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  • T4016BMS-986020BMS986020；AM152；BMS 986020

    BMS-986020 is a selective antagonist of LPA1.

    价 格：￥电议型 号：T4016产 地：中国大陆

  • T39789BMS-986235LAR-1219；BMS-986235

    BMS-986235 (LAR-1219) is a selective, orally active formyl peptide receptor 2 (FPR2) agonist, with EC 50 s of 0.41 nM and 3.4 nM for hFPR2 and mFPR2, respectively. BMS-986235 has potential for the prevention of heart failure.

    价 格：￥电议型 号：T39789产 地：中国大陆

  • T39654AfimetoranAfimetoran；BMS-986256

    Afimetoran is a toll-like receptor antagonist, which can be used in the research of inflammatory and autoimmune diseases [1] .

    价 格：￥电议型 号：T39654产 地：中国大陆

  • T3655BMS-1PD1-PDL1 inhibitor 1；PD-1/PD-L1 inhibitor 1

    PD1-PD-L1 inhibitor 1 (PD1-PD-L1-IN-1) is an inhibitor of the PD1-PD-L1 protein-protein interaction. It also acts as an immunomodulator. Programmed death ligand 1 (PD-L1) is a protein in humans that is encoded by the CD274 gene and the upregulation of PD-

    价 格：￥电议型 号：T3655产 地：中国大陆

  • T35856BMS-986176

    AAK1-IN-1 is a highly selective and potent inhibitor of adaptor associated kinase 1 (AAK1, IC50 = 2 nM).

    价 格：￥电议型 号：T35856产 地：中国大陆

  • T3523Fostemsavir磷坦姆沙韦；BMS-663068

    BMS-663068 is an HIV-1 attachment inhibitor in development for the treatment of HIV-1 infection.

    价 格：￥电议型 号：T3523产 地：中国大陆

  • T3495TasimelteonVEC-162；BMS-214778；他司美琼

    Tasimelteon is a melatonin receptor agonist that is used for the treatment of non-24 hour sleep-wake disorder in blind individuals.

    价 格：￥电议型 号：T3495产 地：中国大陆

  • T3462BMS-582949 hydrochlorideBMS-582949 HCl

    The BMS-582949 hydrochloride is a highly specific p38α MAPK inhibitor (IC50: 13 nM).

    价 格：￥电议型 号：T3462产 地：中国大陆

  • T3146BMS-202PD1-PDL1 inhibitor 2；PD-1/PD-L1 inhibitor 2

    PD1-PDL1 inhibitor 2 is an inhibitor of the PD-1 (Programmed death- 1) /PD-Ll (Programmed death-ligand 1) protein/protein interaction, extracted from patent WO/2015034820 A1.

    价 格：￥电议型 号：T3146产 地：中国大陆

  • T2699BMS 777607BMS777607；BMS-777607；BMS 817378

    BMS-777607 is a Met-related inhibitor for c-Met/Axl/Ron/Tyro3 (IC50: 3.9/1.1/1.8/4.3 nM). BMS-777607 has been investigated for the basic science of Malignant Solid Tumour.

    价 格：￥电议型 号：T2699产 地：中国大陆

  • T26869BMS-986122BMS986122；BMS 986122

    BMS 986122 is a positive allosteric modulator of μ-opioid receptors that increases β-arrestin recruitment stimulated by endomorphin 1 in U2OS-OPRM1 human osteosarcoma cells expressing μ-opioid receptors (EC50 = 3 μM).

    价 格：￥电议型 号：T26869产 地：中国大陆

  • T26859BMS-8BMS8；BMS 8

    BMS-8 is a novel inhibitor of the PD-1/PD-L1 interaction (IC50: 7.2 μM) by binding directly to PD-L1 and inducing the formation of PD-L1 homodimers.

    价 格：￥电议型 号：T26859产 地：中国大陆

  • T2679BMS-265246BMS265246；BMS 265246

    BMS-265246 is a potent and selective CDK1/2 inhibitor.

    价 格：￥电议型 号：T2679产 地：中国大陆

  • T2658BMS-777607

    BMS-777607 is a Met-related inhibitor for c-Met, Axl, Ron and Tyro3.

    价 格：￥电议型 号：T2658产 地：中国大陆

  • T2586Cabozantinib卡博替尼；XL184；BMS-907351

    Cabozantinib (XL184) is a potent pan-tyrosine kinases inhibitor that inhibits VEGFR2, c-Met, Kit, Axl, and Flt3 (IC50s: 0.035, 1.3, 4.6, 7 and 11.3 nM).

    价 格：￥电议型 号：T2586产 地：中国大陆

  • T2576Brivanib (alaninate)丙氨酸布立尼布；BMS-582664；Brivanib Alaninate

    Brivanib Alaninate is the alaninate salt of a vascular endothelial growth factor receptor 2 (VEGFR2) inhibitor with potential antineoplastic activity. Brivanib strongly binds to and inhibits VEGFR2, a tyrosine kinase receptor expressed almost exclusively

    价 格：￥电议型 号：T2576产 地：中国大陆

  • T2419BMS-794833BMS794833

    BMS-794833 is a potent ATP competitive inhibitor of Met/VEGFR2; a prodrug of BMS-817378.

    价 格：￥电议型 号：T2419产 地：中国大陆

  • T2389Dapagliflozin达格列净；BMS-512148

    Dapagliflozin is a selective sodium-glucose co-transporter subtype 2 (SGLT2) inhibitor with antihyperglycemic activity.

    价 格：￥电议型 号：T2389产 地：中国大陆

  • T2349BMS-754807BMS 754807；BMS754807

    Dual IGF-1R/InsR Inhibitor BMS-754807 is an oral small molecule inhibitor of insulin-like growth factor 1 receptor (IGF-1R) and insulin receptor (InsR) tyrosine kinases with potential antineoplastic activity.

    价 格：￥电议型 号：T2349产 地：中国大陆

  • T2337BMS-303141BMS303141；BMS 303141

    BMS-303141 is a potent ATP-citrate lyase (ACL) inhibitor (IC50: 0.13 uM, human recombinant ACL).

    价 格：￥电议型 号：T2337产 地：中国大陆

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