Flumipropyn

Flumipropyn

SCHEMBL7581355

C#CC(C)Oc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl.CCc1cccc(C)c1N(C(=O)CCl)C(C)COC.CS(=O)(=O)c1cc(C(F)(F)F)ccc1C(=O)c1cnoc1C1CC1.C[S+](C)C.O=C(O)CNCP(=O)([O-])O

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
Flumipropyn SCHEMBL7590200 0.96
Flumipropyn SCHEMBL7584140 0.93
Flumipropyn SCHEMBL7581622 0.92
Flumiciorac-Pentyl SCHEMBL7578053 0.91
Flumipropyn SCHEMBL7588253 0.89
Flumipropyn SCHEMBL7578113 0.89
Flumipropyn SCHEMBL7588207 0.89 GRM7 (0.30)
Flumiciorac-Pentyl SCHEMBL7582704 0.86
Flumipropyn SCHEMBL7582703 0.86 MEN1 (0.33)
Isoxaflutole SCHEMBL7580228 0.85

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