Small molecule inhibitors of the PI3-kinase family

Current Topics in Microbiology and Immunology

Volumn 347, Issue 1, 2010, Pages 263-278

  Knight, Zachary A ^a  

^a ROCKEFELLER UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

1 (1 CYANO 1 METHYLETHYL) 3 METHYL 8 (3 QUINOLINYL)IMIDAZO[4,5 C]QUINOLIN 2(1H,3H) ONE; 2 (4 HYDROXYPHENYL) 4 MORPHOLINOPYRIDO[3',2':4,5]FURO[3,2 D]PYRIMIDINE; 2 (6 AMINO 9 PURINYLMETHYL) 5 METHYL 3 (2 METHYLPHENYL) 3H QUINAZOLIN 4 ONE; 2 MORPHOLINO 6 (1 THIANTHRENYL) 4 PYRANONE; 2 MORPHOLINO 8 PHENYLCHROMONE; 5 (6 QUINOXALINYLMETHYLENE) 2,4 THIAZOLIDINEDIONE; 9 (1 ANILINOETHYL) 7 METHYL 2 MORPHOLINOPYRIDO[1,2 A]PYRIMIDIN 4 ONE; ATM PROTEIN; MORPHOLINE; NU 7441; PHOSPHATIDYLINOSITOL 3 KINASE; PHOSPHATIDYLINOSITOL 3 KINASE INHIBITOR; PICTRELISIB; PIK 90; PIK 93; QUERCETIN; UNCLASSIFIED DRUG; WORTMANNIN; XL 147; XL 765; 2-(4-MORPHOLINYL)-8-PHENYL-4H-1-BENZOPYRAN-4-ONE; ADENINE; ANDROSTANE DERIVATIVE; CELL CYCLE PROTEIN; CHROMONE DERIVATIVE; DNA BINDING PROTEIN; DNA DEPENDENT PROTEIN KINASE; DRUG DERIVATIVE; MORPHOLINE DERIVATIVE; NUCLEAR PROTEIN; PRKDC PROTEIN, MOUSE; PROTEIN KINASE INHIBITOR; PROTEIN SERINE THREONINE KINASE; QUINAZOLINE DERIVATIVE; TUMOR SUPPRESSOR PROTEIN;

ANTIINFLAMMATORY ACTIVITY; ARTICLE; CELL CYCLE ARREST; CELL CYCLE G0 PHASE; CELL CYCLE G1 PHASE; CELL PROLIFERATION; CLINICAL TRIAL (TOPIC); CONFORMATIONAL TRANSITION; DRUG DESIGN; DRUG PROTEIN BINDING; DRUG SELECTIVITY; DRUG STRUCTURE; DRUG TARGETING; ENZYME INACTIVATION; ENZYME INHIBITION; HUMAN; HYDROPHOBICITY; INHIBITION KINETICS; MALIGNANT NEOPLASTIC DISEASE; PHARMACOPHORE; PRIORITY JOURNAL; PROTEIN FAMILY; TUMOR XENOGRAFT; ANIMAL; DRUG ANTAGONISM; NEOPLASM; REVIEW;

ADENINE; ANDROSTADIENES; ANIMALS; CELL CYCLE PROTEINS; CHROMONES; DNA-ACTIVATED PROTEIN KINASE; DNA-BINDING PROTEINS; HUMANS; MORPHOLINES; NEOPLASMS; NUCLEAR PROTEINS; PHOSPHATIDYLINOSITOL 3-KINASES; PROTEIN KINASE INHIBITORS; PROTEIN-SERINE-THREONINE KINASES; QUINAZOLINES; TUMOR SUPPRESSOR PROTEINS;

EID: 79952109804     PISSN: 0070217X     EISSN: None     Source Type: Book Series    
DOI: 10.1007/82-2010-44     Document Type: Article

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