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1015-89-0

1015-89-0 Structure

1015-89-0 Structure
IdentificationMore
[Name]

6(5H)-Phenanthridone
[CAS]

1015-89-0
[Synonyms]

2H-BENZ[C]ISOQUINOLIN-1-ONE
6(5H)-PHENANTHRIDINONE
6(5H)-PHENANTHRIDONE
PHENANTHRIDINONE
PHENANTHRIDONE
6(5H)-Phenantridinone
6-Phenanthridinol
6-Phenanthridone
Phenantridone
phenanthridin-6(5H)-one
3,7-DIAMINO-2-METHOXYFLUOREN 98%
6(5H)-PHENANTHRIDINONE 97%
6-PHENANTHRIDINONE
5,6-Dihydrophenanthridin-6-one
5,6-Dihydrophenanthridine-6-one
Benzo[c]quinoline-6(5H)-one
[EINECS(EC#)]

213-804-3
[Molecular Formula]

C13H9NO
[MDL Number]

MFCD00004988
[Molecular Weight]

195.22
[MOL File]

1015-89-0.mol
Chemical PropertiesBack Directory
[Melting point ]

290-292 °C(lit.)
[Boiling point ]

435 °C
[density ]

1.230±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

DMF: 1mg/mL; DMF:PBS (pH 7.2) (1:5): 0.16mg/mL
[form ]

powder to crystal
[pka]

13.27±0.20(Predicted)
[color ]

White to Light yellow to Light orange
[Water Solubility ]

Soluble in DMSO (5 mg/ml). Insoluble in water.
[λmax]

338nm(EtOH)(lit.)
[BRN ]

140641
[CAS DataBase Reference]

1015-89-0(CAS DataBase Reference)
[NIST Chemistry Reference]

6(5H)-phenanthridinone(1015-89-0)
[EPA Substance Registry System]

1015-89-0(EPA Substance)
Safety DataBack Directory
[Safety Statements ]

S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

3
[RTECS ]

SG0370000
[HS Code ]

29337900
Hazard InformationBack Directory
[Uses]

6(5H)-Phenanthridinone is used as a probe into the role of PARP in cellular response to irradiation. Treatment of cells with 6(5H)-Phenanthridinone and various DNA-damaging agents showed a resistance to apoptosis. It acts as a reactant in the synthesis of 5,6-dihydrophenanthridine sulfonamides, oxidative coupling with diphenylacetylene, direct copper acetate-catalyzed N-cyclopropylation of cyclic amides. It is used as HIV-1 integrase inhibitor.
[Uses]

6-Phenanthridone is a poly(ADP-ribose) polymerase (PARP) inhibitor with immunosuppressive effects. 6-Phenanthridone has been shown to inhibit concanavalin A-induced lymphocyte proliferation.
[Definition]

ChEBI: A member of the class of phenanthridines that is phenanthridine with an oxo substituent at position 6. A poly(ADP-ribose) polymerase (PARP) inhibitor, it has been shown to exhibit immunosuppressive activity.
[Synthesis Reference(s)]

Canadian Journal of Chemistry, 35, p. 180, 1957 DOI: 10.1139/v57-027
Journal of the American Chemical Society, 79, p. 1245, 1957 DOI: 10.1021/ja01562a054
[General Description]

6-(5H)-Phenanthridinone is an inhibitor of poly(ADP-ribose)polymerase (PARP)-1 activity. The ability of 6-(5H)-phenanthridinone to potentiate the effect of ionizing radiation on tumour cells was evaluated. Action of 6-(5H)-phenanthridinone, one of the most potent PARP inhibitor, on RDM4 murine lymphoma cells in culture was evaluated.
[storage]

Store at -20°C
Spectrum DetailBack Directory
[Spectrum Detail]

6(5H)-Phenanthridone(1015-89-0)1HNMR
6(5H)-Phenanthridone(1015-89-0)FT-IR
6(5H)-Phenanthridone(1015-89-0)Raman
6(5H)-Phenanthridone(1015-89-0)IR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

6(5H)-Phenanthridinone, 96%(1015-89-0)
[Sigma Aldrich]

1015-89-0(sigmaaldrich)
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