6-[3-(dimethylcarbamoyl)benzenesulfonyl]-4-[(3-methoxyphenyl)amino]-8-methylquinoline-3-carboxamide

• ChemBase ID: 73111
• Molecular Formular: C27H26N4O5S
• Molecular Mass: 518.58414
• Monoisotopic Mass: 518.16239095
• SMILES: c1cc(cc(c1)S(=O)(=O)c1cc(c2c(c1)c(c(cn2)C(=O)N)Nc1cc(ccc1)OC)C)C(=O)N(C)C
• Canonical SMILES: COc1cccc(c1)Nc1c(cnc2c1cc(cc2C)S(=O)(=O)c1cccc(c1)C(=O)N(C)C)C(=O)N
• InChI: InChI=1S/C27H26N4O5S/c1-16-11-21(37(34,35)20-10-5-7-17(12-20)27(33)31(2)3)14-22-24(16)29-15-23(26(28)32)25(22)30-18-8-6-9-19(13-18)36-4/h5-15H,1-4H3,(H2,28,32)(H,29,30)
• InChIKey: JFHROPTYMMSOLG-UHFFFAOYSA-N

NAMES AND DATABASE IDS

Names

• IUPAC name: 6-[3-(dimethylcarbamoyl)benzenesulfonyl]-4-[(3-methoxyphenyl)amino]-8-methylquinoline-3-carboxamide
• IUPAC Traditional name: 6-[3-(dimethylcarbamoyl)benzenesulfonyl]-4-[(3-methoxyphenyl)amino]-8-methylquinoline-3-carboxamide
• Synonyms: GSK-256066; GSK256066

Database IDs

• CAS Number: 801312-28-7
• PubChem SID: 162038031
• PubChem CID: 9827968

CALCULATED PROPERTIES

• Acid pKa: 13.750028
• H Acceptors: 7
• H Donor: 2
• LogD (pH = 5.5): 4.074614
• LogD (pH = 7.4): 4.3255186
• Log P: 4.330044
• Molar Refractivity: 141.4523 cm^3
• Polarizability: 55.361633 Å^3
• Polar Surface Area: 131.69 Å^2
• Rotatable Bonds: 7
• Lipinski's Rule of Five: false

PROPERTIES

Safety Information

• Storage Condition: -20°C

Pharmacology Properties

• Target: PDE

Product Information

• Salt Data: Free Base

DETAILS

Selleck Chemicals - S2620

Research Area

• Description: Cancer

Biological Activity

• Description: GSK256066 is a selective PED4B inhibitor with IC50 of 3.2 pM.
• Targets: PDE4B
• IC50: 3.2 pM ^[1]
• In Vitro: GSK256066 is a slow and tight binding inhibitor of PDE4B with apparent IC50 of 3.2 pM. GSK256066 is an extremely potent inhibitor of LPS-stimulated TNFα production in PBMCs with pIC50 of 11.0 and IC50 of 10 pM and human whole-blood cultures with pIC50 of 9.90 and IC50 of 126 pM. GSK256066 is highly selective for PDE4 (>3.8 × 10^5-fold versus PDE1, PDE2, PDE3, PDE5, and PDE6 and >2.5 × 10^3-fold against PDE7). GSK256066 inhibits PDE4 isoforms A-D with equal affinity. ^[1]
• In Vivo: GSK256066 inhibits the LPS-induced pulmonary neutrophilia with an ED50 of 1.1 μg/kg, achieving maximal inhibition of 72% at 30 μg/kg when given in the aqueous suspension. GSK256066 inhibits the LPS-induced pulmonary neutrophilia with ED50 of 2.9 μg/kg, achieving maximal inhibition of 62% when given in the dry powder formulation. GSK256066 shows a moderate plasma clearance of 39 ml/min/kg, a moderate volume of distribution of 0.8 L/kg, and a relatively short half-life of 1.1 hour in the male CD rat. ^[1] GSK256066 sustains at a high lung concentration of 2.6 μg/g after intra-tracheal administration as an aqueous suspension at a dose of 30 μg/kg in rats. ^[2] GSK256066 (10 μg/kg) is administered intratracheally at different times (2, 6, 12, 18, 24, and 36 hours) before LPS administration, inhibiting LPS-Induced Pulmonary Neutrophilia in rat lipopolysaccharide (LPS)-induced models of acute pulmonary inflammation. GSK256066 (0.3–100 μg/kg) inhibits LPS-induced increases in exhaled nitric oxide with ED50 of 35 μg/kg in rat. GSK256066 (10 μg/kg) is administered half a hour before OVA administration in rat, inhibiting OVA-induced pulmonary eosinophilia with ED50 of 0.4 μg/kg. GSK256066 administered intratracheally as a dry powder blended in respiratory-grade lactose at doses of 3 to 100 μg/kg 2 hours before inhaled LPS challenge in ferrets, inhibiting LPS-induced pulmonary neutrophilia with ED50 of 18 μg/kg without inducing emetic episodes. ^[3]
• Clinical Trials: GSK256066 is currently in phase II clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Protocol

• Protocol: Kinase Assay ^[1]
• SPA assays and fluorescence polarization assays: For SPA assays, 75 μL of PDE enzyme in 50 mM Tris-HCl, pH 7.5, containing 8.3 mM MgCl₂, 1.7 mM EGTA, and 0.05% (w/v) BSA is preincubated with 2 μL of GSK256066 solution or DMSO for 30 min. For PDE1 assays the assay buffer containes additionally 4 μg/mL calmodulin and 1 mM CaCl₂ and does not contain any EGTA. Assays are initiated by the addition of 25 μL of [^3H]cAMP (10 nM final concentration: PDE3, PDE4, and PDE7) or [3H]cGMP (36 nM: PDE1, PDE2, PDE5, and PDE6). After a 1 hour incubation, assays are terminated by addition of 50 μL of aqueous suspension of SPA beads (approximately 1 mg per well) and, after an incubation of at least 30 min, bound radioactivity is measured by liquid scintillation counting. For fluorescence polarization assays, 10 μL of PDE enzyme in 10 mM Tris-HCl buffer, pH 7.2, containing 10 mM MgCl₂, 0.1% (w/v) BSA, and 0.05% (w/v) NaN3 is preincubated with 0.5 μL of inhibitor or DMSO for 30 min. Assays are initiated by the addition of 10 μL of fluorescein-cAMP (40 nM final concentration) and terminated after 40 min by the addition of 60 μL of IMAP binding reagent (1 in 400 dilution of stock suspension in binding buffer). The ratio of parallel to perpendicular light is measured using an Analyst or Aquest plate reader.
• Protocol: Animal Study ^[1]
• Animal Models: Male CD rats
• Formulation: Sterile 0.9% sodium chloride solution
• Doses: 0.1–100 μg/kg
• Administration: Administered intratracheally as an aqueous suspension or a dry powder 2 h before LPS challenge.

References

• References: [1] Tralau-Stewart CJ, et al. J Pharmacol Exp Ther, 2011, 337(1), 145-154.
• References: [2] Woodrow MD, et al. Bioorg Med Chem Lett, 2009, 19(17), 5261-5265.
• References: [3] Nials AT, et al. J Pharmacol Exp Ther, 2011, 337(1), 137-144.

REFERENCES

• Tralau-Stewart CJ, et al. J Pharmacol Exp Ther, 2011, 337(1), 145-154.
• Woodrow MD, et al. Bioorg Med Chem Lett, 2009, 19(17), 5261-5265.
• Nials AT, et al. J Pharmacol Exp Ther, 2011, 337(1), 137-144.