ML221

製品コードS8695 バッチS869501

印刷

化学情報

 Chemical Structure Synonyms N/A Storage
(From the date of receipt)
3 years -20°C powder
1 years -80°C in solvent
化学式

C17H11N3O6S

分子量 385.35 CAS No. 877636-42-5
Solubility (25°C)* 体外 DMSO 9 mg/mL (23.35 mM)
Water Insoluble
Ethanol Insoluble
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

溶剤液(一定の濃度)を調合する

生物活性

製品説明 ML221 is a potent apelin receptor (APJ) functional antagonist in cell-based assays that is >37-fold selective over the closely related angiotensin II type 1 (AT1) receptor. The IC50 values of ML221 are 0.70 and 1.75 μM in a cAMP assay and β-arrestin assay, respectively.
in vitro In a PAMPA permeability assay, ML221 exhibits moderate permeability. ML221 displays moderate plasma and poor microsomal stability, as it is rapidly metabolized in both human and mouse liver homogenates (4.2% and 4.9% remaining at 60 min). It shows no toxicity (>50 μM) toward human hepatocytes. ML221 displays limited cross reactivity against a range of GPCRs[1]. ML221 inhibits endothelial cell proliferation by blocking apelin-APJ signaling without affecting the expression of VEGF and VEGFR2[2].
in vivo Intraperitoneal administration of ML221 inhibits pathological angiogenesis but enhances the recovery of normal vessels into the ischemic regions in the retina of the OIR model mice[2]. A single application of ML221 alleviates mechanical allodynia and heat hyperalgesia 7 days following chronic constriction injury (CCI), in a dose‑dependent manner. Intraspinal delivery of ML221, at the onset of and in fully‑established neuropathic pain, persistently attenuates CCI‑induced pain hypersensitivity, indicating that the apelin‑APJ system is involved in initiating and maintaining pain. Intrathecal ML221 downregulates phosphorylated extracellular signal‑related kinase (ERK) in the rat spinal cord dorsal horn, suggesting that the effect of apelin on neuropathic pain may be mediated via ERK signaling[3].

プロトコル(参考用のみ)

細胞アッセイ 細胞株 bEnd.3 cells
濃度 0–30 μM
反応時間 24 h
実験の流れ

The proliferation of bEnd.3 cells following 24 h incubation with ML221 (0-30 μM) are assessed by the MTT assay and the BrdU incorporation assay. Mouse endothelial cell line bEnd.3 cells are maintained in Dulbecco's modified Eagle's medium supplemented with 10% heat-inactivated fetal bovine serum. The cells are plated at a density of 2.5 × 104/well in 24 well culture plates for the MTT assay and the BrdU incorporation assay. To perform the BrdU incorporation assay, 10 μM BrdU is added to the culture medium. After 2 h, the cells are fixed with 4% paraformaldehyde for 10 minutes. After removing the 4% paraformaldehyde, the cells are incubated with 2 M hydrochloric acid for 10 min at 37℃ for DNA hydrolysis, followed by neutralization with 0.1 M Sodium Borate buffer (pH 8.5) for 30 min at room temperature. Intranuclear BrdU is labeled with mouse anti-BrdU antibodies. The primary antibody is visualized with biotinylated goat anti-mouse IgG antibodies plus streptavidin fluorescein isothiocyanate. Nuclei are detected with Hoechst33342. The BrdU incorporation rate is determined by calculating the numbers of BrdU positive cells per Hoechst positive cells.

動物実験 動物モデル An ischemic retinopathy mouse model (C57BL/6 N mice)
投薬量 10 mg/kg
投与方法 i.p.

Selleckの高級品が、幾つかの出版された研究調査結果(以下を含む)で使われた:

A temperature-regulated circuit for feeding behavior [ Nat Commun, 2022, 13(1):4229] PubMed: 35869064
A temperature-regulated circuit for feeding behavior [ Nat Commun, 2022, 13(1):4229] PubMed: 35869064
MiR-185-5p regulates the development of myocardial fibrosis [ J Mol Cell Cardiol, 2021, S0022-2828(21)00246-7] PubMed: 34973276
A temperature-regulated circuit for feeding behavior [ Research Square, 2021, 10.21203/rs.3.rs-916525/v1] PubMed: None

長期の保管のために-20°Cの下で製品を保ってください。

人間や獣医の診断であるか治療的な使用のためにでない。

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