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Bindarit

SKU: orb1226582

Description

Bindarit exhibits selective inhibition against monocyte chemotactic proteins MCP-1/CCL2, MCP-3/CCL7 and MCP-2/CCL8.(In Vitro):Bindarit (10-300 μM; 48 hours) at 100 μM and 300 μM significantly inhibits platelet derived growth factor-BB (PDGF-BB)-induced rat VSMCs proliferation by 27% and 42%, respectively.(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.

Images & Validation

Key Properties

CAS Number130641-38-2
MW324.37
Purity>98% (HPLC)
FormulaC19H20N2O3
SMILESCC(C)(OCC1=NN(CC2=CC=CC=C2)C3=C1C=CC=C3)C(O)=O
TargetCCR
SolubilityDMSO:65 mg/mL (200.38 mM); Ethanol:65 mg/mL (200.38 mM); Water:<1 mg/mL (<1 mM)

Bioactivity

In Vivo
Animal model: NZB/W F1 female mice (two months of age). Dosage: 50 mg/kg. Administration: Oral administration; every day; for 4 months, 6 months, 8 months. Result: Delayed the onset of proteinuria and significantly protected from renal function impairment.
In Vitro
Cell Viability Assay Cell line: VSMC cells. Concentration: 10 μM, 30 μM, 100 μM, 300 μM. Incubation time: 48 hours. Result: Inhibited PDGF-BB-induced rat VSMCs proliferation.

Storage & Handling

StorageStorage temperature: -20°C. Stability: ≥ 2 years
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

AF 2838

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  • Bindarit [orb1300789]

    98.35%

    130641-38-2

    324.37

    C19H20N2O3

    2 mg, 100 mg, 1 mg, 50 mg, 1 ml x 10 mM (in DMSO), 10 mg, 200 mg, 5 mg, 25 mg
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Bindarit (orb1226582)

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Available Sizes

Select a size below

2 mg
$ 130.00
5 mg
$ 190.00
10 mg
$ 280.00
25 mg
$ 460.00
50 mg
$ 670.00
100 mg
$ 940.00
500 mg
$ 1,890.00