SCHEMBL1134091

SCHEMBL1134091

C[C](C)C(CC1CCC2OC2C1)C1CCC2OC2C1

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
SCHEMBL5698911 0.82
SCHEMBL8407085 0.81 KDM4E (0.34)
SCHEMBL1135356 0.77
SCHEMBL17165008 0.77
SCHEMBL16217682 0.76
SCHEMBL16217677 0.76
SCHEMBL12032236 0.74 PIK3CD (0.32)
SCHEMBL10032080 0.73
SCHEMBL16217680 0.71
SCHEMBL6853326 0.70

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1246859-B1 POLYMERIZABLE DENTAL COMPOSITIONS BASED ON EPOXIES THAT CONTAIN SILICON 3M ESPE AG (DE) 2006-07-26 EP claimed
US-20030035899-A1 Polymerizable preparations based on epoxies that contain silicon 3M INNOVATIVE PROPERTIES COMPANY 2003-02-20 US claimed
US-8436067-B2 Initiator system with biphenylene derivates, method of production and use thereof 3M INNOVATIVE PROPERTIES COMPANY (US) 2013-05-07 US disclosed
US-8314162-B2 Initiator system containing a diarylalkylamine derivate, hardenable composition and use thereof 3M INNOVATIVE PROPERTIES COMPANY (US) 2012-11-20 US disclosed
US-8226737-B2 Fixed abrasive particles and articles made therefrom 3M INNOVATIVE PROPERTIES COMPANY (US) 2012-07-24 US disclosed
EP-1684693-B1 PHOTOINITIATOR SYSTEMS WITH ANTHRACENE-BASED ELECTRON DONORS FOR CURING CATIONICALLY POLYMERIZABLE RESINS CURATORS OF UNIVERSITY OF MISSOURI (US) 2011-09-14 EP disclosed
US-20110124764-A1 INITIATOR SYSTEM WITH BIPHENYLENE DERIVATES, METHOD OF PRODUCTION AND USE THEREOF 3M INNOVATIVE PROPERTIES COMPANY 2011-05-26 US disclosed
EP-2307518-A2 FIXED ABRASIVE PARTICLES AND ARTICLES MADE THEREFROM 3M Innovative Properties Company (US) 2011-04-13 EP disclosed
US-20110077361-A1 INITIATOR SYSTEM CONTAINING A DIARYLALKYLAMINE DERIVATE, HARDENABLE COMPOSITION AND USE THEREOF SOLVENTUM INTELLECTUAL PROPERTIES COMPANY 2011-03-31 US disclosed
EP-2285339-A1 INITIATOR SYSTEM CONTAINING A DIARYLAKYLAMINE DERIVATIVE, HARDENABLE COMPOSITION AND USE THEREOF 3M Innovative Properties Company (US) 2011-02-23 EP disclosed
EP-2285340-A2 INITIATOR SYSTEM WITH BIPHENYLENE DERIVATES, METHOD OF PRODUCTION AND USE THEREOF 3M Innovative Properties Company (US) 2011-02-23 EP disclosed
US-20100000160-A1 FIXED ABRASIVE PARTICLES AND ARTICLES MADE THEREFROM 3M INNOVATIVE PROPERTIES COMPANY 2010-01-07 US disclosed
US-7537452-B2 Photoinitiator systems with anthracene-based electron donors for curing cationically polymerizable resins CURATORS OF THE UNIVERSITY OF MISSOURI (US) 2009-05-26 US disclosed
US-20070287764-A1 Photoinitiator systems with anthracene-based electron donors for curing cationically polymerizable resins 3M INNOVATIVE PROPERTIES COMPANY 2007-12-13 US disclosed
US-7262228-B2 Photoinitiator systems with anthracene-based electron donors for curing cationically polymerizable resins CURATORS OF THE UNIVERSITY OF MISSOURI (US) 2007-08-28 US disclosed
US-20050113477-A1 Photoinitiator systems with anthracene-based electron donors for curing cationically polymerizable resins 3M DEUTSCHLAND GMBH (DE) 2005-05-26 US disclosed
US-20030035899-A1 Polymerizable preparations based on epoxies that contain silicon 3M INNOVATIVE PROPERTIES COMPANY 2003-02-20 US disclosed