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  • T4607CAY 10465CAY10465 Exclusive；CAY10465

    CAY 10465 is a selective and high-affinity AhR agonist, with a Ki of 0.2 nM, and shows no effect on estrogen receptor (Ki >100000 nM).

    价 格：￥电议型 号：T4607产 地：中国大陆

  • T4468WAY 316606

    WAY 316606 is an inhibitor of the secreted protein sFRP-1, an endogenous antagonist of the secreted glycoprotein Wnt.

    价 格：￥电议型 号：T4468产 地：中国大陆

  • T4436RO1138452CAY10441

    RO1138452 is a selective and orally bioavailable antagonist of prostacyclin receptor (pKi: 8.3). It antagonizes the carbaprostacyclin-induced activation of human neuroblastoma adenylate cyclase, blocking cyclic AMP accumulation in a dose-dependent manner.

    价 格：￥电议型 号：T4436产 地：中国大陆

  • T4263BAY 61-36062-[[7-(3,4-二甲氧基苯基)咪唑并[1,2-C]嘧啶-5-基]氨基]-3-吡啶甲酰胺；Syk inhibitor IV

    BAY 61-3606 is a potent, ATP-competitive, reversible, and highly selective inhibitor of Syk tyrosine kinase activity (Ki= 7.5 nM), exhibiting no inhibitory effect against Btk, Fyn, Itk, Lyn, and Src.

    价 格：￥电议型 号：T4263产 地：中国大陆

  • T4097Vardenafil hydrochloride trihydrate盐酸瓦地那非三水合物；Vardenafil HCl Trihydrate；BAY38-9456

    Vardenafil HCl Trihydrate is a new type PDE inhibitor with IC50 of 0.7 and 180 nM for PDE5 and PDE1, respectively.

    价 格：￥电议型 号：T4097产 地：中国大陆

  • T4062CAY10602

    CAY10602 is a SIRT1 activator. CAY10602 was derived from high throughput screening for compounds that increase SIRT1-mediated deacetylation of a SIRT1-specific substrate. Functional assays show that CAY10602 dose-dependently suppresses the NF-κB-dependent

    价 格：￥电议型 号：T4062产 地：中国大陆

  • T3S1850Bayogenin

    Bayogenin is an alfalfa saponin, Bayogenin shows moderate potency of glycogen phosphorylase inhibition.

    价 格：￥电议型 号：T3S1850产 地：中国大陆

  • T3958WAY-200070WAY 200070

    WAY-200070 is a specific agonist of estrogen receptor β (ERRβ, IC50: 2.3 nM).

    价 格：￥电议型 号：T3958产 地：中国大陆

  • T3888ScopolinMurrayin；Scopoloside；东莨菪甙；东莨菪苷

    Scopolin formation is increased by the enhanced activity of PAL. Scopolin can reduce the clinical symptoms of rat AIA by inhibiting inflammation and angiogenesis, and this compound may be a potent agent for angiogenesis related diseases and can serve as a

    价 格：￥电议型 号：T3888产 地：中国大陆

  • T37424CAY10781CAY10781

    CAY10781 is an inhibitor of the protein-protein interaction between neuropilin-1 (NRP-1) and VEGF-A.1It inhibits the interaction by 43% when used at a concentration of 12.5 μM. CAY10781 also inhibits VEGF-A-induced phosphorylation of VEGFR2 in catecholami

    价 格：￥电议型 号：T37424产 地：中国大陆

  • T3713BAY-876BAY 876；BAY876

    BAY-876 is a potent and selective GLUT1 inhibitor.

    价 格：￥电议型 号：T3713产 地：中国大陆

  • T3699Bay 59-3074

    Bay 59-3074 is a CB1/CB2 receptor partial agonist (Ki: 48.3/45.5 nM). In rat models of chronic neuropathic and inflammatory pain, it displays anti-hyperalgesic and antiallodynic properties.

    价 格：￥电议型 号：T3699产 地：中国大陆

  • T36631BAY-6035

    BAY-6035 is an inhibitor of SET and MYND domain-containing protein 3 (SMYD3). It is 100-fold selective for SMYD3 over other histone methyltransferases. BAY-6035 inhibits methylation of MEKK2 peptide in a cell-free assay and in cells (IC50s = 88 and 70 nM,

    价 格：￥电议型 号：T36631产 地：中国大陆

  • T3494LW6HIF-1α inhibitor；LW8；CAY10585

    LW6 is a novel HIF-1 inhibitor.

    价 格：￥电议型 号：T3494产 地：中国大陆

  • T3449Bay 41-4109 racemate

    BAY 41-4109 racemate is a potent inhibitor of human hepatitis B virus (HBV) with an IC50 of 53 nM.

    价 格：￥电议型 号：T3449产 地：中国大陆

  • T3204BML-210BML210；BML 210；CAY10433

    BML-210 is a new-type HDAC inhibitor.

    价 格：￥电议型 号：T3204产 地：中国大陆

  • T3183WAY-181187SAX-187；WAY 181187；WAY181187

    WAY-181187 has high-affinity binding at the human 5-HT6 receptor.

    价 格：￥电议型 号：T3183产 地：中国大陆

  • T3170TroglitazoneRezulin；Romglizone；CS-045；Noscal；Prelay；Romozin；曲格列酮

    Troglitazone is a PPARγ agonist with anti-inflammatory and anti-tumor activity.

    价 格：￥电议型 号：T3170产 地：中国大陆

  • T3156Ciliobrevin AHPI-4；Hedgehog Pathway Inhibitor 4

    Ciliobrevin A is an inhibitor of hedgehog signaling pathway with an IC50 <10 μM.

    价 格：￥电议型 号：T3156产 地：中国大陆

  • T30798CerlapirdineSAM-531；PF05212365；P -05212365；SAM531；SAM 531；WAY-262,531；PF-05212365

    Cerlapirdine is a selective, potent, full antagonist of the 5-hydroxytryptamine 6 (5-HT6) receptor. Cerlapirdine is already in clinical development for the treatment of cognitive disorders related to Alzheimer´s disease and schizophrenia. It works by acti

    价 格：￥电议型 号：T30798产 地：中国大陆

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