C07F9/6587

STING AGONISTS FOR TREATING BLADDER CANCER AND SOLID TUMORS
20210060041 · 2021-03-04 · ·

Methods for treating bladder cancer and solid tumors are disclosed. The methods include administering to a patient a compound of formula 1

##STR00001##

Pharmaceutical compositions of compound 1 are also disclosed.

COMPOUNDS FOR THE TREATMENT OF CANCER

Provided herein are compounds useful for the treatment of cancer.

COMPOUNDS FOR THE TREATMENT OF CANCER

Provided herein are compounds useful for the treatment of cancer.

Drug target for treating veterinary infections and methods of using same

The invention includes a method of treating or preventing a Staphylococcus infection in a mammal or avian species in need thereof. The methods comprise administering to the mammal or avian species a therapeutically effective amount of fosmidomycin. In certain embodiments, the methods treat or prevent a drug-resistant Staphylococccus infection.

Drug target for treating veterinary infections and methods of using same

The invention includes a method of treating or preventing a Staphylococcus infection in a mammal or avian species in need thereof. The methods comprise administering to the mammal or avian species a therapeutically effective amount of fosmidomycin. In certain embodiments, the methods treat or prevent a drug-resistant Staphylococccus infection.

NOVEL STING AGONISTS

The present invention provides compounds of Formula I:

##STR00001##

wherein custom-character, W, X, Y, Z, Z.sub.1, Z.sub.2, R.sub.1, R.sub.2, R.sub.3, R.sub.4 and R.sub.5 are as defined herein, or a stereoisomer, tautomer, pharmaceutically acceptable salt, prodrug ester or solvate form thereof, wherein all of the variables are as defined herein. These compounds are effective at modulating the STING protein and thus can be used as medicaments for treating or preventing disorders affected by the agonism of STING.

NOVEL STING AGONISTS

The present invention provides compounds of Formula I:

##STR00001##

wherein custom-character, W, X, Y, Z, Z.sub.1, Z.sub.2, R.sub.1, R.sub.2, R.sub.3, R.sub.4 and R.sub.5 are as defined herein, or a stereoisomer, tautomer, pharmaceutically acceptable salt, prodrug ester or solvate form thereof, wherein all of the variables are as defined herein. These compounds are effective at modulating the STING protein and thus can be used as medicaments for treating or preventing disorders affected by the agonism of STING.

Macrocyclic ligands and their complexes for bifunctional molecular catalysis

Disclosed herein are embodiments of chiral and achiral macrocyclic polydentate ligands and methods of preparing the same. Disclosed herein are also embodiments of metal coordination complexes derived from these macrocyclic polydentate ligands and methods of preparing the same. The metal coordination complexes described herein, can be used for a variety of catalytic reactions, including hydrogenation and transfer hydrogenation of unsaturated organic compounds, dehydrogenation of alcohols and boranes, an asymmetric Michael-type addition reaction, or an aerobic oxidative kinetic resolution of an organic compound, dehydrogenative couplings and other catalytic transformations.