摘要:
The invention relates to substituted hydroxybiphenyls, the derivatives and the physiologically acceptable salts thereof. The invention relates to the compounds of formula (I), wherein the substituents R1, R2 and A are defined as indicated, and to the physiologically acceptable salts thereof. The inventive compounds are suitable e.g. as hypoglycemic drugs and as drugs for use in the prevention and treatment of diabetes.
摘要:
The invention relates to substituted 3-phenyl-5-alkoxy-1,3,4-oxadiazol-2-ones, of general formula (I), wherein R1 represents C7-C22 alkyl, C2-C4 alkyl that is substituted by C4-C20 alkoxy, C6-C10 aryl, C6-C10 aryloxy or C4-C12-alkoxy-C2-C4-alkoxy, and represents C7-C20 alkenyl, 3β-cholestan-3-yl or substituted phenyl; R2, R3, R4 and R5 represent hydrogen, halogen, nitro, C1-C4 alkyl, C1-C9 alkyloxy, trifluoromethyl, trifluoromethoxy or C6-C10-aryl-C1-C4-alkyloxy, C6-C10 aryloxy, C6-C10 aryl, C3-C8 cycloalkyl or O-C3-C8-cycloalkyl, whereby all of these can be substituted. The invention also relates to methods for producing these compounds. The compounds of formula (I) have an inhibiting effect on the pancreatic lipase and can be used as active substances for treating obesity.
摘要:
The invention relates to substituted hydroxybiphenyls, the derivatives and the physiologically acceptable salts thereof. The invention relates to the compounds of formula (I), wherein the substituents R1, R2 and A are defined as indicated, and to the physiologically acceptable salts thereof. The inventive compounds are suitable e.g. as hypoglycemic drugs and as drugs for use in the prevention and treatment of diabetes.
摘要:
The invention relates to indazole derivatives of general formula (I) or (II), with the meanings as given in the description, the pharmaceutically-acceptable salts and use thereof as medicaments.
摘要:
The invention relates to novel insulin analogs having a basal time-action profile, which are characterized by the following features: a) the B chain end consists of an amidated basic amino acid residue such as lysine or arginine amide; b) the N-terminal amino acid residue of the insulin A chain is a lysine or arginine radical; c) the amino acid position A8 is occupied by a histidine radical; d) the amino acid position A21 is occupied by a glycine radical; and e) one or more substitutions and/or additions of negatively charged amino acid residues are carried out in the positions A5, A15, A18, B-1, B0, B1, B2, B3 and B4.
摘要:
The invention relates to indazole derivatives of general formula (I) or (II), with the meanings as given in the description, the pharmaceutically-acceptable salts and use thereof as medicaments.
摘要:
The invention relates to a yeast strain of Saccharomyces cerevisiae which, due to deletion of the genomic sequences, does not produce any hexose transporters and which as a consequence cannot propagate on substrates that have hexose as the only carbon source. The capability of the strain of propagating on substrates that have hexose as the only carbon source can be re-established by expression of a GLUT4 gene.
摘要:
The invention relates to novel insulin analogs having a basal time-action profile, which are characterized by the addition and/or substitution of negatively and positively charged amino acid residues and by an amidation of the C-terminal carboxy group of the B chain and histidine in position 8 of the insulin A chain. The invention also relates to the production and use thereof.