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：3853216

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

  • T16078Mirk-IN-1化合物 T16078Dyrk1B/A-IN-1

    Mirk-IN-1 is an effective inhibitor of Dyrk1B(Mirk kianse) and Dyrk1A (IC50: 68±48 nM and 22±8 nM respectively).

    价 格：￥电议型 号：T16078产 地：中国大陆

  • T16018MB-07811；化合物MB-07811VK-2809；VK-2809

    MB-07811 (VK-2809) is an orally active HepDirect prodrug of MB07344 with cholesterol and triglycerides lowering activity. MB-07811 is an agonist of liver-targeted THR-β.

    价 格：￥电议型 号：T16018产 地：中国大陆

  • T15978Mal-PEG2-acid；化合物 T15978Mal-PEG2-acid

    Mal-PEG2-acid is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Mal-PEG2-acid can be conjugated to Tubulysin and its derivative cytotoxic molecule[1].

    价 格：￥电议型 号：T15978产 地：中国大陆

  • T15878m-PEG4-CH2COOH；化合物 T15878m-PEG4-CH2COOH

    m-PEG4-CH2COOH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

    价 格：￥电议型 号：T15878产 地：中国大陆

  • T15825LY 178002；化合物 T15825LY 178002

    LY 178002 is an effective inhibitor of 5-lipoxygenase (5-LPO), phospholipase A2 (IC50: 0.6 μM for 5-lipoxygenase). LY 178002 also inhibits cellular production of LTB4 by human polymorphonuclear leukocytes and displays relatively weak inhibition on cyclooxygenase.

    价 格：￥电议型 号：T15825产 地：中国大陆

  • T15789LTURM34；化合物LTURM34LTURM34

    LTURM34 is an inhibitor of DNA-PK with IC50 of 34 nM. LTURM34 displays effective antiproliferative activity in a wide range of tumor cell lines. LTURM34 shows 170-fold selectivity for DNA-PK over PI3K .

    价 格：￥电议型 号：T15789产 地：中国大陆

  • T15788LSZ-102；化合物LSZ-102LSZ102；LSZ102

    LSZ-102 is an effective and selective degrader of estrogen receptor (IC50 = 0.2 nM) and can be used in studies about ERα positive breast cancer.

    价 格：￥电议型 号：T15788产 地：中国大陆

  • T15787LRE1；化合物LRE1LRE1

    LRE1 is a specific and allosteric soluble adenylyl cyclase inhibitor.

    价 格：￥电议型 号：T15787产 地：中国大陆

  • T15786LPA2 antagonist 1；化合物 T15786LPA2 antagonist 1

    LPA2 antagonist 1 is an LPA2 antagonist (IC50: 17 nM).

    价 格：￥电议型 号：T15786产 地：中国大陆

  • T15785LPA1 receptor antagonist 1；LPA1受体拮抗剂1LPA1 R antagonist 1；LPA1 R antagonist 1

    LPA1 receptor antagonist 1(LPA1 R antagonist 1) is a selective and potent lysophosphatidic acid (LPA1) receptor antagonist (IC50 : 25 nM) for the study of idiopathic pulmonary fibrosis.

    价 格：￥电议型 号：T15785产 地：中国大陆

  • T15784LP99；化合物LP99LP99

    LP99 is an epigenetic probe. LP99 disrupts the binding of BRD7 and BRD9 to chromatin in cells. LP99 is an effective and selective inhibitor of the BRD7 and BRD9 bromodomains (Kd: 99 nM against BRD9).

    价 格：￥电议型 号：T15784产 地：中国大陆

  • T15783LP117；化合物 T15783LP117

    LP117 is a novel and effective inhibitor of 5-Lipoxygenase (5-LO) product synthesis (IC50: 1.1 μM).

    价 格：￥电议型 号：T15783产 地：中国大陆

  • T15782Lp-PLA2-IN-1；化合物Lp-PLA2 -IN-1Lp-PLA2 inhibitor 1|||Lp-PLA2 -IN-1；Lp-PLA2 inhibitor 1|||Lp-PLA2 -IN-1

    Lp-PLA2-IN-1 (Lp-PLA2 inhibitor 1) suppresses Lp-PLA2 activity processes for their preparation. Lp-PLA2-IN-1 (Lp-PLA2 inhibitor 1) also inhibits to compositions containing them and to their use in the treatment of diseases associated with the activity of Lp-PLA2, for example, atherosclerosis, Alzheimer´s disease.

    价 格：￥电议型 号：T15782产 地：中国大陆

  • T15781LP-935509；化合物LP-935509LP-935509

    LP-935509 is highly brain-penetrant and reverses fully established pain behavior following the SNL procedure. LP-935509 is an effective inhibitor of BIKE (IC50=14 nM) and a modest inhibitor of cyclin G-associated kinase(GAK, IC50=320 nM). LP-935509 is also a ATP-competitive inhibitor of adapter protein-2 associated kinase 1 (AAK1) (IC50 = 3.3 nM, Ki = 0.9 nM).

    价 格：￥电议型 号：T15781产 地：中国大陆

  • T15780LP-922761；化合物LP-922761LP-922761

    LP-922761 is a potent, selective, and orally active AAK1 inhibitor with inhibitory effects on BMP-2 induced protein kinase (BIKE).

    价 格：￥电议型 号：T15780产 地：中国大陆

  • T1578Pargyline hydrochloride优降宁盐酸盐优降宁盐酸盐|||Pargylamine hydrochloride

    Pargyline hydrochloride (Pargylamine hydrochloride) is an irreversible monoamine oxidase(MAO) inhibitor with antihypertensive properties.

    价 格：￥电议型 号：T1578产 地：中国大陆

  • T15778LP-533401化合物 T15778LP533401|||LP 533401

    LP-533401 is an inhibitor of Tryptophan hydroxylase 1. It is used for regulates serotonin production in the gut.

    价 格：￥电议型 号：T15778产 地：中国大陆

  • T15759Lintitript；林替曲特SR 27897；SR 27897|||林替曲特

    Lintitript (SR 27897) is a selective antagonist of CCK1 with EC50s of 6 nM and 200 nM for CCK1 and CCK2. The Ki value is 0.2 nM for CCK1.

    价 格：￥电议型 号：T15759产 地：中国大陆

  • T15678KZR-504；化合物 T15678KZR-504

    KZR-504 is a selective inhibitor of immunoproteasome low molecular mass polypeptide 2 (LMP2) (IC50s: 51 nM, 4.274 μM for LMP2 and LMP7, respectively).

    价 格：￥电议型 号：T15678产 地：中国大陆

  • T15624JNJ-64619178；化合物JNJ-64619178JNJ-64619178

    JNJ-64619178 is a selective, orally active, and pseudo-irreversible inhibitor of protein arginine methyltransferase 5 (IC50: 0.14 nM). It has effective activity In lung cancer.

    价 格：￥电议型 号：T15624产 地：中国大陆

1195196197198199200201202203204215下一页共215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：3853216

中国彩虹热线

快速导航

返回顶部
在线咨询

提交