SCHEMBL5956549

SCHEMBL5956549

CCC(C)(N)C=O

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
SCHEMBL19199017 0.75 ALDH1A1 (0.32)
SCHEMBL13469356 0.73
SCHEMBL11041361 0.73
SCHEMBL18485720 0.73
SCHEMBL9015181 0.71
SCHEMBL3184028 0.71
SCHEMBL8039499 0.71
SCHEMBL19223413 0.71
SCHEMBL1461748 0.71 FDPS (0.43)
SCHEMBL7049398 0.71

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 41 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20050014730-A1 Anti-fungal formulation of triterpene and essential oil REGENTS OF THE UNIVERSITY OF MINNESOTA 2005-01-20 US claimed
WO-2004089357-A2 ANTI-FUNGAL FORMULATION OF TRITERPENE AND ESSENTIAL OIL REGENTS OF THE UNIVERSITY OF MINNESOTA (US) 2004-10-21 WO claimed
EP-1322661-A1 TRITERPENES HAVING FUNGICIDAL ACTIVITY AGAINST YEAST REGENTS OF THE UNIVERSITY OF MINNESOTA (US) 2003-07-02 EP claimed
US-20020128210-A1 Triterpenes having human antifungal and antiyeast activity REGENTS OF THE UNIVERSITY OF MINNESOTA 2002-09-12 US claimed
WO-2002026761-A1 TRITERPENES HAVING FUNGICIDAL ACTIVITY AGAINST YEAST REGENTS OF THE UNIVERSITY OF MINNESOTA (US) 2002-04-04 WO claimed
US-20230311554-A1 Thermosensitive Recording Material NIPPON KAYAKU KABUSHIKI KAISHA (JP) 2023-10-05 US disclosed
EP-4205990-A1 THERMOSENSITIVE RECORDING MATERIAL Nippon Kayaku Kabushiki Kaisha (JP) 2023-07-05 EP disclosed
EP-2570414-B1 Heterocyclic aromatic compounds useful as growth hormone secretagogues BRISTOL MYERS SQUIBB CO (US) 2017-08-30 EP disclosed
CN-102822413-B To the method that multiple fiber and/or textile material process LIPOTEC, S.A. (ES) 2016-03-09 CN disclosed
CN-102822413-A Process of treatment of fibers and/or textile materials LIPOTEC SA 2012-12-12 CN disclosed
CN-100401400-C Rewritable optical information recording medium and recording/reproducing method, recording/reproducing device SONY CORP MITSUI CHEMICALS INC (JP) 2008-07-09 CN disclosed
US-20060003948-A1 Compositions that include a triterpene and a carrier REGENTS OF THE UNIVERSITY OF MINNESOTA 2006-01-05 US disclosed
CN-1184471-A Aminothiazole derivatives, drug containing the same and intermediate in the production of the compounds ZERIA PHARM CO LTD (JP) 1998-06-10 CN disclosed
US-5698017-A INCLUDES AN AMIDE OR AMINO ESTER XEROX CORPORATION (US) 1997-12-16 US disclosed
US-5614470-A AGRICULTURAL ANTHELMINTIC, ACARICIDE, INSECTICIDE SANKYO COMPANY, LIMITED (JP) 1997-03-25 US disclosed
EP-0675133-A1 13-Substituted milbemycin derivatives, their preparation and use SANKYO COMPANY LIMITED (JP) 1995-10-04 EP disclosed
CN-1098713-A The ortho-ethenylphenylacetic acid derivatives that replaces BASF AG (DE) 1995-02-15 CN disclosed
US-4591459-A Intermediates for 6-(aminoacyloxymethyl) penicillanic acid 1,1-dioxides PFIZER INC. (US) 1986-05-27 US disclosed
EP-0154444-A1 6-(Aminoacyloxymethyl) penicillanic acid 1, 1-dioxides as beta-lactamase inhibitors PFIZER INC. (US) 1985-09-11 EP disclosed
US-4503040-A 6-(Aminoacyloxymethyl)penicillanic acid 1,1-dioxides as beta-lactamase inhibitors PFIZER INC. (US) 1985-03-05 US disclosed