摘要:
Novel fluorinated derivatives of the vinblastine and vinorelbine family of general formula (1) and the therapeutically acceptable salts of these molecules. The invention also concerns the application of said compounds in therapy and their methods of preparation.
摘要:
Novel fluorinated derivatives of the vinblastine and vinorelbine family of general formula (1) and the therapeutically acceptable salts of these molecules. The invention also concerns the application of said compounds in therapy and their methods of preparation.
摘要:
The present invention concerns nitrogenated derivatives of narciclasine and pancratistatin of the following general formula (I) as well as their pharmaceutically acceptable salts. The present invention also concerns the use of these compounds in cancer therapy as well as a method for their preparation.
摘要:
The present invention relates to dimeric derivatives of 10-trifluoromethylated artemisinin of formula (I) below: Formula (I) and the pharmaceutically acceptable salts thereof, and also to the preparation method thereof and to the uses thereof, especially in the treatment of cancer.
摘要:
The present invention relates to dimeric derivatives of 10-trifluoromethylated artemisinin of formula (I) : or a pharmaceutically acceptable salt thereof with B1 and B2 selected from C=O, CHOH and CH2, as well as to their use in treating cancer and to their preparation method.
摘要:
The invention concerns novel halogenated derivatives of the vinblastine and vinorelbine family, corresponding to general formula (1) and their therapeutically acceptable salts. The invention also concerns the application of these compounds in therapy and their methods of preparation. The invention further concerns a novel method for preparing vinflunine or 20',20'-difluoro-3',4'-dihydrovinorelbine, of formula (a).
摘要:
The invention concerns novel halogenated derivatives of the vinblastine and vinorelbine family, corresponding to general formula (1) and their therapeutically acceptable salts. The invention also concerns the application of these compounds in therapy and their methods of preparation. The invention further concerns a novel method for preparing vinflunine or 20',20'-difluoro-3',4'-dihydrovinorelbine, of formula (a).