1.169 g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 80 mg/mL (185.4 mM)
H2O: < 1 mg/mL (insoluble or slightly soluble)
Ethanol: < 1 mg/mL (insoluble or slightly soluble)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.3173 mL11.5867 mL23.1734 mL115.8668 mL
5 mM0.4635 mL2.3173 mL4.6347 mL23.1734 mL
10 mM0.2317 mL1.1587 mL2.3173 mL11.5867 mL
20 mM0.1159 mL0.5793 mL1.1587 mL5.7933 mL
50 mM0.0463 mL0.2317 mL0.4635 mL2.3173 mL
100 mM0.0232 mL0.1159 mL0.2317 mL1.1587 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
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Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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