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：3861608

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

  • T62130IDO-IN-16；化合物 IDO-IN-16IDO-IN-16

    IDO-IN-16 (compound 5) is an IDO inhibitor (IC50: 36 nM).

    价 格：￥电议型 号：T62130产 地：中国大陆

  • T62127AMPA-IN-1；化合物 AMPA-IN-1AMPA-IN-1

    AMPA-IN-1 is a potent inhibitor of AMPA receptors, a widely expressed receptor in the brain with a central role in the regulation of rapid excitatory synaptic transmission and synaptic plasticity. 14).

    价 格：￥电议型 号：T62127产 地：中国大陆

  • T62114JAK3-IN-12；化合物 JAK3-IN-12JAK3-IN-12

    JAK3-IN-12 (compound 15k) is a potent inhibitor of JAK3 (IC50: 9.5 nM) and can be used in the study of rheumatoid arthritis.

    价 格：￥电议型 号：T62114产 地：中国大陆

  • T62103COX-2/PI3K-IN-1；化合物 COX-2/PI3K-IN-1COX-2/PI3K-IN-1

    COX-2/PI3K-IN-1 (compound 5d) is a potent inhibitor of PI3K (IC50: 1.14 nM). COX-2/PI3K-IN-1 is a selective inhibitor of COX-2 (Ki: 3.24 nM).

    价 格：￥电议型 号：T62103产 地：中国大陆

  • T62099LSD1-IN-13；化合物 LSD1-IN-13LSD1-IN-13

    LSD1-IN-13 (compound 7e) is an orally active LSD1 inhibitor (IC50: 24.43 nM) that also activates CD86 expression (EC50: 470 nM).LSD1-IN-13 induces differentiation of AML (acute myeloid leukaemia) cell lines.

    价 格：￥电议型 号：T62099产 地：中国大陆

  • T62096Dyrk1A/α-synuclein-IN-1；化合物 Dyrk1A/α-synuclein-IN-1Dyrk1A/α-synuclein-IN-1

    Dyrk1A/α-synuclein-IN-1 (Compound b1) is a dual inhibitor of Dyrk1A (IC50: 177 nM) and α-synuclein aggregation (IC50: 10.5 μM). CNS permeability and neuroprotective activity.

    价 格：￥电议型 号：T62096产 地：中国大陆

  • T62095TRK-IN-19；化合物 TRK-IN-19TRK-IN-19

    TRK-IN-19 (Compound I-10 ) is a potent inhibitor of TRK with IC50 values of 1.1 nM for TRKA and 5.3 nM for TRKAG595R. TRK-IN-19 has shown potential research value in cancer disease.

    价 格：￥电议型 号：T62095产 地：中国大陆

  • T62093Trk-IN-11；化合物 Trk-IN-11Trk-IN-11

    Trk-IN-11 (Compound 14h) is a potent inhibitor of TRK, with IC50 values of 1.4 nM for TrkA and 1.8 nM for TrkA G595R. Trk-IN-11 has shown research potential in cancer diseases.

    价 格：￥电议型 号：T62093产 地：中国大陆

  • T62078Akt/NF-κB/JNK-IN-1；化合物 Akt/NF-κB/JNK-IN-1Akt/NF-κB/JNK-IN-1

    Akt/NF-κB/JNK-IN-1 (Compound 2i) is an inhibitor of Akt, NF-κB and JNK signalling pathways.Akt/NF-κB/JNK-IN-1 exhibits an inhibitory effect on nitric oxide production (IC50: 3.15 μM) and shows anti-inflammatory effects.

    价 格：￥电议型 号：T62078产 地：中国大陆

  • T62075HSV-1/HSV-2-IN-1；化合物 HSV-1/HSV-2-IN-1HSV-1/HSV-2-IN-1

    HSV-1/HSV-2-IN-1 is an HSV-1 and HSV-2 inhibitor that acts against HSV-1 (KOS) (EC50: 7.6 μM), HSV-2 (G) (EC50: 7.6 μM), HSV-1 TK-KOS ACVr (EC50: 4 μM) and cowpox virus (EC50: 12 μM).

    价 格：￥电议型 号：T62075产 地：中国大陆

  • T62071VEGFR-2-IN-16；化合物 VEGFR-2-IN-16VEGFR-2-IN-16

    VEGFR-2-IN-16 (Compound 15b) is a potent inhibitor of VEGFR-2 (IC50: 86.36 nM) that exhibits antitumour effects.

    价 格：￥电议型 号：T62071产 地：中国大陆

  • T62058αβ-Tubulin-IN-1；化合物 αβ-Tubulin-IN-1αβ-Tubulin-IN-1

    αβ-Tubulin-IN-1 is a potent and orally active inhibitor of αβ-Tubulin. αβ- Tubulin-IN-1 blocks cell cycle at G2/M phase and induces apoptosis. αβ-Tubulin-IN-1 inhibits tumor cell migration and metastasis. αβ-Tubulin-IN-1 exhibits significant antitumor efficacy.

    价 格：￥电议型 号：T62058产 地：中国大陆

  • T62048Topo I-IN-1；化合物 Topo I-IN-1Topo I-IN-1

    Topo I-IN-1 (Compound 14d) is a potent Topo I inhibitor. Topo I-IN-1 exhibits antitumor activity and DNA intercalative capability. Topo I-IN-1 can induce cell apoptosis.

    价 格：￥电议型 号：T62048产 地：中国大陆

  • T62047pan-HER-IN-1；化合物 pan-HER-IN-1pan-HER-IN-1

    pan-HER-IN-1 (Compound C5) is an irreversible, orally active pan- HER inhibitor. pan-HER-IN-1 exhibits IC 50s of 0.38, 1.6, 2.2 and 3.5 nM for EGFR, HER4, EGFR T790M/L858R and HER2, respectively. pan-HER-IN-1 induces apoptosis and exhibits antitumor activities.

    价 格：￥电议型 号：T62047产 地：中国大陆

  • T62043Dyrk1A/B-IN-1；化合物 Dyrk1A/B-IN-1Dyrk1A/B-IN-1

    Dyrk1A/B-IN-1 (compound 3n) is a potent, selective and cell-permeable inhibitor of DYRK1A and DYRK1B. Dyrk1A/B-IN-1 inhibits DYRK1A and DYRK1B with Kis of 67.8 nM and 237.9 nM, and IC 50 s of 1.1 μM and 0.8 μM, respectively.

    价 格：￥电议型 号：T62043产 地：中国大陆

  • T62030BRD4-BD1-IN-1；化合物 BRD4-BD1-IN-1BRD4-BD1-IN-1

    BRD4-BD1-IN-1 (Compound 9a) is a BRD4-BD1 inhibitor(IC50= 38.20 μM).

    价 格：￥电议型 号：T62030产 地：中国大陆

  • T62026hCAIX-IN-11；化合物 hCAIX-IN-11hCAIX-IN-11

    hCAIX-IN-11 (Compound 5d) is a selective carbonic anhydrase IX and XII inhibitor. hCAIX-IN-11 shows K i s of 32.7 and 623.5 nM for hCA IX and hCA XII, respectively.

    价 格：￥电议型 号：T62026产 地：中国大陆

  • T62015PqsR/LasR-IN-1；化合物 PqsR/LasR-IN-1PqsR/LasR-IN-1

    PqsR/LasR-IN-1 (Compound 2a) is a potent inhibitor of LasR and PqsR systems in P. aeruginosa. PqsR/LasR-IN-1 is also a inhibitor of hERG (IC50= 6.77 μM).

    价 格：￥电议型 号：T62015产 地：中国大陆

  • T62013PI3Kδ-IN-10；化合物 PI3Kδ-IN-10PI3Kδ-IN-10

    PI3Kδ-IN-10 is a highly potent and orally active PI3Kδ inhibitor (IC50= 2 nM). In hepatocellular carcinoma models, PI3Kδ-IN-10 robustly suppresses the downstream AKT pathway to induce subsequent apoptosis.

    价 格：￥电议型 号：T62013产 地：中国大陆

  • T62003SOS1-IN-13；化合物 SOS1-IN-13SOS1-IN-13

    SOS1-IN-13 is a potent inhibitor of son of sevenless homolog 1 (SOS1). SOS1-IN-13 shows IC 50 s of 6.5 nM and 327 nM for SOS1 and pERK, respectively. SOS1-IN-13 has research value in anticancer.

    价 格：￥电议型 号：T62003产 地：中国大陆

160616263646566676869101下一页共101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：3861608

中国彩虹热线

快速导航

返回顶部
在线咨询

提交