Name | 5-(4-nitrophenyl)-2-phenyl-4H-pyrazol-3-one |
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Synonyms |
TCS PRP INHIBITOR 13
Necrosulfonamide 1-Phenyl-3-p-nitrophenylpyrazolon 3H-Pyrazol-3-one, 2,4-dihydro-5-(4-nitrophenyl)-2-phenyl- 5-(4-Nitrophenyl)-2-phenyl-2,4-dihydro-3H-pyrazol-3-one |
Description | TCS PrP Inhibitor 13, an antiprion agent, is a cellular prion protein (PrPC) inhibitor. TCS PrP Inhibitor 13, as a protease-resistant form of prion protein (PrP-res) accumulation inhibitor, shows an IC50 value of 3 nM in both ScN2a and F3 cell lines. TCS PrP Inhibitor 13 induces Schwannoma cells apoptosis[1]. |
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Related Catalog | |
Target |
IC50: 3 nM (PrPC in ScN2a and F3 cells)[1] |
In Vitro | TCS PrP Inhibitor 13 (0~500 μM; Schwannoma cells) significantly reduces levels of total ERK1/2, pAKT, total FAK, Cyclin D1, PrPC and significantly increases expression of cleaved caspase-3. TCS PrP Inhibitor 13 (Schwannoma cells) significantly reduces the number of proliferating, Ki67-positive cells and total cell number[2]. |
References |
Density | 1.4±0.1 g/cm3 |
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Boiling Point | 445.1±47.0 °C at 760 mmHg |
Molecular Formula | C15H11N3O3 |
Molecular Weight | 281.27 |
Flash Point | 223.0±29.3 °C |
Exact Mass | 281.080048 |
PSA | 78.49000 |
LogP | 1.92 |
Vapour Pressure | 0.0±1.1 mmHg at 25°C |
Index of Refraction | 1.674 |
HS Code | 2933199090 |
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~82% 34320-83-7 |
Literature: Kimata, Ayako; Nakagawa, Hidehiko; Ohyama, Ryo; Fukuuchi, Tomoko; Ohta, Shigeru; Suzuki, Takayoshi; Miyata, Naoki Journal of Medicinal Chemistry, 2007 , vol. 50, # 21 p. 5053 - 5056 |
~0% 34320-83-7 |
Literature: Azev; Teplyashina Chemistry of Heterocyclic Compounds, 1998 , vol. 34, # 9 p. 1091 - 1092 |
Precursor 4 | |
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DownStream 0 |
HS Code | 2933199090 |
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Summary | 2933199090. other compounds containing an unfused pyrazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |