Phenanthridin-6(5H)-one structure
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Common Name | Phenanthridin-6(5H)-one | ||
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CAS Number | 1015-89-0 | Molecular Weight | 195.22 | |
Density | 1.2±0.1 g/cm3 | Boiling Point | 274.8±7.0 °C at 760 mmHg | |
Molecular Formula | C13H9NO | Melting Point | 290-292 °C(lit.) | |
MSDS | USA | Flash Point | 158.7±3.1 °C |
Use of Phenanthridin-6(5H)-one6(5H)-Phenanthridinone is a potent PARP-1 inhibitor and immunomodulator. 6(5H)-Phenanthridinone inhibits cell proliferation and can be used in cancer research[1]. |
Name | phenanthridone |
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Synonym | More Synonyms |
Description | 6(5H)-Phenanthridinone is a potent PARP-1 inhibitor and immunomodulator. 6(5H)-Phenanthridinone inhibits cell proliferation and can be used in cancer research[1]. |
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Related Catalog | |
References |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 274.8±7.0 °C at 760 mmHg |
Melting Point | 290-292 °C(lit.) |
Molecular Formula | C13H9NO |
Molecular Weight | 195.22 |
Flash Point | 158.7±3.1 °C |
Exact Mass | 195.068420 |
PSA | 32.86000 |
LogP | 2.81 |
Vapour Pressure | 0.0±0.6 mmHg at 25°C |
Index of Refraction | 1.642 |
Storage condition | 2-8°C |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATAMUTATION DATA
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Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Safety Phrases | S22-S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | SG0370000 |
HS Code | 2933990090 |
Precursor 10 | |
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DownStream 10 | |
HS Code | 2933990090 |
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Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
Molecular design, synthesis and docking study of benz[b]oxepines and 12-oxobenzo[c]phenanthridinones as topoisomerase 1 inhibitors.
Bioorg. Med. Chem. Lett. 19 , 2444-7, (2009) Benz[b]oxepines 4a-g and 12-oxobenzo[c]phenanthridines 5a-d were designed and synthesized as constrained forms of 3-arylisoquinolines through an intramolecular radical cyclization reaction. Radical cy... |
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Novel isoquinolinone-derived inhibitors of poly(ADP-ribose) polymerase-1: pharmacological characterization and neuroprotective effects in an in vitro model of cerebral ischemia.
J. Pharmacol. Exp. Ther. 305(3) , 943-9, (2003) Excessive activation of poly(ADP-ribose) polymerase-1 (PARP-1), a nuclear enzyme catalyzing the transfer of ADP-ribose units from NAD to acceptor proteins, induces cellular energy failure by NAD and A... |
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Total synthesis of 7-deoxypancratistatin-1-carboxaldehyde and carboxylic acid via solvent-free intramolecular aziridine opening: phenanthrene to phenanthridone cyclization strategy.
Org. Lett. 10(3) , 361-4, (2008) Solid-state silica-gel-catalyzed opening of aziridine 6 provided phenanthrene 7, whose oxidative cleavage, recyclization, and further elaboration furnished the C-1 aldehyde and carboxylic acid derivat... |
phenanthridone |
6-phenanthridinol |
phenanthridin-6(5H)-one |
EINECS 213-804-3 |
phenanthridin-6-ol |
6-(5H)-Phenanthridinone |
MFCD00004988 |
6-Hydroxyphenanthridine |
5,6-dihydrophenanthridin-6-one |
6(5H)-Phenanthridinone |
6(5H)-Phenanthridone |
5H-phenanthridin-6-one |