SCHEMBL2020575

SCHEMBL2020575

CC(C)(O)C[N+](=O)[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
SCHEMBL3814475 0.82 TSHR (0.40)
SCHEMBL5907560 0.78
SCHEMBL2018465 0.77 ALDH1A1 (0.43)
SCHEMBL20920025 0.76
SCHEMBL20920023 0.76
SCHEMBL12219493 0.75
SCHEMBL9452628 0.75 TSHR (0.44)
SCHEMBL2371528 0.74 TSHR (0.33)
SCHEMBL20919831 0.74 TET2 (0.40)
SCHEMBL5690075 0.74 TSHR (0.33)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109776522-B Substituted heteroaryl compounds, compositions and uses thereof 广东东阳光药业有限公司 2020-12-29 CN disclosed
CN-109776522-A Substituted heteroaryl compound and combinations thereof and purposes 广东东阳光药业有限公司 2019-05-21 CN disclosed
US-20180222906-A1 SUBSTITUTED IMIDAZOQUINOLINES, IMIDAZOPYRIDINES, AND IMIDAZONAPHTHYRIDINES 3M INNOVATIVE PROPERTIES COMPANY 2018-08-09 US disclosed
US-9938275-B2 Substituted imidazoquinolines, imidazopyridines, and imidazonaphthyridines 3M INNOVATIVE PROPERTIES COMPANY (US) 2018-04-10 US disclosed
US-20170129891-A1 SUBSTITUTED IMIDAZOQUINOLINES, IMIDAZOPYRIDINES, AND IMIDAZONAPHTHYRIDINES 3M INNOVATIVE PROPERTIES CO (US) 2017-05-11 US disclosed
US-9550773-B2 Substituted imidazoquinolines, imidazopyridines, and imidazonaphthyridines 3M INNOVATIVE PROPERTIES COMPANY (US) 2017-01-24 US disclosed
EP-2516379-B1 HYDROCARBON FEED FLEXIBLE HIGH PRESSURE NITRATION PLANT DESIGN ANGUS CHEMICAL (US) 2016-12-28 EP disclosed
US-9504933-B2 Hydrocarbon feed flexible high pressure nitration plant design ANGUS CHEMICAL COMPANY (US) 2016-11-29 US disclosed
US-20150218162-A1 SUBSTITUTED IMIDAZOQUINOLINES, IMIDAZOPYRIDINES, AND IMIDAZONAPHTHYRIDINES 3M INNOVATIVE PROPERTIES COMPANY 2015-08-06 US disclosed
CN-102741217-B Design of high pressure nitration plant with flexible hydrocarbon feed DOW GLOBAL TECHNOLOGIES INC 2015-04-15 CN disclosed
US-20110092477-A1 SUBSTITUTED IMIDAZOQUINOLINES, IMIDAZOPYRIDINES, AND IMIDAZONAPHTHYRIDINES 3M INNOVATIVE PROPERTIES COMPANY 2011-04-21 US disclosed
US-7884207-B2 such as 4-[(4-Amino-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)methyl]tetrahydro-2H-pyran-4-ol, used as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases 3M INNOVATIVE PROPERTIES COMPANY (US) 2011-02-08 US disclosed
US-20100010250-A1 METHODS FOR PREPARING 2-METHOXYISOBUTYLISONITRILE AND TETRAKIS(2-METHOXYISOBUTYLISONITRILE)COPPER(I) TETRAFLUOROBORATE Draximage Limited (IE) 2010-01-14 US disclosed
US-7563920-B2 Methods for preparing 2-methoxyisobutylisonitrile and tetrakis(2-methoxyisobutylisonitrile)copper(I) tetrafluoroborate Draximage Limited (IE) 2009-07-21 US disclosed
US-7563920-B2 Methods for preparing 2-methoxyisobutylisonitrile and tetrakis(2-methoxyisobutylisonitrile)copper(I) tetrafluoroborate Draximage Limited (IE) 2009-07-21 US disclosed
US-20080102028-A1 METHODS FOR PREPARING 2-METHOXYISOBUTYLISONITRILE AND TETRAKIS(2-METHOXYISOBUTYLISONITRILE)COPPER(I) TETRAFLUOROBORATE DRAXIS SPECIALTY PHARMACEUTICALS INC. (CA) 2008-05-01 US disclosed
US-20080102028-A1 METHODS FOR PREPARING 2-METHOXYISOBUTYLISONITRILE AND TETRAKIS(2-METHOXYISOBUTYLISONITRILE)COPPER(I) TETRAFLUOROBORATE DRAXIS SPECIALTY PHARMACEUTICALS INC. (CA) 2008-05-01 US disclosed
US-20070287724-A1 Substituted Imidazoquinolines, Imidazopyridines, and Imidazonaphthyridines 3M INNOVATIVE PROPERTIES COMPANY (US) 2007-12-13 US disclosed
US-4561862-A Use of selected beta-nitroalkenes as cetane number boosters for diesel fuel OLIN CORPORATION (US) 1985-12-31 US disclosed
US-3955935-A ELECTROLYTIC DEPOSITION, DIFFUSION GENERAL MOTORS CORPORATION (US) 1976-05-11 US disclosed