Remedy for diabetes
A method of screening a compound having a hypoglycemic effect (hereinafter referred to as “hypoglycemic compound”), a remedy for diabetes which contains a compound having a novel function mechanism, etc. More specifically speaking, a method of screening a hypoglycemic compound capable of binding to the β subunit of a trimeric GTP-binding protein, a remedy for diabetes comprising a hypoglycemic compound, which is characterized by being capable of binding to the β subunit of a trimeric GTP-binding protein, as the active ingredient, etc.
1. A method for screening a hypoglycemic compound, comprising using a compound represented by the following general formula (I) or a pharmaceutically acceptable salt thereof (hereinafter referred to as “said compound”) and a trimeric GTP-binding protein β subunit (hereinafter referred to as “said protein”), by measuring an inhibitory activity of a test substance against binding of the said compound to the said protein:
wherein in the general formula (I), A and B may be the same or different and independently represent an optionally substituted aromatic ring, an optionally substituted heterocyclic ring, or an optionally substituted aliphatic ring;
R 1 represents a lower alkyl group, a lower alkenyl group, a lower alkynyl group, or a lower alkoxy group, the groups being optionally substituted by 1 to 3 substituents;
—X— and —Y— may be the same or different and independently represent a hydrogen atom, —O—, —NR 2 —, —S—, —SO—, —SO 2 —, —CH 2 —, —CR 3 R 4 —, —COO—, —CONR 2 —, or —CO—, in which R 2 represents a hydrogen atom, an optionally substituted lower alkyl group, an optionally substituted acyl group, an optionally substituted alkoxycarbonyl group, an optionally substituted carbamoyl group, or an optionally substituted sulfonyl group, and R 3 and R 4 may be the same or different and independently represent a hydrogen atom, a halogen atom, a hydroxyl group, an alkyl group, a mercapto group, an alkoxy group, an alkylthio group, an alkylsulfonyl group, an acyl group, an acyloxy group, an amino group, an alkylamino group, a carboxyl group, an alkoxycarbonyl group, a carbamoyl group, a nitro group, a cyano group, or a trifluoromethyl group;
—W— represents an optionally substituted alkyl chain having 1 to 20 carbon atoms, and 1 to 10 carbon atoms in the alkyl chain may be replaced by —O—, —NR 5 —, —S—, —SO—, —SO 2 —, or —CO—, in which R 5 represents a hydrogen atom, an optionally substituted lower alkyl group, an optionally substituted acyl group, an optionally substituted alkoxycarbonyl group, an optionally substituted carbamoyl group, or an optionally substituted sulfonyl group;
Q represents a hydrogen atom, biotin, a fluorophore, a chromophore, a chemiluminescent functional group, an enzyme, a solid phase, a diazo group, or an azido group;
one or more atoms in the formula may be (a) radioisotope(s);
with the proviso that:
i) in the optionally substituted groups, each substituent is selected from the group consisting of halogen atoms, a hydroxyl group, alkyl groups, mercapto groups, alkoxy groups, alkylthio groups, alkylsulfonyl groups, acyl groups, acyloxy groups, amino groups, alkylamino groups, a carboxyl group, alkoxycarbonyl groups, carbamoyl groups, a nitro group, a cyano group, a trifluoromethyl group, aryl groups, heteroaryl groups, diazo groups, and azido groups, and the substituent may be labeled with biotin, a fluorophore, a chromophore, a chemiluminescent moiety, or an enzyme;
ii) when —X— is a hydrogen atom, —W—, —Y—, and Q do not exist; and
iii) when —Y— is a hydrogen atom, Q does not exist.
2. A method according to claim 1 , wherein in the lactam compound represented by the general formula (I), —X— and —Y— are other than a hydrogen atom, Q is biotin, a fluorophore, a chromophore, a chemiluminescent functional group, or an enzyme, and each substituent in the optionally substituted groups is not labeled with biotin, a fluorophore, a chromophore, a chemiluminescent moiety, or an enzyme.
3. A method according to claim 1 , wherein in the lactam compound represented by the general formula (I), —X— and —Y— are other than a hydrogen atom, Q is a hydrogen atom, a diazo group, or an azido group, and each substituent in the optionally substituted groups is not labeled with biotin, a fluorophore, a chromophore, a chemiluminescent moiety, or an enzyme.
4. A method according to claim 1 , wherein in the lactam compound represented by the general formula (I), X is a hydrogen atom, and at least one atom in the general formula (I) is a radioisotope.
5. A method according to any one of claims 1 to 4 , comprising the steps of:
(A) contacting the compound represented by the general formula (I) or the pharmaceutically acceptable salt thereof (the said compound) with the trimeric GTP-binding protein β subunit (the said protein);
(B) contacting the said compound with the said protein in the presence of the test substance; and
(C) measuring the inhibitory activity of the test substance against the binding of the said compound to the said protein.
6. A method according to any one of claims 1 to 4 , wherein the method for screening the hypoglycemic compound by measuring the inhibitory activity of the test substance against the binding of the compound represented by the general formula (I) or the pharmaceutically acceptable salt thereof (the said compound) to the trimeric GTP-binding protein β subunit uses a cell, a tissue, or an extract thereof containing the trimeric GTP-binding protein β subunit.