SCHEMBL986572

SCHEMBL986572

CC/C=N/C(C)(C)C

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
SCHEMBL986573 1.00
SCHEMBL13970112 1.00
SCHEMBL22952855 0.75
SCHEMBL7111855 0.75
SCHEMBL7111853 0.75
SCHEMBL987640 0.75 FFAR1 (0.31)
SCHEMBL987638 0.75 FFAR1 (0.31)
SCHEMBL28779510 0.73 ALDH1A1 (0.31)
SCHEMBL18651103 0.73 PPARA (0.31)
SCHEMBL17084275 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 25 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20170279055-A1 ORGANIC ELECTROLUMINESCENCE DEVICE LM CHEM, LTD. (KR) 2017-09-28 US disclosed
US-20170279055-A1 ORGANIC ELECTROLUMINESCENCE DEVICE LM CHEM, LTD. (KR) 2017-09-28 US disclosed
US-9601696-B2 Electroluminescent composition and electric device with high brightness SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2017-03-21 US disclosed
US-9306170-B2 Electronic device and polymer compound SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2016-04-05 US disclosed
US-9299937-B2 Active layer, organic photovoltaic cell comprising the same and manufacturing method thereof LG CHEM, LTD. (KR) 2016-03-29 US disclosed
US-8921506-B2 Copolymer, organic solar cell using the same and manufacturing method thereof LG CHEM, LTD. (KR) 2014-12-30 US disclosed
US-8912308-B2 Copolymer, organic solar cell using the same and manufacturing method thereof LG CHEM, LTD. (KR) 2014-12-16 US disclosed
US-8835475-B2 Compounds as cannabinoid receptor ligands ABBVIE INC. (US) 2014-09-16 US disclosed
US-20140116511-A1 ACTIVE LAYER, ORGANIC PHOTOVOLTAIC CELL COMPRISING THE SAME AND MANUFACTURING METHOD THEREOF LG CHEM, LTD. (KR) 2014-05-01 US disclosed
US-20140039131-A1 ELECTRONIC DEVICE AND POLYMER COMPOUND SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2014-02-06 US disclosed
US-20110082116-A1 NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS ABBOTT LABORATORIES (US) 2011-04-07 US disclosed
US-7872033-B2 N-[(5Z)-4-butyl-2-tert-butylisothiazol-5(2H)-ylidene]-5-chloro-2-methoxybenzamide; CB2 receptors ligand; antiinflammatory, analgesic agent; autoimmune diseases; neuroprotectants ABBOTT LABORATORIES (US) 2011-01-18 US disclosed
US-20100234345-A1 NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS ABBOTT LABORATORIES (US) 2010-09-16 US disclosed
WO-2010054024-A2 NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS ABBOTT LABORATORIES (US) 2010-05-14 WO disclosed
EP-2146973-A2 NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS Abbott Laboratories (US) 2010-01-27 EP disclosed
US-20090062213-A1 Small Molecule Inhibitors of PDZ Interactions ARBOR VITA CORPORATION (US) 2009-03-05 US disclosed
US-20090023789-A1 N-[(5Z)-4-butyl-2-tert-butylisothiazol-5(2H)-ylidene]-5-chloro-2-methoxybenzamide; CB2 receptors ligand; antiinflammatory, analgesic agent; autoimmune diseases; neuroprotectants ABBOTT LABORATORIES (US) 2009-01-22 US disclosed
WO-2008130953-A2 2-IMIN0IS0THIAZ0LE DERIVATIVES AS CANNABINOID RECEPTOR LIGANDS ABBOTT LABORATORIES (US) 2008-10-30 WO disclosed
US-20040152903-A1 6-chloro-3-pyridylmethylpropylamine derivatives, preparation process thereof and bactericides KUREHA CORPORATION (JP) 2004-08-05 US disclosed
EP-1375483-A1 6-CHLORO-3-PYRIDYLMETHYLPROPYLAMINE DERIVATIVES, PREPARATION PROCESS THEREOF AND BACTERICIDES KUREHA KAGAKU KOGYO KABUSHIKI KAISHA (JP) 2004-01-02 EP disclosed