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| | 2-[6-(4-Chloro-phenyl)-1-Methyl-4H-3-oxa-2,5-diaza-benzo[e]azulen-4-yl]-acetaMide Basic information |
| | 2-[6-(4-Chloro-phenyl)-1-Methyl-4H-3-oxa-2,5-diaza-benzo[e]azulen-4-yl]-acetaMide Chemical Properties |
| Boiling point | 622.8±55.0 °C(Predicted) | | density | 1.41±0.1 g/cm3(Predicted) | | storage temp. | Store at -20°C | | solubility | DMSO : 100 mg/mL (273.37 mM; Need ultrasonic) | | form | Powder | | pka | 16.07±0.40(Predicted) | | color | White to off-white | | InChI | InChI=1S/C20H16ClN3O2/c1-11-18-14-4-2-3-5-15(14)19(12-6-8-13(21)9-7-12)23-16(10-17(22)25)20(18)26-24-11/h2-9,16H,10H2,1H3,(H2,22,25)/t16-/m0/s1 | | InChIKey | GCWIQUVXWZWCLE-INIZCTEOSA-N | | SMILES | N1=C(C2=CC=C(Cl)C=C2)C2=CC=CC=C2C2C(C)=NOC=2[C@@H]1CC(N)=O |
| | 2-[6-(4-Chloro-phenyl)-1-Methyl-4H-3-oxa-2,5-diaza-benzo[e]azulen-4-yl]-acetaMide Usage And Synthesis |
| Uses | BET Bromodomain Inhibitor has be shown to inhibit myeloma cell proliferation in clinically relevant models. | | in vivo | Pelabresib (30-60 mg/kg; oral administration; for 28 days; MV-4-11 mouse xenograft model) treatment results in substantial suppression of tumor growth over the time period examined (41%, 80%, and 74% tumor growth inhibition, respectively), without any significant body weight loss in the animals[1]. | Animal Model: | MV-4-11 mouse xenograft model[1] | | Dosage: | 30 mg/kg once daily, 30 mg/kg twice daily, or 60 mg/kg once daily | | Administration: | Oral administration; for 28 days | | Result: | Suppressed of tumor growth, without any significant body weight loss in the animals.
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| | IC 50 | BRD4-BD1: 39 nM (IC50) |
| | 2-[6-(4-Chloro-phenyl)-1-Methyl-4H-3-oxa-2,5-diaza-benzo[e]azulen-4-yl]-acetaMide Preparation Products And Raw materials |
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