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SB-435495 is an orally active, selective and potent Lp-PLA2 inhibitor (IC50 of 0.06 nM) for the study of autoimmune uveitis and atherosclerosis.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $31 | - | In Stock | |
| 5 mg | $74 | - | In Stock | |
| 10 mg | $119 | - | In Stock | |
| 25 mg | $273 | - | In Stock | |
| 50 mg | $447 | - | In Stock | |
| 100 mg | $708 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $116 | - | In Stock |
| Description | SB-435495 is an orally active, selective and potent Lp-PLA2 inhibitor (IC50 of 0.06 nM) for the study of autoimmune uveitis and atherosclerosis. |
| Targets&IC50 | Lp-PLA2:0.06 nM |
| In vitro | SB-435495 inhibits CYP450 3A4 with an IC50 of 10 μM and a membrane permeability of 0.017 cm/h[1]; SB-435495 (5 μM; 24 h) significantly inhibits the expression of Lp-PLA2 protein and simultaneously increases oxLDL-exposed HUVECs. Medium expression levels of AMPKα and phospho-AMPKα (T172); SB-435495 (5 μM; 24-72 h) significantly increased cell viability and NO expression and significantly decreased ET-1 expression in oxLDL-exposed HUVECs[2] . |
| In vivo | SB-435495 (10 mg/kg; p.o.; once) inhibits plasma Lp-PLA2 in WHHL rabbit [1].
SB-435495 (10 mg/kg; i.p.; daily for 28 days) effectively inhibits blood retinal barrier (BRB) disruption in Streptozotocin diabetic Brown Norway rats [3]. |
| Synonyms | SB435495, SB 435495 |
| Molecular Weight | 720.82 |
| Formula | C38H40F4N6O2S |
| Cas No. | 304694-39-1 |
| Smiles | O=C1N=C(SCC2=CC=C(F)C=C2)N(C=C1CC=3C=NN(C3)C)CC(=O)N(CC4=CC=C(C=C4)C=5C=CC(=CC5)C(F)(F)F)CCN(CC)CC |
| Storage | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 80 mg/mL (110.98 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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Dissolve 2 mg of the compound in 100 μL DMSO
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.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
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 ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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