- ETP-46464
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- $34.00
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2026-07-27
- CAS:1345675-02-6
- Purity: 99.56%
- Supply Ability: 10g
- ETP46464
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- $2.00
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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;ETP 46464; ETP46464;2-Methyl-2-(4-(2-oxo-9-(quinolin-3-yl)-2,4-dihydro-1H-[1,3]oxazino[5,4-c]quinolin-1-yl)phenyl);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 | | InChI | 1S/C30H22N4O2/c1-30(2,18-31)23-8-10-24(11-9-23)34-28-22(17-36-29(34)35)16-33-27-12-7-19(14-25(27)28)21-13-20-5-3-4-6-26(20)32-15-21/h3-16H,17H2,1-2H3 | | InChIKey | DPLMXAYKJZOTKO-UHFFFAOYSA-N | | SMILES | CC(C)(C#N)C(C=C1)=CC=C1N(C2=C(CO3)C=NC(C2=C4)=CC=C4C5=CC6=C(C=CC=C6)N=C5)C3=O |
| WGK Germany | WGK 3 | | Storage Class | 11 - Combustible Solids |
| | 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 | | IC 50 | mTOR: 0.6 nM (IC50); ATR: 14 nM (IC50); ATM: 545 nM (IC50); DNA-PK: 36 nM (IC50); PI3Kα: 170 nM (IC50) | | 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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