Cilomilast
CAS No. 153259-65-5
Cilomilast( SB-207499 | SB207499 | SB 207499 )
Catalog No. M12158 CAS No. 153259-65-5
A potent and selective PDE4 inhibitor with IC50 of 95/120 nM for LPDE4/HPDE4.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 41 | In Stock |
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| 5MG | 74 | In Stock |
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| 10MG | 133 | In Stock |
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| 25MG | 241 | In Stock |
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| 50MG | 429 | In Stock |
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| 100MG | 628 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameCilomilast
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NoteResearch use only, not for human use.
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Brief DescriptionA potent and selective PDE4 inhibitor with IC50 of 95/120 nM for LPDE4/HPDE4.
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DescriptionA potent and selective PDE4 inhibitor with IC50 of 95/120 nM for LPDE4/HPDE4; shows selectivity for PDE4 over the other PDE isozymes and is 75-fold more selective than (R)-rolipram with respect to LPDE4 activity versus HPDE4 activity; inhibits antigen-induced bronchoconstriction in conscious guinea pigs at 30 mg/kg and orally acitive.COPD Phase 3 Discontinued(In Vitro):Cilomilast (0.1 nM-10 μM; 5 min) inhibits human neutrophil functions.Cilomilast (0.1 nM-10 μM; 5 min) inhibits eosinophil chemiluminescence response.Cilomilast (0.001-100 μM; 30 min) inhibits the synthesis of TNFα in human monocytes and in human whole blood.(In Vivo):SB-207499 (1-100 mg/kg; p.o.) significantly inhibits the production of human TNFα in a dose-dependent manner in mice.SB-207499 (0.1-100 mg/kg; oral gavage) reverses reserpine-induced hypothermia in mice, with an ED50 of 2.3 mg/kg.SB-207499 (500 μg/ear; b.i.d. for 6 d) inhibits the chronic oxazolone-induced inflammatory response and intralesional IL-4 concentrations in mice.
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In VitroCilomilast (0.1 nM-10 μM; 5 min) inhibits human neutrophil functions.Cilomilast (0.1 nM-10 μM; 5 min) inhibits eosinophil chemiluminescence response.Cilomilast (0.001-100 μM; 30 min) inhibits the synthesis of TNFα in human monocytes and in human whole blood.
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In VivoSB-207499 (1-100 mg/kg; p.o.) significantly inhibits the production of human TNFα in a dose-dependent manner in mice.SB-207499 (0.1-100 mg/kg; oral gavage) reverses reserpine-induced hypothermia in mice, with an ED50 of 2.3 mg/kg.SB-207499 (500 μg/ear; b.i.d. for 6 d) inhibits the chronic oxazolone-induced inflammatory response and intralesional IL-4 concentrations in mice. Animal Model:Male Balb/c mice (18-25 g) are injected with human monocytes and LPS Dosage:1, 5, 10, 50, 100 mg/kg Administration:P.o. after the injection of human monocytes and before LPS challenge Result:Inhibited the production of human TNFα, with an ED50 of 4.9 mg/kg.
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SynonymsSB-207499 | SB207499 | SB 207499
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PathwayAngiogenesis
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TargetPDE
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RecptorHPDE4|LPDE4
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Research AreaInflammation/Immunology
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IndicationCOPD
Chemical Information
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CAS Number153259-65-5
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Formula Weight343.4168
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Molecular FormulaC20H25NO4
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESO=C([C@H]1CC[C@](C2=CC=C(OC)C(OC3CCCC3)=C2)(C#N)CC1)O
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Chemical NameCyclohexanecarboxylic acid, 4-cyano-4-[3-(cyclopentyloxy)-4-methoxyphenyl]-, cis-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Christensen SB, et al. J Med Chem. 1998 Mar 12;41(6):821-35.
2. Barnette MS, et al. J Pharmacol Exp Ther. 1998 Jan;284(1):420-6.
3. Griswold DE, et al. J Pharmacol Exp Ther. 1998 Nov;287(2):705-11.
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