Metolachor

Metolachor

SCHEMBL7579358

CC1(C)OC(c2ccco2)CN1C(=O)C(Cl)Cl.CCOC(=O)/C(Cl)=C/c1cc(N2C(=O)C3=C(CCCC3)C2=O)ccc1Cl.CCc1cccc(C)c1N(C(=O)CCl)C(C)COC.O=C(O)CNCP(=O)(O)O

nearest known ligand 0.00

Full drug profile on Sugi Atlas →

⚠ 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
Metolachor SCHEMBL7588475 0.95
Metolachor SCHEMBL7581925 0.93 MEN1 (0.31)
Alachlor SCHEMBL7583474 0.91
Acetochlor SCHEMBL7584922 0.91 ALDH1A1 (0.32)
Metolachor SCHEMBL7582100 0.90
Metolachor SCHEMBL7582039 0.88 MEN1 (0.36)
Alachlor SCHEMBL7581264 0.87
Acetochlor SCHEMBL7575848 0.86 ALDH1A1 (0.30)
Alachlor SCHEMBL7581569 0.84 TP53 (0.34)
Metolachor SCHEMBL7587654 0.84 MEN1 (0.31)

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