SCHEMBL4913490

SCHEMBL4913490

CCCCC(CC)COc1ccccc1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.54
CYP3A4 P08684 3/20 0.54
CA2 P00918 1/20 0.54
LTA4H P09960 2/20 0.50
LMNA P02545 3/20 0.49
PRSS1 P07477 1/20 0.48
PRSS2 P07478 1/20 0.48
PRSS3 P35030 1/20 0.48
MAPK1 P28482 1/20 0.46
KDM4E B2RXH2 1/20 0.45
L3MBTL1 Q9Y468 2/20 0.45
MEN1 O00255 1/20 0.45
MAPT P10636 1/20 0.45
KMT2A Q03164 1/20 0.45
ALOX5 P09917 1/20 0.43
PPARG P37231 1/20 0.43
PPARA Q07869 1/20 0.43
MAOA P21397 1/20 0.43
PTGS1 P23219 1/20 0.43
KCNA3 P22001 1/20 0.42

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
SCHEMBL7162660 0.93 PRSS1 (0.56) ALDH1A1CYP3A4CA2LTA4HLMNA
SCHEMBL28573281 0.93 PRSS1 (0.56) ALDH1A1CYP3A4CA2LTA4HLMNA
SCHEMBL1357035 0.91 ALDH1A1 (0.50) ALDH1A1CYP3A4CA2LMNAPRSS1
SCHEMBL1356320 0.91 ALDH1A1 (0.50) ALDH1A1CYP3A4CA2LMNAPRSS1
SCHEMBL28029167 0.89 LMNA (0.50) ALDH1A1CYP3A4CA2LTA4HLMNA
SCHEMBL17138127 0.88 CYP3A4 (0.49) ALDH1A1CYP3A4CA2LMNAPRSS1
SCHEMBL8943906 0.88 ALDH1A1 (0.47) ALDH1A1CYP3A4CA2LTA4HLMNA
SCHEMBL18854867 0.88 ALDH1A1 (0.47) ALDH1A1CYP3A4CA2LTA4HLMNA
SCHEMBL11883192 0.86 ALDH1A1 (0.49) ALDH1A1CYP3A4CA2LTA4HLMNA
SCHEMBL20357876 0.86 CYP3A4 (0.47) ALDH1A1CYP3A4CA2LMNAPRSS1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111253285-A High fluorescence quantum efficiency material based on terphenyl derivative and preparation method thereof 南京邮电大学 2020-06-09 CN claimed
CN-104892641-A Neutral cathode buffer layer molecular type material based on N-heterocycle groups as well as preparation method and application of neutral cathode buffer layer molecular type material UNIV SOUTH CHINA TECH 2015-09-09 CN claimed
WO-2025151605-A1 IONIZABLE AMPHIPHILIC JANUS DENDRIMERS, DELIVERY SYSTEMS COMPRISING THEREOF, AND METHODS OF USE THEREOF THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2025-07-17 WO disclosed
CN-112321806-B Conjugated polymer containing thieno [3,4-b ] pyrazine and preparation method and application thereof 天津理工大学 2023-05-02 CN disclosed
CN-112321806-A Conjugated polymer containing thieno [3,4-b ] pyrazine and preparation method and application thereof 天津理工大学 2021-02-05 CN disclosed
CN-111253285-A High fluorescence quantum efficiency material based on terphenyl derivative and preparation method thereof 南京邮电大学 2020-06-09 CN disclosed
CN-110997012-A Polymer nanoparticles for afterglow molecular imaging 南洋理工大学 2020-04-10 CN disclosed
CN-109180475-A A method of without alkali cleaning and washing quick synthesizing dioctyl terephthalate through esterification 华侨大学 2019-01-11 CN disclosed
EP-3242897-A1 ULTRAVIOLET CURABLE LIQUID COMPOSITION, ULTRAVIOLET CURING INKJET INK, ULTRAVIOLET CURING WET ELECTROPHOTOGRAPHIC LIQUID DEVELOPER, ULTRAVIOLET CURING ELECTROSTATIC INKJET INK, AND IMAGE FORMING METHOD USING THEREOF C/o Canon Kabushiki Kaisha (JP) 2017-11-15 EP disclosed
EP-2514736-B1 Intermediates for Polymers BASF SE (DE) 2017-03-01 EP disclosed
CN-106459385-A Organic heteropolymer and method for manufacturing same 株式会社大赛璐 2017-02-22 CN disclosed
WO-2006097717-A1 HIGHLY BRANCHED DENDRIMERS ISIS INNOVATION LIMITED (GB) 2006-09-21 WO disclosed
CN-1729571-A Electrical connection of optoelectronic devices CAMBRIDGE DISPLAY TECH LTD (GB) 2006-02-01 CN disclosed
US-20040166366-A1 Light-emitting fluorene-based copolymers, EL devices comprising the same and method of synthesis thereof KOREA ADVANCED INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) 2004-08-26 US disclosed
US-5446172-A Reacting diarylsulfoxide and aromatic substrate in the presence of phosphorus pentoxide and methanesulfonic acid to produce triarylsulfonium complex, metathesizing with alkali metal hexafluoro metal salt GENERAL ELECTRIC COMPANY (US) 1995-08-29 US disclosed
EP-0455083-B1 Method for making triarylsulfonium hexafluorometal or metalloid salts GEN ELECTRIC (US) 1995-03-01 EP disclosed
US-5144051-A Improved solubility; photinitiators for epoxy compounds or expoxysilanes MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1992-09-01 US disclosed
EP-0486745-A1 Improved solvents for chromogens useful in the manufacture of carbonless copying paper MONSANTO EUROPE S.A./N.V. (BE) 1992-05-27 EP disclosed
EP-0455083-A1 Method for making triarylsulfonium hexafluorometal or metalloid salts GENERAL ELECTRIC COMPANY (US) 1991-11-06 EP disclosed
US-4066707-A METHOD FOR MANUFACTURE OF DIPHENOLS AND MONOALKYL ETHERS OF DIPHENOLS AGENCY OF INDUSTRIAL SCIENCE & TECHNOLOGY (JA) 1978-01-03 US disclosed