US2003060506A1PendingUtilityA1
Bile secretion promoting composition
Est. expiryApr 6, 2020(expired)· nominal 20-yr term from priority
A61P 7/08A61P 41/00A61P 1/18A61P 1/16A61K 31/5585A61K 31/5575A61K 31/558A61K 31/557
42
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Claims
Abstract
Disclosed is a method for promoting bile secretion, which comprises administering and effective amount of a certain 15-keto-prostaglandin compound to a subject having a disease or condition associated with bile secretion deficient. Also disclosed is a method for treatment of a liver to be transplanted in a liver transplantation process, which comprises contacting the liver with a liquid composition comprising the 15-keto-prostaglandin compound as above.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method for promoting bile secretion comprising administering an effective amount of a 15-keto-prostaglandin compound represented by the general formula (I):
wherein W 1 , W 2 and W 3 are carbon or oxygen atoms;
L, M and N are hydrogen, hydroxy, halogen, lower alkyl, lower alkoxy, hydroxy(lower)alkyl or oxo, wherein at least one of L and M is a group other than hydrogen, and the five-membered ring may have one or more double bond(s);
A is —CH 2 OH, —COCH 2 OH, —COOH or its functional derivative;
B is —CH 2 —CH 2 —, —CH═CH— or —C≡C—;
R 1 is a divalent saturated or unsaturated lower-medium aliphatic hydrocarbon residue, which is unsubstituted or substituted by halogen, alkyl, hydroxy, oxo, aryl or heterocyclic group; and
Ra is a saturated or unsaturated lower-medium aliphatic hydrocarbon residue, which is unsubstituted or substituted by halogen, oxo, hydroxy, lower alkyl, lower alkoxy, lower alkanoyloxy, cyclo(lower)alkyl, cyclo(lower)alkyloxy, aryl, aryloxy, heterocyclic group or heterocyclic-oxy group; cyclo(lower)alkyl; cyclo(lower)alkyloxy; aryl; aryloxy; heterocyclic group; or heterocyclic-oxy group, to a subject having a condition or disease associated with bile secretion deficient.
2 . The method of claim 1 , wherein the 5-keto-prostaglandin compound is a 13,14-dihydro-15-keto-prostaglandin compound
3 . The method of claim 1 , wherein the 5-keto-prostaglandin compound is a 15-keto-16-mono or di-halogen-prostaglandin compound.
4 . The method of claim 1 , wherein the 5-keto-prostaglandin compound is a 13,14-dihydro-15-keto-16-mono or di-halogen-prostaglandin compound.
5 . The method of claim 1 , wherein the 15-keto-prostaglandin compound is a 15-keto-16-mono or di-fluoro-prostaglandin compound.
6 . The method of claim 1 , wherein the 15-keto-prostaglandin compound is a 13,14-dihydro-15-keto-16-mono or di-fluoro-prostaglandin compound.
7 . The method of claim 1 , wherein the 15-keto-prostaglandin compound is a 15-keto-prostaglandin E compound.
8 . The method of claim 1 , wherein the 15-keto-prostaglandin compound is 13,14-dihydro-15-keto-16,16-difluoro-18-methyl-prostaglandin E 1.
9 . The method of claim 1 , wherein the 5-keto-prostaglandin compound is 13,14-dihydro-15-keto-16,16-difluoro-17-methyl-prostaglandin E 1 .
10 . A method for treating a liver to be transplanted in a liver transplantation process, which comprises contacting the liver with a liquid composition comprising a 15-keto-prostaglandin compound represented by the general formula (I):
wherein W 1 , W 2 and W 3 are carbon or oxygen atoms;
L, M and N are hydrogen, hydroxy, halogen, lower alkyl, lower alkoxy, hydroxy(lower)alkyl or oxo, wherein at least one of L and M is a group other than hydrogen, and the five-membered ring may have one or more double bond(s);
A is —CH 2 OH, —COCH 2 OH, —COOH or its functional derivative;
B is —CH 2 —CH 2 —, —CH═CH— or —C≡C—;
R 1 is a divalent saturated or unsaturated lower-medium aliphatic hydrocarbon residue, which is unsubstituted or substituted by halogen, alkyl, hydroxy, oxo, aryl or heterocyclic group; and
Ra is a saturated or unsaturated lower-medium aliphatic hydrocarbon residue, which is unsubstituted or substituted by halogen, oxo, hydroxy, lower alkyl, lower alkoxy, lower alkanoyloxy, cyclo(lower)alkyl, cyclo(lower)alkyloxy, aryl, aryloxy, heterocyclic group or heterocyclic-oxy group; cyclo(lower)alkyl; cyclo(lower)alkyloxy; aryl; aryloxy; heterocyclic group; or heterocyclic-oxy group.
11 . The method of claim 10 , wherein the 15-keto-prostaglandin compound is a 13,14-dihydro-15-keto-prostaglandin compound.
12 . The method of claim 10 , wherein the 15-keto-prostaglandin compound is a 15-keto-16-mono or dihalogen-prostaglandin compound.
13 . The method of claim 10 , wherein the 15-keto-prostaglandin compound is a 13,14-dihydro-15-keto-16-mono or di-halogen-prostaglandin compound.
14 . The method of claim 10 , wherein the 15-keto-prostaglandin compound is a 15-keto-16-mono or di-fluoro-prostaglandin compound.
15 . The method of claim 10 , wherein the 15-keto-prostaglandin compound is a 13,14-dihydro-15-keto-16-mono or di-fluoro-prostaglandin compound.
16 . The method of claim 10 , wherein the 15-keto-prostaglandin compound is a 15-keto-prostaglandin E compound.
17 . The method of claim 10 , wherein the 15-keto-prostaglandin compound is 13,14-dihydro-15-keto-16,16-difluoro-18-methyl-prostaglandin E 1 .
18 . The method of claim 10 , wherein the 15-keto-prostaglandin compound is 13,14-dihydro-15-keto-16,16-difluoro-17-methyl-prostaglandin E 1 .
19 . The method of claim 10 , wherein the liquid composition is a preservation solution.
20 . The method of claim 10 , wherein the liquid composition is a perfusate.
21 . The method of claim 10 , wherein the liquid composition is a rinse solution.Join the waitlist — get patent alerts
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