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ChemicalBook--->CAS DataBase List--->158081-99-3

158081-99-3

158081-99-3 Structure

158081-99-3 Structure
IdentificationBack Directory
[Name]

CP-105,696
[CAS]

158081-99-3
[Synonyms]

CP-105,696
Pfizer 105696
UNII-Z7354TW4BM
CP-105,696 >=98% (HPLC)
CP 105696; CP105696; CP-105696; UNII-Z7354TW4BM; PFIZER 105696
1-((3S,4R)-3-([1,1'-biphenyl]-4-ylmethyl)-4-hydroxychroman-7-yl)cyclopentane-1-carboxylic acid
1-[(3S,4R)-4-hydroxy-3-[(4-phenylphenyl)methyl]-3,4-dihydro-2H-chromen-7-yl]cyclopentane-1-carboxylic acid
Cyclopentanecarboxylic acid, 1-[(3S,4R)-3-([1,1'-biphenyl]-4-ylmethyl)-3,4-dihydro-4-hydroxy-2H-1-benzopyran-7-yl]-
[Molecular Formula]

C28H28O4
[MDL Number]

MFCD00934881
[MOL File]

158081-99-3.mol
[Molecular Weight]

428.52
Chemical PropertiesBack Directory
[Boiling point ]

651.2±55.0 °C(Predicted)
[density ]

1.252±0.06 g/cm3(Predicted)
[storage temp. ]

room temp
[solubility ]

Soluble in DMSO
[form ]

powder
[pka]

4.35±0.20(Predicted)
[color ]

white to beige
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P264-P270-P301+P312+P330-P501
Hazard InformationBack Directory
[Uses]

CP-105,696 has been used as a leukotriene B4 receptor (LTB4R) antagonist to study the influence of the LTB4 pathway in the pathogenesis of acute itch flares in irritant calcipotriol (MC903)+ model allergen ovalbumin (OVA) sensitized murine model of atopic dermatitis (AD)-like disease.
[Biochem/physiol Actions]

CP-105,696 is an orally active, potent and selective leukotriene B4 receptor (LTB4R) antagonist (IC50 against [3H]LTB4 = 5.6 nM for binding human neutrophils; IC50 = 9.7 nM & 30.3 nM, respectively using guinea pig spleen or mouse membranes) that targets LTB4R high- and low-affinity binding sites in a LTB4 non-competitive and competitive manner, respectively. CP-105,696 inhibits 5 nM LTB4-induced human neutrophils chemotaxis and CDllb upregualtion (IC50 = 5.2 nM and 430 nM, respectively) without inhibiting cyclooxygenase activity or affecting chemotaxis induced by C5a, PAF, IL-8. Oral administration is efficacious against intradermal LTB4 (100 ng/mouse), but not IL-1, injection-induced neutrophil accumulation in mice and guinea pigs (ED50 = 4.2 and 0.26 mgkg, respectively). CP-105,696 in vivo efficacy is also demonstrated in other animal models, including collagen-induced arthritis (CIA; 0.3-10 mg/kg in mice), allergic encephalomyelitis (ED50= 8.6 mg/kg; mice), and asthma (10-30 mg/kg; primate).
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