您好，欢迎来到易推广！ 请登录 免费注册

上海陶术生物科技有限公司 主营产品：生物试剂,实验服务等

当前位置：易推广 > 上海陶术生物科技有限公司 > 产品展示

企业档案

会员类型：会员

已获得易推广信誉   等级评定
139成长值

(0 -40)基础信誉积累，可浏览访问

(41-90)良好信誉积累，可接洽商谈

(91+  )优质信誉积累，可持续信赖

易推广会员：5年

工商认证 【已认证】

最后认证时间：

注册号： 【已认证】

法人代表： 【已认证】

企业类型：生产商 【已认证】

注册资金：人民币万 【已认证】

产品数：86101

参观次数：3740806

手机网站：http://m.yituig.com/c135739/

旗舰版地址：http://tsbiochem.app17.com

自主品牌

自主品牌

已选条件

  • T68459RO4927350；化合物 RO4927350RO4927350

    RO4927350 is a potent and highly selective non-ATP-competitive MEK1/2 inhibitor. RO4927350 selectively blocks the MAPK pathway signaling both in vitro and in vivo, which results in significant antitumor efficacy in a broad spectrum of tumor models. RO4927350 inhibits not only ERK1/2 but also MEK1/2 phosphorylation. In cancer cells, high basal levels of phospho-MEK1/2 rather than phospho-ERK1/2 seem to correlate with greater sensitivity to RO4927350. Furthermore, RO4927350 prevents a feedback inc

    价 格：￥电议型 号：T68459产 地：中国大陆

  • T68458Fostriecin (free base)；化合物 Fostriecin (free base)Fostriecin (free base)

    Fostriecin (free base) is an inhibitor of the serine/threonine protein phosphatases 2A (PP2A) and 4 (PP4) (IC50s = 3.2 and 3 nM, respectively). It less effectively inhibits topoisomerase II and PP1 (IC50s = 40 and 131 μM, respectively) and does not inhibit PP2B. Through its effects on protein phosphatases, fostriecin increases the level of histone H3 phosphorylation and may alter epigenetic regulation of cell proliferation. On a related note, fostriecin was first identified as an antitumor antib

    价 格：￥电议型 号：T68458产 地：中国大陆

  • T68457GSK812397；化合物 GSK812397GSK812397

    GSK812397 is a potent entry inhibitor of X4-tropic strains of HIV-1, as demonstrated in multiple in vitro cellular assays. GSK812397 is a noncompetitive antagonist of the CXCR4 receptor, with GSK812397 producing a concentration-dependent decrease in both an SDF-1-mediated chemotaxis and intracellular calcium release (IC50s were 0.34+/-0.01 nM and 2.41+/-0.50 nM, respectively). GSK812397 is effective against a broad range of X4- and X4R5-utilizing clinical isolates. The potency and efficacy of GS

    价 格：￥电议型 号：T68457产 地：中国大陆

  • T68456Dexlofexidine HCl；化合物 Dexlofexidine HClDexlofexidine HCl

    Dexlofexidine HCl is the salt form of Dexlofexidine Free Base, an isomer “+“ of lofexidine, which is an agonist of alpha 2-adrenoceptor, but in 10 times less potent than the other isomer, levlofexidine

    价 格：￥电议型 号：T68456产 地：中国大陆

  • T68455AP23846；化合物 AP23846AP-23846；AP-23846

    AP23846 is a novel and potent Src family kinase inhibitor that reduces vascular endothelial growth factor and interleukin-8 expression and abrogates downstream angiogenic processes in human solid tumor cell lines.

    价 格：￥电议型 号：T68455产 地：中国大陆

  • T68454IAV inhibitor 4l；化合物 IAV inhibitor 4lIAV inhibitor 4l

    IAV inhibitor 4l is an IAV inhibitor targeting hemagglutinin and mediates viral entry by preventing HA-membrane fusion.

    价 格：￥电议型 号：T68454产 地：中国大陆

  • T68453HY-52；化合物 HY-52HY-52

    HY-52 is a selective inhibitor of CDC2 kinase.

    价 格：￥电议型 号：T68453产 地：中国大陆

  • T68452H 142-08；化合物 H 142-08H 142-08

    H 142-08 is a partial beta 1-agonist with adrenoreceptor stimulatory effects.

    价 格：￥电议型 号：T68452产 地：中国大陆

  • T68451AG-28262 besylate；化合物 AG-28262 besylateAG-28262 besylate

    AG-28262 besylate is a VEGFR-2 Inhibitorwhich may affect alanine aminotransferase gene expression and enzymatic activity in the liver.

    价 格：￥电议型 号：T68451产 地：中国大陆

  • T68450IDX-989；化合物 IDX-989IDX-989

    IDX-989 is an HIV-1 non-nucleoside reverse transcriptase inhibitor.

    价 格：￥电议型 号：T68450产 地：中国大陆

  • T6845GNE-317；化合物GNE317GNE317；GNE317

    GNE-317, a PI3K/mTOR inhibitor, can pass through the blood-brain barrier (BBB).

    价 格：￥电议型 号：T6845产 地：中国大陆

  • T68449JFD00950；化合物 JFD00950JFD00950

    JFD00950 is a human flap endonuclease 1 (FEN1) inhibitor with in vitro inhibition of flap cleavage activity as well as cytotoxic activity against a colon cancer cell line, DLD-1.

    价 格：￥电议型 号：T68449产 地：中国大陆

  • T68448XAX-162；化合物 XAX-162XAX-162

    XAX-162 is an agonist of Sphingosine 1-phosphate receptor 2 (S1PR2)

    价 格：￥电议型 号：T68448产 地：中国大陆

  • T68447BM-42304；化合物 BM-42304BM-42304

    BM-42304 is an inhibitor of fatty acid oxidation.

    价 格：￥电议型 号：T68447产 地：中国大陆

  • T68446AG-17724；化合物 AG-17724AG-17724

    AG-17724 is a potent peptidyl-prolyl isomerase (PPIase) Pin1 inhibitor.

    价 格：￥电议型 号：T68446产 地：中国大陆

  • T68445Clomoxir；化合物 ClomoxirClomoxir

    Clomoxir is a carnitine palmitoyltransferase I inhibitor that was under development as an antiarrhythmic and antidiabetic.

    价 格：￥电议型 号：T68445产 地：中国大陆

  • T68444Dircin；化合物 DircinDircin

    Dircin is an anti-inflammatory agent, prescribed for osteoarthritis and chronic inflammatory arthritis. It works by inhibiting interleukin-1.

    价 格：￥电议型 号：T68444产 地：中国大陆

  • T68443PI-540；化合物 PI-540PI-540

    PI-540 is a potent and selective inhibitor of class 1A phosphatidylinositide 3-kinases (PI3K).

    价 格：￥电议型 号：T68443产 地：中国大陆

  • T68442Desacetylravidomycin；化合物 DesacetylravidomycinDesacetylravidomycin

    Desacetylravidomycin is a new inhibitor of IL-4 signal transduction, produced by Streptomyces sp. WK-6326.

    价 格：￥电议型 号：T68442产 地：中国大陆

  • T68441SABRAC；化合物 SABRACSABRAC

    SABRAC inhibits acid ceramidase in PC3 MC metastatic prostate cancer cells (IC50 = <1 ?M), as well as induces accumulation of ceramides in the same cells.

    价 格：￥电议型 号：T68441产 地：中国大陆

1345678910111217下一页共17页

展台首页| 公司简介| 供应产品| 产品目录| 公司动态| 荣誉证书| 招聘信息| 技术中心| 联系我们| 会员管理

易推广  设计制作，未经允许翻录必究.Copyright(C) 2009 http://www.yituig.com, All rights reserved.

以上信息由企业自行提供，信息内容的真实性、准确性和合法性由相关企业负责，易推广对此不承担任何责任.   总访问量：3740806

中国彩虹热线

快速导航

返回顶部
在线咨询

提交