SCHEMBL6735674

SCHEMBL6735674

O=CC(S)c1ccco1

nearest known ligand 0.00

⚠ 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
SCHEMBL8141474 0.78 ALDH1A1 (0.46)
SCHEMBL5696508 0.74
SCHEMBL525254 0.74
SCHEMBL10618802 0.74
SCHEMBL9984097 0.74
SCHEMBL29950856 0.74
SCHEMBL1428658 0.74
SCHEMBL4222821 0.74 ALDH1A1 (0.39)
SCHEMBL25278998 0.74
SCHEMBL31094075 0.74 ALDH1A1 (0.45)

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 14 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6683190-B1 CONTACTING RACEMIC HYDANTOIN WITH ENANTIOMERIC SPLITTING AGENT; DECYCLIZATION BAYER CROPSCIENCE S.A. (FR) 2004-01-27 US claimed
EP-0551048-B1 2-imidazoline-5-one and 2-imidazoline-5-thiones derivatives as fungizides AVENTIS CROPSCIENCE SA (FR) 2002-08-07 EP claimed
EP-1076718-B1 NOVEL METHOD FOR PREPARING SYNTHESIS INTERMEDIATES AVENTIS CROPSCIENCE SA (FR) 2002-05-02 EP claimed
EP-0648210-A1 FUNGICIDAL 2-IMIDAZOLINE-5-ONE AND 2-IMIDAZOLINE-5-THIONE DERIVATIVES RHONE-POULENC AGROCHIMIE (FR) 1995-04-19 EP claimed
EP-0629616-A2 Optically aktive 2-imidazolin-5-one and 2-imidazolin-5-thione derivatives as fungicides RHONE-POULENC AGROCHIMIE (FR) 1994-12-21 EP claimed
WO-1994001410-A1 FUNGICIDAL 2-IMIDAZOLINE-5-ONE AND 2-IMIDAZOLINE-5-THIONE DERIVATIVES RHONE POULENC AGROCHIMIE (FR) 1994-01-20 WO claimed
EP-0551048-A1 2-imidazoline-5-one and 2-imidazoline-5-thiones derivatives as fungizides RHONE-POULENC AGROCHIMIE (FR) 1993-07-14 EP claimed
US-6759551-B1 COMPOUND IS DISSOLVED, IN THE FREE AMINO ACID FORM OR IN THE SALIFIED FORM, IN A PH REGION OF LESS THAN APPROXIMATELY 4.5 OR GREATER THAN APPROXIMATELY 9, THEN PH IS GRADUALLY BROUGHT, BY ADDITION OF A BASE OR OF AN ACID RESPECTIVELY, TO NEUTRAL BAYER CROPSCIENCE S.A. (FR) 2004-07-06 US disclosed
US-6683190-B1 CONTACTING RACEMIC HYDANTOIN WITH ENANTIOMERIC SPLITTING AGENT; DECYCLIZATION BAYER CROPSCIENCE S.A. (FR) 2004-01-27 US disclosed
EP-0551048-B1 2-imidazoline-5-one and 2-imidazoline-5-thiones derivatives as fungizides AVENTIS CROPSCIENCE SA (FR) 2002-08-07 EP disclosed
EP-0648210-A1 FUNGICIDAL 2-IMIDAZOLINE-5-ONE AND 2-IMIDAZOLINE-5-THIONE DERIVATIVES RHONE-POULENC AGROCHIMIE (FR) 1995-04-19 EP disclosed
EP-0629616-A2 Optically aktive 2-imidazolin-5-one and 2-imidazolin-5-thione derivatives as fungicides RHONE-POULENC AGROCHIMIE (FR) 1994-12-21 EP disclosed
WO-1994001410-A1 FUNGICIDAL 2-IMIDAZOLINE-5-ONE AND 2-IMIDAZOLINE-5-THIONE DERIVATIVES RHONE POULENC AGROCHIMIE (FR) 1994-01-20 WO disclosed
EP-0551048-A1 2-imidazoline-5-one and 2-imidazoline-5-thiones derivatives as fungizides RHONE-POULENC AGROCHIMIE (FR) 1993-07-14 EP disclosed