摘要:
Utilisation des héparines de bas poids moléculaire pour la prévention et le traitement du trauma du système nerveux central et notamment du traumatisme spinal, crânien ou crânio-spinal.
摘要:
The invention concerns novel azole or triazole derivatives of formula (I), wherein: X, Ar1, Ar3, A, R1, R5, R6, R7 and B are such as defined in the description, their preparation method and their use as antifungal medicines.
摘要:
The invention concerns a pharmaceutical composition comprising trimegestone optionally associated with an oestrogen, characterised in that it comprises a buffer solution whereof the pH, when it is introduced in the composition, ranging essentially between 2 and 5.5. The invention also concerns the methods for making such a composition and the primary package containing them.
摘要:
The present invention relates to acylguanidino derivatives of formula (I), in which R?1, R2, R3¿, A, B, X, Y and n have the meanings indicated in claim 1, their physiologically tolerable salts and their prodrugs. The compounds of the formula (I) are valuable pharmaceutically active compounds. They are vitronectin receptor antagonists and inhibitors of cell adhesion and bone resorption by osteoclasts. This renders them suitable, for example, for the therapy and prophylaxis of illness which are based on the interaction between vitronectin receptors and their ligands in cell-cell or cell-matrix interaction processes or which can be prevented, alleviated or cured by influencing such interactions. For example, they can be applied for treating and preventing osteoporosis, or for inhibiting undesired angiogenesis or proliferation of cells of the vascular smooth muscles. The invention furthermore relates to processes for the preparation of compounds of the formula (I), their use, in particular as pharmaceutical active ingredients, and pharmaceutical compositions comprising them.
摘要:
The invention concerns compounds of formula (I) wherein: m = 1, 2 or 3; n = 1, 2 or 3; R5 represents a group selected among COR6, CO2R6, SO2R6, SO2NHR6, SO2NHCOR6, SO2NHCO2R6, CONH2 and CONHR6; R1, R2, R4, R5, R6 and R7 are as defined in the description, in all their possible isomeric forms, their physiologically acceptable salts, their prodrugs. The invention also concerns the method for preparing them, their use as medicines in particular for treating osteoporosis and pharmaceutical compositions containing them.
摘要:
The invention concerns pharmaceutical compositions containing as active ingredient a compound of formula (I) wherein: R1 represents a -NHCOR4 or -N(R5)-Y-R6 radical; Y is CO or SO2; R4 represents an -alk-SO2R11, -alk-SO2-CH=CH-R11, Het substituted by -SO2R11 or phenyl substituted by -SO2-R11 or -alk-SO2-R11 radical; R5 represents a hydrogen atom or an alkyl radical; R6 represents a phenylalkyl radical, Het or Ar; the novel derivatives of formula (I) and their preparation.
摘要:
The invention concerns a compound of formula (I) wherein R represents a CR1R2 radical, C=C(R5)SO2R6 or C=C(R7)SO2alk, their preparation and pharmaceutical compositions containing them.
摘要:
The invention concerns a pharmaceutical composition comprising trimegestone optionally associated with an oestrogen, characterised in that it comprises a buffer solution whereof the pH, when it is introduced in the composition, ranging essentially between 2 and 5.5. The invention also concerns the methods for making such a composition and the primary package containing them.