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  • T3624A-366A 366；A366

    Potent and selective G9a/GLP histone lysine methyltransferase inhibitor (IC50 = 3.3 nM). Exhibits >1000-fold selectivity for G9a/GLP over 21 other methyltransferases. Decreases levels of lysine 9 dimethylation on histone H3 (H3K9Me2) in PC3 cells.

    价 格：￥电议型 号：T3624产 地：中国大陆

  • T3623CobimetinibGDC-0973；RG7420；XL518；可美替尼；考比替尼

    Cobimetinib is a selective inhibitor of mitogen-activated protein kinase kinase (MEK) (IC50: 0.9 nM). Cobimetinib specifically binds to and inhibits the catalytic activity of MEK1, resulting in inhibition of extracellular signal-related kinase 2 (ERK2) ph

    价 格：￥电议型 号：T3623产 地：中国大陆

  • T3622CP-640186 hydrochlorideCP 640186 HCl；盐酸CP-640186

    CP-640186 HCl is an isozyme-nonselective acetyl-CoA carboxylase (ACC) inhibitor, including rat liver ACC1 (IC50: 53 nM) and rat skeletal muscle ACC2 (IC50: 61 nM); with higher metabolic stability than CP-610431.

    价 格：￥电议型 号：T3622产 地：中国大陆

  • T3621BrigatinibAP-26113；布格替尼

    Brigatinib is a highly potent and selective ALK inhibitor.

    价 格：￥电议型 号：T3621产 地：中国大陆

  • T3620SolcitinibGSK-2586184；GLPG-0778；索西替尼

    Solcitinib (GSK2586184, GLPG0778) is a JAK1 inhibitor. Solcitinib may be potentially used for the treatment of psoriasis, ulcerative colitis, and systemic lupus erythematosus.

    价 格：￥电议型 号：T3620产 地：中国大陆

  • T35862Cucurbit[8]uril

    Cucurbit[8]uril is a potent, low toxicity and orally active supramolecular inducer of protein heterodimerization. Cucurbit[8]uril induces heterodimerization of methylviologen and naphthalene functionalized proteins. Cucurbit[8]uril can induce energy trans

    价 格：￥电议型 号：T35862产 地：中国大陆

  • T3562ValrocemideTV1901；N-Valproylglycinamide；N-丙戊酰基甘氨酰胺；丙戊塞胺

    Valrocemide, also known as TV-1901, is an antiepileptic drug (AED). Valrocemide has a broad spectrum of anticonvulsant activity and promising potential as a new AED. Valrocemide is an anticonvulsant agent under development by Teva and Acorda as a potentia

    价 格：￥电议型 号：T3562产 地：中国大陆

  • T3554RG14620Tyrphostin RG14620；RG 14620

    RG14620 is an epidermal growth factor receptor (EGFR) inhibitor.

    价 格：￥电议型 号：T3554产 地：中国大陆

  • T35362NSC622608

    NSC622608 is a small-molecule ligand for V-domain Ig suppressor of T-cell activation (VISTA) which is an immune checkpoint that affects the ability of T-cells to attack tumors.

    价 格：￥电议型 号：T35362产 地：中国大陆

  • T3518GSK269962AGSK 269962；GSK269962B；GSK269962A HCl

    GSK269962 is a selective ROCK(Rho-associated protein kinase) inhibitor with IC50 values of 1.6 and 4 nM for ROCK1 and ROCK2, respectively.

    价 格：￥电议型 号：T3518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

  • T33762Fosifloxuridine nafalbenamideNUC-3373；NUC 3373；NUC3373

    NUC-3373 (Fosifloxuridine nafalbenamide), a pyrimidine nucleotide analogue, is a Thymidylate synthase inhibitor.NUC-3373 has anticancer activity. NUC-3373 is a ProTide transformation of 5-FU that generates much higher concentrations of FUDR-MP in patients

    价 格：￥电议型 号：T33762产 地：中国大陆

  • T3362EupatilinNSC 122413；异泽兰黄素

    Eupatilin, a flavone derived from Artemisia princepsPampanini, is a PPARα agonist, with pharmacological activity.

    价 格：￥电议型 号：T3362产 地：中国大陆

  • T3283CetilistatATL-962；新利司他

    Cetilistat is a novel inhibitor of pancreatic lipase being developed by Alizyme for the treatment of obesity and associated co-morbidities, including type 2 diabetes.

    价 格：￥电议型 号：T3283产 地：中国大陆

  • T3262Phosphocreatine disodium磷酸肌酸钠；Creatine phosphate disodium salt；Phosphocreatine disodium salt；Disodiu

    Creatine phosphate is a phosphorylated creatine molecule that serves as a rapidly mobilizable reserve of high-energy phosphates in muscle, skeletal, and brain.

    价 格：￥电议型 号：T3262产 地：中国大陆

  • T3162IDE1

    IDE1 can induce definitive endoderm from embryonic stem cells. It has been shown to induce the differentiation of Sox17+/FoxA2+-expressing pancreatic progenitors from human and mouse embryonic stems cells (EC50: 125.5 nM in vitro) by activating the TGF-β

    价 格：￥电议型 号：T3162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

  • T3073PF-670462PF670462

    PF-670462 is a potent (IC50 = 7.7 ± 2.2 nM) and selective (>30-fold with respect to 42 additional kinases) inhibitor of CK1ε in isolated enzyme preparations.

    价 格：￥电议型 号：T3073产 地：中国大陆

  • T3062WIKI4

    WIKI4 is a potent inhibitor of Wnt/β-catenin signaling and tankyrase 2 (TNKS2).

    价 格：￥电议型 号：T3062产 地：中国大陆

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