Keywords: |
unclassified drug; histone deacetylase inhibitor; clinical trial; review; gastrointestinal hemorrhage; nonhuman; antineoplastic agents; drug targeting; protein conformation; protein function; neoplasms; mouse; animals; cell survival; unindexed drug; liver toxicity; breast cancer; cell growth; carboxy terminal sequence; protein binding; weight reduction; cancer cell culture; drug structure; tumor xenograft; structure activity relation; pyrimidines; monoclonal antibody; antibodies, monoclonal; amino terminal sequence; drug mechanism; cell transformation; pyrazole derivative; pyrazoles; cancer cell; heat shock protein 90 inhibitor; heat shock protein 90; hsp90 heat-shock proteins; quinones; malignant neoplastic disease; liver disease; molecular structure; purine derivative; protein-tyrosine kinases; adenosine triphosphate; pyrimidine derivative; triazoles; benzimidazole derivative; benzoquinones; lactams, macrocyclic; 4 [n (2 hydroxyethyl) n [2 (3 indolyl)ethyl]aminomethyl]cinnamohydroxamic acid; acetylation; growth inhibition; geldanamycin; radicicol; cycloproparadicicol; pochonin d; hsp90; binding, competitive; pyrazolopyrimidine derivative; ansamycins; ansamycin derivative; g 3130; novobiocin; coumarin derivative; cnf 1010; mycograb; 17 allylamino 17 demethoxygeldanamycin; fr 901228; lbh 589; ver 49009; resorcinol derivative; kos 953; anticancer therapeutics; pu-class hsp90 inhibitors; radicicol and derivatives; 17 dimethyllamino 17 demethoxygeldanamycin; kf 55823; pu 24 fci; pyrrolopyrimidine derivative; zeranol
|