SCHEMBL8777072

SCHEMBL8777072

NC1(C2CCCCCCC2)CCCCCCC1

nearest known ligand 0.50

Predicted protein targets (top 2)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 1/20 0.34
MAPT P10636 1/20 0.34

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
SCHEMBL7383849 1.00 KDM4E (0.34) KDM4EMAPT
SCHEMBL28477019 1.00 KDM4E (0.34) KDM4EMAPT
SCHEMBL20198577 1.00 KDM4E (0.34) KDM4EMAPT
SCHEMBL2127065 1.00 KDM4E (0.34) KDM4EMAPT
SCHEMBL2125868 1.00 KDM4E (0.34) KDM4EMAPT
SCHEMBL23740127 1.00 KDM4E (0.34) KDM4EMAPT
SCHEMBL2126830 1.00 KDM4E (0.34) KDM4EMAPT
SCHEMBL20104757 1.00 KDM4E (0.34) KDM4EMAPT
SCHEMBL20610083 1.00 KDM4E (0.34) KDM4EMAPT
SCHEMBL28470400 1.00 KDM4E (0.34) KDM4EMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111868842-B Conductive paste with stable viscosity over time 株式会社则武 2021-11-19 CN disclosed
CN-111868842-A Conductive paste with stable viscosity over time 株式会社则武 2020-10-30 CN disclosed
EP-0800513-A1 OPIATE RECEPTOR LIGANDS CHIRON CORPORATION (US) 1997-10-15 EP disclosed
US-5605932-A Opiate receptor ligands CHIRON CORPORATION (US) 1997-02-25 US disclosed
US-5536868-A Opiate receptor ligands CHIRON CORPORATION (US) 1996-07-16 US disclosed
WO-1996020921-A1 OPIATE RECEPTOR LIGANDS CHIRON CORPORATION (US) 1996-07-11 WO disclosed
US-5481020-A Opiate receptor ligands CHIRON CORPORATION (US) 1996-01-02 US disclosed
EP-0008163-B1 A PROCESS FOR PREPARING CIS-2-ARYL-3-AMINOMETHYL-BICYCLO (2,2,2) OCTANES AND THE COMPOUNDS 2-ARYL-3-AMINOMETHYLIDENE-BICYCLO (2,2,2) OCTANES Lilly Industries Limited (GB) 1983-09-21 EP disclosed
US-4215074-A Process for preparing cis-bicyclooctylamines LILLY INDUSTRIES LIMITED (GB) 1980-07-29 US disclosed
US-4215074-A Process for preparing cis-bicyclooctylamines LILLY INDUSTRIES LIMITED (GB) 1980-07-29 US disclosed
EP-0008163-A1 A process for preparing cis-2-aryl-3-aminomethyl-bicyclo (2,2,2) octanes and the compounds 2-aryl-3-aminomethylidene-bicyclo (2,2,2) octanes Lilly Industries Limited (GB) 1980-02-20 EP disclosed