SCHEMBL1964196

SCHEMBL1964196

CCCCCCCCOc1ccccc1OCCCCCCCC

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.62
MEN1 O00255 1/20 0.62
NR1I2 O75469 1/20 0.62
CHRM2 P08172 1/20 0.62
CYP3A4 P08684 1/20 0.62
ADRA2A P08913 1/20 0.62
MAPT P10636 1/20 0.62
OPRK1 P41145 1/20 0.62
HTR2B P41595 1/20 0.62
SLC6A3 Q01959 1/20 0.62
KMT2A Q03164 1/20 0.62
HDAC6 Q9UBN7 1/20 0.62
CYP1A2 P05177 1/20 0.61
CYP2C9 P11712 1/20 0.61
CYP2C19 P33261 1/20 0.61
L3MBTL1 Q9Y468 3/20 0.57
ALDH1A1 P00352 3/20 0.55
LTA4H P09960 1/20 0.53
MCHR1 Q99705 2/20 0.53
TLR8 Q9NR97 2/20 0.53

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
SCHEMBL8974126 1.00 LMNA (0.62) LMNAMEN1NR1I2CHRM2CYP3A4
SCHEMBL30620186 1.00 LMNA (0.62) LMNAMEN1NR1I2CHRM2CYP3A4
SCHEMBL30292285 1.00 LMNA (0.62) LMNAMEN1NR1I2CHRM2CYP3A4
SCHEMBL29868324 1.00 LMNA (0.62) LMNAMEN1NR1I2CHRM2CYP3A4
SCHEMBL9387360 1.00 LMNA (0.62) LMNAMEN1NR1I2CHRM2CYP3A4
SCHEMBL1778134 1.00 LMNA (0.62) LMNAMEN1NR1I2CHRM2CYP3A4
SCHEMBL2245919 1.00 LMNA (0.62) LMNAMEN1NR1I2CHRM2CYP3A4
SCHEMBL2859001 1.00 LMNA (0.62) LMNAMEN1NR1I2CHRM2CYP3A4
SCHEMBL9394792 1.00 LMNA (0.62) LMNAMEN1NR1I2CHRM2CYP3A4
SCHEMBL28106102 1.00 LMNA (0.62) LMNAMEN1NR1I2CHRM2CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108689943-B Ruthenium-containing supramolecular compound and preparation method and application thereof 江苏师范大学 2021-07-30 CN claimed
CN-109939735-A A kind of phase transfer catalyst and its synthetic method 湖南科技大学 2019-06-28 CN claimed
CN-103540157-A Polymeric metal-complex functional dye containing 2-(2'-pyridyl)benzimidazole D-pi-A type structure and preparation method thereof UNIV XIANGTAN 2014-01-29 CN claimed
EP-2723750-B1 DIKETOPYRROLOPYRROLE OLIGOMERS FOR USE IN ORGANIC SEMICONDUCTOR DEVICES CLAP CO LTD (KR) 2022-08-10 EP disclosed
CN-108689943-B Ruthenium-containing supramolecular compound and preparation method and application thereof 江苏师范大学 2021-07-30 CN disclosed
CN-112940276-A Ruthenium-containing supramolecular compound and synthesis method and application thereof 江苏师范大学 2021-06-11 CN disclosed
EP-2751855-B1 DIKETOPYRROLOPYRROLE OLIGOMERS AND COMPOSITIONS, COMPRISING DIKETOPYRROLOPYRROLE OLIGOMERS BASF SE (DE) 2020-10-28 EP disclosed
WO-2020163479-A1 ANTIBIOTIC AMMONIUM COMPOUNDS AND METHODS FOR THE TREATMENT OF BACTERIAL INFECTIONS BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2020-08-13 WO disclosed
US-10323204-B2 Low viscosity, low volatility lubricating oil basestocks EXXONMOBIL RESEARCH AND ENGINEERING COMPANY (US) 2019-06-18 US disclosed
US-10323204-B2 Low viscosity, low volatility lubricating oil basestocks EXXONMOBIL RESEARCH AND ENGINEERING COMPANY (US) 2019-06-18 US disclosed
CN-107629047-A Asymmetric organic small-molecule photovoltaic material based on benzothiadiazole unit and preparation method and application thereof 大连理工大学 2018-01-26 CN disclosed
US-20090176995-A1 Soluble fullerene derivatives NATIONAL UNIVERSITY CORPORATION NAGOYA INSTITUTE OF TECHNOLOGY (JP) 2009-07-09 US disclosed
US-20090176995-A1 Soluble fullerene derivatives NATIONAL UNIVERSITY CORPORATION NAGOYA INSTITUTE OF TECHNOLOGY (JP) 2009-07-09 US disclosed
US-7282742-B2 Organic thin film transistor devices and organic photovoltaic devices TORAY INDUSTRIES, INC. (JP) 2007-10-16 US disclosed
US-20070116984-A1 SPIRO-COMPOUND FOR ELECTROLUMINESCENT DISPLAY DEVICE AND ELECTROLUMINESCENT DISPLAY DEVICE COMPRISING THE SAME DOOSAN CORPORATION (KR) 2007-05-24 US disclosed
US-20040241900-A1 Organic semiconductor material and organic semiconductor element employing the same TORAY INDUSTRIES, INC. (JP) 2004-12-02 US disclosed
EP-1449887-A1 ORGANIC SEMICONDUCTOR MATERIAL AND ORGANIC SEMICONDUCTOR ELEMENT EMPLOYING THE SAME TORAY INDUSTRIES, INC. (JP) 2004-08-25 EP disclosed
EP-1109791-A1 PROCESS FOR MAKING 2-(2-HYDROXY-4-ALKOXYPHENYL)-4,6-BISARYL-1,3,5-TRIAZINES CYTEC TECHNOLOGY CORP. (US) 2001-06-27 EP disclosed
WO-2000014075-A1 PROCESS FOR MAKING 2-(2-HYDROXY-4-ALKOXYPHENYL)-4,6-BISARYL-1,3,5-TRIAZINES CYTEC TECHNOLOGY CORP. (US) 2000-03-16 WO disclosed
WO-1994029243-A1 SYNTHESIS OF SUBSTITUTED TRIPHENYLENES, USEFUL AS DISCOTIC LIQUID CRYSTALS BRITISH TECHNOLOGY GROUP LIMITED (GB) 1994-12-22 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-10323204-B2 Low viscosity, low volatility lubricating oil basestocks TYK2, JAK1, CEL LMNA 2748/4885MEN1 4145/4885NR1I2 735/4885
US-20090176995-A1 Soluble fullerene derivatives SOD1, EPCAM, NDUFV2 LMNA 3745/4885MEN1 2921/4885NR1I2 3362/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.