RA-9 manufacturers
- RA-9
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- $45.00
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2026-07-27
- CAS:919091-63-7
- Purity: 99.31%
- Supply Ability: 10g
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| Product Name: | RA-9 | | Synonyms: | 4-Piperidinone, 3,5-bis[(4-nitrophenyl)methylene]-, (3E,5E)-;RA-9 UPS inhibitor;Unfolded,RA-9,cancer,RA 9,DUBs,Inhibitor,Apoptosis,Response,Deubiquitinase,cells,inhibit,Protein,ovarian,RA9,survival;RA-9, 10 mM in DMSO;(3E,5E)-3,5-Bis[(4-nitrophenyl)methylene]-4-piperidinone | | CAS: | 919091-63-7 | | MF: | C19H15N3O5 | | MW: | 365.34 | | EINECS: | | | Product Categories: | | | Mol File: | 919091-63-7.mol |  |
| Melting point | 230-233 °C(Solv: ethyl ether (60-29-7); acetonitrile (75-05-8)) | | Boiling point | 588.5±50.0 °C(Predicted) | | density | 1.414±0.06 g/cm3(Predicted) | | storage temp. | Store at -20°C | | solubility | DMSO: 4.17 mg/mL (11.41 mM; ultrasonic and warming and heat to 80°C) | | pka | 5.13±0.20(Predicted) | | form | Solid | | color | Light yellow to yellow | | InChI | 1S/C19H15N3O5/c23-19-15(9-13-1-5-17(6-2-13)21(24)25)11-20-12-16(19)10-14-3-7-18(8-4-14)22(26)27/h1-10,20H,11-12H2/b15-9+,16-10+ | | InChIKey | YUYPWAMLWZVHAE-KAVGSWPWSA-N | | SMILES | O=C(/C(CNC/1)=C/C2=CC=C([N+]([O-])=O)C=C2)C1=C\C3=CC=C([N+]([O-])=O)C=C3 |
| WGK Germany | WGK 3 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Oral |
| Uses | RA-9 is a potent and selective proteasome-associated deubiquitinating enzymes (DUBs) inhibitor with favorable toxicity profile and anticancer activity. RA-9 blocks ubiquitin-dependent protein degradation without impacting 20S proteasome proteolytic activity. RA-9 selectively induces onset of apoptosis in ovarian cancer cell lines and primary cultures derived from donors. RA-9 induces endoplasmic reticulum (ER)-stress responses in ovarian cancer cells[1]. | | Biological Activity | RA-9 is a potent and selective inhibitor of cell-permeable proteasome-associated deubiquitinating enzymes (DUBs) with favorable toxicity and anticancer activity. It selectively induces apoptosis in ovarian cancer cell lines. | | in vivo | RA-9 (5 mg/kg; ip; one-day on, two-days off) inhibits human ovarian cancer cell growth in vivo and prolongs survival in a mouse model for ovarian cancer. < td class="col1 fwb"> Animal Model: | Six-week-old female immunodeficient (NCr nu/nu) mice | | Dosage: | 5 mg/kg | | Administration: | Ip; one-day on, two-days off | | Result: | Significant reduction in tumor burden at day 12. | | | target | | Target | Value | DUBs () | table>| References | [1] Coughlin K, et al. Small-molecule RA-9 inhibits proteasome-associated DUBs and ovarian cancer in vitro and in vivo via exacerbating unfolded protein responses. Clin Cancer Res. 2014;20(12):3174-3186. DOI:10.1158/1078-0432.CCR-13-2658 |
| | RA-9 Preparation Products And Raw materials |
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Tag:RA-9(919091-63-7)
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