SCHEMBL1109738

SCHEMBL1109738

Cc1cccc(N(c2ccccc2)c2ccc(-c3ccc(Nc4ccccc4)cc3)cc2)c1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPSR1 Q6W5P4 1/20 0.56
HPGD P15428 2/20 0.47
THRB P10828 2/20 0.43
PKM P14618 1/20 0.43
HSD17B1 P14061 1/20 0.41
HSD17B2 P37059 1/20 0.41
MAPT P10636 5/20 0.41
ALDH1A1 P00352 4/20 0.41
MEN1 O00255 3/20 0.41
KMT2A Q03164 3/20 0.41
AR P10275 1/20 0.41
HSD17B10 Q99714 5/20 0.41
MAPK1 P28482 2/20 0.41
ALOX15 P16050 2/20 0.41
TSHR P16473 2/20 0.41
ALOX12 P18054 2/20 0.41
TDP1 Q9NUW8 2/20 0.41
L3MBTL1 Q9Y468 2/20 0.41
PTGS1 P23219 1/20 0.41
SLC6A2 P23975 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
SCHEMBL3627715 1.00 NPSR1 (0.56) NPSR1HPGDTHRBPKMHSD17B1
SCHEMBL29359258 0.98 NPSR1 (0.53) NPSR1HPGDTHRBPKMHSD17B1
SCHEMBL8587961 0.97 NPSR1 (0.62) NPSR1HPGDTHRBPKMHSD17B1
SCHEMBL8605475 0.95 HPGD (0.50) NPSR1HPGDTHRBPKMHSD17B1
SCHEMBL12012945 0.95 NPSR1 (0.61) NPSR1HPGDTHRBPKMMAPT
SCHEMBL3463650 0.95 NPSR1 (0.61) NPSR1HPGDTHRBPKMMAPT
SCHEMBL5144099 0.95 NPSR1 (0.61) NPSR1HPGDTHRBPKMMAPT
SCHEMBL17426604 0.95 NPSR1 (0.61) NPSR1HPGDTHRBPKMMAPT
SCHEMBL6033820 0.94 NPSR1 (0.62) NPSR1HPGDTHRBPKMHSD17B1
SCHEMBL3461983 0.94 NPSR1 (0.66) NPSR1HPGDTHRBPKMMAPT

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-20030118950-A1 Method of manufacturing full-color organic electro-luminescent device CHAO CHING-IAN (TW) 2003-06-26 US claimed
US-6517996-B1 Method of manufacturing full-color organic electro-luminescent device INDUSTRIAL TECHNOLOGY RESEARCH INSTITUTE (TW) 2003-02-11 US claimed
EP-3127906-A1 COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING SAME Samsung Display Co., Ltd. (KR) 2017-02-08 EP disclosed
EP-2249410-B1 ORGANIC ELECTROLUMINESCENT ELEMENT, AND MANUFACTURING METHOD AND USES THEREFOR SAMSUNG ELECTRONICS CO LTD (KR) 2015-12-02 EP disclosed
EP-2249410-B1 ORGANIC ELECTROLUMINESCENT ELEMENT, AND MANUFACTURING METHOD AND USES THEREFOR SAMSUNG ELECTRONICS CO LTD (KR) 2015-12-02 EP disclosed
US-8017813-B2 Process for production of cycloalkyl alkyl ethers ZEON CORPORATION (JP) 2011-09-13 US disclosed
EP-2279995-A2 Process for producing cycloalkyl alkyl ethers Zeon Corporation (JP) 2011-02-02 EP disclosed
US-20100320455-A1 ORGANIC ELECTROLUMINESCENCE DEVICE, PRODUCTION PROCESS THEREFOR, AND USE THEREOF SHOWA DENKO K.K. (JP) 2010-12-23 US disclosed
US-20100320455-A1 ORGANIC ELECTROLUMINESCENCE DEVICE, PRODUCTION PROCESS THEREFOR, AND USE THEREOF SHOWA DENKO K.K. (JP) 2010-12-23 US disclosed
US-20100320455-A1 ORGANIC ELECTROLUMINESCENCE DEVICE, PRODUCTION PROCESS THEREFOR, AND USE THEREOF SHOWA DENKO K.K. (JP) 2010-12-23 US disclosed
EP-2249410-A1 ORGANIC ELECTROLUMINESCENT ELEMENT, AND MANUFACTURING METHOD AND USES THEREFOR Showa Denko K.K. (JP) 2010-11-10 EP disclosed
EP-1405840-A1 SOLVENTS CONTAINING CYCLOALKYL ALKYL ETHERS AND PROCESS FOR PRODUCTION OF THE ETHERS Zeon Corporation (JP) 2004-04-07 EP disclosed
US-6586876-B2 Organic light-emitting device INDUSTRIAL TECHNOLOGY RESEARCH INSTITUTE (TW) 2003-07-01 US disclosed
US-20030118950-A1 Method of manufacturing full-color organic electro-luminescent device CHAO CHING-IAN (TW) 2003-06-26 US disclosed
US-20030107042-A1 Organic electroluminescent device with a containing fluorine inorganic layer INDUSTRIAL TECHNOLOGY RESEARCH INSTITUTE (TW) 2003-06-12 US disclosed
US-6566805-B1 The titanium dioxide-silicon dioxide composite layer and silicon dioxide protecting layer are formed by ion-assisted electron gun evaporation in the temperature lower than 100 degrees C. INDUSTRIAL TECHNOLOGY RESEARCH INSTITUTE (TW) 2003-05-20 US disclosed
US-20020094422-A1 Organic light-emitting device DISPLAY VECTORS LLC 2002-07-18 US disclosed
US-5763110-A Electroluminescent devices comprising polynuclear arylamines XEROX CORPORATION (US) 1998-06-09 US disclosed
EP-0827367-A2 Electroluminescent devices XEROX CORPORATION (US) 1998-03-04 EP disclosed
US-5378570-A Polyiminocarbonate FUJI XEROX CO., LTD. (JP) 1995-01-03 US disclosed