Structure of Voxtalisib
CAS No.: 934493-76-2
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
Voxtalisib is a potent and highly selective inhibitor of class I PI3Ks with IC50 of 39/110/9/43 nM for PI3Kα/β/γ/δ, also inhibits mTOR with IC50 of 160-910 nM.
Synonyms: XL765; SAR245409
4.5
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CAS No. : | 934493-76-2 |
Formula : | C13H14N6O |
M.W : | 270.29 |
SMILES Code : | CCN1C2=NC(N)=NC(C)=C2C=C(C3=NNC=C3)C1=O |
Synonyms : |
XL765; SAR245409
|
MDL No. : | MFCD20276656 |
InChI Key : | RGHYDLZMTYDBDT-UHFFFAOYSA-N |
Pubchem ID : | 16123056 |
GHS Pictogram: |
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Signal Word: | Warning |
Hazard Statements: | H302 |
Precautionary Statements: | P280-P305+P351+P338 |
Target |
|
In Vitro:
Cell Line
|
Concentration | Treated Time | Description | References |
U87IDHmut cells | 12 μM | 24 hours | To evaluate the effect of XL765 on U87IDHmut cell proliferation, showing a 61.0 ± 10.6% reduction in cell number. | PMC6642106 |
MDA-MB-231 | IC50 75.2 µM | 24 hours | Investigate the effect of XL765 on circRNA and linRNA expression, showing upregulation of circRNA and downregulation of linRNA | PMC10204552 |
MCF-7 | IC50 91.4 µM | 24 hours | Investigate the effect of XL765 on circRNA and linRNA expression, showing upregulation of circRNA and downregulation of linRNA | PMC10204552 |
Chronic lymphocytic leukemia cells | 0.86 µM (IC50) | 48 hours | Therapeutic effect on chronic lymphocytic leukemia through apoptotic caspase-dependent mechanisms and effectively inhibits T-cell-mediated cytokine production | PMC9237521 |
SUM149 and MDA-MB-231 | 0.5 µM | 6 hours | To assess the effect of combination treatment on TNBC cell migration and invasion capabilities | PMC4643087 |
NHAIDHmut cells | 32 μM | 72 hours | To evaluate the effect of XL765 on NHAIDHmut cell proliferation, showing a 55.7 ± 16% reduction in cell number. | PMC6642106 |
GBM 39 | 5.0 μM | 72 hours | Evaluate the cytotoxicity of XL765 on GBM 39 cells, showing a concentration-dependent decrease in cell viability | PMC3064692 |
GBM GS-2 | 7.7 μM | 72 hours | Evaluate the cytotoxicity of XL765 on GBM GS-2 cells, showing a concentration-dependent decrease in cell viability | PMC3064692 |
GBM 12 | 3.7 μM | 72 hours | Evaluate the cytotoxicity of XL765 on GBM 12 cells, showing a concentration-dependent decrease in cell viability | PMC3064692 |
GBM 8 | 5.7 μM | 72 hours | Evaluate the cytotoxicity of XL765 on GBM 8 cells, showing a concentration-dependent decrease in cell viability | PMC3064692 |
SUM149 TNBC cells | 0.005-20 μM | 72 hours | Evaluate the synergistic effect of Voxtalisib with birinapant, results showed no significant synergistic effect observed in SUM149 cells | PMC8747014 |
MDA-MB-231 | 40 nM | 72 hours | To evaluate the synergistic inhibitory effect of PI3K inhibitor SAR245409 combined with MEK inhibitor AS703026 on TNBC cell proliferation | PMC4643087 |
ST88 | 0.25-20 μM | 96 hours | XL765 significantly inhibited MPNST cell growth with an IC50 of 2.49 μM | PMC3416967 |
MPNST642 | 0.25-20 μM | 96 hours | XL765 significantly inhibited MPNST cell growth with an IC50 of 1.93 μM | PMC3416967 |
STS26T | 0.25-20 μM | 96 hours | XL765 significantly inhibited MPNST cell growth with an IC50 of 1.75 μM | PMC3416967 |
MPNST724 | 0.25-20 μM | 96 hours | XL765 significantly inhibited MPNST cell growth with an IC50 of 0.86 μM | PMC3416967 |
S462 | 0.25-20 μM | 96 hours | XL765 significantly inhibited MPNST cell growth with an IC50 of 0.81 μM | PMC3416967 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
Nude mice | U87IDHmut intracranial tumor model | Oral | 30 mg/kg | Twice daily, continuous treatment | To evaluate the effect of XL765 on U87IDHmut intracranial tumor model, showing that XL765 treatment significantly prolonged animal survival. | PMC6642106 |
Mice | Gastrointestinal stromal tumor (GIST) model | Oral gavage | 30 mg/kg (6-hour treatment), 20 mg/kg (7-day treatment) | Single dose for 6-hour treatment or twice daily for 7-day treatment | To evaluate the effect of Voxtalisib on GIST tumor proliferation. Results showed that 6-hour treatment inhibited PI3K signaling (pAKT, pS6, and p4EBP1) but increased MAPK phosphorylation. Seven days of treatment reduced tumor cell proliferation by 70%. | PMC5635919 |
SCID mice | MPNST724 and STS26T xenograft models | Oral | 30 mg/kg/bid | Twice daily, continuous treatment | XL765 significantly inhibited local and metastatic growth of MPNST xenografts | PMC3416967 |
Nude mice | GS-2 and U87-MG GBM orthotopic models | Oral | 30mg/kg voxtalisib twice daily | Twice daily, continuous treatment | To monitor the effect of voxtalisib alone or in combination with TMZ, finding a significantly lower lactate-to-pyruvate ratio post-treatment, associated with enhanced survival | PMC4873419 |
Mice | Aldh5a1−/− mouse model | Intraperitoneal injection | 5 mg/kg/day and 10 mg/kg/day | Once daily until death | To evaluate the effects of mTOR inhibitors on lifespan and body weight in aldh5a1?/? mice. Results showed that Tor2, XL-765, and tat-Bec1 significantly extended lifespan and improved body weight. | PMC5114712 |
Nude mice | Intracranial xenograft GBM 39 model | Oral gavage | 50 mg/kg | Twice daily, 6 hours apart, for 2 weeks | Evaluate the inhibitory effect of XL765 on GBM 39 tumor growth in vivo, showing a 13-fold reduction in median tumor bioluminescence and improvement in median survival compared to control | PMC3064692 |
Clinical Trial:
NCT Number | Conditions | Phases | Recruitment | Completion Date | Locations |
NCT01410513 | Indolent Non-Hodgkin Lymphoma|... More >>Mantle Cell Lymphoma|Chronic Lymphocytic Leukemia Less << | PHASE1 | COMPLETED | 2025-05-14 | Investigational Site Number 84... More >>0004, Aurora, Colorado, 80045, United States|Investigational Site Number 840006, Augusta, Georgia, 30912, United States|Investigational Site Number 840002, Charleston, South Carolina, 29406, United States Less << |
NCT01403636 | Lymphoma | PHASE2 | COMPLETED | 2025-09-14 | Investigational Site Number 84... More >>0012, Los Angeles, California, 90033, United States|Investigational Site Number 840104, Fort Meyers, Florida, 33919, United States|Investigational Site Number 840006, Augusta, Georgia, 30912, United States|Investigational Site Number 840011, Maywood, Illinois, 60153, United States|Investigational Site Number 840010, Kansas City, Kansas, 66160-7321, United States|Investigational Site Number 840013, Lexington, Kentucky, 40536, United States|Investigational Site Number 840007, Paducah, Kentucky, 42002, United States|Investigational Site Number 840004, Boston, Massachusetts, 02115, United States|Investigational Site Number 840015, St Louis, Missouri, 63110, United States|Investigational Site Number 840014, Canton, Ohio, 44718, United States|Investigational Site Number 840001, Philadelphia, Pennsylvania, 19111, United States|Investigational Site Number 840002, Morgantown, West Virginia, 26506, United States|Investigational Site Number 036002, Clayton, 3168, Australia|Investigational Site Number 036001, Hobart, 7001, Australia|Investigational Site Number 036005, Kingswood, 2747, Australia|Investigational Site Number 036003, Perth, 6000, Australia|Investigational Site Number 056003, Bruxelles, 1000, Belgium|Investigational Site Number 056002, Gent, 9000, Belgium|Investigational Site Number 056001, Leuven, 3000, Belgium|Investigational Site Number 250002, Montpellier, 34295, France|Investigational Site Number 250001, Pierre Benite Cedex, 69495, France|Investigational Site Number 250004, Rennes, 35033, France|Investigational Site Number 250005, Rouen Cedex, 76038, France|Investigational Site Number 250003, Villejuif Cedex, 94805, France|Investigational Site Number 276003, Frankfurt Am Main, 60590, Germany|Investigational Site Number 276002, Jena, 07747, Germany|Investigational Site Number 276001, Ulm, 89081, Germany|Investigational Site Number 528001, Amsterdam, 1105 AZ, Netherlands|Investigational Site Number 528003, Groningen, 9713 GZ, Netherlands|Investigational Site Number 528002, Rotterdam, 3075 EA, Netherlands Less << |
NCT01596270 | Neoplasm Malignant | PHASE1 | COMPLETED | 2025-10-14 | Investigational Site Number 84... More >>0001, Detroit, Michigan, 48201, United States|Investigational Site Number 840002, New Brunswick, New Jersey, 08903, United States|Investigational Site Number 840003, Dallas, Texas, 75230, United States Less << |
Tags: Voxtalisib | XL765 | SAR245409 | XL 765 | XL-765 | SAR245409 | SAR 245409 | SAR-245409 | PI3K | mTOR | Phosphoinositide 3-kinase | Mammalian target of Rapamycin | p110α Inhibitor | p110β Inhibitor | p110γ Inhibitor | p110δ Inhibitor | 934493-76-2
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