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- Kasun Wanigasooriya, .et al. Patient Derived Organoids Confirm That PI3K/AKT Signalling Is an Escape Pathway for Radioresistance and a Target for Therapy in Rectal Cancer, Front Oncol, 2022, Jul 4;12:920444 PMID: 35860583
Biological Activity
GDC-0980 (RG7422) is a selective, potent, orally bioavailable inhibitor of Class I PI3 kinase and mTOR kinase (TORC1/2) with in vitro IC50 of 5, 27, 7 and 14 nM for p110 α, β, δ and γ isoforms, respectively.
Targets
| p110α (Cell-free assay) | p110δ (Cell-free assay) | p110γ (Cell-free assay) | mTOR (Cell-free assay) | p110β (Cell-free assay) |
| 5 nM | 7 nM | 14 nM | 17 nM(Ki app) | 27 nM |
| In vitro (25°C) | DMSO | 20 mg/mL (40.11 mM) | |
| Water | Insoluble | ||
| Ethanol | Insoluble | ||
| In vivo | 0.5% methylcellulose+0.2% Tween 80 | 28 mg/mL | |
|
* <1 mg/ml means slightly soluble or insoluble. * Please note that Adooq 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. |
|||
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 0.1 mM | 20.06 mL | 100.28 mL | 200.56 mL |
| 0.5 mM | 4.01 mL | 20.06 mL | 40.11 mL |
| 1 mM | 2.01 mL | 10.03 mL | 20.06 mL |
| 5 mM | 0.4 mL | 2.01 mL | 4.01 mL |
*The above data is based on the productmolecular weight 498.6 . Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
| Catalog Num | A11023 |
|---|---|
| Actions | Inhibitor |
| CAS No. | 1032754-93-0 |
| Formula | C23H30N8O3S |
| M. Wt | 498.6 |
| Purity | >98% |
| Synonyms | GDC0980 |
| SMILES | CC1=C(SC2=C1N=C(N=C2N3CCOCC3)C4=CN=C(N=C4)N)CN5CCN(CC5)C(=O)[[email protected]](C)O |
| Storage | Store lyophilized at -20ºC, keep desiccated. |
Datasheet
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