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Formula | C20H18FN5O2 |
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Molecular Weight | 379.39 | CAS No. | 934343-74-5 | |
Solubility (25°C)* | In vitro | DMSO | 76 mg/mL (200.32 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 | HSP990 (NVP-HSP990) is a novel, potent and selective HSP90 inhibitor for HSP90α/β with IC50 of 0.6 nM/0.8 nM. NVP-HSP990 induces cell cycle arrest and apoptosis. | ||||
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In vitro | NVP-HSP990 is based on a 2-amino-4-methyl-7,8-dihydropyrido[4,3-d]pyrimidin-5(6H)-one scaffold, which is structurally distinct from other known HSP90 inhibitors. NVP-HSP990 binds to the N-terminal ATP-binding domain of HSP90. NVP-HSP990 exhibits single digit nanomolar IC50 values on three of the HSP90 isoforms (HSP90α, HSP90β, and GRP94) and 320 nM IC50 value on the fourth (TRAP-1), with selectivity against unrelated enzymes, receptors, and kinases. NVP-HSP990 dissociates the HSP90-p23 complex, depleted client protein c-Met, and induced Hsp70 in c-Met amplified GTL-16 gastric tumor cells. NVP-HSP990 potently inhibites the growth of human cell lines and primary patient samples from a variety of tumor types. [1] NVP-HSP990 displays dose- and time-dependent effects on HSP90 client proteins. NVP-HSP990 inhibits Glioma tumor-initiating cells (GIC) proliferation in all GIC lines, with IC50 values ranging approximately between 10 and 500 nM. Olig2 is a functional marker associated with cell proliferation and response to NVP-HSP990, as NVP-HSP990 attenuated cell proliferation in Olig2-high GIC lines. In addition, NVP-HSP990 disrupted cell-cycle control mechanism by decreasing CDK2 and CDK4 and elevating apoptosis-related molecules. [2] | ||||
In vivo | NVP-HSP990 exhibits drug-like pharmaceutical and pharmacologic properties with high oral bioavailability. In the GTL-16 xenograft model, a single oral administration of 15 mg/kg of NVP-HSP990 induced sustained downregulation of c-Met and upregulation of Hsp70. In repeat dosing studies, NVP-HSP990 treatment resulted in tumor growth inhibition of GTL-16 and other human tumor xenograft models driven by well-defined oncogenic HSP90 client proteins. [1] | ||||
Features | NVP-HSP990 is an orally available HSP90 inhibitor and is structurally distinct from other clinical HSP90 inhibitors. |
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Data from [Data independently produced by , , Cancer Sci, 2018, 109(2):373-383]
Data from [Data independently produced by , , Am J Transl Res,2015, 7(12):2589-602.]
A novel PET probe to selectively image heat shock protein 90α/β isoforms in the brain [ EJNMMI Radiopharm Chem, 2024, 9(1):19] | PubMed: 38436869 |
Role of heat shock protein 90 as an antiviral target for swine enteric coronaviruses [ Virus Res, 2023, 329:199103] | PubMed: 36963723 |
HSP90 inhibitor NVP-HSP990 alleviates rotavirus infection [ bioRxiv, 2023, 10.1101/2023.06.15.545197] | PubMed: none |
Deciphering the immunopeptidome in vivo reveals new tumour antigens [ Nature, 2022, 607(7917):149-155] | PubMed: 35705813 |
The AhR-SRC axis as a therapeutic vulnerability in BRAFi-resistant melanoma [ EMBO Mol Med, 2022, 14(12):e15677] | PubMed: 36305167 |
A STUB1 ubiquitin ligase/CHIC2 protein complex negatively regulates the IL-3, IL-5, and GM-CSF cytokine receptor common β chain (CSF2RB) protein stability [ J Biol Chem, 2022, 298(10):102484] | PubMed: 36108743 |
Drosophila melanogaster as a model for unraveling unique molecular features of epilepsy elicited by human GABA transporter 1 variants [ Front Neurosci, 2022, 16:1074427] | PubMed: 36741049 |
Deciphering the tumor-specific immunopeptidome in vivo with genetically engineered mouse models [ BioRxiv, 2021, 10.1101/2021.06.30.450516] | PubMed: none |
Hsp90 inhibitor HSP990 in very low dose upregulates EAAT2 and exerts potent antiepileptic activity [ Theranostics, 2020, 10(18):8415-8429] | PubMed: 32724478 |
Targeting NAD+ Biosynthesis Overcomes Panobinostat and Bortezomib-Induced Malignant Glioma Resistance [ Mol Cancer Res, 2020, 18(7):1004-1017] | PubMed: 32238439 |
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