Abstract:
3-Methyl-N-(1-pyrrolin-2-yl)-pyrazole-5-carboxamides and processes for making same. Such compounds lower blood sugar and, hence, are useful as antidiabetic agents.
Abstract:
Novel 2-iminopyrrolidines substituted in the 1-position are prepared from 2-amino- Delta ''-pyrrolines. The novel pyrrolidines are useful as anti-diabetic and hypoglycemic agents since they effect a lowering of the blood sugar content in warm blooded animals.
Abstract:
GUANIDINO OR UREIDO OR THIOUREIDO PYRROLINES (A) PREPARED FROM 2-AMINO-$1-PYRROLINES. (B). BOTH (A) AND (B) LOWER THE BLOOD SUGAR CONTENT IN WARM BLOODED ANIMALS; HENCE, ARE USEFUL AS HYPOLGLYCEMIC AGENTS.
Abstract:
Imidazole derivatives of the formula I wherein R1 and R2 each is lower alkyl, X is a residue of the formula R3 is hydrogen and R4 is hydrogen or lower alkyl or R3 and R4 taken together are an additional carbon-nitrogen bond; R5 is hydrogen or lower alkyl; R6 is hydrogen, lower alkyl, lower alkylthio or a residue of the formula -NR7R8; and R7 and R8 each is lower alkyl or taken together with the nitrogen atom are a 5- or 6-membered saturated heterocycle; and pharmaceutically acceptable acid addition salts thereof are described. The compounds of formula I possess valuable pharmacodynamic properties, especially inflammation-inhibiting and edema-inhibiting properties, so that they can be used for the control or prevention of illnesses, especially for the control or prevention of inflammations and edemas.
Abstract:
1396840 Sulphanilamides F HOFFMANNLA ROCHE & CO AG 19 Oct 1973 [20 Oct 1972] 48787/73 Heading C2C Novel compounds (I) where R is alkyl, allyl or alkoxyalkyl, are made (a) by reacting a compound (II) (R 1 is a leaving atom or group) with a sulphanilamide alkali metal salt, (b) by saponifying compounds (III) and (c) by reducing compounds (IV). The invention also comprises novel compounds (III) and (IV). Pharmaceutical preparations useful for controlling bacterial infections contain (I) as active ingredient. Administration may be orally or parenterally.
Abstract:
Imidazole derivatives of the formula I wherein R1 and R2 each is lower alkyl, X is a residue of the formula R3 is hydrogen and R4 is hydrogen or lower alkyl or R3 and R4 taken together are an additional carbon-nitrogen bond; R5 is hydrogen or lower alkyl; R6 is hydrogen, lower alkyl, lower alkylthio or a residue of the formula -NR7R8; and R7 and R8 each is lower alkyl or taken together with the nitrogen atom are a 5- or 6-membered saturated heterocycle; and pharmaceutically acceptable acid addition salts thereof are described. The compounds of formula I possess valuable pharmacodynamic properties, especially inflammation-inhibiting and edema-inhibiting properties, so that they can be used for the control or prevention of illnesses, especially for the control or prevention of inflammations and edemas.
Abstract:
Imidazole derivatives of the formula I wherein R1 and R2 each is lower alkyl, X is a residue of the formula R3 is hydrogen and R4 is hydrogen or lower alkyl or R3 and R4 taken together are an additional carbon-nitrogen bond; R5 is hydrogen or lower alkyl; R6 is hydrogen, lower alkyl, lower alkylthio or a residue of the formula -NR7R8; and R7 and R8 each is lower alkyl or taken together with the nitrogen atom are a 5- or 6-membered saturated heterocycle; and pharmaceutically acceptable acid addition salts thereof are described. The compounds of formula I possess valuable pharmacodynamic properties, especially inflammation-inhibiting and edema-inhibiting properties, so that they can be used for the control or prevention of illnesses, especially for the control or prevention of inflammations and edemas.