- ETP-46464
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- $34.00 / 2mg
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2024-11-19
- CAS:1345675-02-6
- Min. Order:
- Purity: 99.56%
- Supply Ability: 10g
- ETP46464
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- $2.00 / 1kg
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2019-07-06
- CAS:1345675-02-6
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 100kg
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| | ETP46464 Basic information |
| Product Name: | ETP46464 | | Synonyms: | Benzeneacetonitrile, α,α-dimethyl-4-[2-oxo-9-(3-quinolinyl)-2H-[1,3]oxazino[5,4-c]quinolin-1(4H)-yl]-;alpha,alpha-Dimethyl-4-[2-oxo-9-(3-quinolinyl)-2H-[1,3]oxazino[5,4-c]quinolin-1(4H)-yl]-benzeneacetonitrile ETP46464;2-methyl-2-[4-(2-oxo-9-quinolin-3-yl-4H-[1,3]oxazino[5,4-c]quinolin-1-yl)phenyl]propanenitrile;ETP46464;alpha,alpha-Dimethyl-4-[2-oxo-9-(3-quinolinyl)-2H-[1,3]oxazino[5,4-c]quinolin-1(4H)-yl]-benzeneacetonitrile;2-Methyl-2-(4-(2-oxo-9-(quinolin-3-yl)-2,4-dihydro-1H-[1,3]oxazino[5,4-c]quinolin-1-yl)phenyl);ETP 46464; ETP46464;ETP46464 USP/EP/BP | | CAS: | 1345675-02-6 | | MF: | C30H22N4O2 | | MW: | 470.52 | | EINECS: | | | Product Categories: | Inhibitors;PI3K/Akt/mTOR;Akt;mTOR;PI3K | | Mol File: | 1345675-02-6.mol |  |
| | ETP46464 Chemical Properties |
| Boiling point | 709.3±60.0 °C(Predicted) | | density | 1.310±0.06 g/cm3(Predicted) | | storage temp. | Store at -20°C | | solubility | ≥16.13 mg/mL in DMSO | | form | solid | | pka | 5.10±0.20(Predicted) | | color | Light yellow to yellow |
| | ETP46464 Usage And Synthesis |
| Uses | ETP-46464 is used as an ATR inhibitor in the treatment of cancer-associated mutations. | | Biological Activity | etp-46464 is a potent and selective inhibitor for atr (ic50 = 25 nm).atr (atm- and rad3-related) is a member of pikk (phosphatidylinositol 3-kinase-like kinases) that regulates the dna damage response pathways. it is a dna damage sensor that is activated upon genotoxic stresses (e.g. ionizing radiation, uv radiation and dna replication stalling) and phosphorylates its downstream substrates (e.g. p53, brca1 and chek1).etp-46464 abolished the g2/m checkpoint. it caused the presence of micronuclei or completely fragmented nuclei in cells under ionizing radiation. cells treated simultaneously with hydroxyurea and etp-46464 exhibited elevated atm and chk2 phosphorylation. in u2os cells, etp-46464 promoted the breakage of stalked replication forks. [1] | | target | mTOR | | references | 1. toledo li, murga m, zur r et al. a cell-based screen identifies atr inhibitors with synthetic lethal properties for cancer-associated mutations. nat struct mol biol. 2011 jun;18(6):721-7. |
| | ETP46464 Preparation Products And Raw materials |
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