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  • T16500PF-3450074PF-74

    PF-3450074 acts at an early stage of HIV-1 infection inhibits viral replication by directly competing with the binding of CPSF6 (nuclear host factors cleavage and polyadenylation specific factor 6) and NUP153 (nucleoporin 153), and blocks the uncoating, a

    价 格：￥电议型 号：T16500产 地：中国大陆

  • T1650Chlorzoxazone氯唑沙宗；Chlorzoxazon；Paraflex

    Chlorzoxazone is a Muscle Relaxant. The physiologic effect of chlorzoxazone is by means of Centrally-mediated Muscle Relaxation.

    价 格：￥电议型 号：T1650产 地：中国大陆

  • T16346NS1652

    NS1652 is an anion conductance inhibitor. NS1652 blocks chloride channel has an IC50 of 1.6 μM in human and mouse red blood cells.

    价 格：￥电议型 号：T16346产 地：中国大陆

  • T14687DeucravacitinibBMS-986165

    BMS-986165 inhibits IL-12/23 and type I IFN pathways[1][2]. BMS-986165 is a highly selective, orally bioavailable allosteric TYK2 inhibitor for the treatment of autoimmune diseases. Which selectively binds to TYK2 pseudokinase (JH2) domain (IC50=1.0 nM) a

    价 格：￥电议型 号：T14687产 地：中国大陆

  • T12165nAChR agonist 1DUN71755

    nAChR agonist 1 is a brain-permeable and orally efficacious positive allosteric α7 nicotinic acetylcholine receptor (α7 nAChR)modulator.

    价 格：￥电议型 号：T12165产 地：中国大陆

  • T11657INH154

    INH154 is a potent Nek2 and Hec1 binding (INH) inhibitor with IC50s of 120 nM in MB468 cells and 200 nM in Hela cells for INH.

    价 格：￥电议型 号：T11657产 地：中国大陆

  • T1165EthionamideEthinamide；Bayer 5312；2-ethylthioisonicotinamide；乙硫异烟胺

    Ethionamide is a nicotinamide derivative, with antibacterial activity, used to treat tuberculosis. Although the exact mechanism of action of ethionamide is unknown, it may inhibit the synthesis of mycolic acid, a saturated fatty acid found in the bacteria

    价 格：￥电议型 号：T1165产 地：中国大陆

  • T0165Urapidil乌拉地尔；Eupressyl；Ebrantil；Mediatensyl

    Urapidil, a sympatholytic antihypertensive drug, acts as a 5-HT1A receptor agonist and as an α1-adrenoceptor antagonist.

    价 格：￥电议型 号：T0165产 地：中国大陆

  • T0165UrapidilUrapidil,Ebrantil,Eupressyl

    Urapidil, a sympatholytic antihypertensive drug, acts as a 5-HT1A receptor agonist and as an α1-adrenoceptor antagonist.

    价 格：￥电议型 号：T0165产 地：美洲

  • T13178ToceranibToceranib,SU11654,PHA 291639E

    Toceranib phosphate is an orally active inhibitor of tyrosine kinase (RTK) receptor, and it potently inhibits PDGFR, VEGFR, and Kit(with Kis of 5 and 6 nM for PDGFRβ and Flk-1/KDR, respectively), has antitumor and antiangiogenic activity.

    价 格：￥电议型 号：T13178产 地：美洲

  • T14067A-1165442A-1165442

    A-1165442 is a competitive TRPV1 antagonist. For human TRPV, the IC50 values is 9 nM.

    价 格：￥电议型 号：T14067产 地：美洲

  • T14687BMS-986165BMS-986165

    BMS-986165 inhibits IL-12/23 and type I IFN pathways[1][2]. BMS-986165 is a highly selective, orally bioavailable allosteric TYK2 inhibitor for the treatment of autoimmune diseases. Which selectively binds to TYK2 pseudokinase (JH2) domain (IC50=1.0 nM)

    价 格：￥电议型 号：T14687产 地：美洲

  • T15808Merestinib dihydrochlorideMerestinib dihydrochloride,LY2801653 dihydrochloride,

    Merestinib dihydrochloride is an effective and orally bioavailable c-Met inhibitor (Ki=2 nM). It has anti-tumor activities and also has potent activity against MST1R (IC50=11 nM), FLT3 (IC50=7 nM), AXL (IC50=2 nM), MERTK (IC50=10 nM), TEK (IC50=63 nM), RO

    价 格：￥电议型 号：T15808产 地：美洲

  • T15812LY2979165LY2979165

    LY2979165 is a mGlu2 agonist and is a novel potent agent. It is used as anti-depressants.

    价 格：￥电议型 号：T15812产 地：美洲

  • T16165MyriocinMyriocin

    Myriocin is a fungal metabolite isolated from Myriococcum albomyces, Isaria sinclairi and Mycelia sterilia. Myriocin also is an effective inhibitor of serine-palmitoyl-transferase (SPT) and a key enzyme in de novo synthesis of sphingolipids. Myriocin stro

    价 格：￥电议型 号：T16165产 地：美洲

  • T16346NS1652NS1652

    NS1652 is a reversible anion conductance inhibitor. NS1652 blocks chloride channel has an IC50 of 1.6 μM in human and mouse red blood cells.

    价 格：￥电议型 号：T16346产 地：美洲

  • T1650ChlorzoxazoneChlorzoxazone,Chlorzoxazon,Paraflex

    Chlorzoxazone is a Muscle Relaxant. The physiologic effect of chlorzoxazone is by means of Centrally-mediated Muscle Relaxation.

    价 格：￥电议型 号：T1650产 地：美洲

  • T16501PF-3644022PF-3644022

    PF-3644022 is an effective, selective, and ATP-competitive MAPKAPK2 (MK2) inhibitor (IC50: 5.2 nM and a Ki of 3 nM). PF-3644022 potently inhibits TNFα production and has an anti-inflammatory effect. PF-3644022 also inhibits MK3 and p38 regulated/activated

    价 格：￥电议型 号：T16501产 地：美洲

  • T16503PF-4191834PF-4191834,PF-04191834,

    PF-4191834 is an orally active, noniron chelating, and non-redox inhibitor of the 5-Lipoxygenase (5-LOX) (IC50=229 nM). PF-4191834 shows ~300-fold selectivity for 5-LOX over 12-LOX and 15-LOX and displays no activity toward the cyclooxygenase enzymes. PF-

    价 格：￥电议型 号：T16503产 地：美洲

  • T16506PF-4878691PF-4878691,3M-852A,

    PF-4878691 is an effective and selective Toll-like receptor 7 agonists modelled. It is used to dissociate its antiviral and inflammatory activities.

    价 格：￥电议型 号：T16506产 地：美洲

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