摘要:
in which Z, W, Q, R and Y have the meanings indicated in claim 1, are inhibitors of Tankyrase, and can be employed, inter alia, for the treatment of diseases such as cancer, cardiovascular diseases, central nervous system injury and different forms of inflammation.
摘要:
in which W, X and Y have the meanings indicated in Claim 1, are inhibitors of Tankyrase, and can be employed, inter alia, for the treatment of diseases such as cancer, cardiovascular diseases, central nervous system injury and different forms of inflammation.
摘要:
Compounds of the formula I in which R1-R3 have the meanings indicated in Claim 1, are inhibitors of Tankyrase, and can be employed, inter alia, for the treatment of diseases such as cancer, cardiovascular diseases, central nervous system injury and different forms of inflammation.
摘要:
The invention relates to compounds of formula (I), where R 1 , L and m have the denotations as defined in the claims, and/or to the physiologically harmless salts, tautomers and stereoisomers thereof, including mixtures thereof in all ratios. The compounds of formula (I) can be used for inhibiting serine / threonine protein kinases and for sensitizing cancer cells to anticancer drugs and/or ionizing radiation. A further object of the invention is the use of the compounds of formula (I) in the prophylaxis, therapy or progress monitoring of cancers, tumors, metastases, or angiogenic disorders, in combination with radiotherapy and/or an anticancer drug. The invention further relates to a method for producing the compounds of formula (I) by reacting compounds of formulae (II) and (III) and, if need be, converting a chemical base or acid of the compounds of the formula (I) to one of the salts thereof.
摘要:
Compounds of the formula (I) in which R, R 1 and R 2 are each as defined in claim 1 are PI3K inhibitors and can be used inter alia for treatment of autoimmune disorders, inflammation, cardiovascular disorders, neurodegenerative disorders and tumours.
摘要:
Novel quinazoline amide derivatives of the formula (I), in which R 1 - R 4 and X have the meanings specified in claim 1, are HSP90 inhibitors and can be used for preparing a pharmaceutical for treating diseases, in which the inhibition, regulation and/or modulation of HSP90 plays a part.
摘要:
The invention relates to compounds of the formula (I), where X, R 1 , and R 2 have the meanings specified in claim 1, are PI3K inhibitors, and can be used, inter alia , to treat autoimmune diseases, inflammations, cardiovascular diseases, neurodegenerative diseases, and tumors.
摘要:
The invention relates to a novel quinazolinamide derivatives of the formula (I), where R 1 -R 5 and X have the meanings indicated in Claim 1, that are HSP90-inhibitors and that can be used for producing a medication for treating illnesses for which the prevention, regulation, and/or modulation of HSP90 plays a role.