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LY-2584702 free base
🥰Excellent
Catalog No. T6159Cas No. 1082949-67-4
LY2584702 is a selective, ATP-competitive p70S6K inhibitor(IC50: 4 nM).
LY-2584702 free base
🥰Excellent
Purity: 98.72%
Catalog No. T6159Cas No. 1082949-67-4
LY2584702 is a selective, ATP-competitive p70S6K inhibitor(IC50: 4 nM).
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $39 | In Stock | |
| 2 mg | $54 | In Stock | |
| 5 mg | $116 | In Stock | |
| 10 mg | $150 | In Stock | |
| 25 mg | $332 | In Stock | |
| 50 mg | $448 | In Stock | |
| 100 mg | $658 | In Stock | |
| 500 mg | $1,380 | In Stock |
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Purity:98.72%
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All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.Product Introduction
Bioactivity
Chemical Properties
| Description | LY2584702 is a selective, ATP-competitive p70S6K inhibitor(IC50: 4 nM). |
| Targets&IC50 | p70 S6K:4 nM |
| In vitro | In HCT116 colon cancer cells, LY2584702 inhibits phosphorylation of the S6 ribosomal protein (pS6) with IC50 of 0.1-0.24 μM[1]. Combined with EGFR inhibitor erlotinib or with the mTOR inhibitor everolimus, LY2584702 has significant synergistic effects [2]. |
| In vivo | LY2584702 (12.5 mg/kg BID), shows significant antitumor activity in both U87MG glioblastoma and HCT116 colon carcinoma xenograft models. [1] |
| Molecular Weight | 445.42 |
| Formula | C21H19F4N7 |
| Cas No. | 1082949-67-4 |
| Smiles | CN1C(C2CCN(C3=C4C(=NC=N3)NN=C4)CC2)=NC(=C1)C5=CC(C(F)(F)F)=C(F)C=C5 |
| Relative Density. | no data available |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | ||||||||||
| Solubility Information | DMSO: 1 mg/mL (2.24 mM), Heating is recommended. | ||||||||||
Solution Preparation Table | |||||||||||
DMSO
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(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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