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TMN355

SKU: orb1219292

Description

TMN355 is a potent chemical inhibitor of cyclophilin A and reduces foam cell formation and cytokine secretion,and is used for atherosclerosis. Silencing cyclophilin A in THP-1 cells and human monocytes using siRNA or chemical inhibitor, TMN355 resulted in decrease in lipid uptake by 65-75% even after exposure to oxidized LDL. The expression of scavenger receptors expressed during differentiation process, CD36 and LOX-1 were decreased (p < 0.0001). Levels of extracellular cyclophilin A and other inflammatory cytokines such as TNF-α and MCP-1also significantly reduced. TMN 355 (0.5-10 μM; 3-9 hours) results in 75.9% reduction of cyclophilin A protein expression. And cyclophilin A after 6 h of activation inhibited by TMN 355(1 μM).

Images & Validation

Key Properties

CAS Number1186372-20-2
MW380.8
Purity>98% (HPLC)
FormulaC21H14ClFN2O2
SMILESO=C(NC(NC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O)C4=C(F)C=CC=C4Cl
Targetcyclophilin A
SolubilityDMSO:31.25 mg/mL (82.06 mM; Need ultrasonic)

Bioactivity

In Vitro
TMN 355 (0.5-10 μM; 3-9 hours) results in 75.9% reduction of cyclophilin A protein expression. And 1 μM TMN 355 inhibits cyclophilin A after 6 h of activation. Western blot analysis. Cell line: THP cell lines. Concentration: 0.5, 1, 2.5, 5 and 10 μM Incubation time: 3, 6 and 9 hours. Result: Resulted in 75.9% reduction of cyclophilin A protein expression.

Storage & Handling

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

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    1186372-20-2

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    1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 500 mg, 2 mg, 1 ml x 10 mM (in DMSO)
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TMN355 (orb1219292)

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Available Sizes

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5 mg
$ 220.00
10 mg
$ 320.00
25 mg
$ 540.00
50 mg
$ 820.00
100 mg
$ 1,150.00
500 mg
$ 2,300.00