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LY88074
🥰Excellent
Catalog No. T11915Cas No. 177744-96-6
LY88074 is a raloxifene analog in which the basic side chain has been removed. LY88074 is an agonist of ERβ (EC50 = 232 nM).This compound stimulates uterine cell proliferation.
LY88074
🥰Excellent
Purity: 98.05%
Catalog No. T11915Cas No. 177744-96-6
LY88074 is a raloxifene analog in which the basic side chain has been removed. LY88074 is an agonist of ERβ (EC50 = 232 nM).This compound stimulates uterine cell proliferation.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $197 | In Stock | |
| 5 mg | $478 | In Stock | |
| 10 mg | $654 | In Stock | |
| 25 mg | $990 | In Stock | |
| 50 mg | $1,330 | In Stock | |
| 100 mg | $1,750 | In Stock |
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CitedSelect Batch
Purity:98.05%
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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 | LY88074 is a raloxifene analog in which the basic side chain has been removed. LY88074 is an agonist of ERβ (EC50 = 232 nM).This compound stimulates uterine cell proliferation. |
| Targets&IC50 | ERβ:232 nM(EC50) |
| In vitro | The interaction of LY88074 with collagen matrix, although significant, is less than the interaction found with Raloxifene.Removal of the aminoethylpiperdine moiety, as in LY88074, reduces bone binding, compared to Raloxifene[3]. |
| Molecular Weight | 362.4 |
| Formula | C21H14O4S |
| Cas No. | 177744-96-6 |
| Smiles | C(=O)(C1=C(SC=2C1=CC=C(O)C2)C3=CC=C(O)C=C3)C4=CC=C(O)C=C4 |
| 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: 3.62 mg/mL (10 mM), Sonication 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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