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：3705055

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

  • T2701GSK1292263

    GSK1292263 is a GPR119 agonist and has been investigated for the treatment of DIABETES MELLITUS, TYPE 2.

    价 格：￥电议型 号：T2701产 地：中国大陆

  • T2601Vidofludimus4sc-101；SC12267

    Vidofludimus (4SC-101, SC12267) is a novel small molecule inhibitor of dihydroorotate dehydrogenase (DHODH).

    价 格：￥电议型 号：T2601产 地：中国大陆

  • T22698TLR3-IN-1CU CPT 4a

    CU CPT 4a is a selective TLR3 inhibitor (IC50: 3.44 μM in RAW 264.7 cells). It can inhibit TLR3/dsRNA complex-mediated downstream signaling pathways and inhibit the production of TNF-α and IL-1β in whole cells.

    价 格：￥电议型 号：T22698产 地：中国大陆

  • T22697CS 21001-[[4-Ethyl-5-[5-(4-phenoxyphenyl)-1,2,4-oxadiazol-3-yl]-2-thienyl]methyl]-3-azetidinecarboxy

    CS 2100 is an S1P1 agonist.

    价 格：￥电议型 号：T22697产 地：中国大陆

  • T22694CRANAD 2

    CRANAD-2 is a difluoroboron-derivatized curcumins as near-infrared probe for in vivo detection of amyloid-beta deposits. Upon interacting with Abeta aggregates, CRANAD-2 undergoes a range of changes, which include a 70-fold fluorescence intensity increase

    价 格：￥电议型 号：T22694产 地：中国大陆

  • T2269Pirinixic Acid匹立尼酸；Wy-14643；NSC 310038

    Pirinixic Acid is a synthetic thiacetic acid derivative used in biomedical research, carcinogenic Pirinixic acid is a peroxisome proliferator that activates specific peroxisome proliferator-activated receptors (PPAR).

    价 格：￥电议型 号：T2269产 地：中国大陆

  • T22689CP94253 hydrochlorideCP 94253 hydrochloride

    CP94253 hydrochloride is a potent, selective and centrally active agonist of 5-HT1B receptor with Ki of 2 nM. The Kis are 89, 49, 860, and 1600 nM for 5-HT1A, 5-HT1D, 5-HT1C and 5-HT2 receptors, respectively.

    价 格：￥电议型 号：T22689产 地：中国大陆

  • T2268VER49009VER 49009；CCT0129397；VER-49009

    VER-49009 is an effective HSP90 inhibitor(IC50 =25 nM, Kd=78 nM).

    价 格：￥电议型 号：T2268产 地：中国大陆

  • T226783,5-Bis(4-nitrophenoxy)benzoic acid3,5-二(4-硝基苯氧基)苯甲酸；Compound W

    The compound is an inhibitor of γ-secretase. It also causes a decrease in the released levels of Aβ42 and notch-1 Aβ-like peptide 25 (Nβ25).

    价 格：￥电议型 号：T22678产 地：中国大陆

  • T22677Cobimetinib racemateCobimetinib (racemate)；考比替尼 (外消旋体)

    Cobimetinib racemate (GDC-0973 racemate) is a selective inhibitor of MEK.Cobimetinib racemate is also known as a mitogen-activated protein kinase, is a key component of the RAS/RAF/MEK/ERK pathway.

    价 格：￥电议型 号：T22677产 地：中国大陆

  • T22675Co 102862V 102862

    Co 102862 is a voltage-gated sodium channel blocker. Co 102862 can be used for anticonvulsant studies.

    价 格：￥电议型 号：T22675产 地：中国大陆

  • T22674Co 101244 hydrochloride4-Piperidinol, 1-[2-(4-hydroxyphenoxy)ethyl]-4-[(4-Methylphenyl)Methyl]-,hydr

    Co 101244 hydrochloride is an NR2B-containing NMDA receptor antagonist.

    价 格：￥电议型 号：T22674产 地：中国大陆

  • T2267BQU57

    BQU57 shows selective inhibition for Ral relative to Ras or Rho and inhibit xenograft tumor growth.

    价 格：￥电议型 号：T2267产 地：中国大陆

  • T22665PD 128042CI 976

    CI 976 is a potent orally active and selective ACAT inhibitor(IC50: 73 nM) and a potent lysophospholipid acyltransferase(LPAT) inhibitor. CI 976 inhibits Golgi-associated LPAT activity (IC50: 15 μM) and multiple membrane trafficking steps.

    价 格：￥电议型 号：T22665产 地：中国大陆

  • T22661CHM-1CHM 1

    CHM-1 is an inducer of apoptosis, and displays potent antitumor ability in human hepatocellular carcinoma by activation of Cdc2 kinase activity. CHM-1 inhibits tubulin polymerization in vitro and in vivo.

    价 格：￥电议型 号：T22661产 地：中国大陆

  • T2266SantacruzaMate ACAY-10683

    Santacruzamate A (CAY10683) is a potent and selective HDAC inhibitor.

    价 格：￥电议型 号：T2266产 地：中国大陆

  • T22654Selfotel塞福太；CGS 19755；LY-272541

    CGS 19755 is a selective, competitive NMDA antagonist that inhibits [3H]-3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid binding to NMDA-type receptors with IC50 of 50 nM.

    价 格：￥电议型 号：T22654产 地：中国大陆

  • T2265BimiralisibPQR309；PI3K-IN-2；5-(4,6-dimorpholino-1,3,5-triazin-2-yl)-4-(trifluoromethyl)pyridin-2-ami

    PI3K-IN-2 is an orally bioavailable pan inhibitor of PI3K and inhibitor of the mTOR, with potential antineoplastic activity. PI3K-IN-2 inhibits the PI3K kinase isoforms alpha, beta, gamma and delta and, to a lesser extent, mTOR kinase, which may result in

    价 格：￥电议型 号：T2265产 地：中国大陆

  • T22641CDPPB

    CDPPB is a modulator of mGluR5 positive allosteric(with an EC50 of 27 nM in Chinese hamster ovary cells expressing human mGluR5).

    价 格：￥电议型 号：T22641产 地：中国大陆

  • T2262ItanapracedCHF5074；CSP-1103

    CHF5074, a γ-secretase modulator, reduces Aβ42/40 secretion (IC50: 3.6/18.4 μM).

    价 格：￥电议型 号：T2262产 地：中国大陆

1234567891021下一页共21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：3705055

中国彩虹热线

快速导航

返回顶部
在线咨询

提交