| Identification | Back Directory | [Name]
Capzimin | [CAS]
2084868-04-0 | [Synonyms]
Capzimin dimer >=96% (HPLC)
8,8'-Dithiobis[N-[2-(2-thiazolyl)ethyl]-3-quinolinecarboxamide
3-Quinolinecarboxamide, 8,8'-dithiobis[N-[2-(2-thiazolyl)ethyl]- | [Molecular Formula]
C30H24N6O2S4 | [MDL Number]
MFCD31657375 | [MOL File]
2084868-04-0.mol | [Molecular Weight]
628.81 |
| Chemical Properties | Back Directory | [Boiling point ]
939.4±65.0 °C(Predicted) | [density ]
1.50±0.1 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [solubility ]
DMSO:62.88(Max Conc. mg/mL);100.0(Max Conc. mM) | [form ]
Solid | [pka]
12.48±0.46(Predicted) | [color ]
White to yellow |
| Hazard Information | Back Directory | [Uses]
8,8''-Dithiobis[N-[2-(2-thiazolyl)ethyl]-3-quinolinecarboxamide], is a novel Inhibitor of the Proteasome Subunit Rpn11. | [Biological Activity]
Capzimin can be used as a therapeutic for cancer treatment.''Capzimin dimer is the stable precursor form of capzimin. Capzimin is a selective inhibitor of proteasome isopeptidase Rpn11a proteasomal deubiquitinase th at is part of the proteosome 19S regulatory particle subunit th at removes the polyubiquitin chain from substrates in preparation for degradation. Capzimin was shown to have an IC50 value of 340 nM and have selectivity over related enzymes with 80-fold selectivity for Rpn11 over Csn5ten-fold over AMSH and six-fold over BRCC36. It stabilized proteasome substrates th at would otherwise have been degradedinduced an unfolded protein responseand blocked the proliferation of cancer cellsincluding some th at had become resistant to bortezomib. Capzimin dimer will be quickly reduced to capzimin by glutathione in cell-based systems; DTT should be added to in vitro assays to reduce the disulfide. | [storage]
Store at -20°C |
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| Company Name: |
Energy Chemical
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021-58432009 400-005-6266 |
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http://www.energy-chemical.com |
| Company Name: |
ChemeGen 中國
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18818260767 |
| Website: |
https://www.chemegen.com |
| Company Name: |
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| Tel: |
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www.sangon.com |
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