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  • T12405PentiapinePentiapine,CGS 10746,

    Pentiapine is a novel inhibitor of dopamine release.

    价 格：￥电议型 号：T12405产 地：美洲

  • T12519Sodium metatungstateSodium metatungstate,Sodium polyoxotungstate,POM-1

    Sodium metatungstate is a potent inhibitor of ecto-nucleoside triphosphate diphosphohydrolase (NTPDase)(Ki values of 2.58 μM, 3.26 μM, and 28.8 μM for NTPDase 1, NTPDase 3 and NTPDase 2 respectively).

    价 格：￥电议型 号：T12519产 地：美洲

  • T12571PSI-6206 13CD3PSI-6206 13CD3,RO-2433 13CD3,GS-331007 13CD3

    PSI-6206 13CD3 is the deuterium labeled PSI-6206. PSI-6206 is a potent and selective HCV NS5B polymerase inhibitor.

    价 格：￥电议型 号：T12571产 地：美洲

  • T12962Sofosbuvir impurity GSofosbuvir impurity G

    Sofosbuvir impurity G is a diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.

    价 格：￥电议型 号：T12962产 地：美洲

  • T13086I-BET762 carboxylic acidI-BET762 carboxylic acid,Molibresib carboxylic acid,GSK525762A carboxylic ac

    I-BET762 carboxylic acid is an inhibitor of BRD4(pIC50 of 5.1).

    价 格：￥电议型 号：T13086产 地：美洲

  • T13715LGSK9311GSK9311

    GSK9311 inhibits BRPF bromodomain (pIC50: 6.0 and 4.3 for BRPF1 and BRPF2, respectively). GSK9311 is a less active analogue of GSK6853. It can be used as negative control.

    价 格：￥电议型 号：T13715L产 地：美洲

  • T13727Huangjiangsu AHuangjiangsu A

    ?Huangjiangsu A has hepatoprotective potential against H2O2-induced cytotoxicity and ROS generation and could be promising as potential therapeutic agents for liver diseases.?Huangjiangsu A, pseudoprotodioscin, methyl protobioside, protodioscin, and proto

    价 格：￥电议型 号：T13727产 地：美洲

  • T14525BegacestatBegacestat,GSI-953,

    Begacestat (GSI-953) is an amyloid precursor protein gamma-secretase (IC50Aβ40=15 nM) inhibitor. Which is used for treatment of Alzheimer´s disease.

    价 格：￥电议型 号：T14525产 地：美洲

  • T14774Bragsin1Bragsin1

    Bragsin1 is a potent, selective and noncompetitive inhibitor of the ArfGEF BRAG2. Which inhibits Arf GTPase activation, with an IC50 of 3 μM. Bragsin1 has no effect on the Sec7 domain of human ArfGEFs. Anti-cancer activity[1]. Bragsin1 binds to PH domain

    价 格：￥电议型 号：T14774产 地：美洲

  • T1486Oseltamivir phosphateOseltamivir phosphate,GS 4104,

    Oseltamivir Phosphate is the phosphate salt of oseltamivir, a synthetic derivative prodrug of ethyl ester with antiviral activity. By blocking neuraminidases on the surfaces of influenza viruses, oseltamivir interferes with host cell release of complete v

    价 格：￥电议型 号：T1486产 地：美洲

  • T14944CGS 15943CGS 15943

    CGS 15943 is an orally bioavailable non-xanthine antagonist of Adenosine Receptor. In transfected CHO cells, its Ki for human A1, A2A, A2B, and A3 Adenosine Receptors are 3.5, 4.2, 16, and 50 nM , respectively.

    价 格：￥电议型 号：T14944产 地：美洲

  • T15207Eleclazine hydrochlorideEleclazine hydrochloride,GS 6615 hydrochloride,

    Eleclazine hydrochloride is a novel inhibitorof late Na+ current (IC50: 0.7 uM).

    价 格：￥电议型 号：T15207产 地：美洲

  • T15418GS-6201GS-6201,CVT-6883,

    GS-6201 is a selective antagonist of adenosine A2B receptor. GS-6201 shows high affinity and selectivity for the human adenosine A2B receptors (Ki=22 nM). GS-62013 attenuates the airway reactivity induced by NECA, AMP, or allergen in sensitized mice. GS-6

    价 格：￥电议型 号：T15418产 地：美洲

  • T15422GSK-626616GSK-626616

    GSK-626616 is a potent and orally bioavailable DYRK3 inhibitor (IC50=0.7 nM). GSK-626616 inhibits other members of the DYRK family with similar potency. It is a potential therapy for the treatment of anemia.

    价 格：￥电议型 号：T15422产 地：美洲

  • T15424GSK1379725AGSK1379725A

    GSK1379725A is a selective BPTF ligand (Kd: 2.8 uM). It also showing no binding activity for Brd4.

    价 格：￥电议型 号：T15424产 地：美洲

  • T15425GSK1702934AGSK1702934A

    GSK1702934A modulates cardiac contractility and f arrhythmogenesis by activation of TRPC3. GSK1702934A is a selective agonist of TRPC3.

    价 格：￥电议型 号：T15425产 地：美洲

  • T15427GSK2033GSK2033

    GSK2033 is an antagonist of LXR (pIC50s: 7 and 7.4 for LXRα or LXRβ, respectively).

    价 格：￥电议型 号：T15427产 地：美洲

  • T15429GSK2194069GSK2194069

    GSK2194069 is a potent and specific inhibitor of the β-ketoacyl reductase (KR) activity of hFAS (IC50: 7.7 ± 4.1 nM in an assay detecting released CoA). It is also hFAS inhibitor.

    价 格：￥电议型 号：T15429产 地：美洲

  • T15430GSK2256294AGSK2256294A,GSK 2256294,

    GSK2256294A is a potent, reversible, tight binding inhibitor of isolated recombinant human sEH (soluble epoxide hydrolase) (IC50 = 27 pM; t1/2 = 121 min) and displays potent inhibition against the rat (IC50 = 61 pM) and murine (IC50 = 189 pM) orthologs of

    价 格：￥电议型 号：T15430产 地：美洲

  • T15431NemiralisibNemiralisib,GSK2269557 (free base),

    Nemiralisib is a potent and highly selective inhibitor of PI3Kδ (pKi: 9.9).

    价 格：￥电议型 号：T15431产 地：美洲

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