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847950-09-8

847950-09-8 Structure

847950-09-8 Structure
IdentificationBack Directory
[Name]

PyriMido[5',4':5,6]pyriMido[1,2-a]benziMidazol-5(6H)-one, 6-(2,6-diMethylphenyl)-2-[[4-(4-Methyl-1-piperazinyl)phenyl]aMino]-
[CAS]

847950-09-8
[Synonyms]

Lck Inhibitor
6-(2,6-Dimethylphenyl)-2-[[4-(4-methyl-1-pyrimido[5',4':5,6]pyrimido[1,2-a]benzimidazol-5(6H)-one
6-(2,6-Dimethylphenyl)-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]pyrimido[5',4':5,6]pyrimido[1,2-a]benzimidazol-5(6H)-one
PyriMido[5',4':5,6]pyriMido[1,2-a]benziMidazol-5(6H)-one, 6-(2,6-diMethylphenyl)-2-[[4-(4-Methyl-1-piperazinyl)phenyl]aMino]-
[Molecular Formula]

C31H30N8O
[MDL Number]

MFCD18782603
[MOL File]

847950-09-8.mol
[Molecular Weight]

530.62
Chemical PropertiesBack Directory
[Boiling point ]

809.1±75.0 °C(Predicted)
[density ]

1.36±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
[form ]

crystalline solid
[pka]

7.87±0.42(Predicted)
[color ]

Light yellow to yellow
Hazard InformationBack Directory
[Uses]

TC-S 7003 is a novel, potent and orally active inhibitor of Lymphocyte Specific Kinase (Lck).
[in vivo]

Lck 抑制剂 (0-60 mg/kg;口服每天一次;从第 9 天到第 17 天) 显示出对关节炎的剂量依赖性抑制[1]
Lck 抑制剂 (口服5 mg/kg) 处理显示Cmax、AUC0-∞、tmax和F%分别为82 ng/mL、862 ng h/mL,和 17%,分别[1]

Animal Model:Male Lewis rat (adjuvant-inducedarthritis model) [1]
Dosage:0, 30, and 60 mg/kg
Administration:P.o.; once daily; from day 9 today 17
Result:Showed a dose-dependent inhibition of arthritis, with an ED50 estimated at 24 mg/kg.
Animal Model:Sprague-Dawley Rats[1]
Dosage:P.o. (Pharmacokinetic Analysis)
Administration:5 mg/kg
Result:The Cmax, AUC0-∞, tmax and F% were 82 ng/mL, 862 ng h/mL, and 17%, respectively.
[storage]

Store at -20°C
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