Patent classifications
C07D493/18
COMPOUNDS FROM RENEWABLE RESOURCES
Compounds of formula III:
##STR00001##
and salts thereof are disclosed. Also disclosed are methods for preparing compounds of formula III, intermediates useful for preparing compounds of formula III and methods for preparing compounds and materials from compounds of formula III.
Use of Artemisinin for Treating Tumors Induced by Oncogenic Viruses and for Treating Viral Infections
In certain aspects, the invention relates to methods of treating proliferative cervical disorders (such as cervical cancer and cervical dysplasia) and treating virus infection by administering artemisinin-related compounds. In certain aspects, the invention relates to methods of treating a tumor induced by an oncogenic virus, methods of killing or inhibiting a squamous cell carcinoma, and methods of inhibiting the replication of a virus, by administering artemisinin-related compounds.
Use of Artemisinin for Treating Tumors Induced by Oncogenic Viruses and for Treating Viral Infections
In certain aspects, the invention relates to methods of treating proliferative cervical disorders (such as cervical cancer and cervical dysplasia) and treating virus infection by administering artemisinin-related compounds. In certain aspects, the invention relates to methods of treating a tumor induced by an oncogenic virus, methods of killing or inhibiting a squamous cell carcinoma, and methods of inhibiting the replication of a virus, by administering artemisinin-related compounds.
SHORT SYNTHESES OF (-)-PICROTOXININ AND RELATED COMPOUNDS
The present disclosure relates to concise processes for making (−)-picrotoxinin (1, PXN) and 5-methyl-picrotoxinin (20, 5MePXN), and to 5MePXN, its pharmaceutical compositions, and its method of use for inhibiting GABA.sub.A receptor.
STEREOCHEMICALLY DEFINED POLYPROPIONATES AND METHODS FOR MAKING AND USING THE SAME
The present invention relates to stereochemically defined polypropionates and methods for preparing and using the same. The stereochemically defined polypropionates may be useful in the synthesis of natural products and/or natural product-like libraries.
Hemiacetal compound, polymer, resist composition, and patterning process
A polymer for resist use is obtainable from a hemiacetal compound having formula (1a) wherein R.sup.1 is H, CH.sub.3 or CF.sub.3, R.sup.2 to R.sup.4 each are H or a monovalent hydrocarbon group, X.sup.1 is a divalent hydrocarbon group, ZZ designates a non-aromatic mono- or polycyclic ring of 4 to 20 carbon atoms having a hemiacetal structure, k.sup.1=0 or 1, and k.sup.2=0 to 3. A resist composition comprising the polymer displays controlled acid diffusion and low roughness during both positive and negative tone developments. ##STR00001##
Hemiacetal compound, polymer, resist composition, and patterning process
A polymer for resist use is obtainable from a hemiacetal compound having formula (1a) wherein R.sup.1 is H, CH.sub.3 or CF.sub.3, R.sup.2 to R.sup.4 each are H or a monovalent hydrocarbon group, X.sup.1 is a divalent hydrocarbon group, ZZ designates a non-aromatic mono- or polycyclic ring of 4 to 20 carbon atoms having a hemiacetal structure, k.sup.1=0 or 1, and k.sup.2=0 to 3. A resist composition comprising the polymer displays controlled acid diffusion and low roughness during both positive and negative tone developments. ##STR00001##
Phenylaminopyrimidine-Derived Compounds, Method for Obtaining, Using Said Compounds in the Treatment of Cancer, and Treatment Methods
The present invention relates to novel phenylaminopyrimidine(FAP)-derived compounds of general formulas I and II:
##STR00001##
Where, in formula I, R.sub.1 is:
##STR00002##
Where, in formula II, X.sup.+ is selected among one of the compounds below:
##STR00003##
Where, in formula II, Y is
##STR00004##
The compounds of the present invention are powerful and nonspecific tyrosine kinase inhibitors, and the use of these compounds in the treatment.
Phenylaminopyrimidine-Derived Compounds, Method for Obtaining, Using Said Compounds in the Treatment of Cancer, and Treatment Methods
The present invention relates to novel phenylaminopyrimidine(FAP)-derived compounds of general formulas I and II:
##STR00001##
Where, in formula I, R.sub.1 is:
##STR00002##
Where, in formula II, X.sup.+ is selected among one of the compounds below:
##STR00003##
Where, in formula II, Y is
##STR00004##
The compounds of the present invention are powerful and nonspecific tyrosine kinase inhibitors, and the use of these compounds in the treatment.
Oridonin analogs, compositions, and methods related thereto
Certain embodiments are directed to oridonin analogs or derivatives. In certain aspects, the derivatives are used as anticancer or anti-inflammatory agents.