KC-11404
KC-11404 is an orally active antihistamine and 5-lipoxygenase inhibitor, with an IC50 of 0.9 μM against guinea pig 5-lipoxygenase. KC-11404 inhibits histamine-induced contraction of isolated guinea pig ileum with an IC50 of 0.26 μM. KC-11404 inhibits PAF-induced rabbit platelet aggregation with an IC50 of 2.0 μM. It inhibits the histamine phase of antigen-induced bronchoconstriction and PAF-induced bronchoconstriction in guinea pigs. KC-11404 can be used for the research of asthma.
Nur für Forschungszwecke. Wir verkaufen nicht an Patienten.
- CAS. Nr.: 148490-22-6
- Formel: C28H38N4O
- Molecular Weight:446.63
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Speicherung:
Please store the product under the recommended conditions in the Certificate of Analysis.
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Biologische Aktivität
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Chemical Information
- Reinheit & Dokumentation
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Help & FAQs
Biologische Aktivität
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5-LOX 0.9 μM (IC50) |
KC-11404 potently inhibits histamine-induced contractions of isolated guinea pig ileum with an IC50 of 0.26 μM[1].
KC-11404 inhibits PAF-induced aggregation of rabbit platelets with an IC50 of 2.0 μM[1].
KC-11404 (10 μM) completely inhibits semipurified guinea pig PMN 5-lipoxygenase with an IC50 of 0.9 μM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
KC-11404 (oral administration; single dose) potently inhibits passive cutaneous anaphylaxis in rats, with an ED50 of 0.9 μmol/kg[1].
KC-11404 (oral administration; single dose) inhibits the histamine phase of antigen-induced bronchoconstriction in guinea pigs, with an ED50 of 1.9 μmol/kg[1].
KC-11404 (oral administration; single dose) inhibits PAF-induced bronchoconstriction in guinea pigs, with an ED50 of 2.1 μmol/kg[1].
KC-11404 (50 μmol/kg; p.o.; single administration) exhibits efficacy comparable to that of Zileuton (HY-14164) in inhibiting the leukotriene-dependent phase of antigen-induced bronchoconstriction in guinea pigs at a dose of 50 μmol/kg[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:unspecified strain[1]
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Dosage:50 μmol/kg
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Administration:p.o.; single dose
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Result:Inhibited changes in airway resistance by 53% (5 hours pre-challenge) and 53% (8 hours pre-challenge).
Inhibited changes in dynamic compliance by 31% (5 hours pre-challenge) and 37% (8 hours pre-challenge).
Showed equivalent potency to zileuton, with no significant difference between the two compounds at either time point.
Chemical Information
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CAS. Nr. 148490-22-6
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Molecular Weight 446.63
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Formel C28H38N4O
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SMILES
OC1=CC2=C3C(CCC(CCCC)N3C(C)=C2CCN4CCN(CC4)C5=NC=CC(C)=C5)=C1
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Versand
Room temperature in continental US; may vary elsewhere.
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Speicherung
Please store the product under the recommended conditions in the Certificate of Analysis.
Reinheit & Dokumentation
Verweise
[1]. Paris D, et al. Synthesis, structure-activity relationships, and pharmacological evaluation of pyrrolo[3,2,1-ij]quinoline derivatives: potent histamine and platelet activating factor antagonism and 5-lipoxygenase inhibitory properties. Potential therapeutic application in asthma. J Med Chem. 1995;38(4):669-685. [Content Brief]
Calculators
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)
KC-11404 Related Classifications
HY-182557 Related Classifications
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