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  • T8688(Rac)-X77；化合物CPD77CPD77|||MUN91789；CPD77|||MUN91789

    (Rac)-X77 (MUN91789) is a potent SARS- CoV- 2 main protease inhibitor.

    价 格：￥电议型 号：T8688产 地：中国大陆

  • T8546BD750；化合物BD750BD750

    BD750 is an effective immunosuppressant and a JAK3/STAT5 inhibitor, inhibits IL-2-induced JAK3/STAT5-dependent T cell proliferation(IC50 of 1.5 μM and 1.1 μM in mouse and human T cells, respectively)

    价 格：￥电议型 号：T8546产 地：中国大陆

  • T81175SETD7-IN-1；化合物 SETD7-IN-1SETD7-IN-1

    SETD7-IN-1 (compound 7), a PFI-2 analogue, acts as both a substrate and inhibitor of histone lysine methyltransferase SETD7, exhibiting an inhibitory concentration (IC50) of 0.96 ± 0.10 ?M [1].

    价 格：￥电议型 号：T81175产 地：中国大陆

  • T78801BRD7-IN-2；化合物 BRD7-IN-2BRD7-IN-2

    BRD7-IN-2 (compound 2-77) is a potent selective inhibitor of bromodomain-containing protein 7 (BRD7), exhibiting significant anti-proliferative activity in prostate cancer cells. It demonstrates an IC50 of 5.4 μM for BRD7 while showing weak inhibition for BRD9 with an IC50 of >300 μM.

    价 格：￥电议型 号：T78801产 地：中国大陆

  • T77680BRD7-IN-3；化合物 BRD7-IN-3BRD7-IN-3

    BRD7-IN-3 (compound 1-78) functions as a dual inhibitor targeting the bromodomain-containing proteins BRD7 and BRD9, demonstrating half-maximal inhibitory concentrations (IC50s) of 1.6 μM for BRD7 and 2.7 μM for BRD9, respectively [1].

    价 格：￥电议型 号：T77680产 地：中国大陆

  • T77011Flanvotumab；夫兰妥单抗20D7S|||IMC 20D7S；20D7S|||IMC 20D7S

    Flanvotumab (IMC-20D7S) is a humanized monoclonal antibody directed against tyrosinase-related protein (TYRP1).Flanvotumab exhibits potent antitumor activity and acts through natural killer-mediated and antibody-dependent cell-mediated cytotoxicity (ADCC).

    价 格：￥电议型 号：T77011产 地：中国大陆

  • T7699AZD7325；化合物AZD-7325AZD-7325；AZD-7325

    AZD7325 (AZD-7325) is a GABA-Aα2,3 -selective receptor modulator.

    价 格：￥电议型 号：T7699产 地：中国大陆

  • T756637-Methoxy-β-carboline-1-propionic acid；化合物 7-Methoxy-β-carboline-1-propionic acid7-Methoxy-β-carboli

    7-Methoxy-β-carboline-1-propionic acid (compound 46), known for its cytotoxic and antimalarial properties, is derived from the roots of Eurycoma longifolia [1].

    价 格：￥电议型 号：T75663产 地：中国大陆

  • T7516ZD7288；化合物ZD7288ICI D7288；N-乙基-1,6-二氢-1,2-二甲基-6-(甲基亚氨基)-N-苯基-4-嘧啶胺盐酸盐|||ICI D7288

    ZD7288 (ICI D7288), a selective hyperpolarization-activated cyclic nucleotide-gated channel blocker, inhibits hippocampal synaptic plasticity.

    价 格：￥电议型 号：T7516产 地：中国大陆

  • T740197-Oxotridecanedioic acid；化合物 7-Oxotridecanedioic acid7-Oxotridecanedioic acid

    7-Oxotridecanedioic acid, a biodegradable cationic lipid intermediate, facilitates the formation of lipid nanoparticles. This compound enables the incorporation into lipid particles for the efficient delivery of active agents [1].

    价 格：￥电议型 号：T74019产 地：中国大陆

  • T73444BRD7586；化合物 BRD7586BRD7586

    BRD7586 represents the smallest known anti-CRISPR, functioning as a cell-permeable, small-molecule inhibitor targeting SpCas9.

    价 格：￥电议型 号：T73444产 地：中国大陆

  • T71989CPD7 HCl；化合物 CPD7 HClCPD7 HCl

    CPD7 HCl 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：T71989产 地：中国大陆

  • T71842D719；化合物 D719D719

    D719 is a novel inhibitor of integrase nuclear translocation, showing significant inhibition on virus p24 antigen production.

    价 格：￥电议型 号：T71842产 地：中国大陆

  • T71694BRD73842；化合物 BRD73842BRD73842

    BRD73842 is an inhibitor of Plasmodium PI4K.

    价 格：￥电议型 号：T71694产 地：中国大陆

  • T71484Utatrectinib；化合物 AZD7451AZD-7451；AZD-7451

    Utatrectinib (AZD-7451) is a potent, orally active, and selective inhibitor of Trk. It effectively inhibits TrkC activation and the associated tumorigenic behaviors.

    价 格：￥电议型 号：T71484产 地：中国大陆

  • T71055Albendazole-d7；化合物 Albendazole-d7Albendazole-d7

    Albendazole-d7 is intended for use as an internal standard for the quantification of albendazole by GC- or LC-MS. Albendazole is an orally bioavailable benzimidazole anthelmintic that is active against a variety of helminths, including liver flukes, tapeworms, and roundworms. It eliminates Trichostrongylus in the fourth stomach of cattle and sheep when orally administered at doses ranging from 2.5 to 10 mg/kg as well as other species in the fourth stomach and the small and large intestine. Alben

    价 格：￥电议型 号：T71055产 地：中国大陆

  • T71033ZD7114 free base；化合物 ZD7114 free baseZD7114 free base

    ZD7114, also known as ICI-D7114, is a selective adrenoceptor agonist of brown fat and thermogenesis. ICI D7114 stimulates thermogenesis at doses that have little effect on beta 1 or beta 2 adrenoceptors. Treatment with ICI D7114 activates BAT and thermogenesis even in species and situations where the intrinsic capacity is low. ICI D7114 has beneficial effects in animal models of obesity and disturbed glucose and lipid homeostasis.

    价 格：￥电议型 号：T71033产 地：中国大陆

  • T70927UCD74A HCl；化合物 UCD74A HClUCD74A HCl

    UCD74A HCl is a cell impermeant homolog of UCD38B, inhibitor of uPA (urokinase plasminogen activator).

    价 格：￥电议型 号：T70927产 地：中国大陆

  • T70215BRD7929；化合物 BRD7929BRD7929

    BRD7929 is a multistage antimalarial inhibitor for single-dose treatment of malaria in mouse models.

    价 格：￥电议型 号：T70215产 地：中国大陆

  • T69758Flutamide-d7；化合物 Flutamide-d7Flutamide-d7

    Flutamide-d7 is intended for use as an internal standard for the quantification of flutamide by GC- or LC-MS. Flutamide is an androgen receptor antagonist and prodrug form of 2-hydroxy flutamide. Flutamide is converted to 2-hydroxy flutamide by the cytochrome P450 (CYP) isoform CYP1A2 in human liver microsomes. It is cytotoxic to PC3 and LNCaP prostate cancer cells with IC50 values of 98.8 and 81.8 ?M, respectively. Flutamide (50 mg/kg per day) reduces tumor growth in a PC-82 mouse xenograft mo

    价 格：￥电议型 号：T69758产 地：中国大陆

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