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Formula | C17H11F6N7O |
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Molecular Weight | 443.31 | CAS No. | 1393477-72-9 | |
Solubility (25°C)* | In vitro | DMSO | 89 mg/mL (200.76 mM) | |
Ethanol | 89 mg/mL (200.76 mM) | |||
Water | 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 | Selinexor (KPT-330, ATG-010) is an orally bioavailable selective CRM1 inhibitor. Phase 2. | |
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Targets |
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In vitro | As the clinical candidate analog of KPT-185, KPT-330 exhibits similar effects on the viability of T-ALL cells and elicits rapid apoptotic response. KPT-330 also reduces cell growth in MOLT-4, Jurkat, HBP-ALL, KOPTK-1, SKW-3, and DND-41 cell lines, with IC50 values of 34-203 nM. [1] | |
In vivo | KPT-330 dramatically suppresses the growth of T-ALL cells (MOLT-4) and AML cells (MV4–11) in vivo, with little toxicity to normal haematopoietic cells. [1] In SCID mice with diffuse human MM bone lesions, KPT-330 inhibits MM-induced bone lysis and prolongs survival. Moreover, KPT-330 directly impairs osteoclastogenesis and bone resorption by blocking RANKL-induced NF-κB and NFATc1, with minimal impact on osteoblasts and BMSCs. [2] |
Cell Assay:[1] |
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Animal Study:[1] |
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, , Mol Cancer Ther, 2017, 16(4):717-728
Data from [Data independently produced by , , J Cell Mol Med, 2018, doi:10.1111/jcmm.13886]
Data from [Data independently produced by , , BMC Cancer, 2018, 18(1):764]
Data from [Data independently produced by , , Biochem Biophys Res Commun, 2018, 503(3):1773-1779]
Dual Inhibition of CDK4/6 and XPO1 Induces Senescence With Acquired Vulnerability to CRBN-Based PROTAC Drugs [ Gastroenterology, 2024, S0016-5085(24)00062-3] | PubMed: 38262581 |
p300 nucleocytoplasmic shuttling underlies mTORC1 hyperactivation in Hutchinson-Gilford progeria syndrome [ Nat Cell Biol, 2024, 10.1038/s41556-023-01338-y] | PubMed: 38267537 |
Androgen deprivation induces double-null prostate cancer via aberrant nuclear export and ribosomal biogenesis through HGF and Wnt activation [ Nat Commun, 2024, 15(1):1231] | PubMed: 38336745 |
UCHL1 is a potential molecular indicator and therapeutic target for neuroendocrine carcinomas [ Cell Rep Med, 2024, S2666-3791(23)00610-9] | PubMed: 38244540 |
Phase-separated nuclear bodies of nucleoporin fusions promote condensation of MLL1/CRM1 and rearrangement of 3D genome structure [ Cell Rep, 2023, 42(8):112884] | PubMed: 37516964 |
KPT330 promotes the sensitivity of glioblastoma to olaparib by retaining SQSTM1 in the nucleus and disrupting lysosomal function [ Autophagy, 2023, 1-16.] | PubMed: 37712615 |
Nuclear export inhibition jumbles epithelial-mesenchymal states and gives rise to migratory disorder in healthy epithelia [ Elife, 2023, 12e81048] | PubMed: 36805020 |
Exportin 1-mediated nuclear/cytoplasmic trafficking controls drug sensitivity of classical Hodgkin's lymphoma [ Mol Oncol, 2023, 10.1002/1878-0261.13386] | PubMed: 36727672 |
Cytoplasmic Expression of TP53INP2 Modulated by Demethylase FTO and Mutant NPM1 Promotes Autophagy in Leukemia Cells [ Int J Mol Sci, 2023, 24(2)1624] | PubMed: 36675134 |
Azacitidine Is Synergistically Lethal with XPO1 Inhibitor Selinexor in Acute Myeloid Leukemia by Targeting XPO1/eIF4E/c-MYC Signaling [ Int J Mol Sci, 2023, 24(7)6816] | PubMed: 37047788 |
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