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Formula | C29H40N2O9 |
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Molecular Weight | 560.64 | CAS No. | 30562-34-6 | |
Solubility (25°C)* | In vitro | DMSO | 33 mg/mL (58.86 mM) | |
Water | Insoluble | |||
Ethanol | Insoluble | |||
* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. * Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.) |
Description | Geldanamycin is a natural existing HSP90 inhibitor with Kd of 1.2 μM, specifically disrupts glucocorticoid receptor (GR)/HSP association. Geldanamycin attenuates virus infection-induced ALI (acute lung injury)/ARDS (acute respiratory distress syndrome) by reducing the host's inflammatory responses. | ||||||
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Targets |
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In vitro | Geldanamycin binds in the ATP-binding site in the N-terminus domain of Hsp90s (residues 1-220). Geldanamycin inhibits the ATPase activity of Hsp90 in a dose-dependent manner. [1] Geldanamycin causes a dose-dependent G2 arrest and reversible inhibiton o f entry into the S phase in A2780 human ovarian cell line. This inhibition is accompanied by p53 increase and finally demonstrated to be p53 dependent. [2] Geldanamycin causes polyubiquitination and proteasomal degradation of the p185 receptor protein-tyrosin kinase and shows a IC50 with 70 nM. [3, 4] Geldanamycin is a typical anti-tumor reagent, shows a mean GI50 with 0.18 μM against the panel of 60 human tumor cell lines. [5] | ||||||
In vivo | Geldanamycin (50 mg//kg) shows 30% inhibition on pl85-associated phosphotyrosine levels in FRE/erbB-2 mice. [6] |
Kinase Assay: |
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Cell Assay: |
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Animal Study: |
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Data from [Data independently produced by , , Antimicrob Agents Chemother, 2015, 10.1128/AAC.00946-15]
Data from [Data independently produced by , , PLoS One, 2015, 10(9):e0138936.]
Data from [Data independently produced by , , Radiat Res, 2018, 189(5):519-528]
Inhibition of HSP90 in Driver Oncogene-Defined Lung Adenocarcinoma Cell Lines: Key Proteins Underpinning Therapeutic Efficacy [ Int J Mol Sci, 2023, 24(18)13830] | PubMed: 37762133 |
Development of a First-in-Class Small-Molecule Inhibitor of the C-Terminal Hsp90 Dimerization [ ACS Cent Sci, 2022, 8(5):636-655] | PubMed: 35647282 |
Local Elimination of Senescent Cells Promotes Bone Defect Repair during Aging [ ACS Appl Mater Interfaces, 2022, 10.1021/acsami.1c22138] | PubMed: 35014784 |
Proteome-Wide Deconvolution of Drug Targets and Binding Sites by Lysine Reactivity Profiling [ Anal Chem, 2022, 10.1021/acs.analchem.1c05455] | PubMed: 35147412 |
Hsp90 Regulates GCRV-II Proliferation by Interacting with VP35 as Its Receptor and Chaperone [ J Virol, 2022, 96(19):e0117522] | PubMed: 36102647 |
Hsp90 Regulates GCRV-II Proliferation by Interacting with VP35 as Its Receptor and Chaperone [ Journal of Virology, 2022, Vol. 96, No. 19] | PubMed: None |
Evolution of kinase polypharmacology across HSP90 drug discovery [ Cell Chem Biol, 2021, S2451-9456(21)00221-X] | PubMed: 34077750 |
Antibody-drug conjugate and free geldanamycin combination therapy enhances anti-cancer efficacy [ Int J Pharm, 2021, 610:121272] | PubMed: 34763035 |
Hsp90 is required for snakehead vesiculovirus replication via stabilizing the viral L protein [ J Virol, 2021, JVI0059421] | PubMed: 34037421 |
Solvent-Induced Protein Precipitation for Drug Target Discovery on the Proteomic Scale [ Anal Chem, 2020, 92(1):1363-1371] | PubMed: 31794197 |
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Selleck products are transported at room temperature. If you receive the product at room temperature, please rest assured, the Selleck Quality Inspection Department has conducted experiments to verify that the normal temperature placement of one month will not affect the biological activity of powder products. After collecting, please store the product according to the requirements described in the datasheet. Most Selleck products are stable under the recommended conditions.
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