Inventor

KESICKI EDWARD A

US54 patents

⚠️ This page may combine multiple inventors who share the name “KESICKI EDWARD A”. Patents are grouped by organization below to help distinguish them — per-person disambiguation is on the roadmap.

KESICKI EDWARD A

ICOS CORP

Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta

Inhibitors of human phosphatidyl-inositol 3-kinase delta

Inhibitors of human phosphatidylinositol 3-kinase delta

Inhibitors of human phosphatidylinositol 3-kinase delta

5-fluoro-3-phenyl-2[1-(9H-purin-6-ylamino)propyl]-3H-quinazolin-4-one and 6-fluoro-3-phenyl-2-[1-(9H-purin-6-ylamino)ethyl]-3H-quinazolin-4-one as inhibitors of human phosphatidylinositol 3-kinase delta

6-fluoro-3-phenyl-2-[1-(9H-purin-6-ylamino)ethyl]-3H-quinazolin-4-one as an inhibitor of human phosphatidylinositol 3-kinase delta

Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta

Inhibitors of human phosphatidylinositol 3-kinase delta

5-fluoro-3-phenyl-2-[1-(9H-purin-6-ylamino)propyl]-3H-quinazolin-4-one and 6-fluoro-3-phenyl-2-[1-(9H-purin-6-ylamino)ethyl]-3H-quinazolin-4-one as inhibitors of human phosphatidylinositol 3-kinase delta

6-fluoro-3-phenyl-2-[1-(9H-purin-6-ylamino)-ethyl]-3H-quinazolin-4-one as an inhibitor of human phosphatidylinositol 3-kinase delta

Cyclic AMP-specific phosphodiesterase inhibitors

Inhibitors of human phosphatidylinositol 3-kinase delta

5-fluoro-3-phenyl-2-[1-(9h-purin-6-ylamino)propyl]-3h-quinazolin-4-one as an inhibitor of human phosphatidylinositol 3-kinase delta

Cyclic AMP-specific phosphodie sterase inhibitors

Cyclic AMP-specific phosphodiesterase inhibitors

Compounds useful for inhibiting Chk1

Inhibitors of human phosphatidylinositol 3-kinase delta

Inhibitors of human phosphatidylinositol 3-kinase delta

(S)-2-(1-aminopropyl)-5-fluoro-3-phenylquinazolin-4(3H)-one precursor of a quinazolinone as inhibitor of human phosphatidylinositol 3-kinase delta

Urea or thiourea substituted 1,4-pyrazine compounds useful as anti-cancer agents and for inhibiting Chk1

Tert-butyl (s)-(1-(5-fluoro-4-oxo-3-phenyl-3,4-dihydroquinazolin-2-yl)propyl)carbamate precursor of a quinazolinone inhibitor of human phosphatidylinositol 3-kinase delta and a process for preparing thereof

Cyclic AMP-specific phosphodiesterase inhibitors

Cyclic AMP-specific phosphodiesterase inhibitors

SADHU CHANCHAL

Inhibitors of human phosphatidylinositol 3-kinase delta

Inhibitors of human phosphatidylinositol 3-kinase delta

Inhibitors of human phosphatidylinositol 3-kinase delta

Inhibitors of human phosphatidylinositol 3-kinase delta

Inhibitors of human phosphatidylinositol 3-kinase delta

HIBERCELL INC

Aminopyridine derivatives as phosphatidylinositol phosphate kinase inhibitors

Aminopyrimidine derivatives as phosphatidylinositol phosphate kinase inhibitors

Chromenopyrimidine derivatives as phosphatidylinsitol phosphate kinase inhibitors

Chromenopyridine derivatives as phosphatidylinositol phosphate kinase inhibitors

Aryl-bipyridine amine derivatives as phosphatidylinositol phosphate kinase inhibitors

PROLINX INC

Phenyldiboronic acid reagents and complexes

Phenyldiboronic acid reagents and complexes

Phenyldiboronic acid reagents and complexes

PETRA PHARMA CORP

Allosteric chromenone inhibitors of phosphoinositide 3-kinase (PI3K) for the treatment of disease

Allosteric chromenone inhibitors of phosphoinositide 3-kinase (PI3K) for the treatment of disease

Allosteric chromenone inhibitors of phosphoinositide 3-kinase (PI3K) for the treatment of disease

FOWLER KERRY W

Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta

Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta

ALGOMEDIX INC

TRPA1 modulators

TRPA1 modulators

ICOS

Inhibitors of human phosphatidylinositol 3-kinase delta

LUITPOLD PHARM INC

Materials and methods to potentiate cancer treatment

DUNCAN IAIN W

Tetracycline derivatives with reduced antibiotic activity and neuroprotective benefits

HALBROOK JAMES W

Xanthones, thioxanthones and acridinones as DNA-PK inhibitors

DIAZ FRANK

Heteroaryl urea derivatives useful for inhibiting CHK1

BIO AFFINITY SYSTEMS

Method of thioacylation peptide sequencing with acylation of thiazoloinones

Neumedics

Tetracycline derivatives with reduced antibiotic activity and neuroprotective benefits