1463459-96-2

1463459-96-2 structure
1463459-96-2 structure
  • Name: Ascrinvacumab
  • Chemical Name: Ascrinvacumab
  • CAS Number: 1463459-96-2
  • Molecular Formula:
  • Molecular Weight:
  • Catalog: Signaling Pathways Protein Tyrosine Kinase/RTK ALK
  • Create Date: 2023-01-14 19:11:00
  • Modify Date: 2024-09-17 12:00:40
  • Ascrinvacumab (PF-03446962) is a human IgG2 monoclonal antibody targets ALK-1. Ascrinvacumab shows binding efficiency with human ALK1 with a Kd value of 7 nM. Ascrinvacumab can be used for the research of hepatocellular carcinoma (HCC)[1].

Name Ascrinvacumab
Description Ascrinvacumab (PF-03446962) is a human IgG2 monoclonal antibody targets ALK-1. Ascrinvacumab shows binding efficiency with human ALK1 with a Kd value of 7 nM. Ascrinvacumab can be used for the research of hepatocellular carcinoma (HCC)[1].
Related Catalog
In Vitro Ascrinvacumab 与细胞人 ALK1 结合,Kd 值为 7 nm[1]。 Ascrinvacumab (30 分钟) 阻断 BMP9 和 FCS 诱导的应答,缓解 BMP9 诱导的 Smad1 磷酸化强度和持续时间[1]。 Ascrinvacumab (0.01-10 μg/mL; 2 h) 抑制 BMP9 结合到 ALK1[1]。 Ascrinvacumab (40 μg/mL; 2 h) 有效抑制人脐静脉内皮细胞 (HUVECs) 的内皮萌发[1]。
In Vivo Ascrinvacumab 联合贝伐单抗 (bevacizumab; anti-VEGF) 可降低人血管密度,提高抗肿瘤疗效在小鼠嵌合体肿瘤模型中[1]。
References

[1]. van Meeteren LA, et al. Anti-human activin receptor-like kinase 1 (ALK1) antibody attenuates bone morphogenetic protein 9 (BMP9)-induced ALK1 signaling and interferes with endothelial cell sprouting. J Biol Chem. 2012 May 25;287(22):18551-61.  

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