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  • T11483GSK 256066 TrifluoroacetateGSK 256066 Trifluoroacetate,GSK256066 (2,2,2-trifluoroacetic acid),

    GSK 256066 Trifluoroacetate developed for the treatment of chronic obstructive pulmonary disease.?GSK 256066 Trifluoroacetate ?is a selective and high-affinity phosphodiesterase 4 (PDE) inhibitor, with an IC50 of 3.2 pM for PDE4B.

    价 格：￥电议型 号：T11483产 地：美洲

  • T11486GSK2807 TrifluoroacetateGSK2807 Trifluoroacetate

    GSK2807 Trifluoroacetate is a selective, potent and SAM-competitive inhibitor of SMYD3, with a Ki of 14 nM and an IC50 of 130 nM.?

    价 格：￥电议型 号：T11486产 地：美洲

  • T11487FiboflaponFiboflapon,GSK2190915,AM-803

    Fiboflapon ?is a potent and orally bioavailable 5-lipoxygenase-activating protein (FLAP) inhibitor with a potency of 2.9 nM in FLAP binding, an IC50 of 76 nM for inhibition of LTB4 in human blood.?

    价 格：￥电议型 号：T11487产 地：美洲

  • T11487LFiboflapon sodiumFiboflapon sodium,GSK2190915 sodium salt,AM-803 sodium

    Fiboflapon sodiumis a potent and orally bioavailable 5-lipoxygenase-activating protein (FLAP) inhibitor with a potency of 2.9 nM in FLAP binding, an IC50 of 76 nM for inhibition of LTB4 in human blood.?

    价 格：￥电议型 号：T11487L产 地：美洲

  • T11488GSK2850163GSK2850163

    GSK2850163 is a novel inhibitor of inositol-requiring enzyme-1 alpha (IRE1α) which can inhibit ?RNase activity and IRE1α kinase activity with IC50s of 200 and 20 nM, respectively.

    价 格：￥电议型 号：T11488产 地：美洲

  • T11492GSK2983559 free acidGSK2983559 free acid

    GSK2983559 free acid has excellent activity in blocking many proinflammatory cytokine responses in vivo and in human inflammatory bowel disease explant samples.?GSK2983559 free acid ?is a potent, specific and oral bioavailable receptor interacting protein

    价 格：￥电议型 号：T11492产 地：美洲

  • T11495GSK4028GSK4028

    GSK4028 is the enantiomeric negative control of GSK4027, which is a PCAF/GCN5 bromodomain chemical probe,in a time-resolved fluorescence resonance energy transfer (TR-FRET) assay,?the pIC50 of GSK4028 is 4.9.

    价 格：￥电议型 号：T11495产 地：美洲

  • T11495LGSK 4027GSK 4027

    GSK 4027 is a PCAF/GCN5 bromodomain chemical probe. In a time-resolved fluorescence resonance energy transfer (TR-FRET) assay, it has a pIC50 of 7.4±0.11 for PCAF.

    价 格：￥电议型 号：T11495L产 地：美洲

  • T11496GSK598809GSK598809

    GSK598809 is a selective and potent dopamine D3 Receptor (DRD3) antagonist, with a pKi of 8.9.

    价 格：￥电议型 号：T11496产 地：美洲

  • T11497GSK656GSK656

    GSK656 acting as an inhibitor of Mycobacterium tuberculosis (Mtb) leucyl-tRNA synthetase (LeuRS),?is a potent antitubercular agent, with an IC50 of 0.2 μM.?

    价 格：￥电议型 号：T11497产 地：美洲

  • T11498GSK682753AGSK682753A

    GSK682753A is a selective and highly potent inverse agonist of the epstein-barr virus-induced receptor 2 (EBI2) with an IC50 of 53.6 nM.?

    价 格：￥电议型 号：T11498产 地：美洲

  • T11500GSK3368715GSK3368715,EPZ019997,

    GSK3368715 produces a shift in arginine methylation states, alters exon usage, and has strong anti-cancer activity. GSK3368715 is an orally active, reversible, and S-adenosyl-L-methionine (SAM) uncompetitive type I protein arginine methyltransferases (P

    价 格：￥电议型 号：T11500产 地：美洲

  • T11500LGSK3368715 dihydrochlorideGSK3368715 dihydrochloride,EPZ019997 dihydrochloride,

    GSK3368715 dihydrochloride ?produces a shift in arginine methylation states, alters exon usage, and has strong anti-cancer activity.GSK3368715 dihydrochloride ?is an orally active, reversible, and S-adenosyl-L-methionine (SAM) uncompetitive type I protein

    价 格：￥电议型 号：T11500L产 地：美洲

  • T11504GSTO-IN-2GSTO-IN-2

    GSTO-IN-2 is a glutathione S-transferase inhibitor with IC50s of 1.4, 16.3, and 3.6 μM for GSTP1-1, GSTM1, and GSTA2.?

    价 格：￥电议型 号：T11504产 地：美洲

  • T11505GSTO1-IN-1GSTO1-IN-1

    GSTO1-IN-1 is a potent glutathione S-transferase omega 1 (GSTO1) inhibitor with an IC50 of 31 nM.

    价 格：￥电议型 号：T11505产 地：美洲

  • T11508CamicilCamicil,Camicinal,GSK962040

    Camicinal is a small molecule, selective motilin receptor agonist with pEC50 of 7.9.

    价 格：￥电议型 号：T11508产 地：美洲

  • T11824Lanraplenib succinateLanraplenib succinate,GS-9876 succinate,

    Lanraplenib succinate inhibits SYK activity in platelets via the glycoprotein VI (GPVI) receptor without prolonging bleeding time (BT) in monkeys or humans.?Lanraplenib succinate is a highly selective and orally active SYK inhibitor (IC50=9.5 nM) in devel

    价 格：￥电议型 号：T11824产 地：美洲

  • T11824LLLanraplenibLanraplenib,GS-9876,

    Lanraplenib inhibits SYK activity in platelets via the glycoprotein VI (GPVI) receptor without prolonging bleeding time (BT) in monkeys or humans. Lanraplenib is a highly selective and orally active SYK inhibitor (IC50=9.5 nM) in development for the treat

    价 格：￥电议型 号：T11824LL产 地：美洲

  • T11832Ledipasvir D-tartrateLedipasvir D-tartrate,GS-5885 D-tartrate,

    Ledipasvir D-tartrate with EC50 values of 34 pM against GT1a and 4 pM against GT1b replicon.?is an inhibitor of the hepatitis C virus NS5A.

    价 格：￥电议型 号：T11832产 地：美洲

  • T12311Tirabrutinib hydrochlorideTirabrutinib hydrochloride,ONO-4059 (hydrochloride),GS-4059 (hydrochloride

    Tirabrutinib hydrochloride is a selective and novelBTK with IC50 2.2 nm inhibitor.

    价 格：￥电议型 号：T12311产 地：美洲

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