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LP-261

LP-261
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Purity:99.76%
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LP-261

Catalog No. T9595Cas No. 915412-67-8
LP-261 is a novel tubulin targeting anticancer agent that binds at the colchicine site on tubulin, inducing G2/M arrest.
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Pack SizePriceAvailabilityQuantity
1 mg$32In Stock
2 mg$45In Stock
5 mg$72In Stock
10 mg$122In Stock
25 mg$197In Stock
50 mg$372In Stock
100 mg$556In Stock
1 mL x 10 mM (in DMSO)$79In Stock
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Product Introduction

Bioactivity
Description
LP-261 is a novel tubulin targeting anticancer agent that binds at the colchicine site on tubulin, inducing G2/M arrest.
Targets&IC50
Tubulin polymerization:3.2 μM (EC50)
In vitro
LP-261 was tested as a single agent in colon adenocarcinoma (SW620) and prostate cancer (LNCaP and PC3) xenografts, evaluating several different dosing schedules. LP-261 was also used in combination with bevacizumab in the SW620 xenograft model. LP-261 also exhibited high oral bioavailability and apparent lack of efflux by intestinal transporters such as ABCB1. LP-261 is a very potent inhibitor of angiogenesis, preventing microvessel outgrowth in the rat aortic ring assay and HUVEC cell proliferation at nanomolar concentrations. Complete inhibition of tumor growth was achieved in the PC3 xenograft model and shown to be schedule dependent. Excellent inhibition of tumor growth in the SW620 model was observed, comparable with paclitaxel[1].
In vivo
LP-261 significantly inhibits growth of a human non-small-cell lung tumor (NCI-H522) in a mouse xenograft model[2].
Chemical Properties
Molecular Weight421.47
FormulaC22H19N3O4S
Cas No.915412-67-8
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 22 mg/ml (52.20 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.3726 mL11.8632 mL23.7265 mL118.6324 mL
5 mM0.4745 mL2.3726 mL4.7453 mL23.7265 mL
10 mM0.2373 mL1.1863 mL2.3726 mL11.8632 mL
20 mM0.1186 mL0.5932 mL1.1863 mL5.9316 mL
50 mM0.0475 mL0.2373 mL0.4745 mL2.3726 mL

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