US2010249200A1PendingUtilityA1
Novel Compounds 569
Est. expiryDec 20, 2026(~0.4 yrs left)· nominal 20-yr term from priority
A61P 37/08A61P 43/00A61P 27/16A61P 29/00A61P 11/00A61P 11/08A61P 11/02A61P 11/06C07D 417/12C07D 277/14C07D 285/14
41
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Claims
Abstract
The present invention provides compounds of formula (I) wherein R a , R b , R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 29 are as defined in the specification, processes for their preparation, pharmaceutical compositions containing them and their use in therapy.
Claims
exact text as granted — not AI-modified1 - 14 . (canceled)
15 . A method of treating, or reducing the risk of, a disease or condition in which modulation of β2 adrenoreceptor activity is beneficial which comprises administering to a patient in need thereof a therapeutically effective amount of N-Cyclohexyl-N 3 -[2-(3-fluorophenyl)ethyl]-N-(2-{[2-(4-hydroxy-2-oxo-2,3-dihydro-1,3-benzothiazol-7-yl)ethyl]amino}ethyl)-β-alaninamide or a pharmaceutically acceptable salt thereof.
16 . A method of treating, or reducing the risk of, an inflammatory disease or condition which comprises administering to a patient in need thereof a therapeutically effective amount of N-Cyclohexyl-N 3 -[2-(3-fluorophenyl)ethyl]-N-(2-{[2-(4-hydroxy-2-oxo-2,3-dihydro-1,3-benzothiazol-7-yl)ethyl]amino}ethyl)-β-alaninamide or a pharmaceutically acceptable salt thereof.
17 . A method according to claim 15 or claim 16 , wherein the disease or condition is adult respiratory distress syndrome (ARDS).
18 . (canceled)
19 . A method according to claim 15 or claim 16 , wherein the disease or condition is pulmonary emphysema.
20 . A method according to claim 15 or claim 16 , wherein the disease or condition is bronchitis.
21 . A method according to claim 15 or claim 16 , wherein the disease or condition is bronchiectasis.
22 . A method according to claim 15 or claim 16 , wherein the disease or condition is chronic obstructive pulmonary disease (COPD).
23 . A method according to claim 15 or claim 16 , wherein the disease or condition is asthma.
24 . A method according to claim 15 or claim 16 , wherein the disease or condition is rhinitis.
25 . A method according to claim 15 or claim 16 , wherein the method comprises administering to the patient in need thereof a therapeutically effective amount of N-Cyclohexyl-N 3 -[2-(3-fluorophenyl)ethyl]-N-(2-{[2-(4-hydroxy-2-oxo-2,3-dihydro-1,3-benzothiazol-7-yl)ethyl]amino}ethyl)-β-alaninamide.
26 . A method according to claim 15 or claim 16 , wherein the method comprises administering to the patient in need thereof a therapeutically effective amount of N-Cyclohexyl-N 3 -[2-(3-fluorophenyl)ethyl]-N-(2-{[2-(4-hydroxy-2-oxo-2,3-dihydro-1,3-benzothiazol-7-yl) ethyl]amino}ethyl)-β-alaninamide in the form of a pharmaceutically acceptable salt, wherein the salt is an acid addition salt which is selected from the group consisting of hydrochloride, hydrobromide, sulphate, phosphate, acetate, fumarate, maleate, tartrate, lactate, citrate, pyruvate, succinate, oxalate, methanesulphonate, and p-toluenesulphonate.Cited by (0)
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