跳轉至內容
Merck
全部照片(1)

重要文件

654271

Sigma-Aldrich

MetAP2 Inhibitor, A832234 - Calbiochem

同義詞:

Methionine aminopeptidase-2 Inhibitor, 2-[({2-[(1Z)-3-(Diethylamino)-1-propenyl]-4-fluorophenyl}-sulfonyl)amino]-5,6,7,8-tetrahydro-1-naphthalenecarboxylic Acid, Methionyl aminopeptidase 2 Inhibitor

登入查看組織和合約定價


About This Item

化驗

≥97% (HPLC)

形狀

solid

效力

11 nM IC50

顏色

light beige

溶解度

DMSO: 5 mg/mL, pale yellow

一般說明

A cell-permeable anthranilic acid sulfonamide compound that acts as a potent and reversible inhibitor of methionine aminopetidase-2 (MetAP2, IC50 = 11 nM). Acts by directly targeting the active site of MetAP2 without any significant binding to human serum albumin. Also shown to inhibit cellular MetAP2 activity (EC50 = 5.3 nM) and block the proliferation of HT1080 fibrosarcoma cells (EC50 = 6 nM).
The MetAP2 Inhibitor, A832234 controls the biological activity of MetAP2.

生化/生理作用

MetAP2

重構

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

儲存類別代碼

10-13 - German Storage Class 10 to 13


分析證明 (COA)

輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號,寫有 ‘Lot’或‘Batch’.。

已經擁有該產品?

您可以在文件庫中找到最近購買的產品相關文件。

存取文件庫

George S Sheppard et al.
Journal of medicinal chemistry, 49(13), 3832-3849 (2006-06-23)
Methionine aminopeptidase-2 (MetAP2) is a novel target for cancer therapy. As part of an effort to discover orally active reversible inhibitors of MetAP2, a series of anthranilic acid sulfonamides with micromolar affinities for human MetAP2 were identified using affinity selection

我們的科學家團隊在所有研究領域都有豐富的經驗,包括生命科學、材料科學、化學合成、色譜、分析等.

聯絡技術服務