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：3649408

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

  • T72868ADAMTS-5-IN-2；化合物 ADAMTS-5-IN-2ADAMTS-5-IN-2

    ADAMTS-5-IN-2 is a potent inhibitor of ADAMTS-5, exhibiting an IC50 of 0.71 ?M, and holds potential for osteoarthritis research.

    价 格：￥电议型 号：T72868产 地：中国大陆

  • T72862PARP-2/1-IN-2化合物 PARP-2/1-IN-2ABT-888对映体

    PARP-2/1-IN-2, an enantiomer of Veliparib, serves as a potent inhibitor of PARP, demonstrating inhibition constants (Kis) of 2 nM for PARP-2 and 5 nM for PARP-1. This compound exhibits a half-maximal effective concentration (EC50) of 3 nM in cell-based assays evaluating PARP activity [1].

    价 格：￥电议型 号：T72862产 地：中国大陆

  • T72828α-Amylase-IN-2；化合物 α-Amylase-IN-2α-Amylase-IN-2

    α-Glucosidase-IN-3, an oxime ester derivative of oleanolic acid (OA), exhibits inhibitory activity against α-glucosidase (IC50 = 1.28 ?M) and α-amylase (IC50 = 3.8 ?M).

    价 格：￥电议型 号：T72828产 地：中国大陆

  • T72759c-Met/HDAC-IN-2；化合物 c-Met/HDAC-IN-2c-Met/HDAC-IN-2

    c-Met/HDAC-IN-2 is a potent dual inhibitor of c-Met and HDAC, exhibiting IC50 values of 5.40 nM for c-Met and 18.49 nM for HDAC1, respectively. It demonstrates antiproliferative effects on various cancer cell lines, induces G2/M-phase arrest, and triggers apoptosis in HCT-116 cells, making it a promising candidate for anti-cancer resistance research.

    价 格：￥电议型 号：T72759产 地：中国大陆

  • T72746(R)-eIF4A3-IN-2；化合物 (R)-eIF4A3-IN-2(R)-eIF4A3-IN-2

    (R)-eIF4A3-IN-2, a less active enantiomer of eIF4A3-IN-2, is a highly selective and noncompetitive inhibitor of the eukaryotic initiation factor 4A-3 (eIF4A3) with an IC50 of 110 nM.

    价 格：￥电议型 号：T72746产 地：中国大陆

  • T72721PD-1/PD-L1-IN-29；化合物 PD-1/PD-L1-IN-29PD-1/PD-L1-IN-29

    PD-1/PD-L1-IN-29 (S4-1) is a potent inhibitor of the PD-1/PD-L1 interaction, with an IC50 value of 6.1 nM. It effectively binds to PD-L1, inhibiting the PD-1/PD-L1 interaction, promotes PD-L1 dimerization and its internalization, enhances localization to the endoplasmic reticulum, and facilitates PD-L1´s entry into the endoplasmic reticulum, demonstrating anticancer activity.

    价 格：￥电议型 号：T72721产 地：中国大陆

  • T72719Tubulin/MMP-IN-2；化合物 Tubulin/MMP-IN-2Tubulin/MMP-IN-2

    Tubulin/MMP-IN-2, a dual inhibitor of tubulin and matrix metalloproteinases (MMPs), effectively inhibits tubulin polymerization and induces cell apoptosis. It demonstrates inhibitory activities against MMP-2, MMP-3, and MMP-9, with IC50 values of 24.95 μM, 31.60 μM, and 22.37 μM, respectively. This compound is utilized in cancer research.

    价 格：￥电议型 号：T72719产 地：中国大陆

  • T72700Cavα2δ1&NET-IN-2；化合物 Cavα2δ1&NET-IN-2Cavα2δ1&NET-IN-2

    Cavα2δ1&NET-IN-2 . Cavα2δ1&NET-IN-2 inhibits Ca v α2δ-1 with a K i of 454 nM. Cavα2δ1&NET-IN-2 inhibits NET with a K i of 59 nM and IC 50 of 7 nM. Cavα2δ1&NET-IN-2 can be used for research of pain [1] .

    价 格：￥电议型 号：T72700产 地：中国大陆

  • T72691PD-1/PD-L1-IN-28；化合物 PD-1/PD-L1-IN-28PD-1/PD-L1-IN-28

    PD-1/PD-L1-IN-28, an inhibitor of the PD-1/PD-L1 signaling pathway (IC 50 = 0.744 ?M), demonstrates promising research potential in tumor immunity. This immune checkpoint inhibitor effectively blocks the interaction within the pathway, offering insights into cancer treatment strategies.

    价 格：￥电议型 号：T72691产 地：中国大陆

  • T72680PD-1/PD-L1-IN-27；化合物 PD-1/PD-L1-IN-27PD-1/PD-L1-IN-27

    PD-1/PD-L1-IN-27 is a potent inhibitor of PD-1/PD-L1, exhibiting an IC50 of 134 nM and demonstrating antitumor effects with minimal T cell cytotoxicity. It activates CD8+ T cells and mitigates T cell exhaustion [1].

    价 格：￥电议型 号：T72680产 地：中国大陆

  • T72675PD-1/PD-L1-IN-23；化合物 PD-1/PD-L1-IN-23PD-1/PD-L1-IN-23

    PD-1/PD-L1-IN-23 is a potent, orally active ester prodrug of L7, a benzooxadiazole derivative, and functions as an inhibitor of PD-1/PD-L1. It has been biologically evaluated for its inhibitory effects on PD-L1, demonstrating significant antitumor effects in both syngeneic tumor models and PD-L1 humanized mice.

    价 格：￥电议型 号：T72675产 地：中国大陆

  • T72668PD-1/PD-L1-IN-26；化合物 PD-1/PD-L1-IN-26PD-1/PD-L1-IN-26

    PD-1/PD-L1-IN-26 (Compound II-14) is a potent PD-1/PD-L1 inhibitor, demonstrating an IC50 of 0.0380 μM. It enhances the immune microenvironment by facilitating CD4+ T cell infiltration into tumor tissues, indicating potential use in cancer research [1].

    价 格：￥电议型 号：T72668产 地：中国大陆

  • T72662NMDAR/TRPM4-IN-2；化合物NMDAR/TRPM4-IN-2NMDAR/TRPM4-IN-2

    NMDAR/TRPM4-IN-2 is a potent interfacial inhibitor of NMDAR/TRPM4 interaction.NMDAR/TRPM4-IN-2 protects against MCAO-induced brain damage and NMDA-induced retinal ganglion cell loss in mice.NMDAR/TRPM4-IN-2 has neuroprotective activity against NMDA-induced hippocampal neuronal cell death and mitochondrial dysfunction. NMDAR/TRPM4-IN-2 showed neuroprotective activity against NMDA-induced cell death and mitochondrial dysfunction in hippocampal neurons with an IC50 value of 2.1 μM.

    价 格：￥电议型 号：T72662产 地：中国大陆

  • T7263SMS2-IN-2；化合物SMS2-IN-2SMS2 inhibitors；SMS2 inhibitors

    SMS2-IN-2 (SMS2 inhibitors) is a potent, selective and orally active sphingomyelin synthase 2 (SMS2) inhibitor, (IC50s of 100 and 56 μM for SMS2 and SMS1, respectively). SMS2-IN-2 has anti-chronic inflammatory activity.

    价 格：￥电议型 号：T7263产 地：中国大陆

  • T72629PfGSK3/PfPK6-IN-2；化合物 PfGSK3/PfPK6-IN-2PfGSK3/PfPK6-IN-2

    PfGSK3/PfPK6-IN-2, an effective dual inhibitor targeting Plasmodium falciparum GSK3/PK6 (PfGSK3/PfPK6), exhibits potent inhibitory activity with IC50 values of 172 nM for PfGSK3 and 11 nM for PfPK6, respectively. This compound is utilized in malaria research.

    价 格：￥电议型 号：T72629产 地：中国大陆

  • T72624Kallikrein 5-IN-2；化合物 Kallikrein 5-IN-2Kallikrein 5-IN-2

    Kallikrein 5-IN-2 is a potent inhibitor of Kallikrein KLK5, exhibiting selectivity with a pIC50 value of 7.1. By inhibiting KLK5, it has the potential to normalize epidermal shedding, thereby reducing associated inflammation and itching.

    价 格：￥电议型 号：T72624产 地：中国大陆

  • T72608VEGFR-2/BRAF-IN-2；化合物 VEGFR-2/BRAF-IN-2VEGFR-2/BRAF-IN-2

    VEGFR-2/BRAF-IN-2, as a dual VEGFR-2 and BRAF kinase inhibitor, exhibits potent IC50 values of 0.111 ?M, 0.089 ?M, and 0.071 ?M against VEGFR-2, BRAF V600E, and BRAF WT, respectively. This compound effectively induces apoptosis and predominantly arrests the cell cycle in the G1 phase.

    价 格：￥电议型 号：T72608产 地：中国大陆

  • T72581SARS-CoV MPro-IN-2；化合物 SARS-CoV MPro-IN-2SARS-CoV MPro-IN-2

    SARS-CoV MPro-IN-2 effectively inhibits the SARS-CoV-2 main protease (M pro), crucial for the virus´s replication and transcription in host cells, with an IC50 value of 72.07 nM. Given its significant role in processing viral polyproteins, M pro is regarded as a key target in drug discovery efforts. Consequently, SARS-CoV MPro-IN-2 holds promise for COVID-19 research.

    价 格：￥电议型 号：T72581产 地：中国大陆

  • T72557Transketolase-IN-2；化合物 Transketolase-IN-2Transketolase-IN-2

    Transketolase-IN-2 is a potent inhibitor of Transketolase, demonstrating significant inhibitory effects on Digitaria sanguinalis and Amaranthus retroflexus, with over 90% inhibition at 200 mg/L and approximately 80% at 100 mg/L. This compound is relevant for research in weed control.

    价 格：￥电议型 号：T72557产 地：中国大陆

  • T72554ARTD10/PARP10-IN-2；化合物 ARTD10/PARP10-IN-2ARTD10/PARP10-IN-2

    ARTD10/PARP10-IN-2 is a potent, non-selective inhibitor of mono-ADP-ribosyltransferases ARTD10/PARP10 and poly(ADP-ribose) polymerase-1 ARTD1/PARP1, exhibiting IC50 values of 2.0 μM and 9.7 μM, respectively.

    价 格：￥电议型 号：T72554产 地：中国大陆

12425262728293031323370下一页共70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：3649408

中国彩虹热线

快速导航

返回顶部
在线咨询

提交