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95933-75-8

95933-75-8 Structure

95933-75-8 Structure
IdentificationBack Directory
[Name]

Trimidox (hydrochloride) Exclusive
[CAS]

95933-75-8
[Synonyms]

Reaxys ID: 25792093
KBKNXSNOQYLIRI-UHFFFAOYSA-N
Trimidox (hydrochloride) Exclusive
[Molecular Formula]

C7H9ClN2O4
[MDL Number]

MFCD18382080
[MOL File]

95933-75-8.mol
[Molecular Weight]

220.61
Chemical PropertiesBack Directory
[solubility ]

DMF: 1 mg/ml; DMSO: 2 mg/ml; Ethanol: 0.25 mg/ml; PBS (pH 7.2): 5 mg/ml
[form ]

A crystalline solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P321-P362+P364-P332+P313-P337+P313-P403+P233-P405-P501
Hazard InformationBack Directory
[Description]

Ribonucleotide reductase, the rate-limiting enzyme for de novo DNA synthesis, is a common target for chemotherapy. Its increased activity in cancer cells is associated with malignant transformation and proliferation.1 Trimidox is a specific ribonucleotide reductase inhibitor that reduces levels of dGTP and dCTP in HL-60 cells, inducing apoptosis via activation of caspases without altering the cell cycle distribution.1,2 Trimidox inhibits growth of human promyelocytic leukemia HL-60 cells with an IC50 value of 35 μM.1
[Uses]

Trimidox hydrochloride (VF-233) is a ribonucleotide reductase inhibitor with antileukemic activities. Trimidox hydrochloride inhibits the growth of human promyelocytic leukemia HL-60 cells with an IC50 of 35 μM[1].
[References]

1. Szekeres, T., Fritizer, M., Strobl, H., et al. Synergistic growth inhibitory and differentiating effects of trimidox and tiazofurin in human promyelocytic leukemia HL-60 cells Blood 84(12),4316-4321(1994).
2. Kanno, S.I., Uwai, K., Tomizawa, A., et al. Trimidox induces apoptosis via cytochrome c release in NALM-6 human B cell leukaemia cells Basic Clin. Pharmacol. Toxicol. 98,44-50(2006).
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