天堂网亚洲,天天操天天搞,91视频高清,菠萝蜜视频在线观看入口,美女视频性感美女视频,95丝袜美女视频国产,超高清美女视频图片

Ispinesib (SB-715992)

別名: CK0238273 中文名稱:伊斯平斯

Ispinesib (SB-715992, CK0238273)是一種有效的,特異性的,可逆kinesin spindle protein (KSP)抑制劑,無細胞試驗中Kiapp為1.7 nM,對CENP-E, RabK6, MCAK, MKLP1,KHC和Kif1A沒有抑制作用。Ispinesib可誘導有絲分裂阻滯和細胞的凋亡。

Ispinesib (SB-715992) Chemical Structure

Ispinesib (SB-715992) Chemical Structure

CAS: 336113-53-2

規(guī)格 價格 庫存 購買數(shù)量
10mM (1mL in DMSO) 2170 現(xiàn)貨
1mg 794.43 現(xiàn)貨
10mg 2621.56 現(xiàn)貨
50mg 7941.69 現(xiàn)貨
200mg 20229.3 現(xiàn)貨
1g 54873 現(xiàn)貨
更大包裝 有超大折扣

400-668-6834

info@selleck.cn

免費分裝
免費預溶

Ispinesib (SB-715992)相關產(chǎn)品

相關信號通路圖

細胞實驗數(shù)據(jù)示例

細胞系 實驗類型 給藥濃度 孵育時間 活性描述 文獻信息
LXFS 538 Antitumor assay 6 mg/kg Antitumor activity against human LXFS 538 cells xenografted in NMRI nu/nu mouse assessed as tumor regression at 6 mg/kg, ip measured on day 13 23394180
HCT116 Growth inhibition assay 72 hrs Growth inhibition of human HCT116 cells after 72 hrs by MTS assay, IC50=0.0011μM 26396688
MCF7 Antiproliferative assay 48 hrs Antiproliferative activity against human MCF7 cells after 48 hrs by MTT assay, IC50=1.3μM 24184776
HeLa Antiproliferative assay 48 hrs Antiproliferative activity against human HeLa cells after 48 hrs by MTT assay, IC50=1μM 24184776
NCI-H1299 Growth inhibition assay 72 hrs Growth inhibition of human NCI-H1299 cells after 72 hrs by Alamar blue assay, GI50=0.082μM 23394180
BxPC3 Growth inhibition assay 72 hrs Growth inhibition of human BxPC3 cells after 72 hrs by Alamar blue assay, GI50=0.08μM 23394180
PC3 Growth inhibition assay 72 hrs Growth inhibition of human PC3 cells after 72 hrs by Alamar blue assay, GI50=0.05μM 23394180
HCT116 Growth inhibition assay 72 hrs Growth inhibition of human HCT116 cells after 72 hrs by Alamar blue assay, GI50=0.025μM 23394180
LNCAP Growth inhibition assay 72 hrs Growth inhibition of human LNCAP cells after 72 hrs by Alamar blue assay, GI50=0.022μM 23394180
NCI-H1299 Antiproliferative assay 72 hrs Antiproliferative activity against human NCI-H1299 cells after 72 hrs by Alamar blue assay, GI50=0.082μM 22248262
BxPC3 Antiproliferative assay 72 hrs Antiproliferative activity against human BxPC3 cells after 72 hrs by Alamar blue assay, GI50=0.08μM 22248262
K562 Antiproliferative assay 72 hrs Antiproliferative activity against human K562 cells after 72 hrs by Alamar blue assay, GI50=0.071μM 22248262
hTERT-HME1 Antiproliferative assay 72 hrs Antiproliferative activity against human hTERT-HME1 cells after 72 hrs by Alamar blue assay, GI50=0.032μM 22248262
HCT116 Antiproliferative assay 72 hrs Antiproliferative activity against human HCT116 cells after 72 hrs by Alamar blue assay, GI50=0.025μM 22248262
Rh30 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Rh30 cells 29435139
RD qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for RD cells 29435139
U-2 OS qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for U-2 OS cells 29435139
Rh41 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Rh41 cells 29435139
TC32 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for TC32 cells 29435139
MG 63 (6-TG R) qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for MG 63 (6-TG R) cells 29435139
BT-37 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for BT-37 cells 29435139
DAOY qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for DAOY cells 29435139
BT-12 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for BT-12 cells 29435139
SK-N-MC qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for SK-N-MC cells 29435139
A673 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for A673 cells) 29435139
OHS-50 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for OHS-50 cells 29435139
BT-12 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for BT-12 cells 29435139
LAN-5 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for LAN-5 cells 29435139
Saos-2 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Saos-2 cells 29435139
NB-EBc1 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for NB-EBc1 cells 29435139
SK-N-MC qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-MC cells 29435139
A673 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for A673 cells 29435139
SJ-GBM2 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SJ-GBM2 cells 29435139
DAOY qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for DAOY cells 29435139
TC32 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for TC32 cells 29435139
Saos-2 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Saos-2 cells 29435139
SK-N-SH qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for SK-N-SH cells 29435139
點擊查看更多細胞系數(shù)據(jù)

生物活性

產(chǎn)品描述 Ispinesib (SB-715992, CK0238273)是一種有效的,特異性的,可逆kinesin spindle protein (KSP)抑制劑,無細胞試驗中Kiapp為1.7 nM,對CENP-E, RabK6, MCAK, MKLP1,KHC和Kif1A沒有抑制作用。Ispinesib可誘導有絲分裂阻滯和細胞的凋亡。
特性 Ispinesib是一種有效可逆的特定有絲分裂驅動蛋白(KSP)變構抑制劑。
靶點
KSP (HsEg5) [1]
(Cell-free assay)
1.7 nM(Ki app)
體外研究(In Vitro)
體外研究活性

Ispinesib 是有效可逆的特定KSP變構抑制劑,KSP與微管的結合性能,通過抑制ADP釋放而不改變微管中KSP-ADP復合體的釋放,而擾亂KSP的運動。[1] Ispinesib作用于一系列腫瘤細胞系, 包括Colo205, Colo201, HT-29, M5076, Madison-109,和MX-1, IC50為1.2 nM 到 9.5 nM,具有很強細胞毒性。[2] 15 nM 和 30 nM Ispinesib作用于PC-3前列腺癌細胞, 通過調節(jié)控制凋亡,細胞增殖,細胞周期,和信號的基因表達水平,如EGFR, p27, p15, 和IL-11,而抑制細胞增殖和誘導凋亡。[3] 7.4 nM–600 nM Ispinesib 作用于一組53種乳腺癌細胞系,具有廣譜抑制活性。150 nM Ispinesib 作用于BT-474 和MDA-MB-468細胞,誘導凋亡, 提高凋亡細胞比例,降低抗凋亡的Bcl-XL水平,和提高促凋亡的Bax和Bid 水平。[4]

激酶實驗 人類KSP ATP酶活性和Ispinesib抑制的穩(wěn)定動力學分析
使用丙酮酸激酶-乳酸脫氫酶檢測體系進行驅動蛋白的特異性分析,伴隨著NADH氧化產(chǎn)生ADP。在340 nm處檢測吸光度的變化。使用納摩爾濃度KSP進行穩(wěn)態(tài)研究, 使用一個敏感的熒光為基礎的檢測系統(tǒng),利用丙酮酸激酶,丙酮酸氧化酶,辣根過氧化物酶(HRP)耦合的檢測體系, 伴隨著Amplex紅色熒光試劑氧化為試鹵靈而生成ADP。通過熒光檢測產(chǎn)生的試鹵靈。在含10 μM 紫杉醇的PEM25 buffer [25 mM Pipes-K+ (pH 6.8), 2 mM MgCl2, 1 mM EGTA]中進行穩(wěn)態(tài)生化試驗。在含500 μM ATP, 5 μM 微管,和1 nM KSP的PEM25 buffer中測定抑制穩(wěn)定的IC50值。通過劑量-反應曲線獲得Ispinesib的Ki?app(明顯的抑制劑解離常數(shù))值, 通過使用Morrison方程明確糾正酶濃度。在穩(wěn)態(tài)情況下測定抑制劑形態(tài)(競爭性,非競爭性,無競爭力的,或者混合生物)。
細胞實驗 細胞系 Breast 乳腺癌細胞,包括MCF-7, HCC1954, MDA-MB-468,和KPL4
濃度 0.085 nM-33 μM
孵育時間 72小時
方法

指數(shù)生長期細胞接種在96孔板上,用Ispinesib處理72小時。然后使用CellTiter-Glo測量細胞生長, 并使用BioTek FLx800測定熒光值。分析數(shù)據(jù),計算IC50值。

體內研究(In Vivo)
體內研究活性

Ispinesib按4.5 mg/kg-15 mg/kg劑量作用于攜帶移植瘤的小鼠模型,有效抑制Colo205, Colo201, HT-29細胞,但是不抑制MX-1細胞。SB-715992按6 mg/kg-10 mg/kg劑量處理,也抑制小鼠實體瘤,包括 Madison 109 肺癌, M5076肉瘤,及L1210和P388白血病。[2] Ispinesib 按8 mg/kg-10 mg/kg劑量作用于攜帶乳腺癌細胞MCF-7, HCC1954, MDA-MB-468,和KPL4移植瘤的小鼠,抑制腫瘤生長。[4]

動物實驗 Animal Models 攜帶MCF7, KPL4,和HCC1954細胞的(nu/nu)裸鼠模型,攜帶MDA-MB-468 細胞的SCID小鼠模型
Dosages 10 mg/kg作用于裸鼠,8 mg/kg作用于SCID 鼠
Administration 3倍劑量腹腔注射,每隔四天進行一次
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT00607841 Terminated
Breast Neoplasms
Cytokinetics
December 2007 Phase 1
NCT00354250 Completed
Recurrent Renal Cell Cancer|Stage III Renal Cell Cancer|Stage IV Renal Cell Cancer
National Cancer Institute (NCI)
May 2006 Phase 2
NCT00097409 Completed
Ovarian Cancer
GlaxoSmithKline
December 2004 Phase 2
NCT00119171 Completed
Solid Tumor Cancer
GlaxoSmithKline
November 2004 Phase 1

化學信息&溶解度

分子量 517.06 分子式

C30H33ClN4O2

CAS號 336113-53-2 SDF Download Ispinesib (SB-715992) SDF
Smiles CC1=CC=C(C=C1)C(=O)N(CCCN)C(C2=NC3=C(C=CC(=C3)Cl)C(=O)N2CC4=CC=CC=C4)C(C)C
儲存條件(自收到貨起)

體外溶解度
批次:

DMSO : 103 mg/mL ( (199.2 mM) ;DMSO吸濕會降低化合物溶解度,請使用新開封DMSO)

Ethanol : 103 mg/mL (199.2 mM)

Water : Insoluble

摩爾濃度計算器

體內溶解度
批次:

現(xiàn)配現(xiàn)用,請按從左到右的順序依次添加,澄清后再加入下一溶劑

動物體內配方計算器

實驗計算

摩爾濃度計算器

質量 濃度 體積 分子量

動物體內配方計算器(澄清溶液)

第一步:請輸入基本實驗信息(考慮到實驗過程中的損耗,建議多配一只動物的藥量)

mg/kg g μL

第二步:請輸入動物體內配方組成(配方適用于不溶于水的藥物;不同批次藥物配方比例不同,請聯(lián)系Selleck為您提供正確的澄清溶液配方)

% DMSO % % Tween 80 % ddH2O
%DMSO %

計算結果:

工作液濃度: mg/ml;

DMSO母液配制方法: mg 藥物溶于μL DMSO溶液(母液濃度mg/mL,:如該濃度超過該批次藥物DMSO溶解度,請先聯(lián)系Selleck);

體內配方配制方法:μL DMSO母液,加入μL PEG300,混勻澄清后加入μL Tween 80,混勻澄清后加入μL ddH2O,混勻澄清。

體內配方配制方法:μL DMSO母液,加入μL Corn oil,混勻澄清。

注意:1. 首先保證母液是澄清的;
2.一定要按照順序依次將溶劑加入,進行下一步操作之前必須保證上一步操作得到的是澄清的溶液,可采用渦旋、超聲或水浴加熱等物理方法助溶。

技術支持

在訂購、運輸、儲存和使用我們的產(chǎn)品的任何階段,您遇到的任何問題,均可以通過撥打我們的熱線電話400-668-6834,或者技術支持郵箱tech@selleck.cn,直接聯(lián)系到我們。我們會在24小時內盡快聯(lián)系您。

操作手冊

如果有其他問題,請給我們留言。

* 必填項

請輸入您的姓名
請輸入您的郵箱地址 請輸入一個有效的郵箱地址
請寫點東西給我們
Tags: buy Ispinesib (SB-715992) | Ispinesib (SB-715992) supplier | purchase Ispinesib (SB-715992) | Ispinesib (SB-715992) cost | Ispinesib (SB-715992) manufacturer | order Ispinesib (SB-715992) | Ispinesib (SB-715992) distributor
在線咨詢
聯(lián)系我們