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C3a Receptor Agonist

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Catalog No. T38287Cas No. 944997-60-8
Alias Complement 3a Receptor Agonist, C3a receptor agonist 1

C3a Receptor Agonist (C3a receptor agonist 1) binds the G protein-coupled C3a receptors (C3aRs) in the immune system complement pathway. Activation of C3aR prevents neutrophils from being mobilized in a model of intestinal ischemia-reperfusion injury. C3aRs are expressed on neural progenitor cells and immature neurons in adult mice. C3a stimulates differentiation of neural progenitor cells in vitro.

C3a Receptor Agonist

C3a Receptor Agonist

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Purity: 99.76%
Catalog No. T38287Alias Complement 3a Receptor Agonist, C3a receptor agonist 1Cas No. 944997-60-8
C3a Receptor Agonist (C3a receptor agonist 1) binds the G protein-coupled C3a receptors (C3aRs) in the immune system complement pathway. Activation of C3aR prevents neutrophils from being mobilized in a model of intestinal ischemia-reperfusion injury. C3aRs are expressed on neural progenitor cells and immature neurons in adult mice. C3a stimulates differentiation of neural progenitor cells in vitro.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$89In StockIn Stock
5 mg$318In StockIn Stock
10 mg$538In StockIn Stock
25 mg$868In StockIn Stock
50 mg$1,170In StockIn Stock
100 mg$1,580-In Stock
500 mg$3,170-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:99.76%
Appearance:Solid
Color:White
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Product Introduction

C3a Receptor Agonist AI Summary
C3a Receptor Agonist exhibits bioactivities including C3a receptor agonist activity with an EC50 value of 1995.26 nM and the ability to displace [125I]C3a from the human C3a receptor with an IC50 of 794.33 nM. It shows moderate permeability across Caco-2 cells, with a permeability value of 12.0 x 10^-6 cm/s. In terms of metabolism and excretion, the compound has a clearance of 500.0 μL/min in rat microsomes and 33.0 μL/min in rat hepatocytes. It has an elimination half-life of 0.2 hours in rats at a dose of 1 mg/kg (both intravenous and oral) and demonstrates 5.0% oral bioavailability at the same dose..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
C3a Receptor Agonist (C3a receptor agonist 1) binds the G protein-coupled C3a receptors (C3aRs) in the immune system complement pathway. Activation of C3aR prevents neutrophils from being mobilized in a model of intestinal ischemia-reperfusion injury. C3aRs are expressed on neural progenitor cells and immature neurons in adult mice. C3a stimulates differentiation of neural progenitor cells in vitro.
SynonymsComplement 3a Receptor Agonist, C3a receptor agonist 1
Chemical Properties
Molecular Weight433.59
FormulaC27H35N3O2
Cas No.944997-60-8
SmilesO=C(CCc1cccnc1)N1CCC(CC1)NC(=O)C(C1CCCCC1)c1ccccc1
Relative Density.1.15 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMF: 30 mg/mL (69.19 mM), Sonication is recommended.
DMSO: 40 mg/mL (92.25 mM), Sonication is recommended.
Ethanol: 30 mg/mL (69.19 mM), Sonication is recommended.
Solution Preparation Table
DMF/Ethanol/DMSO
1mg5mg10mg50mg
1 mM2.3063 mL11.5316 mL23.0633 mL115.3163 mL
5 mM0.4613 mL2.3063 mL4.6127 mL23.0633 mL
10 mM0.2306 mL1.1532 mL2.3063 mL11.5316 mL
20 mM0.1153 mL0.5766 mL1.1532 mL5.7658 mL
50 mM0.0461 mL0.2306 mL0.4613 mL2.3063 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

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