2762739-36-4

2762739-36-4 structure
2762739-36-4 structure
  • Name: BT7480
  • Chemical Name: BT7480
  • CAS Number: 2762739-36-4
  • Molecular Formula: C331H467N73O89S10
  • Molecular Weight: 7213.34
  • Catalog: Research Areas Cancer
  • Create Date: 2023-06-17 19:39:09
  • Modify Date: 2025-08-27 14:40:53
  • BT7480 (BCY11863) is one of the Bicycle tumor-targeted immune cell agonists (Bicycle TICAs). BT7480 is an angonist of CD137 (4-1BB). BT7480 consists of a poly(ethylene glycol) (PEG)-based linker, and a synthetic Bicycle peptide targeting CD137 conjugated to Bicycles targeting Nectin-4. Nectin-4 is a cell adhesion molecule, overexpressing in multiple tumor cells. BT7480 elicits significant CD137 agonism and potent antitumor activity in syngeneic mouse models[1][2].

Name BT7480
Description BT7480 (BCY11863) is one of the Bicycle tumor-targeted immune cell agonists (Bicycle TICAs). BT7480 is an angonist of CD137 (4-1BB). BT7480 consists of a poly(ethylene glycol) (PEG)-based linker, and a synthetic Bicycle peptide targeting CD137 conjugated to Bicycles targeting Nectin-4. Nectin-4 is a cell adhesion molecule, overexpressing in multiple tumor cells. BT7480 elicits significant CD137 agonism and potent antitumor activity in syngeneic mouse models[1][2].
Related Catalog
Target

CD137 (4-1BB)[1]

In Vitro BT7480 导致原代人免疫细胞中促炎细胞因子 IFNγ 和 IL-2 的分泌呈剂量依赖性增加 (EC50=0.22 nM 和 0.36 nM),而 HT1376 肿瘤细胞与来自健康供体的人外周血单核细胞 (PBMC) 共培养并用抗 CD3 处理以刺激 CD137 在免疫细胞上的表达[1]。
In Vivo BT7480(5 mg/kg;腹腔注射;每天一次,持续 10 天)在 CT26-Nectin-4/huCD137 小鼠模型中表现出抗肿瘤活性[1]。 BT7480(2 mg/kg;静脉注射;单剂量)的 CL 为 8.5 mL/min/kg,终末半衰期为 3.6 小时[1]。 BT7480(1、5、10 和 30 mg/kg;腹腔注射;单剂量)导致 CD-1 小鼠的暴露量 (AUCinf) 剂量依赖性增加[1] 。 BT7480(1 和 10 mg/kg;腹腔注射;每天 3 次,持续 40 天)在小鼠 MC38-Nectin-4 肿瘤模型中导致肿瘤消退[1]。 在食蟹猴 MC38 同基因模型中的药代动力学分析[1] Route Dose (mg/kg) CLlast (mL/min/kg) Vdss (L/kg) t1/2 (h) i.v. 1 3.3 0.62 5.3 Animal Model: Mice bearing subcutaneous MC38-Nectin-4 tumors[1] Dosage: 1 mg/kg and 10 mg/kg Administration: IP; 3 times per days for 40 days Result: Led efficacious tumor growth reduction and complete responses (CRs) induction, with the rate of CRs ranging from 4/6 (1 mg/kg) to 6/6 (10 mg/kg) by day 40.
References

[1]. Upadhyaya P, et al. Discovery and Optimization of a Synthetic Class of Nectin-4-Targeted CD137 Agonists for Immuno-oncology. J Med Chem. 2022 Jul 28;65(14):9858-9872.  

[2]. Hurov K, et al. A novel fully synthetic dual targeted Nectin-4/4-1BB Bicycle (R) peptide induces tumor localized 4-1BB agonism[J]. J. Immunother. Cancer, 2019, 7.

Molecular Formula C331H467N73O89S10
Molecular Weight 7213.34
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