1. Cancer
  2. Cancer Targeted Therapy

Cancer Targeted Therapy (肿瘤靶向治疗)

Cancer targeted therapy is the foundation of precision medicine; it uses drugs or other substances to target specific genes and proteins that control cancer cells’ growth, division and spreading. Compared to traditional chemotherapy drugs, targeted-drugs can specifically act on cancer cells with high efficacy without damaging normal cells. Drugs used in cancer targeted therapy mainly includes small molecules and macromolecules (e.g., monoclonal antibodies), which can target cancer cells and constituents in the tumor microenvironment to activate the immune system. Anti-angiogenesis drugs, such as those targeting vascular endothelial growth factor (VEGF), epidermal growth factor receptor (EGFR), transforming growth factor (TGF)-α, TGF-β, Tumor necrosis factor (TNF)-α, and platelet-derived endothelial growth factor (PDGFR) inhibit the proliferation and metastasis of cancer cells. In recent years, the proportion of antibody drugs in cancer treatment has gradually become prominent. Antibody-drug conjugates (ADCs) are a new type of targeted drugs that are composed of monoclonal antibody, cytotoxic drug and linker. ADCs can deliver drugs to tumor cells and minimize the toxicity to normal tissues. Proteolysis-targeting chimera (PROTAC) is a useful technology for targeted protein degradation. PROTAC exploits the ubiquitin-proteasome system and forms a ternary complex with a hijacked E3 ubiquitin ligase and target protein, leading to polyubiquitination and degradation of the target protein.

Targeted therapy is a useful strategy in treatment of cancer either alone or in combination with standard chemotherapy. At present, targeted therapy has proved significant clinical success in the treatment of many types of cancer, including breast cancer, colorectal cancer, leukemia, ovarian cancer and lung cancer.

Cancer Targeted Therapy 相关产品 (36407):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-RI00667A
    hsa-miR-3200-3p antagomir
    hsa-miR-3200-3p antagomir 是一种经过特殊化学修饰的成熟miRNA的互补单链,全链进行甲氧基修饰,在5'端和3'端分别有2个和4个硫代骨架修饰,并在3'端连接有高亲和性胆固醇修饰。miRNA antagomir通过特异性结合成熟miRNA,阻止miRNA与其靶基因的互补配对,从而抑制miRNA的功能。相比于miRNA inhibitor,miRNA antagomir在动物实验中具有更高的稳定性和抑制效果,更易通过细胞膜、组织间隙而富集于靶细胞。
    hsa-miR-3200-3p antagomir
  • HY-RI00551A
    hsa-miR-3120-3p antagomir
    hsa-miR-3120-3p antagomir 是一种经过特殊化学修饰的成熟miRNA的互补单链,全链进行甲氧基修饰,在5'端和3'端分别有2个和4个硫代骨架修饰,并在3'端连接有高亲和性胆固醇修饰。miRNA antagomir通过特异性结合成熟miRNA,阻止miRNA与其靶基因的互补配对,从而抑制miRNA的功能。相比于miRNA inhibitor,miRNA antagomir在动物实验中具有更高的稳定性和抑制效果,更易通过细胞膜、组织间隙而富集于靶细胞。
    hsa-miR-3120-3p antagomir
  • HY-RI03425
    mmu-miR-6417 inhibitor
    mmu-miR-6417 inhibitor 是一种全链经过甲氧基修饰的成熟miRNA的互补单链。miRNA inhibitor通过特异性结合成熟miRNA,阻止miRNA与其靶基因的互补配对,从而抑制miRNA的功能,可用于miRNA 功能缺失性(loss-of-function)研究。
    mmu-miR-6417 inhibitor
  • HY-RI01676A
    hsa-miR-548bb-5p antagomir
    hsa-miR-548bb-5p antagomir 是一种经过特殊化学修饰的成熟miRNA的互补单链,全链进行甲氧基修饰,在5'端和3'端分别有2个和4个硫代骨架修饰,并在3'端连接有高亲和性胆固醇修饰。miRNA antagomir通过特异性结合成熟miRNA,阻止miRNA与其靶基因的互补配对,从而抑制miRNA的功能。相比于miRNA inhibitor,miRNA antagomir在动物实验中具有更高的稳定性和抑制效果,更易通过细胞膜、组织间隙而富集于靶细胞。
    hsa-miR-548bb-5p antagomir
  • HY-N4332
    Rivulariapeptolides 1121
    Rivulariapeptolides 1121 是一种高效的选择性丝氨酸蛋白酶抑制剂,其对胰凝蛋白酶、弹性蛋白酶和蛋白酶 K 的 IC50 值分别为 35.52 nM、13.24 nM 和 48.05 nM。
    Rivulariapeptolides 1121
  • HY-173603
    FAK-IN-27
    FAK-IN-27 (compound 8A) 是一种有效的 FAK 选择性抑制剂,其IC50 为 4.968 nM。FAK-IN-27 对 H1299 细胞增殖有抑制作用,IC50 为 0.28 μM。FAK-IN-27 可用于 NSCLC 的研究。
    FAK-IN-27
  • HY-174329
    mrt-5702D
    mrt-5702D 是一种靶向 cereblon (CRBN) 的分子胶降解剂。mrt-5702D 与 CRBN 和 G3BP2 形成三元复合物,激活泛素-蛋白酶体系统,从而降解 G3BP2。mrt-5702D 有望用于 G3BP2 相关癌症 (如乳腺癌、肺癌) 和神经退行性疾病的研究。
    mrt-5702D
  • HY-RI03583
    mmu-miR-6930-5p inhibitor
    mmu-miR-6930-5p inhibitor 是一种全链经过甲氧基修饰的成熟miRNA的互补单链。miRNA inhibitor通过特异性结合成熟miRNA,阻止miRNA与其靶基因的互补配对,从而抑制miRNA的功能,可用于miRNA 功能缺失性(loss-of-function)研究。
    mmu-miR-6930-5p inhibitor
  • HY-RI00318
    hsa-miR-15a-3p inhibitor
    hsa-miR-15a-3p inhibitor 是一种全链经过甲氧基修饰的成熟miRNA的互补单链。miRNA inhibitor通过特异性结合成熟miRNA,阻止miRNA与其靶基因的互补配对,从而抑制miRNA的功能,可用于miRNA 功能缺失性(loss-of-function)研究。
    hsa-miR-15a-3p inhibitor
  • HY-155671
    HDAC6-IN-18
    HDAC6-IN-18 (Compound 4) 是第一个不可逆的 HDAC6 亚型选择性抑制剂,具有有效的抗多发性骨髓瘤活性。 HDAC6-IN-18 在 RPMI8266、U266 和 MM.1S 细胞中具有 HDAC6 抑制活性,IC50 值分别为 0.17、0.7 和 0.42 μM[1 ]
    HDAC6-IN-18
  • HY-RI01247A
    hsa-miR-4678 antagomir
    hsa-miR-4678 antagomir 是一种经过特殊化学修饰的成熟miRNA的互补单链,全链进行甲氧基修饰,在5'端和3'端分别有2个和4个硫代骨架修饰,并在3'端连接有高亲和性胆固醇修饰。miRNA antagomir通过特异性结合成熟miRNA,阻止miRNA与其靶基因的互补配对,从而抑制miRNA的功能。相比于miRNA inhibitor,miRNA antagomir在动物实验中具有更高的稳定性和抑制效果,更易通过细胞膜、组织间隙而富集于靶细胞。
    hsa-miR-4678 antagomir
  • HY-132077
    THP-PEG16-THP
    THP-PEG16-THP 是一种 PROTAC linker,属于 PEG 类。可用于合成 PROTAC 分子。
    THP-PEG16-THP
  • HY-P99464
    Bectumomab

    贝妥莫单抗

    158318-63-9
    Bectumomab (IMMU-LL 2) 是一种针对人 CD22 (抗原) 的人源化 IgG2a 单抗。Bectumomab 也是一种抗淋巴瘤抗体片段。Bectumomab 可与锝 99 (Tc99m LL2 Fab) 联合用于成像。此外,Bectumomab 能够检查复发性或新诊断的非霍奇金淋巴瘤 (NHL) 的分期,并在放射免疫研究 (RIT) 前评估靶向性。
    Bectumomab
  • HY-RI00313A
    hsa-miR-154-3p antagomir
    hsa-miR-154-3p antagomir 是一种经过特殊化学修饰的成熟miRNA的互补单链,全链进行甲氧基修饰,在5'端和3'端分别有2个和4个硫代骨架修饰,并在3'端连接有高亲和性胆固醇修饰。miRNA antagomir通过特异性结合成熟miRNA,阻止miRNA与其靶基因的互补配对,从而抑制miRNA的功能。相比于miRNA inhibitor,miRNA antagomir在动物实验中具有更高的稳定性和抑制效果,更易通过细胞膜、组织间隙而富集于靶细胞。
    hsa-miR-154-3p antagomir
  • HY-RI02165
    hsa-miR-6800-5p inhibitor
    hsa-miR-6800-5p inhibitor 是一种全链经过甲氧基修饰的成熟miRNA的互补单链。miRNA inhibitor通过特异性结合成熟miRNA,阻止miRNA与其靶基因的互补配对,从而抑制miRNA的功能,可用于miRNA 功能缺失性(loss-of-function)研究。
    hsa-miR-6800-5p inhibitor
  • HY-RI04472
    rno-miR-450b-5p inhibitor
    rno-miR-450b-5p inhibitor 是一种全链经过甲氧基修饰的成熟miRNA的互补单链。miRNA inhibitor通过特异性结合成熟miRNA,阻止miRNA与其靶基因的互补配对,从而抑制miRNA的功能,可用于miRNA 功能缺失性(loss-of-function)研究。
    rno-miR-450b-5p inhibitor
  • HY-W605935
    2-Amino-6-chloropurine-9-beta-d-(2'-deoxy-3',5'-di-o-benzoyl-2'-fluoro)arabinoriboside 118373-61-8
    2-Amino-6-chloropurine -9-beta-D-(2’-deoxy-3’,5’-di-O-benzoyl-2’-fluoro)arabinoriboside 是一种嘌呤核苷类似物。嘌呤核苷类似物具有广泛的抗肿瘤活性,靶向惰性淋巴系统恶性肿瘤。这一过程中的抗癌机制依赖于抑制 DNA 合成,诱导细胞凋亡 (apoptosis) 等。
    2-Amino-6-chloropurine-9-beta-d-(2'-deoxy-3',5'-di-o-benzoyl-2'-fluoro)arabinoriboside
  • HY-RI04227
    rno-miR-133b-5p inhibitor
    rno-miR-133b-5p inhibitor 是一种全链经过甲氧基修饰的成熟miRNA的互补单链。miRNA inhibitor通过特异性结合成熟miRNA,阻止miRNA与其靶基因的互补配对,从而抑制miRNA的功能,可用于miRNA 功能缺失性(loss-of-function)研究。
    rno-miR-133b-5p inhibitor
  • HY-RI03082
    mmu-miR-3535 inhibitor
    mmu-miR-3535 inhibitor 是一种全链经过甲氧基修饰的成熟miRNA的互补单链。miRNA inhibitor通过特异性结合成熟miRNA,阻止miRNA与其靶基因的互补配对,从而抑制miRNA的功能,可用于miRNA 功能缺失性(loss-of-function)研究。
    mmu-miR-3535 inhibitor
  • HY-147710
    PIN1 inhibitor 2 2417101-28-9
    PIN1 inhibitor 2 (compound 12) 是一种有效的 PIN1 抑制剂。PIN1 inhibitor 2 显示出抗肿瘤活性,对 MCF7 细胞的 IC50 为 9.55 µM。PIN1 inhibitor 2 具有研究乳腺癌的潜力。
    PIN1 inhibitor 2