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

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:86095

参观次数:4041526

手机网站:http://m.yituig.com/c135739/

旗舰版地址:http://tsbiochem.app17.com

自主品牌

产品分类

  • T6092SapitinibAZD-8931;沙普替尼

    AZD8931, a reversible, ATP competitive inhibitor of EGFR(IC50=4 nM), ErbB2(IC50=3 nM) and ErbB3(IC50=4 nM), is more effective over Gefitinib or Lapatinib against NSCLC cell, 100-fold more specific for the ErbB family over MNK1 and Flt.

    价 格:¥电议型 号:T6092产 地:中国大陆

  • T6091CP-673451CP 673451;CP673451

    CP-673451 is a specific inhibitor of PDGFRα/β (IC50: 10/1 nM) with antiangiogenic and antitumor activity and the selectivity is higher 450-fold than other angiogenic receptors.

    价 格:¥电议型 号:T6091产 地:中国大陆

  • T6090BelnacasanVX-765

    VX-765 is an orally active IL-converting enzyme/caspase-1 inhibitor.

    价 格:¥电议型 号:T6090产 地:中国大陆

  • T6089NeflamapimodVX-745

    VX-745, a specific and effective inhibitor of p38α(IC50=10 nM), is 22-fold greater specificity against p38β and no inhibition activity to p38γ.

    价 格:¥电议型 号:T6089产 地:中国大陆

  • T6088Anidulafungin阿尼芬净;Ecalta;Eraxis;LY303366

    Anidulafungin (LY303366) is an echinocandin derivative used as an antifungal drug. It inhibits glucan synthase activity.

    价 格:¥电议型 号:T6088产 地:中国大陆

  • T6087AZD 6482KIN 193;AZD6482

    AZD 6482 is a potent and selective p110β inhibitor with IC50 of 0.69 nM and a PI3Kβ inhibitor with IC50 of 10 nM.

    价 格:¥电议型 号:T6087产 地:中国大陆

  • T6084RabusertibLY2603618;IC-83

    Rabusertib is an inhibitor of the cell cycle checkpoint kinase 2 (chk2) with potential chemopotentiating activity. Rabusertib has been used in trials studying the treatment of Cancer, Solid Tumors, Advanced Cancer, Pancreatic Neoplasms, and Non-Small Cell

    价 格:¥电议型 号:T6084产 地:中国大陆

  • T6083AZD8330ARRY-424704;ARRY-704

    AZD8330 is a novel, selective, non-ATP competitive MEK 1/2 inhibitor with IC50 of 7 nM. Phase 1.

    价 格:¥电议型 号:T6083产 地:中国大陆

  • T6082SSR128129ESSR

    SSR128129E is an allosteric and orally-active FGFR1 inhibitor (IC50: 1.9 μM), but not affecting other related RTKs.

    价 格:¥电议型 号:T6082产 地:中国大陆

  • T6081MilciclibPHA-848125

    Milciclib (PHA-848125) is a potent, ATP-competitive CDK inhibitor for CDK2 with IC50 of 45 nM. It is >3-fold more selective for CDK2 than CDK1, 2, 4, 5, and 7. Phase 2.

    价 格:¥电议型 号:T6081产 地:中国大陆

  • T6080NVP-AEW541AEW541

    NVP-AEW541, a potent inhibitor of IGF-1R(IC50=150 nM) and InsR(IC50=140 nM), exhibits excellent efficiency and specificity for IGF-1R in a cell-based assay.

    价 格:¥电议型 号:T6080产 地:中国大陆

  • T6079NVP-ADW742GSK 552602A;ADW;ADW742

    NVP-ADW742 is an IGF-1R inhibitor with IC50 of 0.17 μM, >16-fold more potent against IGF-1R than InsR; little activity to HER2, PDGFR, VEGFR-2, Bcr-Abl and c-Kit.

    价 格:¥电议型 号:T6079产 地:中国大陆

  • T6078SaracatinibAZD0530;塞卡替尼

    Saracatinib (AZD0530) is an effective Src inhibitor (IC50: 2.7 nM), and effective to Lck, Fyn, Lyn, Blk, Fgr and c-Yes.

    价 格:¥电议型 号:T6078产 地:中国大陆

  • T6077ZM-447439ZM 447439

    ZM 447439 is a selective and ATP-competitive inhibitor for Aurora A and Aurora B with IC50 of 110 nM and 130 nM, respectively. It is more than 8-fold selective for Aurora A/B than MEK1, Src, Lck and has little effect against CDK1/2/4, Plk1, Chk1, etc.

    价 格:¥电议型 号:T6077产 地:中国大陆

  • T6076EPZ015666GSK3235025

    EPZ015666 is an orally available inhibitor of PRMT5 enzymatic activity.

    价 格:¥电议型 号:T6076产 地:中国大陆

  • T6075Epothilone B帕妥匹隆;EPO 906;Patupilone

    Epothilone B is a compound isolated from the myxobacterium Sorangium cellulosum. Similar to paclitaxel, patupilone induces microtubule polymerization and stabilizes microtubules against depolymerization conditions. In addition to promoting tubulin polymer

    价 格:¥电议型 号:T6075产 地:中国大陆

  • T6074KPT276KPT-276;KPT 276

    KPT-276 is an orally bioavailable selective inhibitor of nuclear export (SINE) that irreversibly bind to CRM1 and block the function of CRM1.

    价 格:¥电议型 号:T6074产 地:中国大陆

  • T6073OG-L002

    OG-L002 is an effective and selective LSD1 inhibitor (IC50: 20 nM), showing 69- and 36-fold selectivity over MAO-A and MAO-B, respectively.

    价 格:¥电议型 号:T6073产 地:中国大陆

  • T6072LBGT226BGT226 free base;NVP-BGT226

    Bgt226 is a novel dual PI3K / mTOR inhibitor, it acts on PI3K α/β/γ with IC50 of 4 nM / 63 nM / 38 nM, respectively.

    价 格:¥电议型 号:T6072L产 地:中国大陆

  • T6072BGT226 maleateNVP-BGT226 (maleate);NVP-BGT226;BGT226

    BGT226 (NVP-BGT226) is a class I PI3K/mTOR inhibitor for PI3Kα/β/γ (IC50: 4/63/38 nM) .

    价 格:¥电议型 号:T6072产 地:中国大陆

快速导航

在线咨询

提交