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：3698834

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

  • T6272Fosbretabulin DisodiumFosbretabulin Disodium,CA 4P,Combretastatin A4 disodium phosphate

    Fosbretabulin (Combretastatin A4 Phosphate (CA4P)) Disodium, a water-soluble prodrug of Combretastatin A4 (CA4), is a microtubule-targeting agent that binds β-tubulin (Kd: 0.4 μM). Fosbretabulin Disodium inhibits the polymerization of tubulin (IC50: 2.4 μ

    价 格：￥电议型 号：T6272产 地：美洲

  • T8476RSVA405；化合物RSVA 405RSVA 405；RSVA 405

    RSVA405 is an AMPK activator (EC50 = 1 μM), and is STAT3 inhibitor

    价 格：￥电议型 号：T8476产 地：中国大陆

  • T83847SP-A (196-215) (human) TFA；化合物 SP-A (196-215) (human) TFASurfactant Protein A|||SPA4；Surfactant Prot

    Surfactant protein A (SP-A) (196-215) is a synthetic peptide derived from the C-terminal carbohydrate recognition domain of human SP-A, specifically amino acids 196-215. This peptide suppresses LPS-induced TNF-α release in JAWSII mouse dendritic cells at 1 and 10 ?M concentrations and promotes phagocytosis of P. aeruginosa at a 75 ?M concentration. Furthermore, intratracheal administration of SP-A (196-215) at a dose of 50 ?g per animal reduces disease severity and lung colony-forming units in m

    价 格：￥电议型 号：T83847产 地：中国大陆

  • T833324,27-Dimethyl withaferin A；化合物 4,27-Dimethyl withaferin A4,27-Dimethyl withaferin A

    4,27-Dimethyl withaferin A, a synthetic analog of withanolide natural products, exhibits potential in the study of neurodegenerative diseases[1].

    价 格：￥电议型 号：T83332产 地：中国大陆

  • T833194-epi-Withaferin A；化合物 4-epi-Withaferin A4-epi-Withaferin A

    4-epi-Withaferin A (compound 28), an analogue of Withaferin A, exhibits enhanced cytotoxicity and cytoprotective heat-shock-inducing activity (HSA). It shows promise for the investigation of protein aggregation-associated diseases through the stimulation of cellular defense mechanisms [1].

    价 格：￥电议型 号：T83319产 地：中国大陆

  • T833164-Methyl withaferin A；化合物 4-Methyl withaferin A4-Methyl withaferin A

    4-Methylwithaferin A, a withaferin A analog, exhibits antitumor activity [1].

    价 格：￥电议型 号：T83316产 地：中国大陆

  • T83225A4333；化合物 A4333A4333

    A4333, a biotinylated derivative of A3373, selectively inhibits Phospholipase D1 (PLD1) while sparing PLD2. It is noted for its significant role in antitumor activity [1].

    价 格：￥电议型 号：T83225产 地：中国大陆

  • T81574PAA4；化合物 PAA4PAA4

    PAA4, a methide carbon-centered polynuclear Au(I) cluster, exhibits antiproliferative activity and induces pH2AX expression in a time-dependent manner. It also demonstrates an anti-tumor effect in an orthotopic bladder cancer mouse model [1].

    价 格：￥电议型 号：T81574产 地：中国大陆

  • T81534PDE11A4-IN-1；化合物 PDE11A4-IN-1PDE11A4-IN-1

    PDE11A4-IN-1 (compound 23b) is a potent, selective inhibitor of PDE11A4, demonstrating an IC50 of 12 nM and exhibiting high selectivity against PDE1, PDE2, PDE7, PDE8, and PDE9 [1].

    价 格：￥电议型 号：T81534产 地：中国大陆

  • T81149SMA4；化合物 SMA4SMA4

    SMA4, a selective activator of PKG1α, exhibits a basal EC50 of 29 μM, enhances phosphorylation of the PKG1 substrate VASP, and inhibits proliferation of hPASMCs. It is utilized in cardiovascular disease research [1].

    价 格：￥电议型 号：T81149产 地：中国大陆

  • T79343hCYP3A4-IN-1；化合物 hCYP3A4-IN-1hCYP3A4-IN-1

    hCYP3A4-IN-1 (compound C6) is a potent, orally active inhibitor of hCYP3A4, exhibiting IC50 values of 43.93 nM in human liver microsomes (HLMs) and 153.00 nM in the CHO-3A4 stably transfected cell line. It competitively inhibits the CYP3A4-mediated hydroxylation of N-ethyl-1,8-naphthalimide (NEN) with a Ki of 30.00 nM [1].

    价 格：￥电议型 号：T79343产 地：中国大陆

  • T78808NDNA4；化合物 NDNA4NDNA4

    NDNA4 (compound 17) is a selective Hsp90α inhibitor (IC50: 0.34 μM), characterized by its permanent charge and low membrane permeability. It exhibits minimal cytotoxicity against Ovcar-8 and MCF-10A cell lines (IC50 >100 μM) and maintains hERG channel maturation without eliciting a heat shock response or degrading Hsp90α-dependent client proteins [1].

    价 格：￥电议型 号：T78808产 地：中国大陆

  • T78334Surzebiclimab；化合物 SurzebiclimabBGB-A425；BGB-A425

    Surzebiclimab (BGB-A425), a humanized variant IgG1 monoclonal antibody, targets and binds with high affinity (K D = 0.36 nM) and specificity to the extracellular domain of T-cell immunoglobulin and mucin-domain containing-3 (TIM-3). This compound is utilized in cancer research [1].

    价 格：￥电议型 号：T78334产 地：中国大陆

  • T77698hCYP3A4 Fluorogenic substrate 1；化合物 hCYP3A4 Fluorogenic substrate 1hCYP3A4 Fluorogenic substrate 1

    hCYP3A4 Fluorogenic substrate 1 is a phthalimide derivative and shows low activity against COX.

    价 格：￥电议型 号：T77698产 地：中国大陆

  • T76447[DAla4] Substance P (4-11)；化合物 [DAla4] Substance P (4-11)[DAla4] Substance P (4-11)

    [DAla4] Substance P (4-11), an analog of Substance P (Substance P), effectively inhibits the binding of 125I-Bolton Hunter-conjugated Eledoisin (Eledoisin) and 125I-Bolton Hunter-conjugated Substance P to rat brain cortex membranes, with IC50 values of 0.5 μM and 0.15 μM, respectively [1].

    价 格：￥电议型 号：T76447产 地：中国大陆

  • T75933d[Cha4]-AVP TFA；化合物 d[Cha4]-AVP TFAd[Cha4]-AVP TFA

    d[Cha4]-AVP TFA is a potent and selective agonist for the vasopressin (AVP) V1b receptor, displaying a high affinity with a K i of 1.2 nM. It exhibits greater selectivity for the V1b receptor over the V1a receptor, V2 receptor, and oxytocin receptors, demonstrating its specificity in targeting the human V1b receptor [1] [2].

    价 格：￥电议型 号：T75933产 地：中国大陆

  • T72900Indolokine A4；化合物 Indolokine A4Indolokine A4

    Indolokine A4, a catabolite of indole-3-pyruvate (I3P), is a potent AhR agonist [1] .

    价 格：￥电议型 号：T72900产 地：中国大陆

  • T71854AA43279；化合物 AA43279AA43279

    AA43279 is a novel selective Nav1.1 activator, increasing the firing activity of parvalbumin-expressing, fast-spiking GABAergic interneurons and increasing the spontaneous inhibitory post-synaptic currents (sIPSCs) recorded from pyramidal neurons.

    价 格：￥电议型 号：T71854产 地：中国大陆

  • T69933VA4 TG2 inhibitor；化合物 VA4 TG2 inhibitorVA4 TG2 inhibitor

    VA4 is a novel irreversible TG2 transamidase site-specific inhibitor.

    价 格：￥电议型 号：T69933产 地：中国大陆

  • T68316GAC0003A4；化合物 GAC0001E5GAC0001E5；GAC0001E5

    GAC0003A4 is a potent LXR inverse agonist with antitumor activity that inhibits the transcription of LXR proteins.GAC0003A4 degrades LXRβ proteins and inhibits the proliferation of PDAC cells in a dose-dependent manner.GAC0003A4 has been used in the study of advanced pancreatic cancers and other recalcitrant malignancies.

    价 格：￥电议型 号：T68316产 地：中国大陆

1234567下一页共7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：3698834

中国彩虹热线

快速导航

返回顶部
在线咨询

提交