SCHEMBL989755

SCHEMBL989755

CCCCCCCCCCCCOc1cc(N)cc(OCCCCCCCCCCCC)c1OCCCCCCCCCCCC

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.50
TLR8 Q9NR97 2/20 0.46
MCHR1 Q99705 2/20 0.43
CYP1A2 P05177 1/20 0.43
CYP2C9 P11712 1/20 0.43
CYP2C19 P33261 1/20 0.43
MEN1 O00255 2/20 0.42
MAPT P10636 2/20 0.42
KMT2A Q03164 2/20 0.42
NR1I2 O75469 1/20 0.42
LMNA P02545 1/20 0.42
CHRM2 P08172 1/20 0.42
CYP3A4 P08684 1/20 0.42
ADRA2A P08913 1/20 0.42
OPRK1 P41145 1/20 0.42
HTR2B P41595 1/20 0.42
SLC6A3 Q01959 1/20 0.42
HDAC6 Q9UBN7 1/20 0.42
CHUK O15111 1/20 0.42
DAPK3 O43293 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
SCHEMBL28103222 1.00 TSHR (0.50) TSHRTLR8MCHR1CYP1A2CYP2C9
SCHEMBL14706339 0.90 TSHR (0.45) TSHRTLR8MCHR1CYP1A2CYP2C9
SCHEMBL6608551 0.86 KMT2A (0.53) TSHRTLR8MCHR1CYP1A2CYP2C9
SCHEMBL1010950 0.82 THRB (0.42) TLR8MEN1MAPTKMT2ANR1I2
SCHEMBL14405204 0.82 THRB (0.42) TLR8MEN1MAPTKMT2ANR1I2
SCHEMBL1237686 0.81 SPIN1 (0.43) TSHRTLR8MEN1MAPTKMT2A
SCHEMBL13836995 0.81 SPIN1 (0.43) TSHRTLR8MEN1MAPTKMT2A
SCHEMBL5268487 0.81 THRA (0.44) THRATHRB
SCHEMBL5266338 0.81 THRA (0.44) THRATHRB
SCHEMBL5269365 0.81 THRA (0.41) TLR8MEN1MAPTKMT2ANR1I2

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
US-8841454-B2 Functionalized carbon nanostructures which are soluble in hydrocarbons and method for preparation EXXONMOBIL RESEARCH AND ENGINEERING COMPANY (US) 2014-09-23 US disclosed
US-20140221664-A1 COUPLED HETEROARYL COMPOUNDS VIA REARRANGEMENT OF HALOGENATED HETEROAROMATICS FOLLOWED BY OXIDATIVE COUPLING (ELECTRON WITHDRAWING GROUPS) GEORGIA TECH RESEARCH CORPORATION (US) 2014-08-07 US disclosed
EP-2742024-A1 COUPLED HETEROARYL COMPOUNDS VIA REARRANGEMENT OF HALOGENATED HETEROAROMATICS FOLLOWED BY OXIDATIVE COUPLING (ELECTRON WITHDRAWING GROUPS) Georgia Tech Research Corporation (US) 2014-06-18 EP disclosed
US-8435931-B2 Reduced friction lubricating oils containing functionalized carbon nanomaterials EXXONMOBIL RESEARCH AND ENGINEERING COMPANY (US) 2013-05-07 US disclosed
US-20130102785-A1 METHOD OF MAKING COUPLED HETEROARYL COMPOUNDS VIA REARRANGEMENT OF HALOGENATED HETEROAROMATICS FOLLOWED BY OXIDATIVE COUPLING GEORGIA TECH RESEARCH CORPORATION (US) 2013-04-25 US disclosed
US-8378336-B2 Liquid crystalline organic semiconductor material and organic electron device FUJIFILM CORPORATION (JP) 2013-02-19 US disclosed
WO-2013023106-A1 COUPLED HETEROARYL COMPOUNDS VIA REARRANGEMENT OF HALOGENATED HETEROAROMATICS FOLLOWED BY OXIDATIVE COUPLING (ACYL MOIETIES) GEORGIA TECH RESEARCH CORPORATION (US) 2013-02-14 WO disclosed
WO-2013023109-A1 COUPLED HETEROARYL COMPOUNDS VIA REARRANGEMENT OF HALOGENATED HETEROAROMATICS FOLLOWED BY OXIDATIVE COUPLING (COUPLED TRICYCLIC CORE COMPOUNDS) GEORGIA TECH RESEARCH CORPORATION (US) 2013-02-14 WO disclosed
WO-2013023108-A1 COUPLED HETEROARYL COMPOUNDS VIA REARRANGEMENT OF HALOGENATED HETEROAROMATICS FOLLOWED BY OXIDATIVE COUPLING (HETEROARYLENE SPACER MOIETY) GEORGIA TECH RESEARCH CORPORATION (US) 2013-02-14 WO disclosed
WO-2013023107-A1 COUPLED HETEROARYL COMPOUNDS VIA REARRANGEMENT OF HALOGENATED HETEROAROMATICS FOLLOWED BY OXIDATIVE COUPLING (ELECTRON WITHDRAWING GROUPS) GEORGIA TECH RESEARCH CORPORATION (US) 2013-02-14 WO disclosed
WO-2011098495-A1 METHOD OF MAKING COUPLED HETEROARYL COMPOUNDS VIA REARRANGEMENT OF HALOGENATED HETEROAROMATICS FOLLOWED BY OXIDATIVE COUPLING GEORGIA TECH RESEARCH CORPORATION (US) 2011-08-18 WO disclosed
US-20110015423-A1 Functionalized Carbon Nanostructures Which are Soluble in Hydrocarbons and Method for Preparation EXXONMOBIL RESEARCH AND ENGINEERING COMPANY (US) 2011-01-20 US disclosed
US-20110015106-A1 Reduced Friction Lubricating Oils Containing Functionalized Carbon Nanomaterials EXXONMOBIL RESEARCH AND ENGINEERING COMPANY (US) 2011-01-20 US disclosed
WO-2011009025-A1 REDUCED FRICTION LUBRICATING OILS CONTAINING FUNCTIONALIZED CARBON NANOMATERIALS EXXONMOBIL RESEARCH AND ENGINEERING COMPANY (US) 2011-01-20 WO disclosed
WO-2011009026-A1 FUNCTIONALIZED CARBON NANOSTRUCTURES WHICH ARE SOLUBLE IN HYDROCARBONS AND METHOD FOR PREPARATION EXXONMOBIL RESEARCH AND ENGINEERING COMPANY (US) 2011-01-20 WO disclosed
EP-1313735-B1 LIQUID CRYSTALLINE 3,4:9,10-PERYLENETETRACARBOXYLIC ACID DIIMIDES BASF SE (DE) 2008-04-23 EP disclosed
US-6806368-B2 FOR ELECTRONIC, OPTOELECTRONIC AND PHOTONIC APPLICATIONS, FOR COLORATION OF MACROMOLECULAR ORGANIC AND OF INORGANIC MATERIALS BASF AKTIENGESELLSCHAFT (DE) 2004-10-19 US disclosed
US-20030181721-A1 Liquid crystalline 3,4:9,10-perylenetetacarbocylic acid diimides BASF AKTIENGESELLSCHAFT (DE) 2003-09-25 US disclosed
EP-1313735-A1 LIQUID CRYSTALLINE 3,4:9,10-PERYLENETETRACARBOXYLIC ACID DIIMIDES BASF AKTIENGESELLSCHAFT (DE) 2003-05-28 EP disclosed
WO-2002014318-A1 LIQUID CRYSTALLINE 3,4:9,10-PERYLENETETRACARBOXYLIC ACID DIIMIDES BASF AKTIENGESELLSCHAFT (DE) 2002-02-21 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 (3 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-20110015423-A1 Functionalized Carbon Nanostructures Which are Soluble in Hydrocarbons and Method for Preparation ALKBH3, HCCS, CCL11 TSHR 3669/4885TLR8 278/4885MCHR1 1006/4885
US-20030181721-A1 Liquid crystalline 3,4:9,10-perylenetetacarbocylic acid diimides CCR9, CLTA, HAO2 TSHR 2200/4885TLR8 1344/4885MCHR1 858/4885
US-20130102785-A1 METHOD OF MAKING COUPLED HETEROARYL COMPOUNDS VIA REARRANGEMENT OF HALOGENATED HETEROAROMATICS FOLLOWED BY OXIDATIVE COUPLING NOX5, KAT5, PRXL2A TSHR 337/4885TLR8 2647/4885MCHR1 1524/4885

“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.