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SKU | Size | Availability | Price | Qty |
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B646521-5mg | 5mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $300.90 | |
B646521-10mg | 10mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $480.90 | |
B646521-50mg | 50mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $1,450.90 |
Specifications & Purity | ≥99% |
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Biochemical and Physiological Mechanisms | BI-4394 (MMP13-IN-3) is a potent, selective, and orally active MMP-13 inhibitor ( IC 50 =1 nM) for the potential treatment of osteoarthritis. BI-4394 is >1000 selective over other MMPs. |
Storage Temp | Store at -20°C |
Shipped In | Ice chest + Ice pads |
Product Description | BI-4394 (MMP13-IN-3) is a potent, selective, and orally active MMP-13 inhibitor ( IC 50 =1 nM ) for the potential treatment of osteoarthritis . BI-4394 is >1000 selective over other MMPs In Vitro BI-4394 (Compound 15) is potent in a full-length MMP-13 collagen degradation assay (11 nM) and is able to inhibit degradation of bovine nasal cartilage with an IC 50 of 31 nM. BI-4394 inhibits MMP-2, MMP-9, MMP-10 and MMP-14 with IC 50 s of 18, 8.9, 16 and 8.3 μM, respectively. MCE has not independently confirmed the accuracy of these methods. They are for reference only. In Vivo When dosed orally at 10 mg/kg or i.v. 1 mg/kg, BI-4394 (Compound 15) reaches micromolar plasma levels (AUC=1109±64 nM h/mL), displays modest clearance (CL=34 mL/min/kg), and shows acceptable bioavailability (39%). The V ss is quite low at 0.26 mL/mi/kg rat pharmacokinetic profile. BI-4394 has short terminal elimination half-life (t 1/2 =0.47 h for rat (1 mg/kg, i.v.) and rat (10 mg/kg, orally), respectively) . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Srapgue Dally Rats Dosage: 10 mg/kg (oral gavage); 1 mg/kg (i.v.) Administration: Dosed orally (10 mg/kg); i.v. (1 mg/kg)(Pharmacokinetic Analysis) Result: T 1/2 =0.47 h for rat (1 mg/kg, i.v.) and rat (10 mg/kg, orally) , respectively. Form:Solid IC50& Target:MMP-13 1 nM (IC 50 ) MMP-14 8.3 μM (IC 50 ) MMP-9 8.9 μM (IC 50 ) MMP-10 16 μM (IC 50 ) MMP-2 18 μM (IC 50 ) |
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IUPAC Name | 4-[[[5-(2-ethoxycarbonyl-1H-indol-5-yl)-1-methylpyrazole-3-carbonyl]amino]methyl]benzoic acid |
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INCHI | InChI=1S/C24H22N4O5/c1-3-33-24(32)20-11-17-10-16(8-9-18(17)26-20)21-12-19(27-28(21)2)22(29)25-13-14-4-6-15(7-5-14)23(30)31/h4-12,26H,3,13H2,1-2H3,(H,25,29)(H,30,31) |
InChi Key | MMJPVSDTLGFIQW-UHFFFAOYSA-N |
Canonical SMILES | CCOC(=O)C1=CC2=C(N1)C=CC(=C2)C3=CC(=NN3C)C(=O)NCC4=CC=C(C=C4)C(=O)O |
Isomeric SMILES | CCOC(=O)C1=CC2=C(N1)C=CC(=C2)C3=CC(=NN3C)C(=O)NCC4=CC=C(C=C4)C(=O)O |
PubChem CID | 45376872 |
Molecular Weight | 446.46 |
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Solubility | DMSO : 100 mg/mL (223.98 mM; ultrasonic and warming and heat to 60°C) |
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