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  • T76677Dacetuzumab；化合物 DacetuzumabDacetuzumab

    Dacetuzumab (SGN-40), a humanized IgG1 anti-CD40 monoclonal antibody, exhibits anti-lymphoma activity by inducing tumor cell death through immune effector functions (antibody-dependent cellular cytotoxicity and phagocytosis [ADCC/ADCP]). It is utilized in research on multiple myeloma [1].

    价 格：￥电议型 号：T76677产 地：中国大陆

  • T76676Cusatuzumab；化合物 CusatuzumabCusatuzumab

    Cusatuzumab, a human αCD70 monoclonal antibody, exhibits cytotoxic activity and enhances antibody-dependent cellular cytotoxicity. It reduces leukemia stem cells (LSCs), triggers gene signatures associated with myeloid differentiation and apoptosis, and holds potential for Acute myeloid leukemia (AML) research [1].

    价 格：￥电议型 号：T76676产 地：中国大陆

  • T76675Clazakizumab；化合物 ClazakizumabClazakizumab

    Clazakizumab, a monoclonal antibody, demonstrates high affinity and specificity towards the interleukin-6 (IL-6) cytokine, potentially inhibiting the cytokine response in COVID-19 caused by SARS-CoV-2. It is also under research for treating psoriatic arthritis (PsA) and renal antibody-mediated rejection [1] [2].

    价 格：￥电议型 号：T76675产 地：中国大陆

  • T76674Cibisatamab；赛必妥单抗Cibisatamab

    Cibisatamab is a T-cell bispecific antibody that acts as a T-cell splicer.Cibisatamab targets carcinoembryonic antigen (CEA) on cancer cells and CD3 on T-cells, and triggers T-cell killing when the CEA on the surface of the cancer cells ranges from intermediate to high levels.Cibisatamab may be used to study solid cancers such as colorectal cancer.

    价 格：￥电议型 号：T76674产 地：中国大陆

  • T76673Bemarituzumab；贝玛妥珠单抗FPA144；FPA144

    Bemarituzumab is a novel humanized IgG1 monoclonal antibody targeting FGFR2b. Bemarituzumab prevents FGFR2b from binding to FGF and activation. Potential applications of Bemarituzumab in cancer research.

    价 格：￥电议型 号：T76673产 地：中国大陆

  • T76672Aprutumab阿普卢妥单抗FGFR-moAb|||FGFR2-TTC|||BAY 1179470

    Aprutumab (BAY 1179470) is a human FGFR2 monoclonal antibody with affinity to FGFR2 isoforms FGFR2-IIIB and FGFR2-IIIC. Aprutumab is commonly used to synthesize antibody-drug conjugates.

    价 格：￥电议型 号：T76672产 地：中国大陆

  • T76671Amatuximab；阿麦妥单抗MORab-009；MORab-009

    Amatuximab (MORab-009) is a chimeric IgG1/k monoclonal antibody humanized against cell surface mesoleptin (MSLN) with antitumor activity for the treatment of solid tumors.

    价 格：￥电议型 号：T76671产 地：中国大陆

  • T76670hMC1R agonist 1；化合物 hMC1R agonist 1hMC1R agonist 1

    hMC1R agonist 1, with an EC 50 of 3 nM, exhibits at least 300-fold higher selectivity for hMC1R compared to hMC3R (EC 50 >902 nM), hMC4R (EC 50 >915 nM), and hMC5R (EC 50 >1000 nM). This compound demonstrates potential for therapeutic applications in targeting the melanocortin family [1].

    价 格：￥电议型 号：T76670产 地：中国大陆

  • T7667R1487；化合物R1487R1487

    R1487 is an orally bioavailable and highly selective p38α mitogen-activated protein kinase inhibitor.

    价 格：￥电议型 号：T7667产 地：中国大陆

  • T76667Z-Arg-SBzl；化合物 Z-Arg-SBzlZ-Arg-SBzl

    Z-Arg-SBzl is a substrate of both bovine and activated human protein C [1] .

    价 格：￥电议型 号：T76667产 地：中国大陆

  • T75667Neamine；化合物 NeamineNeamine

    Neamine, a broad-spectrum aminoglycoside antibiotic derived from Neomycin, exhibits potent antibacterial, antitumor, and neuroprotective activities. As an anti-angiogenesis agent, it specifically targets angiogenin [1] [2].

    价 格：￥电议型 号：T75667产 地：中国大陆

  • T74667KTX-612；化合物 KTX-612KTX-612

    KTX-612 is a compound that serves as an orally active IRAK4 degrader, exhibiting a DC50 value of 7 nM. It is primarily utilized in oncology research [1].

    价 格：￥电议型 号：T74667产 地：中国大陆

  • T74213BAY-6672 hydrochloride；化合物 BAY-6672 hydrochlorideBAY-6672 hydrochloride

    BAY-6672 hydrochloride is a potent, selective antagonist of the human Prostaglandin F (FP) receptor, exhibiting an IC50 value of 11 nM.

    价 格：￥电议型 号：T74213产 地：中国大陆

  • T73667Motapizone；化合物 MotapizoneMotapizone

    Motapizone (NAT 05-239) is a selective PDE3 inhibitor that not only moderately reduces cytokine release in lipopolysaccharide (LPS)-stimulated alveolar macrophages but also suppresses human platelet aggregation by elevating intracellular cAMP levels [1] [2].

    价 格：￥电议型 号：T73667产 地：中国大陆

  • T70667KF 20274；化合物 KF 20274KF 20274

    KF 20274 is an adenosine A1 antagonist; purinergic receptor antagonist.

    价 格：￥电议型 号：T70667产 地：中国大陆

  • T70369PF-06672131；化合物 PF-06672131PF-06672131

    PF-06672131 is a selective EGFR kinase inhibitor.

    价 格：￥电议型 号：T70369产 地：中国大陆

  • T6977SB-366791；化合物SB366791SB366791；SB366791

    SB-366791 is a new and selective cinnamide TRPV1 antagonist.

    价 格：￥电议型 号：T6977产 地：中国大陆

  • T69667IAG-10 HCl；化合物 IAG-10 HClIAG-10 HCl

    IAG-10 is a Novel potent and selective inhibitor of human DNA polymerase kappa (hpol κ).

    价 格：￥电议型 号：T69667产 地：中国大陆

  • T68667Oxanosine；化合物 OxanosineOxanosine

    Oxanosine is an analog of guanosine that has been found in S. capreolus and has diverse biological activities, including antibacterial, antiviral, and anticancer properties. It is active against a variety of bacteria, including S. flexneri, P. mirabilis, and E. coli (MICs = 6.25, 12.5, 25 ?g/ml, respectively, on peptone, but not nutrient, agar). Oxanosine inhibits replication of the HIV-1 strain IIIb in infected CEM and U937, but not H9, cells (EC50s = 7, 27, and >500 ?g/ml, respectively). It al

    价 格：￥电议型 号：T68667产 地：中国大陆

  • T67667Ethyl (Z)-3-aminobut-2-enoate；化合物 Ethyl (Z)-3-aminobut-2-enoateEthyl (Z)-3-aminobut-2-enoate

    Ethyl (Z)-3-aminobut-2-enoate is a useful organic compound for research related to life sciences and the catalog number is T67667.

    价 格：￥电议型 号：T67667产 地：中国大陆

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