SCHEMBL238630

SCHEMBL238630

CCC1COCN1

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
SCHEMBL14197970 1.00
SCHEMBL1117526 0.80
SCHEMBL1117502 0.77
SCHEMBL1006247 0.75
SCHEMBL22433362 0.75
SCHEMBL1006882 0.75
SCHEMBL16953 0.75
SCHEMBL1117476 0.75 ALDH1A1 (0.43)
SCHEMBL18040167 0.74
SCHEMBL3785497 0.74

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20120004272-A1 BIOCIDAL COMPOSITION OF 2,6-DIMETHYL-M-DIOXANE-4-OL ACETATE AND METHODS OF USE JI KATHY J (CN) 2012-01-05 US claimed
EP-2346327-A2 BIOCIDAL COMPOSITIONS AND METHODS OF USE Dow Global Technologies LLC (US) 2011-07-27 EP claimed
EP-1751199-B1 NOVEL PHENOLIC RESINS ANGUS CHEMICAL (US) 2010-11-24 EP claimed
WO-2010108324-A1 BIOCIDAL COMPOSITION OF 2,6-DIMETHYL-M-DIOXANE-4-OL ACETATE AND METHODS OF USE DOW GLOBAL TECHNOLOGIES INC. (US) 2010-09-30 WO claimed
WO-2010039923-A2 BIOCIDAL COMPOSITIONS AND METHODS OF USE DOW GLOBAL TECHNOLOGIES INC. (US) 2010-04-08 WO claimed
US-20100078393-A1 BIOCIDAL COMPOSITIONS AND METHODS OF USE DOW GLOBAL TECHNOLOGIES LLC 2010-04-01 US claimed
US-7319131-B2 Phenolic resins ANGUS CHEMICAL COMPANY (US) 2008-01-15 US claimed
US-5460797-A Method for fixing tissues and cells for analysis using oxazolidine compounds STRECK LABORATORIES, INC. (US) 1995-10-24 US claimed
US-4042520-A EXOTHERMIC REDOX REACTIONS OF HYDROGEN PEROXIDE AND OXAZOLIDINES IMC CHEMICAL GROUP, INC. (US) 1977-08-16 US claimed
US-10189841-B2 Purinones as ubiquitin-specific protease 1 inhibitors FORMA THERAPEUTICS, INC. (US) 2019-01-29 US disclosed
US-20180170944-A1 USE OF THE FL-ONE HUNDRED EIGHTEEN CORE CHEMICAL STRUCTURE PLATFORM TO GENERATE FL-ONE HUNDRED EIGHTEEN DERIVATIVES FOR TREATMENT OF HUMAN DISEASE CANGET BIOTEKPHARMA, LLC (US) 2018-06-21 US disclosed
US-20170145012-A1 PURINONES AS UBIQUITIN-SPECIFIC PROTEASE 1 INHIBITORS FORMA THERAPEUTICS, INC. 2017-05-25 US disclosed
US-20130137709-A1 Compounds that modulate EGFR activity and methods for treating or preventing conditions therewith Gatekeeper Pharmaceuticals, Inc. 2013-05-30 US disclosed
CN-101684078-B Chemical synthesis method for of 2-amino-butanamide hydrochloride UNIV ZHEJIANG TECHNOLOGY 2013-01-16 CN disclosed
US-20070027147-A1 Biarylurea derivatives MSD K.K. (JP) 2007-02-01 US disclosed
WO-2005108453-A1 NOVEL PHENOLIC RESINS ANGUS CHEMICAL COMPANY (US) 2005-11-17 WO disclosed
US-20050054787-A1 Novel phenolic resins ANGUS CHEMICAL COMPANY 2005-03-10 US disclosed
US-5460797-A Method for fixing tissues and cells for analysis using oxazolidine compounds STRECK LABORATORIES, INC. (US) 1995-10-24 US disclosed
US-4088655-A ANTIMICROBIAL AGENTS IMC CHEMICAL GROUP, INC. (US) 1978-05-09 US disclosed
US-4042520-A EXOTHERMIC REDOX REACTIONS OF HYDROGEN PEROXIDE AND OXAZOLIDINES IMC CHEMICAL GROUP, INC. (US) 1977-08-16 US disclosed