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  • T71653GS-9256；化合物 GS-9256GS-9256

    GS-9256 is a selective inhibitor of the HCV NS3 protease, exhibiting favorable pharmacokinetic properties and antiviral activity [1].

    价 格：￥电议型 号：T71653产 地：中国大陆

  • T70925GS-5759；化合物 GS-5759GS-5759

    GS-5759 is a bifunctional ?2-Adrenoceptor Agonist and Phosphodiesterase 4 Inhibitor for Chronic Obstructive Pulmonary Disease with a Unique Mode of Action.

    价 格：￥电议型 号：T70925产 地：中国大陆

  • T70633GR-92549；化合物 GR-92549GR-92549

    GR-92549 is an HMG-CoA reductase inhibitor.

    价 格：￥电议型 号：T70633产 地：中国大陆

  • T70031ER-38925；化合物 ER-38925ER-38925

    ER-38925 is a retinoic acid receptor (rar) subtype α-selective agonist

    价 格：￥电议型 号：T70031产 地：中国大陆

  • T69925NVR3-778 hydrate；化合物 NVR3-778 hydrateNVR3-778 hydrate

    NVR 3-778 is the first capsid assembly modulator (CAM) that has demonstrated antiviral activity in hepatitis B virus (HBV)-infected patients. NVR 3-778 inhibited the generation of infectious HBV DNA-containing virus particles with a mean antiviral 50% effective concentration (EC50) of 0.40??M in HepG2.2.15 cells. The antiviral profile of NVR 3-778 indicates pan-genotypic antiviral activity and a lack of cross-resistance with nucleos(t)ide inhibitors of HBV replication.

    价 格：￥电议型 号：T69925产 地：中国大陆

  • T69808ABT-925 fumarate；化合物 ABT-925 fumarateABT-925 fumarate

    ABT-925, also known as A-37203, BSF-201640; DAT-201; Lu-201640; and A-437203, is a selective dopamine D3 receptor (DRD3) antagonist with an approximately 100-fold higher in vitro affinity for dopamine D? versus D? receptors. ABT-925 was tested in schizophrenia. ABT-925 is a selective dopamine D? receptor antagonist with an approximately 100-fold higher in vitro affinity for dopamine D? versus D? receptors.

    价 格：￥电议型 号：T69808产 地：中国大陆

  • T69259NCS-356 sodium；化合物 NCS-356 sodiumNCS-356 sodium

    NCS-356 sodium is a GHB receptor agonist.

    价 格：￥电议型 号：T69259产 地：中国大陆

  • T69258PPI-2458；化合物 PPI-2458PPI-2458

    PPI-2458 is a synthetic derivative of fumagillin with antineoplastic and cytotoxic properties. PPI-2458 irreversibly inhibits the enzyme methionine aminopeptidase type 2 (MetAP2), thereby preventing abnormal cell growth and angiogenesis. PPI-2458 is reported to have a better toxicity profile compared to other agents of its class.

    价 格：￥电议型 号：T69258产 地：中国大陆

  • T69257Methotrexate diethyl ester；化合物 Methotrexate diethyl esterMethotrexate diethyl ester

    Methotrexate diethyl ester is an antineoplastic antimetabolite with immunosuppressant properties. It is an inhibitor of tetrahydrofoltae dehydrogenase and prevents the formation of tetrahydrofolate, necessary for synthesis of thymidylate, an essential component of DNA.

    价 格：￥电议型 号：T69257产 地：中国大陆

  • T69255MRS-2339；化合物 MRS-2339MRS-2339

    MRS-2339 is a P2X receptor activator.

    价 格：￥电议型 号：T69255产 地：中国大陆

  • T69254Ajmalicine hydrochloride；化合物 Raubasine hydrochlorideRaubasine hydrochloride；Raubasine hydrochloride

    Ajmalicine (Raubasine) hydrochloride, a potent adrenolytic compound, selectively inhibits α1-adrenoceptors and acts as a reversible, non-competitive full inhibitor of nicotine receptors with an IC50 of 72.3 μM. This chemical also serves as an anti-hypertensive and exhibits sedative activity, making it useful in various therapeutic applications.

    价 格：￥电议型 号：T69254产 地：中国大陆

  • T69253FMP-401319-3；化合物 FMP-401319-3FMP-401319-3

    FMP-401319-3 is a concentration-dependent inhibitor of CRF1R-pPL cotranslational translocation at the level of the Sec61 complex.

    价 格：￥电议型 号：T69253产 地：中国大陆

  • T69252CPD26；化合物 CPD26CPD26

    CPD26 is a novel non-RBD binding modulator to inhibit SARS-CoV-2 by prohibiting the conformational change of the spike (S) protein.

    价 格：￥电议型 号：T69252产 地：中国大陆

  • T69251Methamilane methiodide；化合物 Methamilane methiodideMethamilane methiodide

    Methamilane methiodide is a Muscarinic agonist.

    价 格：￥电议型 号：T69251产 地：中国大陆

  • T69250JMX0312；化合物 JMX0312JMX0312

    JMX0312 is a salicylamide derivative used as a potent inhibitor of HAdV infection. JMX0312 showed significantly improved anti-HAdV activities with nanomolar to submicromolar IC50 values and high selectivity indexes (SI > 100), indicating better safety windows, compared to those of the lead compound niclosamide.

    价 格：￥电议型 号：T69250产 地：中国大陆

  • T6925P005091；化合物P005091P5091；P5091

    P005091 (P5091) is a selective and potent inhibitor of ubiquitin-specific protease 7 (USP7) with EC50 of 4.2 μM.

    价 格：￥电议型 号：T6925产 地：中国大陆

  • T68925Maroxepin；化合物 MaroxepinMaroxepin

    Maroxepin is a locust neuronal octopamine receptor antagonist.

    价 格：￥电议型 号：T68925产 地：中国大陆

  • T68723FPL-59257；化合物 FPL-59257FPL-59257

    FPL-59257 is a leukotriene antagonist that has been shown to abolish cough response & partly inhibit bronchoconstriction produced by leukotrienes C & D.

    价 格：￥电议型 号：T68723产 地：中国大陆

  • T68688CID-1792579；化合物 CID-1792579CID-1792579

    CID-1792579 is a selective agonist of GPR55.

    价 格：￥电议型 号：T68688产 地：中国大陆

  • T67925Nampt activator-1；化合物Nampt activator-1Nampt activator-1

    NAMPT Activator-1 (compound 1) is an effective and specific activator of niacinamide phosphotransferase (Compound 1) with a wide range of EC50 (3.3-3.7 μM). NAMPT activator-1 effectively protects cultured cells from FK866-mediated toxicity and is a potential neuroprotective compound.

    价 格：￥电议型 号：T67925产 地：中国大陆

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