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
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2MG 41 In Stock
5MG 74 In Stock
10MG 133 In Stock
25MG 241 In Stock
50MG 429 In Stock
100MG 628 In Stock
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Biological Information

  • Product Name
    Cilomilast
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent and selective PDE4 inhibitor with IC50 of 95/120 nM for LPDE4/HPDE4.
  • Description
    A 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.
  • 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. 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.
  • Synonyms
    SB-207499 | SB207499 | SB 207499
  • Pathway
    Angiogenesis
  • Target
    PDE
  • Recptor
    HPDE4|LPDE4
  • Research Area
    Inflammation/Immunology
  • Indication
    COPD

Chemical Information

  • CAS Number
    153259-65-5
  • Formula Weight
    343.4168
  • Molecular Formula
    C20H25NO4
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    O=C([C@H]1CC[C@](C2=CC=C(OC)C(OC3CCCC3)=C2)(C#N)CC1)O
  • Chemical Name
    Cyclohexanecarboxylic acid, 4-cyano-4-[3-(cyclopentyloxy)-4-methoxyphenyl]-, cis-

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • 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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