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

抗体-药物偶联物 (ADC) 是一种通过化学接头与高细胞毒性小分子 (有效载荷) 偶联的人源化或人类单克隆抗体,是一种新型治疗形式,具有在癌症化疗中实现范式转变的巨大潜力。这种基于抗体的分子平台能够选择性地将强效的细胞毒性有效载荷递送至目标癌细胞,与传统化疗相比,可提高疗效、降低全身毒性并实现更佳的药代动力学 (PK)/药效学 (PD) 和生物分布。

ADC 的所有三个组成部分,即抗体、细胞毒性剂和连接它们的接头,都是其设计中的关键元素。抗体部分应该对选择性表达在癌细胞上或相对于正常细胞在癌细胞上过度表达的细胞表面靶分子具有特异性。ADC 的有效载荷必须具有高度的细胞毒性,这样它才能在 ADC 分布到实体肿瘤组织后达到细胞内浓度时杀死肿瘤细胞,并且因为只有有限数量的有效载荷可以连接到抗体分子(通常平均每个抗体 3-4 个有效载荷)而不会严重损害其生物物理和药代动力学特性。细胞毒性化合物包括卡奇霉素的衍生物,一类通过引起 DNA 双链断裂杀死细胞的高细胞毒性烯二炔抗生素,以及强效抗有丝分裂微管破坏剂、多拉司他汀 10(奥瑞他汀)和美登素的衍生物。

ADC 的第三个重要组成部分是形成有效载荷和抗体之间化学连接的接头。连接子在循环中应足够稳定,以允许有效载荷在循环中分布到组织(包括实体肿瘤组织)时保持与抗体的连接,但一旦 ADC 被癌细胞吸收,应允许有效释放活性细胞杀伤剂。连接子可分为可裂解连接子和不可裂解连接子。

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.

Antibody-Drug Conjugates (ADCs) 相关产品 (104):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-171682
    Anti-CCL2 (Carlumab)-McMMAF
    Anti-CCL2 (Carlumab)-McMMAF 是一种抗体-药物偶联物 (ADC),由人源性抗 CCL2 (趋化因子配体 2) 抗体 Carlumab (HY-P99188) 与保护基团 maleimidocaproyl 和微管蛋白 (tubulin) 抑制剂 MMAF (HY-15579) 缀合而成。ADC 毒性分子和 linker 部分是 McMMAF (HY-15578)。 Anti-CCL2 (Carlumab)-McMMAF 可诱导细胞凋亡 (Apoptosis) 并用于癌症的研究。
    Anti-CCL2 (Carlumab)-McMMAF
  • HY-172820
    Trastuzumab envedotin
    Trastuzumab envedotin (DP303c) 是一种抗人表皮生长因子受体 2 (HER2) 抗体-药物偶联物 (ADC)。Trastuzumab envedotin 是由微管蛋白聚合抑制剂 Monomethyl auristatin E (MMAE) (HY-15162) 通过可切割的连接体与抗 HER2 抗体 DP001 组成。Trastuzumab envedotin 可用于 HER2 阳性实体肿瘤的研究,如乳腺癌、结直肠癌、胃癌。
    Trastuzumab envedotin
  • HY-171683
    Anti-CCL2 (Carlumab)-VcMMAE
    Anti-CCL2 (Carlumab)-VcMMAE 是一种抗体-药物偶联物 (ADC),由人源性抗 CCL2 (趋化因子配体 2) 抗体 Carlumab (HY-P99188) 与 valine-citrulline (vc) 和微管蛋白 (tubulin) 抑制剂 MMAE (HY-15162) 缀合而成。ADC 毒性分子和 linker 部分是 McMMAE (HY-15575) 。Anti-CCL2 (Carlumab)-VcMMAE 可诱导细胞凋亡 (Apoptosis) 并用于癌症的研究。
    Anti-CCL2 (Carlumab)-VcMMAE
  • HY-164919
    Calotatug ginistinag
    Calotatug ginistinag (XMT-2056) 是一种靶向 HER2 的抗体偶联药物 (Antibody-Drug Conjugates),通过 linker (XMT-1519 conjugate-1, HY-148067) 与 STING 激动剂 (STING agonist-20, HY-148068) 组成的有效载荷相连,具有潜在的免疫激活和抗肿瘤活性。
    Calotatug ginistinag