US2010120800A1PendingUtilityA1
Agent for preventing recurrence of cerebrovascular disorder and agent for ameliorating troubles following cerebrovascular disorder and inhibiting progress thereof
Est. expiryJul 21, 2019(expired)· nominal 20-yr term from priority
A61P 9/10A61P 43/00A61P 9/08A61K 31/00A61P 25/28A61K 31/4188A61P 25/18A61K 31/4245A61P 25/00
45
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Claims
Abstract
There is provided an agent for preventing the recurrence of cerebrovascular disorder and an agent for ameliorating troubles following cerebrovascular disorder and inhibiting the progress thereof which contain a compound having an angiotensin II antagonistic activity, a prodrug thereof or a salts thereof.
Claims
exact text as granted — not AI-modified1 - 13 . (canceled)
14 . A method for preventing recurrence of cerebrovascular disorder in a mammal, which comprises administering an effective amount of a compound having an angiotensin II antagonistic activity, a prodrug thereof or a salt thereof to the mammal, provided that the compound having an angiotension II antagonistic activity is not a compound represented by formula (I):
wherein R 1 represents a group capable of forming an anion or being converted into said group, X indicates that the phenylene group and the phenyl group are bound to each other directly or via a spacer of a chain made of 2 or less atoms, n is an integer of 1 or 2, ring A represents a benzene ring which may further have substituent(s), R 2 represents a group capable of forming an anion or being converted into said group, and R 3 represents a hydrocarbon residue which may be bound via a heteroatom and may have substituent(s).
15 . A method for ameliorating troubles following cerebrovascular disorder or inhibiting progress thereof in a mammal, which comprises administering an effective amount of a compound having an angiotensin II antagonistic activity, a prodrug thereof or a salt thereof to the mammal.
16 - 17 . (canceled)
18 . The method according to claim 14 , wherein the compound having an angiotensin II antagonistic activity is a non-peptide compound.
19 . The method according to claim 14 , wherein the compound having an angiotensin II antagonistic activity is a compound having an oxygen atom in the molecule.
20 . The method according to claim 14 , wherein the compound having an angiotensin II antagonistic activity is a compound having an ether bond or a carbonyl group.
21 . The method according to claim 14 , wherein the compound having an angiotensin II antagonistic activity is Losartan, Eprosartan, Valsartan, Telmisartan, Irbesartan, Olmesartan or Tasosartan.
22 . The method according to claim 14 , wherein the cerebrovascular disorder caused nerve symptoms.
23 . The method according to claim 14 , wherein the cerebrovascular disorder caused mental symptoms.
24 . The method according to claim 14 , wherein the cerebrovascular disorder caused subjective symptoms.
25 . The method according to claim 14 , wherein the cerebrovascular disorder caused obstacles in activities of daily living.
26 . The method according to claim 15 , wherein the compound having an angiotensin II antagonistic activity is a non-peptide compound.
27 . The method according to claim 15 , wherein the compound having an angiotensin II antagonistic activity is a compound having an oxygen atom in the molecule.
28 . The method according to claim 15 , wherein the compound having an angiotensin II antagonistic activity is a compound having an ether bond or a carbonyl group.
29 . The method according to claim 15 , wherein the compound having an angiotensin II antagonistic activity is a compound represented by the formula (I):
wherein R 1 represents a group capable of forming an anion or being converted into said group, X indicates that the phenylene group and the phenyl group are bound to each other directly or via a spacer of a chain made of 2 or less atoms, n is an integer of 1 or 2, ring A represents a benzene ring which may further have substituent(s), R 2 represents a group capable of forming an anion or being converted into said group, and R 3 represents a hydrocarbon residue which may be bound via a heteroatom and may have substituent(s).
30 . The method according to claim 15 , wherein the compound having an angiotensin II antagonistic activity is Losartan, Eprosartan, Candesartan cilexetil, Candesartan, Valsartan, Telmisartan, Irbesartan, Olmesartan or Tasosartan.
31 . The method according to claim 15 , wherein the compound having an angiotensin II antagonistic activity is 2-ethoxy-1-[[2′-(1H-tetrazole-5-yl)biphenyl-4-yl]methyl]benzimidazole-7-carboxylic acid.
32 . The method according to claim 15 , wherein the compound having an angiotensin II antagonistic activity is 1-(cyclohexyloxycarbonyloxy)ethyl 2-ethoxy-1-[[2′-(1H-tetrazole-5-yl)biphenyl-4-yl]methyl]benzimidazole-7-carboxylate.
33 . The method according to claim 15 , wherein the compound having an angiotensin II antagonistic activity is 2-ethoxy-1-[[2′-(2,5-dihydro-5-oxo-1,2,4-oxadiazole-3-yl)biphenyl-4-yl]methyl]benzimidazole-7-carboxylic acid.
34 . The method according to claim 15 , wherein the troubles following cerebrovascular disorder are nerve symptoms.
35 . The method according to claim 15 , wherein the troubles following cerebrovascular disorder are mental symptoms.
36 . The method according to claim 15 , wherein the troubles following cerebrovascular disorder are subjective symptoms.
37 . The method according to claim 15 , wherein the troubles following cerebrovascular disorder are obstacles in activities of daily living.Join the waitlist — get patent alerts
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