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Asapiprant

Asapiprant (S-555739) is a potent and selective DP1 receptor antagonist (Ki: 0.44 nM) . It exhibited high affinity and selectivity for the DP1 receptor. (In Vivo) :Oral administration of Asapiprant to sheep at 1 and 3 mg/kg significantly (P<0.01) suppresses the increase in nasal resistance by 82% and 92%, respectively. Oral administration of Asapiprant to sheep at 5 mg/kg suppresses Prostaglandin (PG) D2 (PGD) 2-induced nasal resistance by 86%. When orally administered 1 h before the antigen challenge in pigs, Asapiprant (3, 10, and 30 mg/kg) suppresses immediate airway response (IAR) by 52%, 57%, and 96%, and late airway response (LAR) by 67%, 50%, and 79%, respectively. Orally administered with Asapiprant (5 mg/kg) for 4 days, the Asapiprant significantly (P<0.01) suppresses antigen-induced nasal resistance by 73% in sheep. Treatment with 3 and 30 mg/kg of Asapiprant in pigs significantly (P<0.01) suppresses nasal secretion by 53% and 72%, respectively. Treatment with Asapiprant in rats at 10 mg/kg significantly (P<0.05) reduces airway hyper-responsiveness (AHR), infiltration of inflammatory cells, and mucin production in bronchoalveolar lavage fluid (BALF), although treatment with Asapiprant at 0.1 mg/kg does not have a significant effect on any responses.

Product Specifications

CAS Number

932372-01-5

Purity

>98% (HPLC)

Solubility

DMSO: 10 mg/mL (19.94 mM)

Smiles

CC (C) Oc1ccc (cc1) S (=O) (=O) N1CCN (CC1) c1ccc (-c2ncco2) c (OCC (O) =O) c1

Molecular Formula

C24H27N3O7S

Molecular Weight

501.55

Storage Conditions

Storage temperature: -20°C. Stability: ≥ 2 years

Notes

For research use only.

Other Product Names

2- (5- (4- ((4-isopropoxyphenyl) sulfonyl) piperazin-1-yl) -2- (oxazol-2-yl) phenoxy) acetic acid

Available Sizes

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