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 (36400):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-RI03011A
    mmu-miR-3112-3p antagomir
    mmu-miR-3112-3p 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。
    mmu-miR-3112-3p antagomir
  • HY-150072A
    (2S,4R)-DS89002333
    (2S,4R)-DS89002333 是 DS89002333 (HY-150072) 的对映异构体。DS89002333 是一种具有口服活性的 PRKACA 抑制剂,IC50 为 0.3 nM。
    (2S,4R)-DS89002333
  • HY-160709
    Wnt/β-catenin-IN-2 1397006-01-7
    Wnt/β-catenin-IN-2 (Compound 3235-0367) 是一种 Wnt/β-catenin 信号通路抑制剂,IC50KD 值分别为 7.1 和 2.5 μM。Wnt/β-catenin-IN-2 可用于癌症研究。
    Wnt/β-catenin-IN-2
  • HY-152328
    7-Ethyl-7,8-dihydro-8-oxo-9-(β-D-xylofuranosyl)guanine 2389988-43-4
    7-Ethyl-7,8-dihydro-8-oxo-9-(β-D-xylofuranosyl)guanine 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。
    7-Ethyl-7,8-dihydro-8-oxo-9-(β-D-xylofuranosyl)guanine
  • HY-168307
    Me-Thalidomide-O-C8-NH2 2550393-20-7
    Me-Thalidomide-O-C8-NH2 是一种 E3 泛素酶配体-连接子偶联物 (E3 ligase ligand-linker conjugate)。Me-Thalidomide-O-C8-NH2 可用于合成 MS154N (HY-157579)。
    Me-Thalidomide-O-C8-NH2
  • HY-RI01127
    hsa-miR-450b-3p inhibitor
    hsa-miR-450b-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-450b-3p inhibitor
  • HY-RI04349
    rno-miR-324-3p inhibitor
    rno-miR-324-3p 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。
    rno-miR-324-3p inhibitor
  • HY-169324
    APL-1092 2921735-91-1
    APL-1092 (Mal-Exo-EEVC-Exatecan) 是一种 可用于 ADC 合成的药物-Linker 偶联物,结构中包含 Exatecan (HY-13631) (ADC payload) 和 linker。
    APL-1092
  • HY-RI04351
    rno-miR-327 inhibitor
    rno-miR-327 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-327 inhibitor
  • HY-130960
    Tubulysin IM-3 1639986-05-2
    Tubulysin IM-3 是微管蛋白 (Microtubule/Tubulin) 抑制剂,可作为 ADC 细胞毒素 (ADC Cytotoxin) 及抗微管毒素 (anti-microtubule toxins) 用于 ADC 合成。
    Tubulysin IM-3
  • HY-RI00283A
    hsa-miR-1468-3p antagomir
    hsa-miR-1468-3p 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-1468-3p antagomir
  • HY-RI03966A
    mmu-miR-7214-5p antagomir
    mmu-miR-7214-5p 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。
    mmu-miR-7214-5p antagomir
  • HY-158197
    RC-106 1346216-50-9
    RC-106 是一种蛋白酶体抑制剂 (IC50: 35 μM) 和 Sigma 受体调节剂,具有抗癌活性。RC-106 对包括胶质母细胞瘤 (GB) 和多发性骨髓瘤 (MM) 在内的癌细胞具有抗增殖活性。
    RC-106
  • HY-10201S1
    Sorafenib-d4

    索拉非尼-d4

    1207560-07-3
    Sorafenib-d4 是 Sorafenib 的氘代化合物。Sorafenib 是一种多激酶抑制剂,抑制 Raf-1,B-RafVEGFR-3 的 IC50 分别为6 nM,20 nM,22 nM。
    Sorafenib-d<sub>4</sub>
  • HY-W014605R
    Diphenylcyclopropenone (Standard)

    二苯基环丙烯酮 (Standard)

    886-38-4
    Diphenylcyclopropenone (Standard)是 Diphenylcyclopropenone 的分析标准品。本产品用于研究及分析应用。Diphenylcyclopropenone (Diphencyprone) 是一种局部免疫调节剂,可用于斑秃的研究。
    Diphenylcyclopropenone (Standard)
  • HY-N4322R
    Decursinol angelate (Standard)

    紫花前胡醇当归酸酯 (Standard)

    130848-06-5
    Decursinol angelate (Standard) 是 Decursinol angelate 的分析标准品。本产品用于研究及分析应用。Decursinol angelate 是从 Angelica gigas 根部分离得到的一种细胞毒性物质,是 PKC 激酶的激活剂,拥有抗肿瘤和抗炎活性。
    Decursinol angelate (Standard)
  • HY-RI01370A
    hsa-miR-4755-5p antagomir
    hsa-miR-4755-5p 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-4755-5p antagomir
  • HY-163697
    WEE1-IN-7 2924006-98-2
    WEE1-IN-7 (compound 12h) 是一种有效的具有口服活性的 WEE1 抑制剂,其IC50值为 2.1 nM。WEE1-IN-7 诱导细胞凋亡 (apoptosis) 和细胞周期停滞于 S 期。WEE1-IN-7 具有抗肿瘤活性。
    WEE1-IN-7
  • HY-154148
    N6-Isopentenyl-2’-deoxy adenosine, 2’-deoxy riboprine 25775-85-3
    N6-Isopentenyl-2’-deoxy adenosine, 2’-deoxy riboprine 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。
    N6-Isopentenyl-2’-deoxy adenosine, 2’-deoxy riboprine
  • HY-139104
    Thailanstatin D 1609105-89-6
    Thailanstatin D 是 Thailanstatin A 的类似物,通过干扰 U2AF65 和 SAP155 之间的相互作用,阻止它们与位于分支点和 3' 剪接位点之间的多嘧啶束结合,能够抑制 AR-V7 基因剪接。Thailanstatin D 对人 CRPC 异种移植瘤具有明显的抑瘤作用,可导致细胞凋亡 (apoptosis)。
    Thailanstatin D