Bindarit (AF2838)
This product is for research use only, not for human use. We do not sell to patients.
For small sizes, please check our retail website as below: www.invivochem.com
Size | Price | Stock |
---|---|---|
250mg | $860 | Check With Us |
500mg | $1450 | Check With Us |
1g | $2175 | Check With Us |
Cat #: V2026 CAS #: 130641-38-2 Purity ≥ 98%
Description: Bindarit (also known as AF-2838; AF 2838) is a potent and selective inhibitor of monocyte chemotactic proteins MCP-1/CCL2, MCP-3/CCL7 and MCP-2/CCL8 with anti-inflammatory activity.
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- Related Biological Data
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Molecular Weight (MW) | 324.37 |
---|---|
Molecular Formula | C19H20N2O3 |
CAS No. | 130641-38-2 |
Storage | -20℃ for 3 years in powder formr |
-80℃ for 2 years in solvent | |
Solubility In Vitro | DMSO: 65 mg/mL (200.4 mM)r |
Water: <1 mg/mLr | |
Ethanol: 65 mg/mL (200.4 mM) | |
Solubility In Vivo | 0.5% CMC: 7 mg/mL |
Synonyms | AF-2838; AF2838; AF 2838 |
Protocol | In Vivo | Bindarit (50 mg/kg; oral administration; every day; for 4 months, 6 months, 8 months; NZB/W F1 female mice) delays the onset of proteinuria and significantly protects from renal function impairment. Bindarit completely prevents monocyte chemoattractant protein (MCP-1) up-regulation |
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Animal model | NZB/W F1 female mice ( two months of age) | |
Dosages | 50 mg/kg | |
Administration | Oral administration; every day; for 4 months, 6 months, 8 months |
These protocols are for reference only. InvivoChem does not
independently validate these methods.
Solvent volume to be added | Mass (the weight of a compound) | |||
---|---|---|---|---|
Mother liquor concentration | 1mg | 5mg | 10mg | 20mg |
1mM | 3.0829 mL | 15.4145 mL | 30.8290 mL | 61.6580 mL |
5mM | 0.6166 mL | 3.0829 mL | 6.1658 mL | 12.3316 mL |
10mM | 0.3083 mL | 1.5414 mL | 3.0829 mL | 6.1658 mL |
20mM | 0.1541 mL | 0.7707 mL | 1.5414 mL | 3.0829 mL |
The molarity calculator equation
Mass(g) = Concentration(mol/L) × Volume(L) × Molecular Weight(g/mol)
Mass
=
Concentration
×
Volume
×
Molecular Weight*
The dilution calculator equation
Concentration(start)
×
Volume(start)
=
Concentration(final)
×
Volume(final)
This equation is commonly abbreviated as: C1 V1 = C2 V2
Concentration(start)
C1
×
Volume(start)
V1
=
Concentration(final)
C2
×
Volume(final)
V2
Step One: Enter information below
Dosage mg/kg
Average weight of animals g
Dosing volume per animal µL
Number of animals
Step Two: Enter the in vivo formulation
%DMSO
+
%
+
%Tween 80
+
%ddH2O
Calculation Results:
Working concentration:
mg/ml;
Method for preparing DMSO master liquid:
mg
drug pre-dissolved in
µL
DMSO(Master liquid concentration
mg/mL)
,Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation:
Take
µL
DMSO master liquid, next add
µL
PEG300, mix and clarify, next add
µL
Tween 80,mix and clarify, next add
µL
ddH2O,mix and clarify.
Note:
- (1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
- (2) Be sure to add the solvent(s) in order.