US2012178726A1PendingUtilityA1
Novel compounds
Est. expiryOct 4, 2027(~1.2 yrs left)· nominal 20-yr term from priority
A61P 5/44A61P 43/00A61P 37/08A61P 11/00A61P 11/02A61P 11/06C07J 71/0047
40
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Claims
Abstract
The present invention provides compounds of formula (I) wherein n, p, R 1 , R 2 , X 1 , X 2 , X 3 , X 4 , X 5 , R 3a , R 3b , R 4 , R 5 and R 6 are as defined in the specification, a process for their preparation, pharmaceutical compositions containing them and their use in therapy.
Claims
exact text as granted — not AI-modified1 - 16 . (canceled)
17 . A compound or a pharmaceutically acceptable salt thereof, wherein the compound has the structure:
18 . A pharmaceutically acceptable salt of the compound of claim 17 , wherein the pharmaceutically acceptable salt comprises a hydrochloride, hydrobromide, trifluoroacetate, sulphate, phosphate, acetate, fumarate, maleate, tartrate, lactate, citrate, pyruvate, succinate, oxalate, methanesulphonate or p-toluenesulphonate salt.
19 . A pharmaceutical composition comprising a compound or pharmaceutically acceptable salt thereof as claimed in claim 17 and a pharmaceutically acceptable adjuvant, diluent or carrier.
20 . A pharmaceutical composition as claimed in claim 19 , wherein the composition is an inhalation composition.
21 . A process for the preparation of a pharmaceutical composition as claimed in claim 19 which comprises mixing the compound or pharmaceutically acceptable salt thereof with a pharmaceutically acceptable adjuvant, diluent or carrier.
22 . A method of treating, or reducing the risk of, an obstructive airways disease or condition which comprises administering to a patient in need thereof a therapeutically effective amount of a compound or pharmaceutically acceptable salt thereof as claimed in claim 17 .
23 . A method as claimed in claim 22 , wherein the disease or condition is chronic obstructive pulmonary disease.
24 . A method as claimed in claim 22 , wherein the disease or condition is asthma.
25 . A method of treating allergic rhinitis which comprises administering to a patient in need thereof a therapeutically effective amount of a compound or pharmaceutically acceptable salt thereof as claimed in claim 17 .
26 . The method as claimed in claim 22 , wherein the therapeutically effective amount of the compound or pharmaceutically acceptable salt thereof is administered by a dry powder inhaler.
27 . A combination comprising a compound according to claim 17 , or a pharmaceutically acceptable salt thereof, and one or more agents independently selected from:
a non-steroidal glucocorticoid receptor agonist; a selective β2 adrenoreceptor agonist; a phosphodiesterase inhibitor; a protease inhibitor; a glucocorticoid; an anticholinergic agent; a modulator of chemokine receptor function; and an inhibitor of kinase function.Cited by (0)
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