BM213

Synonyms:

BM213, a selective C5aR1 agonist with an EC50 of 59 nM, induces C5aR1-mediated calcium mobilization and pERK1/2 signaling but not β-arrestin recruitment. BM213 is much more stable in serum and displays no cytotoxicity on SHSY-5Y cells.

BM213 Chemical Structure

BM213 Chemical Structure

CAS:

Purity & Quality Control

Batch: P121501 Water] 100 mg/mL] false] ] ] false] ] ] false Purity: 98%
98

BM213 Related Products

Biological Activity

Description BM213, a selective C5aR1 agonist with an EC50 of 59 nM, induces C5aR1-mediated calcium mobilization and pERK1/2 signaling but not β-arrestin recruitment. BM213 is much more stable in serum and displays no cytotoxicity on SHSY-5Y cells.
In vitro
In vitro

BM213 is a potent and stable peptide C5aR1 agonists that display no C5aR2 activity and over 1000-fold selectivity for C5aR1 over C3aR. BM213 induces C5aR1-mediated calcium mobilization and pERK1/2 signaling but not β-arrestin recruitment. BM213 is functionally similar to C5a in human macrophage cytokine release assays and in a murine in vivo neutrophil mobilization assay.[1]

Cell Research Cell lines HMDMs, SHSY-5Y cells
Concentrations 0.1-100 μM
Incubation Time 0-6 h, 24 h
Method

HMDMs are stimulated with LPS (10 ng/mL) alone or in the presence of BM213. The supernatant content of cytokines after 24 h stimulation is quantified using ELISA. For MTT cell survival assay, differentiated SH-SY5Y cells are treated with varying concentrations of BM213 following a 2.5 h incubation.

In Vivo
In vivo

BM213 shows antitumor activity in a mouse model of mammary carcinoma.[1]

Animal Research Animal Models Mammary carcinoma model mice bearing with EMT-6 cells
Dosages 1mg/kg
Administration IOCV

Chemical Information & Solubility

Molecular Weight Formula
CAS No. SDF --
Density 95.0~105.0%
Storage (From the date of receipt) 3 years-20°C powder

In vitro
Batch:

Water : 100 mg/mL


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