1. Signaling Pathways
  2. Antibody-drug Conjugate/ADC Related
  3. Antibody-Drug Conjugates (ADCs)

Antibody-Drug Conjugates (ADCs) (抗体偶联药物)

Antibody-Drug Conjugates

The antibody-drug conjugate (ADC), a humanized or human monoclonal antibody conjugated with highly cytotoxic small molecules (payloads) through chemical linkers, is a novel therapeutic format and has great potential to make a paradigm shift in cancer chemotherapy. This antibody-based molecular platform enables selective delivery of a potent cytotoxic payload to target cancer cells, resulting in improved efficacy, reduced systemic toxicity, and preferable pharmacokinetics (PK)/pharmacodynamics (PD) and biodistribution compared to traditional chemotherapy.

All three component parts of an ADC, the antibody, the cytotoxic agent, and the linker that joins them, are critical elements in its design. The antibody moiety should be specific for a cell surface target molecule that is selectively expressed on cancer cells, or overexpressed on cancer cells relative to normal cells. The payload of an ADC must be highly cytotoxic so that it can kill tumor cells at the intracellular concentrations achievable following distribution of the ADC into solid tumor tissue, and because only a limited number of payloads can be linked to an antibody molecule (typically an average of 3-4 payloads per antibody) without severely compromising its biophysical and pharmacokinetic properties. The cytotoxic compounds include derivatives of calicheamicin, a class of highly cytotoxic enediyne antibiotics which kill cells by causing DNA double-strand breaks, and derivatives of the potent antimitotic microtubule-disrupting agents, dolastatin 10 (auristatins) and maytansine.

The third vital component of an ADC is the linker that forms a chemical connection between the payload and the antibody. The linker should be sufficiently stable in circulation to allow the payload to remain attached to the antibody while in circulation as it distributes into tissues (including solid tumor tissue), yet should allow efficient release of an active cell-killing agent once the ADC is taken up into the cancer cells. Linkers can be characterized as either cleavable, or as non-cleavable.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-152963
    Tisotumab vedotin 99.47%
    Tisotumab vedotin 是一种靶向组织因子 (tissue factor, TF) 的抗体-药物偶联物 (ADC)。Tisotumab vedotin 由组织因子的全人源单克隆抗体(TF-011) 与 Monomethyl Auristatin E (MMAE) 结合而成。Tisotumab vedotin 具有较好的抗肿瘤活性,可用于晚期或转移性实体瘤的研究。
    Tisotumab vedotin
  • HY-P99107A
    Brentuximab vedotin (solution) 99.23%
    Brentuximab vedotin 溶液是 Brentuximab vedotin (HY-P99107) 的溶液形式。Brentuximab vedotin (cAC10-vcMMAE) 是一种抗体-药物偶联物 (ADC),包含抗 CD30 抗体和细胞毒性剂单甲基 auristatin E (MMAE)。
    Brentuximab vedotin (solution)
  • HY-P99612
    Farletuzumab ecteribulin
    Farletuzumab ecteribulin (MORAb-202) 是一种抗体-活性分子偶联物 (ADC),由人源化抗人叶酸受体 α (FRA) 抗体 Farletuzumab (HY-P99153) 通过还原的链间二硫键与 Mal-PEG2-Val-Cit-PAB-eribulin 偶联而成。Farletuzumab ecteribulin 的活性分子抗体比为 4.0。Farletuzumab ecteribulin 在体外对 FRA 阳性细胞具有高度细胞毒性。Farletuzumab ecteribulin 具有有效的抗肿瘤活性。
    Farletuzumab ecteribulin
  • HY-141604
    Glembatumumab vedotin 99.41%
    Glembatumumab vedotin (CDX-011) 是一种 ADC (Antibody-Drug Conjugates (ADCs)),包含针对糖蛋白 NMB (GPNMB) 的全人 IgG2 单克隆抗体 (CR011),并通过蛋白酶敏感的 vc 接头与强效微管蛋白结合细胞毒剂 MMAE 偶联。Glembatumumab vedotin 具有强大的抗癌作用。
    Glembatumumab vedotin
  • HY-P4073
    ANG1005 98.83%
    ANG1005 (Paclitaxel trevade) 是一种可透过血脑屏障的肽-药物偶联物。ANG1005 是一种紫杉烷衍生物,由三个紫杉醇 (HY-B0015) 分子与 Angiopep-2 共价连接组成,旨在通过低密度脂蛋白受体相关蛋白 (LRP1) 运输系统穿过血脑和血脑脊髓屏障,并穿透恶性细胞。
    ANG1005
  • HY-P99547
    Trastuzumab duocarmazine 99.87%
    Trastuzumab duocarmazine ((vic)-Trastuzumab duocarmazine) 是一种 HER2 靶向ADC, 可以在肿瘤细胞中被组织蛋白酶 B 识别并裂解,选择性靶向肿瘤细胞。Trastuzumab duocarmazine 具有抗肿瘤活性,可以用于子宫和卵巢癌肉瘤等相关癌症研究。
    Trastuzumab duocarmazine
  • HY-P99493
    Cantuzumab ravtansine 98.71%
    Cantuzumab ravtansine (IMGN242; huC242-DM4) 是一种 ADC,由一种人源化单克隆抗体 huC242,通过二硫键与 DM4 (DM4; HY-12454) 共价连接。Cantuzumab ravtansine 对一系列 CanAg 阳性人肿瘤异种移植物具有广泛的抗肿瘤功效。
    Cantuzumab ravtansine
  • HY-P99829
    Cofetuzumab pelidotin 99.67%
    Cofetuzumab pelidotin (PF-06647020) 是一种靶向 PTK7ADC,包含人源化抗 PTK7 mAb (hu6M024;IgG1),通过可裂解的缬氨酸-瓜氨酸 (vc) 的 linker 与 auristatin 微管抑制剂 Auristatin-0101 (Aur0101;HY-12522) 连接。Cofetuzumab pelidotin 的 DAR 为 4。Cofetuzumab pelidotin 与细胞表面 PTK7 结合的 EC50 为 1153 pM (通过流式细胞术检测)。Cofetuzumab pelidotin 具有用于实体瘤研究的潜力。
    Cofetuzumab pelidotin
  • HY-P99956
    Zilovertamab vedotin 98.15%
    Zilovertamab vedotin (VLS-101) 是一种新型抗体-活性分子偶联物 (ADC),包含人源化单克隆抗体 zilovertamab 和抗微管细胞毒素单甲基 vedotin。Zilovertamab vedotin 与肿瘤细胞 ROR1 结合导致快速内化、转运至溶酶体、抗体-活性分子偶联物裂解和单甲基 vedotin 释放。Zilovertamab vedotin 诱导细胞凋亡。Zilovertamab vedotin 可用于癌症研究。
    Zilovertamab vedotin
  • HY-P99593A
    Sofituzumab vedotin (solution)
    Sofituzumab vedotin (DMUC5754A) (solution) 是一种抗体-药物偶联物 (ADC),包含人源化 IgG1 抗 MUC16 单克隆抗体和一种有效的抗有丝分裂剂 MMAE,通过蛋白酶可切割的连接子连接。
    Sofituzumab vedotin (solution)
  • HY-P99492
    Cantuzumab mertansine

    莫坎妥珠单抗

    Cantuzumab mertansine (SB-408075; huC242-DM1) 是一种 ADC,是强效美登素衍生物 (DM1; HY-19792) 和针对 CanAg 的人源化单克隆抗体 (huC242) 的免疫偶联物。Cantuzumab mertansine 对结肠癌细胞具有细胞毒性,并且对一系列 CanAg 阳性人肿瘤异种移植物具有广泛的抗肿瘤活性。
    Cantuzumab mertansine
  • HY-132254A
    Sacituzumab govitecan (solution)
    Sacituzumab govitecan (IMMU-132) 是一种抗体-活性分子偶联物 (ADC),靶向 Trop-2 传递 SN-38。Sacituzumab govitecan 具有抗癌活性。
    Sacituzumab govitecan (solution)
  • HY-P99255
    Moxetumomab pasudotox
    Moxetumomab pasudotox (CAT 8015) 是一种抗 CD22 免疫毒素,含有抗 CD22 FvPseudomonas exotoxinCD22 是在多种恶性 B 细胞上表达的细胞表面受体。Moxetumomab pasudotox 可用于毛细胞白血病 (HCL) 的研究。
    Moxetumomab pasudotox
  • HY-156712
    Depatuxizumab MMAE
    Depatuxizumab MMAE 是一种抗体-活性分子偶联物 (ADC),由抗 EGFR 抗体 (Depatuxizumab) 和 Monomethyl auristatin E (MMAE) 组成。Depatuxizumab 抑制突变型 EGFRvIII 和野生型 EGFR 异种移植瘤模型的生长。
    Depatuxizumab MMAE
  • HY-P99593
    Sofituzumab vedotin

    维汀-索非妥珠单抗

    98.72%
    Sofituzumab vedotin (DMUC5754A) 是一种含有 MMAE 的抗 MUC16 抗体-药物偶联物 (ADC),具有蛋白酶切割连接子。Sofituzumab vedotin 可用于癌症研究。
    Sofituzumab vedotin
  • HY-132259
    Depatuxizumab mafodotin
    Depatuxizumab mafodotin 是一种抗体-药物偶联物 (ADC),能够特异性的靶向表皮生长因子受体 (EGFR)。Depatuxizumab mafodotin 可以用于癌症的研究。
    Depatuxizumab mafodotin
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