Mesotrione

Mesotrione

SCHEMBL7575641

C#CCOc1cc(-n2nc(C(C)(C)C)oc2=O)c(Cl)cc1Cl.CCc1cccc(C)c1N(C(=O)CCl)C(C)COC.CP(=O)(O)CCC(N)C(=O)O.CS(=O)(=O)c1ccc(C(=O)C2C(=O)CCCC2=O)c([N+](=O)[O-])c1

nearest known ligand 0.00

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⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Mesotrione SCHEMBL7579805 0.94 MEN1 (0.34)
Mesotrione SCHEMBL7582251 0.90
Mesotrione SCHEMBL7583736 0.89
Mesotrione SCHEMBL7580678 0.88 PPOX (0.34)
Metolachor SCHEMBL7583879 0.88 PPOX (0.36)
Mesotrione SCHEMBL7576731 0.87
Mesotrione SCHEMBL7581465 0.86 PPOX (0.40)
Mesotrione SCHEMBL7579347 0.85
Mesotrione SCHEMBL7587655 0.84 MEN1 (0.35)
Mesotrione SCHEMBL7581748 0.84

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 1 patent. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20020004457-A1 Herbicidal composition SYNGENTA PARTICIPATIONS AG (CH) 2002-01-10 US disclosed