Drug intelligence / Profile preview

Mo4Zol2Mn

Development stage
Preclinical
Lead developer
Northeast Normal University
Modality
Small Molecules
Administration
Intravenous
01

Overview

Mo4Zol2Mn is a heterometallic coordination complex composed of molybdenum (Mo), manganese (Mn), and the bisphosphonate zoledronic acid (Zol). It is a preclinical research compound investigated for its anti-tumor properties, particularly in the treatment of breast cancer (DOID_1612). The complex is designed to leverage the pharmacological activity of zoledronic acid—a potent inhibitor of farnesyl pyrophosphate synthase (FPPS) in the mevalonate pathway—while potentially enhancing its efficacy through the synergistic biological effects of the molybdenum and manganese metal centers. Preclinical studies have demonstrated that Mo4Zol2Mn exhibits significant cytotoxicity against breast cancer cell lines, such as MCF-7, by inducing apoptosis and inhibiting cell proliferation and migration. This coordination complex represents an effort to develop multi-targeted metallodrugs that can address both primary tumor growth and associated bone complications in cancer patients.

Other names
molybdenum-manganese-zoledronate complex[Mo4O12(Zol)2Mn(H2O)4]·2H2OMo4Zol2Mn2Mo-4Zol2Mn2Mo 4Zol2Mn2[Mo4O12(Zol)2Mn2(H2O)8]·4H2O
02

Targets

FDPS (Farnesyl pyrophosphate synthase)

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