SCHEMBL7525264

SCHEMBL7525264

CCCCCCCCn1c(C)c(C2(c3c(C)n(CCCC)c4ccccc34)OC(=O)c3ccccc32)c2ccccc21

nearest known ligand 0.47

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
CNR2 P34972 14/20 0.47
CNR1 P21554 8/20 0.47
SLC6A3 Q01959 1/20 0.45
PGR P06401 1/20 0.44
RORA P35398 1/20 0.44
RORC P51449 1/20 0.44
RORB Q92753 1/20 0.44
KDM4E B2RXH2 2/20 0.42
MAPT P10636 1/20 0.42
ALDH1A1 P00352 3/20 0.41
LMNA P02545 1/20 0.41
HPGD P15428 1/20 0.41
HTT P42858 1/20 0.41

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

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
SCHEMBL11003866 1.00 CNR2 (0.47) CNR2CNR1SLC6A3PGRRORA
SCHEMBL311993 0.99 CNR2 (0.47) CNR2CNR1SLC6A3PGRRORA
SCHEMBL29576122 0.99 CNR2 (0.47) CNR2CNR1SLC6A3PGRRORA
SCHEMBL3234369 0.99 CNR2 (0.47) CNR2CNR1SLC6A3PGRRORA
SCHEMBL2048334 0.98 CNR2 (0.47) CNR2CNR1SLC6A3PGRRORA
SCHEMBL29361500 0.97 PGR (0.47) CNR2CNR1SLC6A3PGRRORA
SCHEMBL27560 0.97 PGR (0.47) CNR2CNR1SLC6A3PGRRORA
SCHEMBL18516808 0.95 CNR2 (0.44) CNR2CNR1SLC6A3PGRRORA
SCHEMBL8608974 0.94 PGR (0.44) CNR2CNR1SLC6A3PGRRORA
SCHEMBL29056525 0.93 CFTR (0.46) CNR2CNR1SLC6A3KDM4EMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2023085225-A1 METHOD FOR MANUFACTURING RECYCLED RESIN COMPOSITION 住友化学株式会社 2023-05-19 WO disclosed
US-20210323333-A1 IMAGING MEDIUM HEWLETT-PACKARD DEVELOPMENT COMPANY, L.P. 2021-10-21 US disclosed
US-20210039414-A1 IMAGING MEDIUM HEWLETT-PACKARD DEVELOPMENT COMPANY, L.P. 2021-02-11 US disclosed
US-20210023867-A1 IMAGING MEDIUM HEWLETT-PACKARD DEVELOPMENT COMPANY, L.P. 2021-01-28 US disclosed
WO-2020117255-A1 IMAGING MEDIA HEWLETT-PACKARD DEVELOPMENT COMPANY, L.P. (US) 2020-06-11 WO disclosed
US-8446660-B2 Electrochromic display device FUNAI ELECTRIC ADVANCED APPLIED TECHNOLOGY RESEARCH INSTITUTE INC. (JP) 2013-05-21 US disclosed
US-7995262-B2 Electrochromic display device FUNAI ELECTRIC ADVANCED APPLIED TECHNOLOGY RESEARCH INSTITUTE INC. (JP) 2011-08-09 US disclosed
US-20110141544-A1 Electrochromic Display Device Funai Electric Advanced Applied Technology Research Institute Inc., (JP) 2011-06-16 US disclosed
US-20100134865-A1 Electrochromic Display Device FUNAI ELECTRIC ADVANCED APPLIED TECHNOLOGY RESEARCH INSTITUTE INC. (JP) 2010-06-03 US disclosed
EP-1179435-A1 Reversible thermochromic composition having improved light-fastness and product comprising same The Pilot Ink Co., Ltd. (JP) 2002-02-13 EP disclosed
EP-0757628-B1 PROCESS FOR FIXING AN IMAGE POLAROID CORP (US) 1998-12-02 EP disclosed
EP-0665119-B1 Thermochromic colour-memory composition PILOT INK CO LTD (JP) 1997-12-03 EP disclosed
US-5582956-A EXPOSING MEDIUM HAVING ACID GENERATING LAYER CONTAINING SUPERACID PRECURSOR, SENSITIZER, SECONDARY ACID GENERATOR, COLOR CHANGE LAYER CONTAINING IMAGE DYE TO ACTINIC RADIATION, HEATING, MIXING LAYERS, FIXING IMAGE BY DESTROYING PRECURSOR POLAROID CORPORATION (US) 1996-12-10 US disclosed
US-5558699-A COLOR IS RETAINED AFTER HEATING OR COOLING IS WITHDRAWN, REACTION MEDIUM IS ALKYL OR ALKYLARYL KETONE THE PILOT INK CO., LTD. (JP) 1996-09-24 US disclosed
EP-0665119-A1 Thermochromic colour-memory composition THE PILOT INK CO., LTD. (JP) 1995-08-02 EP disclosed
EP-0334663-A2 Photographic material THE MEAD CORPORATION (US) 1989-09-27 EP disclosed