Method for modulating claudin mediated functions
AssigneesSucampo AG, Osaka University
InventorsRyuji Ueno, Sachiko Tsukita
Life of this patent
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Abstract
Disclosed is a method for modulating a claudin-mediated function in a mammalian subject which comprises administering to a subject in need thereof an effective amount of a specific fatty acid derivative. The application also discloses a method for treating a dermatological disease and a method for modulating an expression of a claudin in a mammalian subject using the same fatty acid derivative as above.
Claims21
A method for treating a dermatological disease in a mammalian subject, which comprises administering to the subject in need thereof an effective amount of a fatty acid derivative represented by the formula (I):
- wherein L, M and N are hydrogen atom, hydroxy, halogen atom, lower alkyl, hydroxy(lower) alkyl, lower alkanoyloxy or oxo, wherein at least one of L and M is a group other than hydrogen, and the five-membered ring may have at least one double bond;
- A is —CH-A, or —CH2OH, —COCH2OH, —COOH or a functional derivative thereof;
- B is single bond, —CH2—CH2—, —CH═CH—, —C═C—, —CH2—CH2—CH2—, —CH═CH—CH, —, —CH2—CH═CH—, —C═C—CH2— or —CH2—C═C—;
- Z is
- or single bond
- wherein R4 and R5 are hydrogen, hydroxy, halogen, lower alkyl, lower alkoxy or hydroxy(lower)alkyl, wherein R4 and R5 are not hydroxy and lower alkoxy at the same time;
- R1 is a saturated or unsaturated bivalent lower or medium aliphatic hydrocarbon residue, which is unsubstituted or substituted with halogen, lower alkyl, hydroxy, oxo, aryl or heterocyclic group, and at least one of carbon atom in the aliphatic hydrocarbon is optionally substituted by oxygen, nitrogen or sulfur;
- and
- Ra is a saturated or unsaturated lower or medium aliphatic hydrocarbon residue, which is unsubstituted or substituted with halogen, oxo, hydroxy, lower alkyl, lower alkoxy, lower alkanoyloxy, cyclo(lower)alkyl, cyclo(lower)alkyloxy, aryl, aryloxy, heterocyclic group or hetrocyclic-oxy group;
- lower alkoxy;
- lower alkanoyloxy;
- cyclo(lower)alkyl;
- cyclo(lower)alkyloxy;
- aryl;
- aryloxy;
- heterocyclic group;
- heterocyclic-oxy.
A method for modulating a claudin-mediated function in a mammalian subject, which comprises administering to the subject in need thereof an effective amount of a fatty acid derivative represented by the formula (I):
- wherein L, M and N are hydrogen atom, hydroxy, halogen atom, lower alkyl, hydroxy(lower)alkyl, lower alkanoyloxy or oxo, wherein at least one of L and M is a group other than hydrogen, and the five-membered ring may have at least one double bond;
- A is —CH3, or —CH2OH, —COCH2OH, —COOH or a functional derivative thereof;
- B is single bond, —CH2—CH2—, —CH═CH—, —C═C—, —CH2—CH2—CH2—, —CH_CH—CH2—, —CH2—CH═CH—, —C≡C—CH2— or —CH2—C═C—;
- Z is
- or single bond
- wherein R4 and R5 are hydrogen, hydroxy, halogen, lower alkyl, lower alkoxy or hydroxy(lower)alkyl, wherein R4 and R5 are not hydroxy and lower alkoxy at the same time;
- R1 is a saturated or unsaturated bivalent lower or medium aliphatic hydrocarbon residue, which is unsubstituted or substituted with halogen, lower alkyl, hydroxy, oxo, aryl or heterocyclic group, and at least one of carbon atom in the aliphatic hydrocarbon is optionally substituted by oxygen, nitrogen or sulfur;
- and
- Ra is a saturated or unsaturated lower or medium aliphatic hydrocarbon residue, which is unsubstituted or substituted with halogen, oxo, hydroxy, lower alkyl, lower alkoxy, lower alkanoyloxy, cyclo(lower)alkyl, cyclo(lower)alkyloxy, aryl, aryloxy, heterocyclic group or hetrocyclic-oxy group;
- lower alkoxy;
- lower alkanoyloxy;
- cyclo(lower)alkyl;
- cyclo(lower)alkyloxy;
- aryl;
- aryloxy;
- heterocyclic group;
- heterocyclic-oxy.
A method for modulating an expression of a claudin in a mammalian subject, which comprises administering to the subject in need thereof an effective amount of a fatty acid derivative represented by the formula (I):
- wherein L, M and N are hydrogen atom, hydroxy, halogen atom, lower alkyl, hydroxy(lower)alkyl, lower alkanoyloxy or oxo, wherein at least one of L and M is a group other than hydrogen, and the five-membered ring may have at least one double bond;
- A is —CH3, or —CH2OH, —COCH2OH, —COOH or a functional derivative thereof;
- B is single bond, —CH2—CH2—, —CH═CH—, —C═C—, —CH2—CH2—CH2—, —CH═CH—CH2—, —CH2—CH═CH—, —C═C—CH2— or —CH2—C═C—;
- Z is
- or single bond
- wherein R4 and R5 are hydrogen, hydroxy, halogen, lower alkyl, lower alkoxy or hydroxy(lower)alkyl, wherein R4 and R5 are not hydroxy and lower alkoxy at the same time;
- R1 is a saturated or unsaturated bivalent lower or medium aliphatic hydrocarbon residue, which is unsubstituted or substituted with halogen, lower alkyl, hydroxy, oxo, aryl or heterocyclic group, and at least one of carbon atom in the aliphatic hydrocarbon is optionally substituted by oxygen, nitrogen or sulfur;
- and
- Ra is a saturated or unsaturated lower or medium aliphatic hydrocarbon residue, which is unsubstituted or substituted with halogen, oxo, hydroxy, lower alkyl, lower alkoxy, lower alkanoyloxy, cyclo(lower)alkyl, cyclo(lower)alkyloxy, aryl, aryloxy, heterocyclic group or hetrocyclic-oxy group;
- lower alkoxy;
- lower alkanoyloxy;
- cyclo(lower)alkyl;
- cyclo(lower)alkyloxy;
- aryl;
- aryloxy;
- heterocyclic group;
- heterocyclic-oxy.
Dependencies are inferred from the claim text.