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  • T11199Endothelial lipase inhibitor-1Endothelial lipase inhibitor-1

    Endothelial lipase inhibitor-1 is a potent endothelial lipase inhibitor with an IC50 of 49 nM.?

    价 格：￥电议型 号：T11199产 地：美洲

  • T11500GSK3368715GSK3368715,EPZ019997,

    GSK3368715 produces a shift in arginine methylation states, alters exon usage, and has strong anti-cancer activity. GSK3368715 is an orally active, reversible, and S-adenosyl-L-methionine (SAM) uncompetitive type I protein arginine methyltransferases (P

    价 格：￥电议型 号：T11500产 地：美洲

  • T11500LGSK3368715 dihydrochlorideGSK3368715 dihydrochloride,EPZ019997 dihydrochloride,

    GSK3368715 dihydrochloride ?produces a shift in arginine methylation states, alters exon usage, and has strong anti-cancer activity.GSK3368715 dihydrochloride ?is an orally active, reversible, and S-adenosyl-L-methionine (SAM) uncompetitive type I protein

    价 格：￥电议型 号：T11500L产 地：美洲

  • T1171MethylprednisoloneMethylprednisolone,U 7532,NSC-19987

    Methylprednisolone is a PREDNISOLONE derivative with similar anti-inflammatory action.

    价 格：￥电议型 号：T1171产 地：美洲

  • T11993MEK inhibitorMEK inhibitor

    MEK inhibitor is a potent MEK inhibitor with antitumor potency.

    价 格：￥电议型 号：T11993产 地：美洲

  • T11996MELK-8a hydrochlorideMELK-8a hydrochloride

    MELK-8a hydrochloride is a novel maternal embryonic leucine zipper kinase (MELK) inhibitor.(IC50:2 nM).?

    价 格：￥电议型 号：T11996产 地：美洲

  • T12199NB-598 MaleateNB-598 Maleate

    NB-598 Maleate is a competitive squalene epoxidase (SE) inhibitor.

    价 格：￥电议型 号：T12199产 地：美洲

  • T15199EdicotinibEdicotinib,JNJ-40346527,JNJ-527

    Edicotinib shows less inhibitory effects on KIT and FLT3 (IC50: 20 nM and 190 nM, respectively). Edicotinib is a brain penetrant and orally active inhibitor of colony-stimulating factor-1 receptor (IC50: 3.2 nM). Edicotinib limits microglial expansion an

    价 格：￥电议型 号：T15199产 地：美洲

  • T1990(R)-P7C3-Ome(R)-P7C3-Ome

    P7C3 is a drug related to latrepirdine (dimebon), which has neuroprotective and proneurogenic effects, and may be potentially useful for the treatment of Alzheimer´s disease and similar neurodegenerative disorders. The precise mechanism of action through

    价 格：￥电议型 号：T1990产 地：美洲

  • T1992MertansineMertansine,Maytansinoid DM1,DM1

    Mertansine refers to the thiol-containing maytansinoid, DM1 (N2’-deacetyl-N2’-(3-mercapto-1-oxopropyl)maytansine) attached to a monoclonal antibody through reaction of the thiol group with the SPP (N-succinimidyl 4-(2-pyridyldithio)) linker to create an a

    价 格：￥电议型 号：T1992产 地：美洲

  • T1993J147J147

    J147 is an experimental drug with reported effects against both Alzheimer´s disease and ageing in mouse models of accelerated aging. It is a curcumin derivative and a potent neurogenic and neuroprotective drug candidate initially developed for the treatme

    价 格：￥电议型 号：T1993产 地：美洲

  • T1994PictilisibPictilisib,GDC-0941,RG7321

    Pictilisib (GDC-0941) is a potent pan inhibitor of class I catalytic subunits of PI3K (IC50s: 3/33/3/75 nM for p110α/β/δ/γ).

    价 格：￥电议型 号：T1994产 地：美洲

  • T1995FedratinibFedratinib,SAR 302503,TG-101348

    Fedratinib (TG101348) is an ATP-competitive inhibitor of JAK2 (IC50: 3 nM) with significantly less potent activity against JAK3.

    价 格：￥电议型 号：T1995产 地：美洲

  • T1997JNJ-31020028JNJ-31020028,JNJ31020028,JNJ 31020028

    JNJ-31020028 is a selective brain penetrant antagonist of neuropeptide Y2 receptor with high affinity(pIC50=8.07, human; pIC50=8.22, rat); it exhibits >100-fold selectivity for Y2 versus human Y1/Y4/Y5 receptors.

    价 格：￥电议型 号：T1997产 地：美洲

  • T1998CHS 828CHS 828,GMX1778,

    GMX1778(CHS-828), a pyridyl cyanoguanidine, is an effective inhibitor of NAD+ biosynthesis enzyme NAMPT (IC50 <25 nM).

    价 格：￥电议型 号：T1998产 地：美洲

  • T1999TaselisibTaselisib,RG-7604,GDC-0032

    Taselisib is an orally bioavailable inhibitor of the class I phosphatidylinositol 3-kinase (PI3K) alpha isoform (PIK3CA), with potential antineoplastic activity.

    价 格：￥电议型 号：T1999产 地：美洲

  • T2119ABT-199ABT-199,ABT199,ABT 199

    ABT-199 is a selective inhibitor of Bcl-2 (Ki < 0.010 nM), binding over 3 orders of magnitude less avidly to Bcl-xL, and Bcl-W (Kis = 48 and 245 nM, respectively).

    价 格：￥电议型 号：T2119产 地：美洲

  • T2199MyclobutanilMyclobutanil,Systhane,

    Myclobutanil is a triazole chemical used as a fungicide. It is a steroid demethylation inhibitor, specifically inhibiting ergosterol biosynthesis. Ergosterol is a critical component of fungal cell membranes.

    价 格：￥电议型 号：T2199产 地：美洲

  • T4S1990CarvacrolCarvacrol,cymophenol,O-Thymol

    1. 5-Isopropyl-2-methylphenol presents anxiolytic effects. 2. 5-Isopropyl-2-methylphenol presents antinociceptive activity. 3. 5-Isopropyl-2-methylphenol presents antidepressant effects, seems to be dependent on its interaction with the dopaminergic sy

    价 格：￥电议型 号：T4S1990产 地：美洲

  • T4S1999ValepotriateValepotriate,Valtrate,

    Valepotriate fraction can have sedative effects and affect behavioral parameters related to recognition memory. Valepotriates, a new class of cytotoxic and antitumor agents, they are very potent cytotoxic agents for the HTC hepatoma cells. Valepotriates m

    价 格：￥电议型 号：T4S1999产 地：美洲

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