SCHEMBL6744197

SCHEMBL6744197

Fc1cc(-c2cccs2)ccc1-c1cccs1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KCNH2 Q12809 1/20 0.52
PDK2 Q15119 1/20 0.49
ERN1 O75460 2/20 0.47
KDM4E B2RXH2 1/20 0.45
MAPT P10636 1/20 0.45
SLC6A11 P48066 1/20 0.45
LTA4H P09960 1/20 0.44
PGR P06401 2/20 0.41
FLT3 P36888 1/20 0.41
HTR1D P28221 1/20 0.40
HTR1B P28222 1/20 0.40
CYP2E1 P05181 1/20 0.40
CYP3A4 P08684 1/20 0.40
CYP2A6 P11509 1/20 0.40
CYP2C9 P11712 1/20 0.40
CYP2B6 P20813 1/20 0.40
PRMT6 Q96LA8 1/20 0.40
CYP17A1 P05093 1/20 0.40
CYP11B1 P15538 1/20 0.40
CYP11B2 P19099 1/20 0.40

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
SCHEMBL29945114 1.00 KCNH2 (0.52) KCNH2PDK2ERN1KDM4EMAPT
SCHEMBL6318301 0.84 KCNH2 (0.55) KCNH2PDK2ERN1KDM4EMAPT
SCHEMBL4207045 0.82 MAPT (0.47) ERN1KDM4EMAPTCYP3A4CYP2C9
SCHEMBL25165727 0.82 ESR1 (0.42) KCNH2PDK2ERN1KDM4EMAPT
SCHEMBL2782222 0.81 NPC1 (0.46) KCNH2ERN1KDM4EMAPTLTA4H
SCHEMBL7056060 0.79 ERN1 (0.58) KCNH2PDK2ERN1KDM4EMAPT
SCHEMBL27740028 0.79 KCNH2 (0.50) KCNH2PDK2ERN1KDM4EMAPT
SCHEMBL22578266 0.79 KCNH2 (0.50) KCNH2PDK2ERN1KDM4EMAPT
SCHEMBL7157852 0.79 ESR1 (0.57) ERN1ESR1ESR2
SCHEMBL27684417 0.79 HPGD (0.43) PDK2ERN1KDM4EMAPTCYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6699621-B2 ELECTROPOLYMERIZING MONOMERS ON TO A SUBSTRATE IN A POLYMERIZATION SOLUTION; ELECTROCHEMICALLY CONDITIONING POLYMER SO AS TO INCREASE DISCHARGE EFFICIENCY AND CHARGE CAPACITY; DOPING TO IMPART A NON-NEUTRAL CHARGE JOHNS HOPKINS UNIVERSITY 2004-03-02 US claimed
US-20030143461-A1 METHOD FOR ELECTROCHEMICAL CONDITIONING POLYMERIC ELECTRODEDS JOHNS HOPKINS UNIVERSITY 2003-07-31 US claimed
US-6120940-A BATTERY COMPRISING AN ELECTRICALLY CONDUCTIVE POLYTHIOPHENE FLUOROPOLYMER; HIGH CHARGE CAPACITIES, AND EXCELLENT CYCLING EFFICIENCY; POLYELECTROLYTES THE JOHNS HOPKINS UNIVERSITY (US) 2000-09-19 US claimed
US-11133479-B2 Organic solar cell comprising a phenyldithiophene polymer donor and a non-fullerene acceptor LG CHEM, LTD. (KR) 2021-09-28 US disclosed
US-20200028098-A1 ORGANIC SOLAR CELL LG CHEM, LTD. (KR) 2020-01-23 US disclosed
EP-3557640-A1 ORGANIC SOLAR CELL LG Chem, Ltd. (KR) 2019-10-23 EP disclosed
US-6699621-B2 ELECTROPOLYMERIZING MONOMERS ON TO A SUBSTRATE IN A POLYMERIZATION SOLUTION; ELECTROCHEMICALLY CONDITIONING POLYMER SO AS TO INCREASE DISCHARGE EFFICIENCY AND CHARGE CAPACITY; DOPING TO IMPART A NON-NEUTRAL CHARGE JOHNS HOPKINS UNIVERSITY 2004-03-02 US disclosed
US-20030143461-A1 METHOD FOR ELECTROCHEMICAL CONDITIONING POLYMERIC ELECTRODEDS JOHNS HOPKINS UNIVERSITY 2003-07-31 US disclosed
US-6120940-A BATTERY COMPRISING AN ELECTRICALLY CONDUCTIVE POLYTHIOPHENE FLUOROPOLYMER; HIGH CHARGE CAPACITIES, AND EXCELLENT CYCLING EFFICIENCY; POLYELECTROLYTES THE JOHNS HOPKINS UNIVERSITY (US) 2000-09-19 US disclosed
US-6120940-A BATTERY COMPRISING AN ELECTRICALLY CONDUCTIVE POLYTHIOPHENE FLUOROPOLYMER; HIGH CHARGE CAPACITIES, AND EXCELLENT CYCLING EFFICIENCY; POLYELECTROLYTES THE JOHNS HOPKINS UNIVERSITY (US) 2000-09-19 US disclosed
WO-1999023711-A9 AN ELECTROCHEMICAL STORAGE CELL CONTAINING AT LEAST ONE ELECTRODE FORMULATED FROM A PHENYLENE-THIENYL BASED POLYMER UNIV JOHNS HOPKINS (US) 1999-08-12 WO disclosed
WO-1999023711-A1 AN ELECTROCHEMICAL STORAGE CELL CONTAINING AT LEAST ONE ELECTRODE FORMULATED FROM A PHENYLENE-THIENYL BASED POLYMER THE JOHNS HOPKINS UNIVERSITY (US) 1999-05-14 WO disclosed