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  • T6352(-)-Dizocilpine maleate(-)-MK 801 (Maleate)；C13737；(-)-MK 801 Maleate；(-)-MK 801马来酸

    MK-801 is a potent, selective and non-competitive NMDA receptor antagonist with Kd of 37.2 nM in rat brain membranes.

    价 格：￥电议型 号：T6352产 地：中国大陆

  • T6351MGCD-265 analogGlesatinib；MGCD-265

    MGCD-265-analog (structurally related to MGCD-265) is an orally bioavailable multitargeted tyrosine kinase inhibitor with potential antineoplastic activity with IC50 of 29 nM and 10 nM for c-Met and VEGFR2, respectively.

    价 格：￥电议型 号：T6351产 地：中国大陆

  • T6350CHIR-124CHIR 124；CHIR124

    CHIR-124 is an effective Chk1 inhibitor (IC50: 0.3 nM). It has 2, 000-fold selectivity against Chk2, 500- to 5, 000-fold less activity against Cdc2 and CDK2/4.

    价 格：￥电议型 号：T6350产 地：中国大陆

  • T5635CH7057288

    CH7057288 is an effective and selective TRK inhibitor with an IC50 value of 1.1 nM, 7.8 nM and 5.1 nM for TRKA, TRKB and TRKC, respectively.

    价 格：￥电议型 号：T5635产 地：中国大陆

  • T5392TP0463518

    TP-0463518 is a highly potent HIF prolyl hydroxylase (PHD) inhibitor (IC50s: 13 nM and 18 nM for human and rat PHD2, respectively).

    价 格：￥电议型 号：T5392产 地：中国大陆

  • T4635RalinepagAPD811

    Ralinepag is a potent, orally bioavailable and non-prostanoid prostacyclin (IP) receptor agonist, with EC50s of 8.5 nM, 530 nM and 850 nM for human and rat IP receptor and human DP1 receptor, respectively.

    价 格：￥电议型 号：T4635产 地：中国大陆

  • T4265AZD4635HTL1071

    AZD4635 is a new-type adenosine 2A receptor (A2AR) inhibitor(Ki=1.7 nM).

    价 格：￥电议型 号：T4265产 地：中国大陆

  • T39635Obafistat

    Obafistat is a potent aldo-keto reductase AKR1C3 inhibitor with an IC 50 of 1.2 nM for human AKR1C3 (patent WO2017202817A1, example 4) [1] .

    价 格：￥电议型 号：T39635产 地：中国大陆

  • T3635IQ 1IQ-1；IQ1

    Maintains embryonic stem cell (ESC) pluripotency in Wnt3a-treated cells; enables Wnt/β-catenin-driven expansion of mouse ESCs and prevents spontaneous differentiation. Upregulates expression of Oct4 and Sox2 transcription factors. Binds to serine/threonin

    价 格：￥电议型 号：T3635产 地：中国大陆

  • T3119JNJ-63533054JNJ63533054；JNJ 63533054

    JNJ-63533054 is a potent and selective agonist of hGPR139 with an EC50 = 16 nM.

    价 格：￥电议型 号：T3119产 地：中国大陆

  • T2S16353-Isomangostin

    3-Isomangostin is an acetylcholinesterase selective inhibitor and a potent human aldose reductase inhibitor with an IC50 of 3.48 uM. 3-Isomangostin has free radical scavenging activity and inhibits MutT homolog 1 (MTH1) with an IC50 of 52 nM. It shows ant

    价 格：￥电议型 号：T2S1635产 地：中国大陆

  • T28804Slingshot inhibitor D3JHN76359

    Slingshot inhibitor D3 is a potent inhibitor of the Protein Phosphatase Slingshot.

    价 格：￥电议型 号：T28804产 地：中国大陆

  • T27635IsoxepacOlopatadine USP Related Compound C

    Isoxepac is a non-steroidal anti-antiphlogistic agent and analgesic.

    价 格：￥电议型 号：T27635产 地：中国大陆

  • T26357Pitstop 2

    Pitstop 2 is a inhibitor of clathrin, and inhibits clathrin-mediated endocytosis (CME) by associating with the terminal domain of clathrin. It has the potential for anti-cancer research.

    价 格：￥电议型 号：T26357产 地：中国大陆

  • T2631WAY-100635 Maleate

    WAY-100635 is a specific and effective 5-HT receptor antagonist (IC50=0.95 nM).

    价 格：￥电议型 号：T2631产 地：中国大陆

  • T25635LateritinBassiatin

    Lateritin is An Acyl-CoA:cholesterol acyltransferase (ACAT) inhibitor and a platelet aggregation inhibitor from the mycelial cake of Gibberella lateritium. Bassiatin is the (3S,6R) isomer.

    价 格：￥电议型 号：T25635产 地：中国大陆

  • T2514LinifanibRG3635；ABT-869；AL-39324

    Linifanib (ABT-869) is a novel, potent ATP-competitive VEGFR/PDGFR inhibitor for KDR (IC50: 4 nM), CSF-1R (IC50: 3 nM), Flt-1/3 (IC50: 3/4 nM) and PDGFRβ (IC50: 66 nM). Linifanib may exhibit potent antiproliferative and apoptotic effects on tumor cells wh

    价 格：￥电议型 号：T2514产 地：中国大陆

  • T21635PD184161

    PD184161 is a novel, orally-active MEK inhibitor. PD184161 inhibited MEK activity (IC50 = 10-100 nM) in a time- and concentration-dependent manner[1].

    价 格：￥电议型 号：T21635产 地：中国大陆

  • T16359NU6140

    NU6140 is a selective inhibitor of CDK2-cyclin A (IC50, 0.41 μM). It shows 10- to 36-fold selectivity over other CDKs. NU6140 also effectively inhibits Aurora A and Aurora B (IC50s: 67 and 35 nM, respectively). It also enhances the apoptotic effect and ha

    价 格：￥电议型 号：T16359产 地：中国大陆

  • T16355NSC781406

    NSC781406 is a highly effective inhibitor of PI3K and mTOR (IC50: 2 nM for PI3Kα).

    价 格：￥电议型 号：T16355产 地：中国大陆

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