ChemicalBook--->CAS DataBase List--->2734853-80-4

2734853-80-4

2734853-80-4 Structure

2734853-80-4 Structure
IdentificationBack Directory
[Name]

INDEX NAME NOT YET ASSIGNED
[CAS]

2734853-80-4
[Synonyms]

Fludarabine-Cl
Fludarabine Phosphate Impurity 35
[Molecular Formula]

C10H11ClFN5O3
[MOL File]

2734853-80-4.mol
[Molecular Weight]

303.68
Chemical PropertiesBack Directory
[Boiling point ]

711.5±70.0 °C(Predicted)
[density ]

2.12±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[form ]

Solid
[pka]

12.96±0.70(Predicted)
[color ]

White to off-white
[Water Solubility ]

Water : 5 mg/mL (16.46 mM; ultrasonic and warming and heat to 60°C)
Hazard InformationBack Directory
[Uses]

Fludarabine-Cl has an inhibitory effect on RNA adenosine deaminase 1 (ADAR1) with an IC50 of 0.87 μM and can be used to prevent and/or study cancer or tumor-related diseases[1].
[Biological Activity]

Fludarabine-Cl has inhibition effect on RNA adenosine deaminase 1(ADAR1), and can be used for preventing and/or treating cancer or tumor-related diseases[1].
[in vivo]

Fludarabine-Cl (104.9-400 mg/kg, intraperitoneal injection, twice a day, for one day) has some toxicity in mice, with an LD50 of 186.5641 mg/kg[1].
Fludarabine-Cl (10-20 mg/kg, intraperitoneal injection, twice a day, for 29 days) inhibits tumor proliferation in mice[1].

Animal Model:ICR mice[1]
Dosage:104.9, 131.1, 163.8, 204.8, 256, 320, 400 mg/kg; twice a day; one day
Administration:Intraperitoneal injection (i.p.)
Result:Was somewhat toxic and could cause death in mice at higher doses, but no abnormality in organs.
Animal Model:BALB/c mice induced by Du-145[1]
Dosage:10, 20 mg/kg; twice a day; 29 days
Administration:Intraperitoneal injection (i.p.)
Result:Inhibited tumor growth and had no effect on mouse body weight.
[IC 50]

ADAR1: 0.87 μM (IC50)
[References]

[1]. Polysubstituted purine compound and preparation method and application thereof. CN113549076A.
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