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  • T11541HCV-IN-30

    HCV-IN-30 is an HCV NS5A replication complex inhibitor (IC50s: 901 and 102 nM for genotypes 1a and 1b replicons).

    价 格：￥电议型 号：T11541产 地：中国大陆

  • T0154Nebivolol hydrochloride盐酸奈必洛尔；R-65824；R 065824 hydrochloride；Nebivolol HCl

    Nebivolol hydrochloride is a cardioselective ADRENERGIC BETA-1 RECEPTOR ANTAGONIST (beta-blocker) that functions as a VASODILATOR through the endothelial L-arginine/ NITRIC OXIDE system. It is used to manage HYPERTENSION and chronic HEART FAILURE in elder

    价 格：￥电议型 号：T0154产 地：中国大陆

  • T0154Nebivolol hydrochlorideNebivolol hydrochloride,R 065824 hydrochloride,Nebivolol HCl

    Nebivolol hydrochloride is a cardioselective ADRENERGIC BETA-1 RECEPTOR ANTAGONIST (beta-blocker) that functions as a VASODILATOR through the endothelial L-arginine/ NITRIC OXIDE system. It is used to manage HYPERTENSION and chronic HEART FAILURE in elder

    价 格：￥电议型 号：T0154产 地：美洲

  • T11544HDACs/mTOR Inhibitor 1HDACs/mTOR Inhibitor 1

    HDACs/mTOR Inhibitor 1 stimulates cell cycle arrest in G0/G1 phase and induce tumor cell apoptosis with low toxicity in vivo.?HDACs/mTOR Inhibitor 1 is a dual Histone Deacetylases (HDACs) and mammalian target of Rapamycin (mTOR) target inhibitor for treat

    价 格：￥电议型 号：T11544产 地：美洲

  • T11546hDHODH-IN-1hDHODH-IN-1

    hDHODH-IN-1 has anti-inflammatory effect.?hDHODH-IN-1 is a human dihydroorotate dehydrogenase (hDHODH) inhibitor.?

    价 格：￥电议型 号：T11546产 地：美洲

  • T11549Helioxanthin 8-1Helioxanthin 8-1,Helioxanthin analogue 8-1,

    Helioxanthin 8-1 is an analogue of helioxanthin, exhibites significant in vitro anti-HBV/HCV/HSV-1/HIV activity with EC50 of >5/10/1.4/15 uM. IC50 value: >5/10/1.4/15 uM(HBV/HCV/HSV-1/HIV) Target: Antiviral agent The cyclic hydrazide 28(Helioxanthin 8-1)

    价 格：￥电议型 号：T11549产 地：美洲

  • T12154N-Desethyl amodiaquineN-Desethyl amodiaquine

    N-Desethyl amodiaquine dihydrochloride is an antiparasitic agent,is the major biologically active Amodiaquine metabolite .

    价 格：￥电议型 号：T12154产 地：美洲

  • T12934SMAP-2SMAP-2,DT-1154,

    SMAP-2 is an orally bioavailable activator of phosphatase 2A (PP2A) which binds to the PP2A Aα scaffold subunit to drive conformational changes in PP2A. It inhibits the growth of KRAS-mutant lung cancers .

    价 格：￥电议型 号：T12934产 地：美洲

  • T1540Doxepin hydrochlorideDoxepin hydrochloride,Doxepin HCl,Novoxapin

    Doxepin Hydrochloride is a dibenzoxepin tricyclic compound. It displays a range of pharmacological actions including maintaining adrenergic innervation. Its mechanism of action is not fully understood, but it appears to block reuptake of monoaminergic neu

    价 格：￥电议型 号：T1540产 地：美洲

  • T15400GNE-272GNE-272

    GNE-272 is a potent and selective inhibitor of CBP/EP300 (IC50: 0.02, 0.03 and 13 μM for CBP, EP300 and BRD4, respectively) and it is also selective in vivo probe for CBP/EP300.

    价 格：￥电议型 号：T15400产 地：美洲

  • T15404GNE-6468GNE-6468

    GNE-6468 is a potent and selective agonist of RORγ(RORc) (EC50: 13 nM for HEK-293 cell).

    价 格：￥电议型 号：T15404产 地：美洲

  • T15405GNE-781GNE-781

    GNE-781 is a highly potent and selective inhibitor of CBP (IC50: 0.94 nM in TR-FRET assay). GNE-781 also inhibits BRET and BRD4(1) (IC50s: 6.2 nM and 5100 nM, respectively).

    价 格：￥电议型 号：T15405产 地：美洲

  • T15407GNE 0723GNE 0723

    GNE 0723 is an NMDAR brain permeable positive allosteric modulator (EC50: 21 nM for GluN2A; 7.4 and 6.2 μM for GluN2C and GluN2D, respectively).

    价 格：￥电议型 号：T15407产 地：美洲

  • T1541DrospirenoneDrospirenone,Dihydrospirorenone,ZK 3059

    Drospirenone is a synthetic spironolactone analogue and progestin with progestational and anti-mineralocorticoid activity.

    价 格：￥电议型 号：T1541产 地：美洲

  • T15410GNF351GNF351

    GNF351 is a full antagonist of the aryl hydrocarbon receptor (AHR). GNF351 is minimal toxicity in mouse or human keratinocytes. GNF351 competes with a photoaffinity AHR ligand for binding to the AHR (IC50: 62 nM).

    价 格：￥电议型 号：T15410产 地：美洲

  • T15411GPNA hydrochlorideGPNA hydrochloride

    GPNA hydrochloride is specific glutamine (Gln) transporter ASCT2 inhibitor. GPNA reversibly induces apoptosis in A549 cells. GPNA hydrochloride is a well-known substrate of the enzyme γ-glutamyltransferase (GGT). GPNA hydrochloride also inhibits Na+-depe

    价 格：￥电议型 号：T15411产 地：美洲

  • T15412GPP78GPP78,CAY10618,

    GPP78 is cytotoxic to neuroblastoma cell line SH-SY5Y cells (IC50 of 3.8 nM by inducing autophagy). GPP78 is a potent inhibitor of Nampt (IC50 of 3.0 nM for nicotinamide adenine dinucleotide (NAD) depletion). GPP78 has anti-cancer and anti-inflammatory ef

    价 格：￥电议型 号：T15412产 地：美洲

  • T15413GPR120-IN-1GPR120-IN-1

    GPR120-IN-1 is a selective agonist of Gpr120 ( logEC50: ?7.62).

    价 格：￥电议型 号：T15413产 地：美洲

  • T15416GR148672XGR148672X

    GR148672X is an inhibitor of triacyglycerol hydrolase (TGH) (IC50: 4 nM).

    价 格：￥电议型 号：T15416产 地：美洲

  • T15418GS-6201GS-6201,CVT-6883,

    GS-6201 is a selective antagonist of adenosine A2B receptor. GS-6201 shows high affinity and selectivity for the human adenosine A2B receptors (Ki=22 nM). GS-62013 attenuates the airway reactivity induced by NECA, AMP, or allergen in sensitized mice. GS-6

    价 格：￥电议型 号：T15418产 地：美洲

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