
Emactuzumab
CAS No. 1448221-67-7
Emactuzumab( —— )
Catalog No. M36711 CAS No. 1448221-67-7
Emactuzumab(RG 7155) is a monoclonal antibody against colony-stimulating factor-1 receptor targeting tumor-associated macrophages (TAMs) Emactuzumab has antitumor activity and inhibits activation of colony-stimulating factor 1 receptor (CSF1R) Emactuzumab has a high affinity for CSF-1R with a Ki value of 0.2 nM.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 499 | Get Quote |
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5MG | 710 | Get Quote |
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10MG | 1102 | Get Quote |
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25MG | 1582 | Get Quote |
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50MG | 2107 | Get Quote |
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100MG | 2808 | Get Quote |
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500MG | Get Quote | Get Quote |
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Biological Information
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Product NameEmactuzumab
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NoteResearch use only, not for human use.
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Brief DescriptionEmactuzumab(RG 7155) is a monoclonal antibody against colony-stimulating factor-1 receptor targeting tumor-associated macrophages (TAMs) Emactuzumab has antitumor activity and inhibits activation of colony-stimulating factor 1 receptor (CSF1R) Emactuzumab has a high affinity for CSF-1R with a Ki value of 0.2 nM.
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DescriptionEmactuzumab(RG 7155) is a specific monoclonal antibody that inhibits colonystimulating factor 1 receptor (CSF1R) activation. Emactuzumab has high affinity for CSF-1R with Ki value of 0.2 nM to blocks CSF-1R dimerization. Emactuzumab can be used for the research of several diseases, such as diffuse-type tenosynovial giant cell tumour (dt-GCT) .
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In VitroEmactuzumab (RG 7155) binds to human and cynomolgus CSF-1R with high affinity (Kd = 0.2 nM) to blocks CSF-1R dimerization.RG7155 (0-10 μg/mL, 7 days) potently inhibited the viability of CSF-1-differentiated macrophages with an IC50 of 0.3 nM by inducing cell death.RG7155 (30 μg/mL, 6 days) induces cell death of in vitro-differentiated human M2-like macrophages.Cell Viability Assay Cell Line:CSF-1 and/or GM-CSF Macrophages Concentration:0-10 μg/mL Incubation Time:7 days Result:Resulted cell death of CSF-1-differentiated macrophages.
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In VivoEmactuzumab(RG 7155) (i.v.; 0.1、1、10、30 and 100 mg/kg; once) increases CSF-1 concentration in nonhuman primates’ peripheral blood.RG7155 (i.v.; 0, 30, and 100 mg/kg; once weekly; for 2 weeks) depletes CSF-1R+CD163+ macrophages in vivo.Animal Model:cynomolgus monkeys Macaca fascicularis Dosage:0.1, 1, 10, 30 and 100 mg/kg (male cynomolgus monkeys)0, 30, and 100 mg/kg (male and female cynomolgus) Administration:i.v., once (male cynomolgus monkeys) i.v., once weekly, for 2 weeks(male and female cynomolgus) Result:Increased CSF-1 concentration in serum.Efficiently reduced CSF-1R and CD68+163+ macrophages in the liver (Kupffer cells) and colon of cynomologus monkeys.
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Synonyms——
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PathwayTyrosine Kinase
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TargetCSF1R
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Recptorc-Fms | TAM Receptor
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Research Area——
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Indication——
Chemical Information
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CAS Number1448221-67-7
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Formula Weight
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Molecular Formula——
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Purity>98% (HPLC)
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Solubility——
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SMILES——
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Philippe A Cassier, et al. CSF1R inhibition with emactuzumab in locally advanced diffuse-type tenosynovial giant cell tumours of the soft tissue: a dose-escalation and dose-expansion phase 1 study. Lancet Oncol. 2015 Aug;16(8):949-56.?
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