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Agnuside

カタログ番号GC40750

Agnuside は Vitex negundo から分離された化合物で、炎症誘発性メディエーターである PGE2 および LTB4 をダウンレギュレートし、サイトカインの発現を低下させ、抗関節炎活性を示します 。

Products are for research use only. Not for human use. We do not sell to patients.

Agnuside 化学構造

Cas No.: 11027-63-7

サイズ 価格 在庫数 個数
1mg
$58.00
在庫あり
5mg
$160.00
在庫あり
10mg
$263.00
在庫あり
25mg
$582.00
在庫あり

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

Agnuside is an iridoid glycoside originally isolated from V. rotundifolia fruit that has diverse biological activities. It inhibits COX-2 with an IC50 value of 0.026 mg/ml but exhibits less than 10% inhibition of COX-1 at this concentration. It also inhibits 46.3, 66.8, and 82.1% of P-glycoprotein (P-gp) ATPase activity at concentrations of 5, 25, and 100 μM, respectively. Agnuside (0.1-10 μM) induces proliferation of MCF-7 breast cancer cells, an effect that is inhibited by the estrogen receptor antagonist fulvestrant . In vivo, agnuside (50 mg/kg) reduces acetic acid-induced writhing in mice indicating analgesia. It also suppresses production of the pro-inflammatory mediators prostaglandin E2 (PGE2) and leukotriene B4 and the T cell-mediated cytokines IL-2, TNF-α, INF-γ, IL-4, IL-10, and IL-17 in splenocytes and arthritic paw tissue from arthritic adrenalectomized rats.

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Average Rating: 5 ★★★★★ (Based on Reviews and 27 reference(s) in Google Scholar.)

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