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Lasofoxifene

🥰Excellent
Catalog No. T62119Cas No. 180916-16-9
Alias CW-008, CW008

Lasofoxifene (CP-336156) is a selective oestrogen receptor modulator/antagonist that reduces serum IL-6 levels and inhibits joint inflammation and osteoporosis. It suppresses primary tumour growth and metastasis, making it suitable for breast cancer research.

Lasofoxifene

Lasofoxifene

🥰Excellent
Purity: 99.6%
Catalog No. T62119Alias CW-008, CW008Cas No. 180916-16-9
Lasofoxifene (CP-336156) is a selective oestrogen receptor modulator/antagonist that reduces serum IL-6 levels and inhibits joint inflammation and osteoporosis. It suppresses primary tumour growth and metastasis, making it suitable for breast cancer research.
Pack SizePriceAvailabilityQuantity
2 mg$34In Stock
5 mg$53In Stock
10 mg$74In Stock
50 mg$187In Stock
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Purity:99.6%
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Product Introduction

Bioactivity
Description
Lasofoxifene (CP-336156) is a selective oestrogen receptor modulator/antagonist that reduces serum IL-6 levels and inhibits joint inflammation and osteoporosis. It suppresses primary tumour growth and metastasis, making it suitable for breast cancer research.
In vivo
Methods: Lasofoxifene (1, 5, and 10 mg/kg, 5 times per week) was administered subcutaneously to NSG mice with established human-derived xenograft models (MIND models) to assess the antitumor activity of lasofoxifene in endocrine therapy-resistant ER+ breast cancer mouse models. Results: Lasofoxifene demonstrated superior efficacy in inhibiting tumor growth and metastasis compared to fulvestrant, especially in Y537S and D538G mutant tumors, where lasofoxifene showed stronger inhibitory effects. [1]
SynonymsCW-008, CW008
Chemical Properties
Molecular Weight413.55
FormulaC28H31NO2
Cas No.180916-16-9
SmilesOC=1C=C2C([C@H]([C@H](CC2)C3=CC=CC=C3)C4=CC=C(OCCN5CCCC5)C=C4)=CC1
ColorWhite
AppearanceSolid
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 6.5 mg/mL (15.72 mM), when pH is adjusted to 4 with 1M HCl. Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.4181 mL12.0904 mL24.1809 mL120.9044 mL
5 mM0.4836 mL2.4181 mL4.8362 mL24.1809 mL
10 mM0.2418 mL1.2090 mL2.4181 mL12.0904 mL

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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (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 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 μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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