RVX-297

RVX-297 is an inhibitor of the bromodomain and extra-terminal domain (BET) family protein bromodomain 2 (BD2). It inhibits BD2 in bromodomain-containing protein 2 (BRD2), BRD3, and BRD4, (IC50s = 0.08, 0.05, and 0.02 µM, respectively) and is selective for BD2 over BD1 (IC50s = 3.76, 2.34, and 1.16 µM for BRD2, BRD3, and BRD4, respectively), as well as CREB-binding protein (CREBBP) and p300 (IC50s = >50 µM for both). RVX-297 (10 and 30 µM) decreases levels of the mRNAs encoding IL-6 and vascular cell adhesion molecule-1 (VCAM-1) in primary synovial fibroblasts isolated from patients with rheumatoid arthritis. It prevents LPS-induced increases in IL-6 and Ifn-gamma serum levels in a mouse model of LPS-induced endotoxemia when administered at a dose of 75 mg/kg. RVX-297 (25, 50, and 75 mg/kg twice per day) inhibits collagen-induced increases in ankle and knee diameter, cartilage damage, the ankle tissue levels of mRNA encoding IL-1beta, matrix metalloproteinase-3 (Mmp-3), Mmp-13, and Rankl, and ankle joint protein levels of IL-6 and VCAM-1 in a rat model of collagen-induced rheumatoid arthritis. It improves gait and mobility and reverses body weight loss, as well as decreases the number of spinal cord inflammatory foci and apoptotic cells and reduces spinal nerve demyelination in a mouse model of experimental autoimmune encephalomyelitis (EAE) when administered at doses of 75 and 125 mg/kg per day.Formal Name: 2-[3,5-dimethyl-4-[2-(1-pyrrolidinyl)ethoxy]phenyl]-5,7-dimethoxy-4(3H)-quinazolinone. CAS Number: 1044871-04-6. Molecular Formula: C24H29N3O4. Formula Weight: 423.5. Purity: >95%. Formulation: (Request formulation change), A solid. Solubility: Methanol: Soluble. SMILES: O=C1N=C(C2=CC(C)=C(OCCN3CCCC3)C(C)=C2)NC4=C1C(OC)=CC(OC)=C4. InChi Code: InChI=1S/C24H29N3O4/c1-15-11-17(12-16(2)22(15)31-10-9-27-7-5-6-8-27)23-25-19-13-18(29-3)14-20(30-4)21(19)24(28)26-23/h11-14H,5-10H2,1-4H3,(H,25,26,28). InChi Key: PQZDYFRDRHRZGF-UHFFFAOYSA-N.