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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 |
| Color | White |
| Appearance | Solid |
| 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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