Abstract: The present invention relates to a 3-aryl-4 catechol-pyrrole-n-propanol compound and the derivatives thereof having General Formula (I), wherein:—R1 is an aryl group, particularly a phenyl, optionally substituted by one or more (C1-C2)alkyl groups, one or more halogens, one or more —OH, —CN or CF3 groups, or a combination of same, and—R2 is a (C1-C6)alkyl group, a hydroxy(C1-C6)alkyl group, a (C1-C4)alcoxy(C1-C6)alkyl group, or a pharmaceutically acceptable hydrate or solvate of same. The invention also relates to the methods for preparing said compound and derivatives, to the pharmaceutical compositions containing same, and to the use of same as a drug or in the form of a prodrug converted via dimerization, particularly via oxidative coupling in the presence of a superoxide anion, in the treatment of cancer and diseases related to excessive angiogenesis.

Abstract: The present invention relates to a 3-aryl-4 catechol-pyrrole-n-propanol compound and the derivatives thereof having General Formula (I), wherein:—R1 is an aryl group, particularly a phenyl, optionally substituted by one or more (C1-C2)alkyl groups one or more halogens, one or more —OH, —CN or CF3 groups, or a combination of same, and—R2 is a (C1-C2)alkyl group, a hydroxy(C1-C8)alkyl group, a (C1-C4)alocoxy(C1-C8)alkyl group, or a pharmaceutically acceptable hydrate or solvate of same. The invention also relates to the methods for preparing said compound and derivatives, to the pharmaceutical compositions containing same, and to the use of same as a drug or in the form of a prodrug converted via dimerization, particularly via oxidative coupling in the presence of a superoxide anion, in the treatment of cancer and diseases related to excessive angiogenesis.

Abstract: The present invention relates to the use of biguanide derivatives of general formula I below: in which: the groups R1 and R2 represent, independently of each other, a hydrogen atom, a C1–C7, alkyl group, a cycloalkyl group, a heterocycle, a C2–C7 alkenyl group, an aryl group, an aralkyl group, an aryloxyalkyl group or a heteroaryl group, or R1 and R2, taken together, represent a C2–C7 alkylene which may contain one or more hetero atoms, and the group R3 represents a primary, secondary or tertiary amine, or pharmaceutically acceptable salts thereof, to manufacture a medicinal product with cicatrizing action, the said medicinal product being in a pharmaceutical form for topical use.

Abstract: The present invention relates to the use of biguanide derivatives of general, formula I below; 1