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：3795025

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

  • T62304Minzasolmin；化合物Minzasolmin(R)-NPT200-11|||UCB0599|||DLX-313；(R)-NPT200-11|||UCB0599|||DLX-313

    Minzasolmin(DLX-313) is an alpha-synuclein misfolding inhibitor for the study of Parkinson´s disease.

    价 格：￥电议型 号：T62304产 地：中国大陆

  • T60976Bezuclastinib；化合物BezuclastinibCGT9486|||PLX 9486；CGT9486|||PLX 9486

    Bezuclastinib (CGT9486) is a novel, potent and highly selective tyrosine kinase and c-kit D816V inhibitor for the study of advanced mastocytosis.

    价 格：￥电议型 号：T60976产 地：中国大陆

  • T6044Telotristat Etiprate；特罗司他马尿酸盐LX1606 (Hippurate)|||LX 1606 Hippurate；LX1606 (Hippurate)|||LX 1606 Hip

    Telotristat Etiprate (LX 1606 Hippurate) is an orally bioavailable, tryptophan hydroxylase (TPH) inhibitor with potential antiserotonergic activity.

    价 格：￥电议型 号：T6044产 地：中国大陆

  • T5600Darovasertib；化合物LXS196LXS196；LXS196

    Darovasertib (LXS196) is a potent, selective and orally active protein kinase C (PKC) inhibitor(IC50 values of 1.9 nM, 0.4 nM and 3.1 μM for PKCα, PKCθ and GSK3β, respectively).

    价 格：￥电议型 号：T5600产 地：中国大陆

  • T5317LCridanimod sodium；化合物 T5317LXBIO-101|||XBIO 101|||Cycloferon|||Sodium Cridanimod|||Cridanimod Na|||X

    Cridanimod can increase progesterone receptor (PR) expression, with potential antineoplastic adjuvant activity. Cridanimod is able to induce the expression of PR in endometrial cancer. In combination with a progestin, cancer cells could be eradicated through increased PR-mediated signaling, leading to an inhibition of luteinizing hormone release from the pituitary gland, via a negative feedback mechanism, and, eventually, an inhibition of estrogen released from the ovaries.

    价 格：￥电议型 号：T5317L产 地：中国大陆

  • T4973Paraxanthine1,7-二甲基黄嘌呤1,7-二甲基黄嘌呤|||1,7-DIMETHYLXANTHINE

    Paraxanthine (1,7-dimethylxanthine) is a metabolite of caffeine (sc-202514) which functions as an adenosine receptor ligand and a PARP-1 inhibitor in pulmonary epithelial cells. Studies suggest that Paraxanthine is structurally similar to caffeine and possibly mediates the physiological effects of caffeine. Also Paraxanthine acts as a competitive phosphodiesterase inhibitor, which increases intracellular cAMP, activates PKA, inhibits TNF-α and leukotriene synthesis. In addition, Paraxanthine act

    价 格：￥电议型 号：T4973产 地：中国大陆

  • T47001,3,5-Trihydroxy-4-prenylxanthone；化合物 T47001,3,5-Trihydroxy-4-prenylxanthone

    1,3,5-Trihydroxy-4-prenylxanthone is a relatively potent inhibitor of phosphodiesterase type 5 (PDE5), with an IC50 value of 3.0 μM; it shows in vitro inhibitory activity against acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), with IC50 values of 56.3plusmn;0.4 and 46.0plusmn;0.3 M, respectively. 1,3,5-Trihydroxy-4-prenylxanthone inhibits LPS-induced NF-κB and AP-1 activations by interfering with the posttranslational modification (phosphorylation and/or ubiquitinylation) of IRAK-1

    价 格：￥电议型 号：T4700产 地：中国大陆

  • T4398LX2343；化合物LX2343LX2343

    LX2343 is a BACE1 enzyme inhibitor with an IC50 value of 11.43±0.36 μM. LX2343 acts as a non-ATP competitive PI3K inhibitor with an IC50 of 15.99±3.23 μM. LX2343 stimulates autophagy in its promotion of Aβ clearance.

    价 格：￥电议型 号：T4398产 地：中国大陆

  • T4067VLX1570；化合物VLX1570VLX1570

    VLX1570 is a competitive inhibitor of proteasome DUB activity with IC50 ranging from 4.2 uM to 8.6 uM. It has potent inhibition for USP14.

    价 格：￥电议型 号：T4067产 地：中国大陆

  • T39740Acoramidis hydrochloride；盐酸橡酰胺AG10 hydrochloride|||Alxn2060 hydrochloride；AG10 hydrochloride|||Alxn2

    Acoramidis hydrochloride (Alxn2060 hydrochloride) is an orally active and selective kinetic stabilizer of WT and V122I- TTR (transthyretin) . Acoramidis hydrochloride is used in the study for transthyretin amyloidosis.

    价 格：￥电议型 号：T39740产 地：中国大陆

  • T39555Belumosudil mesylateBelumosudil mesylateSLx-2119mesylate|||KD025 mesylate

    Belumosudil mesylate (KD025 mesylate) is a compound that selectively inhibits ROCK2, demonstrating IC50 values of 105 nM for ROCK2 and 24 μM for ROCK1. It possesses anti-fibrotic properties.

    价 格：￥电议型 号：T39555产 地：中国大陆

  • T39493VemircopanVemircopanACH0145228|||ACH-5228|||ALXN2050

    Vemircopan is a complement factor D inhibitor.

    价 格：￥电议型 号：T39493产 地：中国大陆

  • T39214LLXE408 fumarate；化合物LXE408 fumarateLXE408 fumarate (1799330-15-6 Free base)；LXE408 fumarate (1799330-

    LXE408 fumarate is an orally active, non-competitive and kinetoplastid-selective?proteasome?inhibitor. LXE408 fumarate has an?IC50?of 0.04 μM for?L. donovani?proteasome and an?EC50?of 0.04 μM for?L. donovani. LXE408 fumarate has a low propensity to cross the blood brain barrier. LXE408 fumarate has the potential for visceral leishmaniasis (VL) research.

    价 格：￥电议型 号：T39214L产 地：中国大陆

  • T39194PLX647 dihydrochloride；PLX647 dihydrochloridePLX647 dihydrochloride

    PLX647 dihydrochloride is a potent and selective dual inhibitor of FMS and KIT kinases, with IC50 values of 28 nM and 16 nM, respectively. At a concentration of 1 μM, PLX647 dihydrochloride demonstrates superior selectivity against a wide range of 400 kinases, except FLT3 and KDR, where IC50 values are 91 nM and 130 nM, respectively. This orally active compound holds great potential for targeted kinase inhibition.

    价 格：￥电议型 号：T39194产 地：中国大陆

  • T38495Gypenoside LXXV；绞股蓝皂苷LXXVGypenoside LXXV

    Gypenoside LXXV, derived from Gynostemma pentaphyllum, is a deglycosylated form of ginsenoside Rb1. This compound effectively decreases cancer cell viability and exhibits potent anti-cancer properties.

    价 格：￥电议型 号：T38495产 地：中国大陆

  • T37273BLX3887；BLX3887BLX3887

    BLX3887 is an inhibitor of 15-lipoxygenase type 1 (15-LO-1; IC50 = 32 nM in a cell-free enzyme assay).1 It is selective for 15-LO-1 over 15-LO-2, which it does not inhibit, 5-LO (IC50 = 472 nM), and 12-LO (IC50 = 3,310 nM). BLX3887 inhibits the production of 15-LO metabolites selectively in eosinophils over neutrophils when used at a concentration of 10 μM. It also inhibits endocytosis in, and the migration of, isolated human peripheral blood mononuclear cell-derived dendritic cells in vitro.

    价 格：￥电议型 号：T37273产 地：中国大陆

  • T36404LPRLX-93936 HCL；化合物 PRLX-93936 hclPRLX-93936 hcl(903499-49-0 Free base)；PRLX-93936 hcl(903499-49-0 Fr

    PRLX-93936 HCL is an analog of erastin and demonstrated synergistic effects against non-small cell lung cancer (NSCLC) cells with cisplatin.

    价 格：￥电议型 号：T36404L产 地：中国大陆

  • T36404PRLX-93936；PRLX-93936PRLX-93936

    PRLX-93936 is an analog of erastin that has antitumor activity. It inhibits the hypoxia-inducible factor 1 (HIF-1) signaling pathway under hypoxic conditions (IC50 = 0.09 μM in a cell-based reporter assay). PRLX-93936 (1 μM) also inhibits hypoxia-induced increases in HIF-1α expression in ME-180 cervical cancer cells. It inhibits the growth of HT-1080 fibrosarcoma, OVCAR-5 ovarian cancer, BJELR tumorigenic primary fibroblast, and PANC-1 pancreatic cancer cells with IC50 values of less than 100 nM

    价 格：￥电议型 号：T36404产 地：中国大陆

  • T36275xStAx-VHLL；xStAx-VHLLxStAx-VHLL

    Selective peptide-based β-catenin Degrader. Comprises a β-catenin-targeted stapled peptide, xStAx, linked to a VHL-binding peptide. Reduces β-catenin levels in HEK293T cells and colorectal cancer cell lines. Selectively degrades β-catenin over other Wnt signaling pathway components. Inhibits tumor growth in APCmin/+ mice, with constitutively active Wnt signaling, and reduces survival of patient-derived colorectal cancer cell organoids.

    价 格：￥电议型 号：T36275产 地：中国大陆

  • T36052Lipoxin A4 methyl ester；Lipoxin A4 methyl esterLXA4 methyl ester；LXA4 methyl ester

    Lipoxin A4 methyl ester (LXA4 methyl ester) is a more lipid soluble, prodrug formulation of the transcellular metabolite LXA4. LXA4 is a trihydroxy fatty acid containing a conjugated tetraene, produced by the metabolism of 15-HETE or 15-HpETE with human leukocytes.[1] LXA4 is equipotent to leukotriene B4 (LTB4) in inducing superoxide generation in human neutrophils at 0.1 μM.[2] LXA4 is associated with several other biological functions including leukocyte activation, chemotaxis effects, natural

    价 格：￥电议型 号：T36052产 地：中国大陆

12345678910下一页共10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：3795025

中国彩虹热线

快速导航

返回顶部
在线咨询

提交