BMS-813160

≥99%

Reagent Code: #57675
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CAS Number 1286279-29-5

science Other reagents with same CAS 1286279-29-5

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scatter_plot Molecular Information
Weight 484.64 g/mol
Formula C₂₅H₄₀N₈O₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

BMS-813160 is a potent and selective CCR2 (C-C chemokine receptor type 2) antagonist primarily investigated for its potential therapeutic applications in oncology. CCR2 plays a crucial role in tumor growth, metastasis, and immune response modulation by recruiting pro-tumorigenic monocytes to the tumor microenvironment. By inhibiting CCR2, BMS-813160 aims to disrupt this microenvironment, limiting cancer progression and enhancing immunotherapies like PD-1 inhibitors. Preclinical studies highlight its utility in combination treatments for solid tumors, reducing immunosuppressive signals and promoting anti-tumor immunity. Clinical trials are ongoing to assess safety, pharmacokinetics, and efficacy as a novel cancer therapy. It has also shown promise in inflammatory conditions like fibrosis.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿10,161.00
inventory 2mg
10-20 days ฿5,643.00

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BMS-813160
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BMS-813160 is a potent and selective CCR2 (C-C chemokine receptor type 2) antagonist primarily investigated for its potential therapeutic applications in oncology. CCR2 plays a crucial role in tumor growth, metastasis, and immune response modulation by recruiting pro-tumorigenic monocytes to the tumor microenvironment. By inhibiting CCR2, BMS-813160 aims to disrupt this microenvironment, limiting cancer progression and enhancing immunotherapies like PD-1 inhibitors. Preclinical studies highlight its util

BMS-813160 is a potent and selective CCR2 (C-C chemokine receptor type 2) antagonist primarily investigated for its potential therapeutic applications in oncology. CCR2 plays a crucial role in tumor growth, metastasis, and immune response modulation by recruiting pro-tumorigenic monocytes to the tumor microenvironment. By inhibiting CCR2, BMS-813160 aims to disrupt this microenvironment, limiting cancer progression and enhancing immunotherapies like PD-1 inhibitors. Preclinical studies highlight its utility in combination treatments for solid tumors, reducing immunosuppressive signals and promoting anti-tumor immunity. Clinical trials are ongoing to assess safety, pharmacokinetics, and efficacy as a novel cancer therapy. It has also shown promise in inflammatory conditions like fibrosis.

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