Assay ID | Title | Year | Journal | Article |
AID266548 | Inhibition of human SKBR3 cell growth | 2006 | Journal of medicinal chemistry, Jul-27, Volume: 49, Issue:15
| Design, synthesis, and biological evaluation of hydroquinone derivatives of 17-amino-17-demethoxygeldanamycin as potent, water-soluble inhibitors of Hsp90. |
AID266553 | Upregulation of Hsp70 in SKOV3 cells | 2006 | Journal of medicinal chemistry, Jul-27, Volume: 49, Issue:15
| Design, synthesis, and biological evaluation of hydroquinone derivatives of 17-amino-17-demethoxygeldanamycin as potent, water-soluble inhibitors of Hsp90. |
AID273351 | Induction of Hsp90-mediated AKT degradation in human LS174T cells in presence of HuCC49deltaCH2-beta galactosidase conjugate by Western blotting at 2 uM | 2006 | Journal of medicinal chemistry, Oct-19, Volume: 49, Issue:21
| Enzyme specific activation of benzoquinone ansamycin prodrugs using HuCC49DeltaCH2-beta-galactosidase conjugates. |
AID273354 | Induction of Hsp90-mediated AKT degradation in human LS174T cells in absence of HuCC49deltaCH2-beta galactosidase by Western blotting at 10 uM | 2006 | Journal of medicinal chemistry, Oct-19, Volume: 49, Issue:21
| Enzyme specific activation of benzoquinone ansamycin prodrugs using HuCC49DeltaCH2-beta-galactosidase conjugates. |
AID465301 | Apparent volume of distribution in tumor of mouse bearing human A2780 cells at 80 mg/kg, ip administered as DMSO/egg phospholipid formulation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID201632 | Inhibition of oncogene product p185 erbB-2 from human breast cancer cells(SK-BR-3 cells) at 50 mg/kg dose. | 1995 | Journal of medicinal chemistry, Sep-15, Volume: 38, Issue:19
| Inhibition of the oncogene product p185erbB-2 in vitro and in vivo by geldanamycin and dihydrogeldanamycin derivatives. |
AID273353 | Induction of Hsp90-mediated AKT degradation in human LS174T cells in presence of HuCC49deltaCH2-beta galactosidase conjugate by Western blotting at 10 uM | 2006 | Journal of medicinal chemistry, Oct-19, Volume: 49, Issue:21
| Enzyme specific activation of benzoquinone ansamycin prodrugs using HuCC49DeltaCH2-beta-galactosidase conjugates. |
AID266552 | Upregulation of Hsp70 in SKBR3 cells | 2006 | Journal of medicinal chemistry, Jul-27, Volume: 49, Issue:15
| Design, synthesis, and biological evaluation of hydroquinone derivatives of 17-amino-17-demethoxygeldanamycin as potent, water-soluble inhibitors of Hsp90. |
AID465298 | AUC in tumor of mouse bearing human A2780 cells at 80 mg/kg, ip administered as DMSO/egg phospholipid formulation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID465315 | AUC in human at 220 mg/m2 administered as DMSO/egg phospholipid formulation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID465306 | Half life in plasma of mouse bearing human A2780 cells at 80 mg/kg, ip administered as DMSO/egg phospholipid formulation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID465314 | Half life in human at 220 mg/m2 administered as DMSO/egg phospholipid formulation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID465299 | AUC in liver of mouse bearing human A2780 cells at 80 mg/kg, ip administered as DMSO/egg phospholipid formulation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID201635 | In vitro inhibition of p185 erbB-2 oncoprotein in human breast cancer SK-BR-3 cells | 1995 | Journal of medicinal chemistry, Sep-15, Volume: 38, Issue:19
| erbB-2 oncogene inhibition by geldanamycin derivatives: synthesis, mechanism of action, and structure-activity relationships. |
AID266546 | Inhibition of BODIPY-AG binding to human HSP90 | 2006 | Journal of medicinal chemistry, Jul-27, Volume: 49, Issue:15
| Design, synthesis, and biological evaluation of hydroquinone derivatives of 17-amino-17-demethoxygeldanamycin as potent, water-soluble inhibitors of Hsp90. |
AID465300 | Apparent volume of distribution in plasma of mouse bearing human A2780 cells at 80 mg/kg, ip administered as DMSO/egg phospholipid formulation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID465281 | Inhibition of HSP90-mediated client protein HER2 degradation in human MCF7 cells | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID465312 | Cmax in human at 220 mg/m2 administered as DMSO/egg phospholipid formulation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID266550 | Degradation of Her2 in SKBR3 cells | 2006 | Journal of medicinal chemistry, Jul-27, Volume: 49, Issue:15
| Design, synthesis, and biological evaluation of hydroquinone derivatives of 17-amino-17-demethoxygeldanamycin as potent, water-soluble inhibitors of Hsp90. |
AID115733 | In vivo inhibition of p185 phosphotyrosine in nu/nu nude mice bearing Fisher rat embryo cells transfected with human erbB-2 at 400 mg/kg | 1995 | Journal of medicinal chemistry, Sep-15, Volume: 38, Issue:19
| erbB-2 oncogene inhibition by geldanamycin derivatives: synthesis, mechanism of action, and structure-activity relationships. |
AID465295 | Cmax in tumor of mouse bearing human A2780 cells at 80 mg/kg, ip administered as DMSO/egg phospholipid formulation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID465308 | Half life in liver of mouse bearing human A2780 cells at 80 mg/kg, ip administered as DMSO/egg phospholipid formulation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID266547 | Inhibition of BODIPY-AG binding to dog Grp94 | 2006 | Journal of medicinal chemistry, Jul-27, Volume: 49, Issue:15
| Design, synthesis, and biological evaluation of hydroquinone derivatives of 17-amino-17-demethoxygeldanamycin as potent, water-soluble inhibitors of Hsp90. |
AID465317 | Volume of distribution at steady state in human at 220 mg/m2 administered as DMSO/egg phospholipid formulation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID465307 | Half life in tumor of mouse bearing human A2780 cells at 80 mg/kg, ip administered as DMSO/egg phospholipid formulation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID254267 | Binding affinity for human heat shock protein 90 in scintillation proximity assay | 2005 | Bioorganic & medicinal chemistry letters, Nov-15, Volume: 15, Issue:22
| Structure-based design of 7-carbamate analogs of geldanamycin. |
AID201637 | In vitro inhibition of phospho-p185erbB-2 expression in human breast cancer cells(SK-BR-3 cells) at 100 mg/kg dose. | 1995 | Journal of medicinal chemistry, Sep-15, Volume: 38, Issue:19
| Inhibition of the oncogene product p185erbB-2 in vitro and in vivo by geldanamycin and dihydrogeldanamycin derivatives. |
AID307450 | Cell viability of mouse P19 derived neurons at 1 nM by XTT reduction assay relative to control | 2007 | Bioorganic & medicinal chemistry letters, May-15, Volume: 17, Issue:10
| Geldanamycin derivatives and neuroprotective effect on cultured P19-derived neurons. |
AID465289 | Binding affinity to HSP90 under reducing conditions in presence of TECP | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID465303 | Clearance in plasma of mouse bearing human A2780 cells at 80 mg/kg, ip administered as DMSO/egg phospholipid formulation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID465294 | Cmax in plasma of mouse bearing human A2780 cells at 80 mg/kg, ip administered as DMSO/egg phospholipid formulation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID201640 | In vitro inhibition of phospho-p185erbB-2 expression in human breast cancer cells(SK-BR-3 cells) at 200 mg/kg dose. | 1995 | Journal of medicinal chemistry, Sep-15, Volume: 38, Issue:19
| Inhibition of the oncogene product p185erbB-2 in vitro and in vivo by geldanamycin and dihydrogeldanamycin derivatives. |
AID255773 | Cytotoxicity against SKBr3 cells | 2005 | Bioorganic & medicinal chemistry letters, Nov-15, Volume: 15, Issue:22
| Structure-based design of 7-carbamate analogs of geldanamycin. |
AID350567 | Cytotoxicity against human SKBR3 cells after 72 hrs by celltiter-glo assay | 2009 | Journal of medicinal chemistry, May-28, Volume: 52, Issue:10
| Potent cytotoxic C-11 modified geldanamycin analogues. |
AID350568 | Binding affinity to human recombinant HSP90 | 2009 | Journal of medicinal chemistry, May-28, Volume: 52, Issue:10
| Potent cytotoxic C-11 modified geldanamycin analogues. |
AID465305 | Clearance in liver of mouse bearing human A2780 cells at 80 mg/kg, ip administered as DMSO/egg phospholipid formulation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID266551 | Degradation of Her2 in SKOV3 cells | 2006 | Journal of medicinal chemistry, Jul-27, Volume: 49, Issue:15
| Design, synthesis, and biological evaluation of hydroquinone derivatives of 17-amino-17-demethoxygeldanamycin as potent, water-soluble inhibitors of Hsp90. |
AID465283 | Inhibition of HSP90-mediated client protein HER2 degradation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID465302 | Apparent volume of distribution in liver of mouse bearing human A2780 cells at 80 mg/kg, ip administered as DMSO/egg phospholipid formulation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID465293 | Binding affinity to HSP90 under non-reducing conditions in absence of TECP | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID465304 | Clearance in tumor of mouse bearing human A2780 cells at 80 mg/kg, ip administered as DMSO/egg phospholipid formulation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID273352 | Induction of Hsp90-mediated AKT degradation in human LS174T cells in absence of HuCC49deltaCH2-beta galactosidase by Western blotting at 2 uM | 2006 | Journal of medicinal chemistry, Oct-19, Volume: 49, Issue:21
| Enzyme specific activation of benzoquinone ansamycin prodrugs using HuCC49DeltaCH2-beta-galactosidase conjugates. |
AID266549 | Inhibition of human SKOV3 cell growth | 2006 | Journal of medicinal chemistry, Jul-27, Volume: 49, Issue:15
| Design, synthesis, and biological evaluation of hydroquinone derivatives of 17-amino-17-demethoxygeldanamycin as potent, water-soluble inhibitors of Hsp90. |
AID465297 | AUC in plasma of mouse bearing human A2780 cells at 80 mg/kg, ip administered as DMSO/egg phospholipid formulation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID465313 | Tmax in human at 220 mg/m2 administered as DMSO/egg phospholipid formulation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
AID465296 | Cmax in liver of mouse bearing human A2780 cells at 80 mg/kg, ip administered as DMSO/egg phospholipid formulation | 2010 | Journal of medicinal chemistry, Jan-14, Volume: 53, Issue:1
| Heat shock protein 90: inhibitors in clinical trials. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |