Flumipropyn

Flumipropyn

SCHEMBL7585263

C#CC(C)Oc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl.CCNc1nc(Cl)nc(NC(C)C)n1.CCc1cccc(C)c1N(C(=O)CCl)C(C)COC.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 SCHEMBL7579175 0.95 MAPT (0.32)
Flumipropyn SCHEMBL7582703 0.93 MEN1 (0.33)
Flumipropyn SCHEMBL7578236 0.92 MAPT (0.34)
Flumipropyn SCHEMBL7588634 0.91
Flumipropyn SCHEMBL7578397 0.91 MAPT (0.31)
Flumiciorac-Pentyl SCHEMBL7577598 0.89 PPOX (0.30)
Flumipropyn SCHEMBL7579107 0.88
Flumioxazin SCHEMBL7589268 0.88
Flumipropyn SCHEMBL7589670 0.88
Flumipropyn SCHEMBL7586311 0.88 MEN1 (0.35)

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