SCHEMBL734929

SCHEMBL734929

CCCCCCCCc1ccc2ccccc2c1CCCCCCCC

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TYR P14679 2/20 0.47
LIPG Q9Y5X9 1/20 0.46
MAPT P10636 4/20 0.46
KDM4E B2RXH2 4/20 0.46
ALDH1A1 P00352 4/20 0.46
GAA P10253 4/20 0.46
CYP3A4 P08684 2/20 0.46
HPGD P15428 2/20 0.46
USP2 O75604 1/20 0.46
GLA P06280 1/20 0.46
CASP1 P29466 1/20 0.46
CASP7 P55210 1/20 0.46
HSD17B10 Q99714 1/20 0.46
NCEH1 Q6PIU2 1/20 0.46
HTT P42858 4/20 0.45
MEN1 O00255 3/20 0.45
KMT2A Q03164 3/20 0.45
TP53 P04637 1/20 0.45
ALOX5 P09917 1/20 0.45
ALOX15 P16050 1/20 0.45

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
SCHEMBL734618 1.00 TYR (0.47) TYRLIPGMAPTKDM4EALDH1A1
SCHEMBL283798 1.00 TYR (0.47) TYRLIPGMAPTKDM4EALDH1A1
SCHEMBL284720 1.00 TYR (0.47) TYRLIPGMAPTKDM4EALDH1A1
SCHEMBL284188 1.00 TYR (0.47) TYRLIPGMAPTKDM4EALDH1A1
SCHEMBL283786 1.00 TYR (0.47) TYRLIPGMAPTKDM4EALDH1A1
SCHEMBL236078 1.00 TYR (0.47) TYRLIPGMAPTKDM4EALDH1A1
SCHEMBL284699 1.00 TYR (0.47) TYRLIPGMAPTKDM4EALDH1A1
SCHEMBL234512 1.00 TYR (0.47) TYRLIPGMAPTKDM4EALDH1A1
SCHEMBL11381159 1.00 TYR (0.47) TYRLIPGMAPTKDM4EALDH1A1
SCHEMBL232844 1.00 TYR (0.47) TYRLIPGMAPTKDM4EALDH1A1

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 22 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118271147-A Method for preparing long-chain alkyl naphthalene by alkylating naphthalene and long-chain alpha-olefin 大连理工大学 2024-07-02 CN disclosed
CN-106463627-B Photovoltaic element 东丽株式会社 2019-06-28 CN disclosed
CN-109824467-A It is a kind of to utilize the ionic liquid-catalyzed method and its application for preparing more alkylnaphthalenes 太原理工大学 2019-05-31 CN disclosed
CN-108701770-A Photovoltaic element 东丽株式会社 2018-10-23 CN disclosed
EP-2067782-B2 HETEROACENE DERIVATIVE, TETRAHALOTERPHENYL DERIVATIVE, AND THEIR PRODUCTION METHODS TOSOH CORP (JP) 2018-06-27 EP disclosed
CN-106463627-A Photovoltaic element 东丽株式会社 2017-02-22 CN disclosed
CN-102224157-B Novel compound, process for producing the compound, organic semiconductor material, and organic semiconductor device HIROSHIMA UNIVERSITY (JP) 2014-10-22 CN disclosed
EP-2067782-B1 HETEROACENE DERIVATIVE, TETRAHALOTERPHENYL DERIVATIVE, AND THEIR PRODUCTION METHODS TOSOH CORP (JP) 2014-08-13 EP disclosed
US-8138355-B2 Heteroacene derivative, tetrahaloterphenyl derivative, and processes for producing the same TOSOH CORPORATION (JP) 2012-03-20 US disclosed
CN-102224157-A Novel compound, process for producing the compound, organic semiconductor material, and organic semiconductor device UNIV HIROSHIMA 2011-10-19 CN disclosed
EP-2067782-A1 HETEROACENE DERIVATIVE, TETRAHALOTERPHENYL DERIVATIVE, AND THEIR PRODUCTION METHODS Tosoh Corporation (JP) 2009-06-10 EP disclosed
US-20050222000-A1 Lubricating oil composition MITSUBISHI HEAVY INDUSTRIES, LTD. (JP) 2005-10-06 US disclosed
US-5910269-A GENERATES A LARGE SHEAR STRESS AND LOW CURRENT DENSITY, EXHIBITS EXCELLENT WITHSTANDING DIELECTRIC BREAKDOWN STRENGTH, EXHIBITS EXCELLENT FLUIDITY AND REDISPERSABILITY IN THE ABSENCE OF AN ELECTRIC FIELD NIPPON SHOKUBAI CO., LTD. (JP) 1999-06-08 US disclosed
US-5331032-A Hydrophilic aromatic polyester fiber TEIJIN LIMITED (JP) 1994-07-19 US disclosed
US-5262460-A Blend with polyoxyethylene glycol for antistatic fibers, films or sheets TEIJIN LIMITED (JP) 1993-11-16 US disclosed
US-4943656-A SULFONATION OF POLYALKYLAROMATIC COMPOUNDS, SEPARATION INTO LAYERED LIQUID PHASES KING INDUSTRIES, INC. (US) 1990-07-24 US disclosed
EP-0168778-B1 PROCESS FOR THE PRODUCTION OF POLYALKYLAROMATIC POLYSULFONIC ACIDS AND RECOVERY BY HEAVY PHASE SEPARATION KING INDUSTRIES, INC. (US) 1988-11-23 EP disclosed
EP-0168778-A2 Process for the production of polyalkylaromatic polysulfonic acids and recovery by heavy phase separation KING INDUSTRIES, INC. (US) 1986-01-22 EP disclosed
US-4128565-A Process for preparing methyltin chlorides SANKYO ORGANIC CHEMICALS COMPANY LIMITED (JP) 1978-12-05 US disclosed
US-3960688-A AMINOPLAST CROSSLINKING AGENT, POLYMER, AROMATIC SULFONIC ACID CATALYST AMERICAN CYANAMID COMPANY (US) 1976-06-01 US disclosed