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research use only
Cat.No.S8163
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In vitro |
DMSO
: 5 mg/mL
(13.07 mM)
Water : Insoluble Ethanol : Insoluble |
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In vivo |
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )
Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
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| Molecular Weight | 382.42 | Formula | C18H22N8O2 |
Storage (From the date of receipt) | |
|---|---|---|---|---|---|
| CAS No. | 1382979-44-3 | Download SDF | Storage of Stock Solutions |
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| Synonyms | RG7666 | Smiles | CC1(C2=NC3=C(N2CCO1)N=C(N=C3N4CCOCC4)C5=CN=C(N=C5)N)C | ||
| Targets/IC50/Ki |
PI3Kα
(Cell-free assay) 2 nM(Ki app)
PI3Kδ
(Cell-free assay) 3 nM(Ki app)
PI3Kγ
(Cell-free assay) 10 nM(Ki app)
PI3Kβ
(Cell-free assay) 46 nM(Ki app)
mTOR
(Cell-free assay) 70 nM(Ki app)
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| In vitro |
Paxalisib (GDC-0084) has excellent human metabolic stability in microsomal and hepatocyte incubations and demonstrated inhibition of pAKT, a key signal within the PI3K pathway, in normal brain tissue. This compound is shown to inhibit the proliferation of several glioma cells in vitro with IC50 ranging from 0.3 to 1.1 μM. Its binding to plasma proteins is low, with a free fraction (%) of 29.5±2.7 (n=3) in CD-1 mouse plasma, when tested at 5 μM. Binding to brain tissues from CD-1 mice is higher, with a free fraction of 6.7% (±1; n=3).
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| In vivo |
Paxalisib (GDC-0084) markedly inhibits the PI3K pathway in mouse brain, causing up to 90% suppression of the pAkt signal. It achieves significant tumor growth inhibition of 70% and 40% against the U87 and GS2 orthotopic models, respectively. This compound's distribution throughout the brain and intracranial tumors leads to potent inhibition of the PI3K pathway. It is being evaluated in patients, and exposures reached at tolerated doses are consistent with those associated with efficacious doses in mouse models.
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References |
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(data from https://clinicaltrials.gov, updated on 2024-05-22)
| NCT Number | Recruitment | Conditions | Sponsor/Collaborators | Start Date | Phases |
|---|---|---|---|---|---|
| NCT05012670 | Completed | Healthy |
Kazia Therapeutics Limited|Quotient Sciences |
August 18 2021 | Phase 1 |
| NCT03696355 | Completed | Brain and Central Nervous System Tumors |
St. Jude Children''s Research Hospital|Kazia Therapeutics Limited |
November 19 2018 | Phase 1 |
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