| Field | Specification |
|---|---|
| CAS no. | |
| Applications | |
| Molecular weight | |
| Molecular formula | C24H28N4O5 |
| Purity | |
| SMILES | |
| Form | Solid |
| Storage | |
| Shipping | |
| Catalog no. (Mfr.) | |
| Main SKU |
Compound Overview
ABBV-712 is a selective, orally active inhibitor of tyrosine kinase 2 (TYK2), with EC50 values of 0.01 μM against TYK2 JH2, 0.19 μM in TYK2 cells, and 0.17 μM in human whole blood. It has anti-inflammatory activity and can be used in autoimmune disease research[1]. It is supplied as an off-white to light yellow solid (C24H28N4O5, MW 452.50) at 99.94% purity.
Physical & Chemical Properties
| CAS Number | 2368945-27-9 |
|---|---|
| Molecular Formula | C24H28N4O5 |
| Molecular Weight | 452.50 g/mol |
| Purity | 99.94% |
| Appearance | Solid |
| Color | Off-white to light yellow |
| SMILES | CC(NC1=CC2=C(C=N1)N(C=C2C3=NC([C@]4(COCC4)OC)=CC(COC)=C3)C5COC5)=O |
| Signaling Pathway | Epigenetics; Stem Cell/Wnt; Protein Tyrosine Kinase/RTK; JAK/STAT Signaling |
| Solubility | In Vitro: DMSO: 250 mg/mL (552.49 mM; Requires sonication; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO) |
| Storage | Powder: -20°C, 3 years; 4°C, 2 years. In solvent: -80°C, 6 months; -20°C, 1 month. |
| Shipping | Room temperature in continental US; may vary elsewhere. |
Literature Cited
Sources cited in this description and in the In Vitro & In Vivo Data tab. Peer-reviewed publications that used this product are listed under References.
Safety
For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with the Safety Data Sheet and your institution's chemical hygiene plan.
In Vitro
| Solvent | Solubility | Notes |
|---|---|---|
| DMSO | 250 mg/mL (552.49 mM) | requires sonication; use freshly opened DMSO (absorbed moisture lowers solubility) |
Aliquot the stock solution and store it at -80°C (up to 6 months) or -20°C (up to 1 month); avoid repeated freeze-thaw cycles.
Data provided by the manufacturer.
In Vivo
In the mouse ear dermatitis model, ABBV-712, administered orally at 100 mg/kg (BID/QD; 5 days), has a protective effect and can reduce ear thickness[1]. In mice stimulated with IL-12/IL-18, ABBV-712 (10-600 mg/kg; oral administration; single dose) can inhibit IFN-γ production in a dose-dependent manner[1].
Pharmacokinetic Analysis in Rats[1]
| Route | Dose (mg/kg) | CLb,u (L/h/kg) | T1/2 (h) | VSS (L/kg) | F (%) |
| p.o. and i.v. | 1 | 4.1 | 0.6 | 1.9 | 19 |
Data provided by the manufacturer. Numbered citations refer to the Literature Cited list in the product description.
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