Metyltetraprole
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Metyltetraprole is a quinone outside inhibitor fungicide sold under the brand name Pavecto by its inventor, Sumitomo Chemical. ISSN-Lbr>0385-1559
/ref> It is the only tetrazolinone fungicide and the only one in the
Fungicide Resistance Action Committee Fungicides are pesticides used to kill parasitic fungi or their spores. Fungi can cause serious damage in agriculture, resulting in losses of yield and quality. Fungicides are used both in agriculture and to fight fungal infections in animals, in ...
's subgroup 11A.


Development

Metyltetraprole was developed specifically to find an a.i. with the same
mode of action In pharmacology and biochemistry, mode of action (MoA) describes a functional or anatomical change, resulting from the exposure of a living organism to a substance. In comparison, a mechanism of action (MOA) describes such changes at the molecul ...
(a QI) but with sufficiently different chemistry as to avoid "critical" QI resistance increasing around the world.


Target pathogens

Metyltetraprole is highly effective against '' Alternaria triticina''.


Resistance

Developed because of increasing resistance to the main group of QIs. See
Development Development or developing may refer to: Arts *Development (music), the process by which thematic material is reshaped * Photographic development *Filmmaking, development phase, including finance and budgeting * Development hell, when a proje ...
above.


Cross-resistance

It does not suffer cross-resistance with the resistance against 11 conferred by the
cytochrome b Cytochrome b is a protein found in the membranes of aerobic cells. In eukaryotic mitochondria (inner membrane) and in aerobic prokaryotes, cytochrome b is a component of respiratory chain complex III () — also known as the bc1 complex or ubiq ...
mutation G143A. Cross-resistance against F129L is unassessed.


Binding Mode

The structure of the tetrazolinone pharmacophore is very similar to the triazolone pharmacophore of an inhibitor developed by AgoEva, for which the binding mode has been elucidated in the structure deposited a
3L73
in the protein databank.


References

{{agriculture-stub Fungicides Tetrazoles 4-Chlorophenyl compounds Pyrazoles