CS1P1
CS1P1 is a brain-penetrant and selective S1PR1 antagonist and PET radiotracer, with human S1PR1 IC50 values of 2.1 nM. CS1P1 binds specifically to S1PR1 to enable in vivo receptor expression quantification. CS1P1 can be used as PET radiotracer when labelled with 11C. CS1P1 can be used for the research of multiple sclerosis, neointimal hyperplasia, vascular inflammation.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- CAS 番号: 1246526-29-3
- 分子式: C27H23F4N3O3
- 分子量:513.48
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
生物活性
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S1PR1 2.1 nM (IC50) |
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Sprague Dawley (male and female)[2]
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Dosage:0.3 mg/kg
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Administration:i.v.; single bolus
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Result:Allowed all rats to survive to scheduled euthanasia.
Caused no CS1P1-related effects on body weights, hematology parameters, clinical chemistry parameters, organ weights, or gross pathology findings at either Day 2 or Day 15.
Showed no CS1P1-related histopathology.
化学情報
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CAS 番号 1246526-29-3
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分子量 513.48
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分子式 C27H23F4N3O3
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SMILES
O=C(CCN(CC1=C(F)C=C(C2=NOC(C3=CC(C(F)(F)F)=C(C4=C(C)C=CC=C4)C=C3)=N2)C=C1)C)O
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
[1]. Qiu L, et al. Discovery of a Promising Fluorine-18 Positron Emission Tomography Radiotracer for Imaging Sphingosine-1-Phosphate Receptor 1 in the Brain. J Med Chem. 2023;66(7):4671-4688. [Content Brief]
[2]. Liu H, et al. Acute Rodent Tolerability, Toxicity, and Radiation Dosimetry Estimates of the S1P1-Specific Radioligand [11C]CS1P1. Mol Imaging Biol. 2020;22(2):285-292. [Content Brief]
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)