Names | |
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IUPAC name
1-[2-[[1-(4-chlorophenyl)pyrazol-3-yl]oxymethyl]-3-methylphenyl]-4-methyltetrazol-5-one
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Identifiers | |
3D model (
JSmol)
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ChEBI | |
ChemSpider | |
PubChem
CID
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UNII | |
CompTox Dashboard (
EPA)
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Properties | |
C19H17ClN6O2 | |
Molar mass | 396.84 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
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Metyltetraprole is a quinone outside inhibitor fungicide sold under the brand name Pavecto by its inventor, Sumitomo Chemical. [1] It is the only tetrazolinone fungicide and the only one in the Fungicide Resistance Action Committee's subgroup 11A. [2]
Metyltetraprole was developed specifically to find an a.i. with the same mode of action (a QoI) but with sufficiently different chemistry as to avoid "critical" QoI resistance increasing around the world. [3]
Metyltetraprole is highly effective against Alternaria triticina. [1]
Developed because of increasing resistance to the main group of QoIs. See §Development above.
It does not suffer cross-resistance with the resistance against 11 conferred by the cytochrome b mutation G143A. Cross-resistance against F129L is unassessed. [2]
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 as 3L73 in the protein databank.