A mitochondrial complex I inhibitor from A. muricata (IC50 = 54.8 nM); induces ATP depletion

Annonacin – 1 mg

Brand:
Cayman
CAS:
111035-65-5
Storage:
-20
UN-No:
Non-Hazardous - /

Annonacin is a potent and lipophilic acetogenin from A. muricata that inhibits mitochondrial complex I (IC50 = 54.8 nM).{37049},{37050} Annonacin induces ATP depletion, tau pathologies, and dopaminergic cell death in rats (EC50s = 134, 44.1, and 60.8 nM, respectively). Quantities of annonacin in the fruit and teas made from leaves of A. muricata are such that a cumulative dose sufficient to induce murine neurodegeneration can be attained in humans by regular consumption within one year. This implicates annonacin in the etiology of taupathologies identified in regions of A. muricata consumption. Annonacin also reduces cell survival (ED50 = 0.31 µM in MCF-7 cells) and decreases MCF-7 xenograft tumor size in nude mice at a dose of 50 mg/kg per day.{37051}  

 

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Description

A mitochondrial complex I inhibitor from A. muricata (IC50 = 54.8 nM); induces ATP depletion, tau pathologies, and dopaminergic cell death in rats (EC50s = 134, 44.1, and 60.8 nM, respectively); reduces cell survival (ED50 = 0.31 µM in MCF-7 cells); decreases MCF-7 xenograft tumor size in nude mice at a dose of 50 mg/kg per day

Formal name: 5S-5-methyl-3-[(2R,8R,13R)-2,8,13-trihydroxy-13-[(2R,5R)-tetrahydro-5-[(1R)-1-hydroxytridecyl]-2-furanyl]tridecyl]-2(5H)-furanone

Synonyms: 

Molecular weight: 596.9

CAS: 111035-65-5

Purity: ≥98%

Formulation: A powder

Product Type|Biochemicals|Natural Products||Product Type|Biochemicals|Small Molecule Inhibitors|Oxidative Phosphorylation||Research Area|Cancer||Research Area|Cell Biology|Mitochondrial Biology||Research Area|Neuroscience

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