目錄:愛(ài)必信(上海)生物科技有限公司>>生化試劑>>小分子化合物>> abs47026288BV-6 1001600-56-1
| 參考價(jià) | ¥1075-¥3225 |
參考價(jià):¥1075 ~ ¥3225
10mg 50mg
CAS:1001600-56-1 純度:>98% 分子量:1205.57 分子式:C70H96N10O8 供貨周期:現(xiàn)貨 規(guī)格:10mg 貨號(hào):abs47026288 應(yīng)用領(lǐng)域:化工,生物產(chǎn)業(yè),農(nóng)林牧漁,制藥/生物制藥,綜合 主要用途:induces autoubiquitination
>| 10mg | 1075元 | 999mg可售 |
| 50mg | 3225元 | 999mg可售 |
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| CAS | 1001600-56-1 | 純度 | >98% |
|---|---|---|---|
| 分子量 | 1205.57 | 分子式 | C70H96N10O8 |
| 供貨周期 | 現(xiàn)貨 | 規(guī)格 | 10mg |
| 貨號(hào) | abs47026288 | 應(yīng)用領(lǐng)域 | 化工,生物產(chǎn)業(yè),農(nóng)林牧漁,制藥/生物制藥,綜合 |
| 主要用途 | induces autoubiquitination |
BV-6 1001600-56-1
| 產(chǎn)品描述 | |
| 描述 | BV6 induces autoubiquitination and subsequent proteasomal degradation of cIAP1 and cIAP2, and greatly sensitizes cells to TNF-induced necrosis. BV6 significantly enhances the radiosensitization of HCC193 and H460 cells in vitro. BV6 sensitizes both cell lines to radiation (HCC193-DER = 1.38, p < 0.05 at 1 μM BV6; H460-DER = 1.42, p < 0.05 at 5 μM BV6), but a higher concentration of and longer incubation time with BV6 was necessary for H460 cells. |
| 純度 | >98% |
| 儲(chǔ)存/保存方法 | Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution. |
| 基本信息 | |
| 別名 | BV 6;BV-6 |
| 外觀 | White to off-white solid |
| 可溶性/溶解性 | DMSO: ≥58 mg/mL |
| 生物活性 | |
| 靶點(diǎn) | IAP |
| In vitro(體外研究) | HCC193 has an IC50 of 7.2 μM in MTS assays, while H460 cells are not reduced to 50% viability even with 30 μM BV6 treatment. Administration of 1 μM BV6 to HCC193 cells induces complete depletion of cIAP1 levels at 1 hour post-treatment, while a decrease in XIAP levels is not seen until 24 hours following addition of drug. Similarly, 5 μM BV6 fully depletes cIAP1 at 1 hour and begin to reduce XIAP at 24 hours in H460 cells. In parallel findings, cIAP1 levels are decreased in response to a small dose of 0.25 μM BV6 in both cell lines, whereas trace amounts of XIAP are still present at 5μM BV6. HCC193 cells demonstrates noticeable cleaved caspase-3 levels beginning 12 hours post-incubation with 1μM BV6, and cleaved caspase-3 levels continued to increase in a time-dependent manner over 48 hours. Treatment of HCC193 cells with 1 μM BV6 for 24 hours causes a significant survival curve shift in HCC193 cells relative to DMSO-treated cells, with a DER=1.38 (p. BV6 (2 and 5 µM) significantly represses BrdU incorporation in ectopic and eutopic (disease-free and myomas) ESCs. An ~30% decrease of BrdU incorporation is observed in both groups after treatment with 5 µM BV6. |
| In vivo(體內(nèi)研究) | Murine cIAP-1, cIAP-2 and XIAP expressions are clearly observed in the cytoplasm of both epithelial and stromal cells of implants, whereas Survivin is mainly expressed in the nuclei BV6 treatment for 4 weeks attenuated the intensity of IAPs expression. The size of lesions range from ~2 to 7 mm in diameter. The monolayer epithelial cell lining of the cyst is shown. After immunohistochemical staining, cytokeratin and vimentin are positively stained, whereas calretinin is negative. After BV6 treatment for 4 weeks, the total number of lesions (4.6 versus 2.8/mouse), the average weight (78.1 versus 32.0 mg/mouse) and the surface area (44.5 versus 24.6 mm2/mouse) of lesions are significantly less than in the controls. In the endometrial gland epithelia or stroma, the percentage of Ki67-positive cells decreases after BV6 treatment. |
| 研究領(lǐng)域 | |
| 研究領(lǐng)域 | Apoptosis Drug DiscoverySmall Molecule DrugLead Compound Discovery |
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