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  • T0097LPazopanibPazopanib,GW786034,

    Pazopanib, a small molecule inhibitor, inhibits multiple protein tyrosine kinases with potential antineoplastic activity. Pazopanib selectively inhibits VEGFR-1, -2 and -3, c-kit and PDGF-R, which may result in inhibition of angiogenesis in tumors in whic

    价 格：￥电议型 号：T0097L产 地：美洲

  • T11518GW274150 phosphateGW274150 phosphate

    GW274150 phosphate displays less potency for both humans or rats endothelial NOS (eNOS) and neuronal NOS (nNOS). GW274150 phosphate exerts a protective role in an acute model of lung injury inflammation.?GW274150 phosphate is a potent, selective, orally a

    价 格：￥电议型 号：T11518产 地：美洲

  • T11518LGW274150GW274150

    GW274150 shows less potency for both humans or rats endothelial NOS (eNOS) and neuronal NOS (nNOS). GW274150 is a selective and NADPH-dependent inhibitor of human inducible nitric oxide synthase (iNOS) (IC50=2.19 μM; Kd=40 nM) and rat iNOS (ED50=1.15 μM).

    价 格：￥电议型 号：T11518L产 地：美洲

  • T11520GW806742XGW806742X

    GW806742X has activity against VEGFR2.?GW806742X is a Mixed Lineage Kinase Domain-Like protein (MLKL) inhibitor which binds the MLKL pseudokinase domain with a Kd value of 9.3 μM and has anti-necroptosis activity.?

    价 格：￥电议型 号：T11520产 地：美洲

  • T11521GW 766994GW 766994,GW 994,

    GW 766994 has has the potential for asthma and eosinophilic bronchitis treatment.GW 766994 is a specific and oral chemokine receptor-3 (CCR3) antagonist.

    价 格：￥电议型 号：T11521产 地：美洲

  • T11525GW311616GW311616

    GW-311616 is a orally bioavailable,potent , long duration and selective human neutrophil elastase (HNE) inhibitor with IC50 value of 22 nM and Ki value of 0.31 nM.

    价 格：￥电议型 号：T11525产 地：美洲

  • T11525LGW311616 hydrochlorideGW311616 hydrochloride,GW311616A,

    GW-311616 is a potent, long duration,orally bioavailable and selective human neutrophil elastase (HNE) inhibitor with IC50 value of 22 nM and Ki value of 0.31 nM.

    价 格：￥电议型 号：T11525L产 地：美洲

  • T12683Radafaxine hydrochlorideRadafaxine hydrochloride,GW-353162A,BW-306U

    Radafaxine hydrochloride is an inhibitor of DAT and NET transporters, and nAChR family modulator.

    价 格：￥电议型 号：T12683产 地：美洲

  • T12720PrinoxodanPrinoxodan,RGW2938,

    Prinoxodan is an inhibitor of phosphodiesterase.

    价 格：￥电议型 号：T12720产 地：美洲

  • T12850DilmapimodDilmapimod,SB-681323,GW 681323

    Dilmapimod is a potent inhibitor of p38 MAPK ,it potentially suppresses inflammation in chronic obstructive pulmonary disease.

    价 格：￥电议型 号：T12850产 地：美洲

  • T12970SolabegronSolabegron,GW 427353,

    Solabegron is a selective agonist of β3-adrenergic receptor, stimulating cAMP accumulation in Chinese hamster ovary cells expressing the human β3-AR(EC50 : 22 nM). It is used for treatment of overactive bladder and irritable bowel syndrome.

    价 格：￥电议型 号：T12970产 地：美洲

  • T13335WEHI-345 alogWEHI-345 alog,WEHI-345 analog,

    WEHI-345 analog is an inhibitor of Src.

    价 格：￥电议型 号：T13335产 地：美洲

  • T15689L-798106L-798106,CM9,GW671021

    L-798106 is an effective and highly selective prostanoid EP3 receptor antagonist (Ki=0.3 nM). It also has micromolar activities at EP4, EP1, and EP2 receptors (Ki: 916 nM, >5000 nM and >5000 nM at EP4, EP1 and EP2, respectively).

    价 格：￥电议型 号：T15689产 地：美洲

  • T1781GW 9508GW 9508

    GW9508 is a potent and selective agonist for FFA1 (GPR40), stimulates insulin secretion in a glucose-sensitive manner.

    价 格：￥电议型 号：T1781产 地：美洲

  • T1800GW 788388GW 788388

    GW788388 is a potent and selective inhibitor of ALK5, also inhibits TGF-(beta) type II receptor and activin type II receptor activities.

    价 格：￥电议型 号：T1800产 地：美洲

  • T1978GW 627368XGW 627368X,GW627368,

    GW627368X is a novel, potent and selective antagonist of prostanoid EP4 receptor.

    价 格：￥电议型 号：T1978产 地：美洲

  • T2020RGW 611RGW 611

    Detail unknown.

    价 格：￥电议型 号：T2020产 地：美洲

  • T2233GW 4064GW 4064

    GW 4064 is an effective farnesoid X receptor (FXR) agonist (EC50 =65 nM).

    价 格：￥电议型 号：T2233产 地：美洲

  • T2260GW 9662GW 9662,TIMTEC-BB SBB006523,

    GW9662 is a specific PPARγ antagonist (IC50: 3.3 nM, in a cell-free assay), with 100 to 1000-fold functional selectivity for PPARγ than PPARα/δ in cells.

    价 格：￥电议型 号：T2260产 地：美洲

  • T2277LosmapimodLosmapimod,GW856553X,SB856553

    Losmapimod (GW856553X; SB856553; GSK-AHAB) is a specific, potent, and orally active p38 MAPK inhibitor (pKi: 8.1/7.6 for p38α/β).

    价 格：￥电议型 号：T2277产 地：美洲

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