BH400
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You can also order by e-mail: info@biomol.com
Larger quantity required? Request bulk
A PPARalpha agonist and STING inhibitor (IC50 = 8.1 µM), induces transactivation of PPARalpha in... more
Product information "BH400"
A PPARalpha agonist and STING inhibitor (IC50 = 8.1 µM), induces transactivation of PPARalpha in a reporter assay using THP-1 cells (EC50 = 1.2 µM), inhibits 4-HNE- or H2O2-induced decreases in viability in 661W cells at 10 µM, prevents LPS-induced increases in phosphorylated TBK1 and IL-6 levels and LPS-induced decreases in PGC-1alpha levels in HMC3 cells at 10 µM. Formulation: A solid. InChI: InChI=1S/C20H16FNO3/c21-16-7-5-15(6-8-16)14-3-1-13(2-4-14)12-22-17-9-10-19(23)18(11-17)20(24)25/h1-11,22-23H,12H2,(H,24,25). InChIKey: PEWZEZWZGJQFKN-UHFFFAOYSA-N. SMILES: FC(C=C1)=CC=C1C(C=C2)=CC=C2CNC3=CC=C(O)C(C(O)=O)=C3
| Keywords: | 5-(((4'-fluoro-[1,1'-biphenyl]-4-yl)methyl)amino)-2-hydroxybenzoic acid |
| Supplier: | Cayman Chemical |
| Supplier-Nr: | 41892 |
Properties
| Application: | PPARalpha agonist, STING inhibitor |
| Immunogen: | 337.4 |
| MW: | 337.4 D |
| Formula: | C20H16FNO3 |
| Purity: | >95% |
| Format: | Solid |
Database Information
| KEGG ID : | K12654 | Matching products |
Handling & Safety
| Storage: | -20°C |
| Shipping: | +20°C (International: -20°C) |
| Signal Word: | Warning |
| GHS Hazard Pictograms: |
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| H Phrases: | H302, H413 |
| P Phrases: | P264, P270, P273, P301+310, P330, P501 |
Caution
Our products are for laboratory research use only: Not for administration to humans!
Our products are for laboratory research use only: Not for administration to humans!
Information about the product reference will follow.
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