SCHEMBL6685708

SCHEMBL6685708

CCCCCCCOCc1ccccc1

nearest known ligand 0.58

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 4/20 0.58
TDP1 Q9NUW8 2/20 0.58
TSHR P16473 3/20 0.54
CETP P11597 3/20 0.51
LTA4H P09960 1/20 0.47
ALDH1A1 P00352 2/20 0.46
MAPK1 P28482 2/20 0.46
CYP3A4 P08684 1/20 0.46
DNM1 Q05193 1/20 0.46
APAF1 O14727 1/20 0.46
HRH4 Q9H3N8 1/20 0.45
HRH3 Q9Y5N1 1/20 0.45
HPGD P15428 1/20 0.45
MEN1 O00255 1/20 0.44
TP53 P04637 1/20 0.44
KMT2A Q03164 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
EPHX2 P34913 1/20 0.44

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
SCHEMBL7517468 1.00 L3MBTL1 (0.58) L3MBTL1TDP1TSHRCETPLTA4H
SCHEMBL7120703 1.00 L3MBTL1 (0.58) L3MBTL1TDP1TSHRCETPLTA4H
SCHEMBL7641859 1.00 L3MBTL1 (0.58) L3MBTL1TDP1TSHRCETPLTA4H
SCHEMBL16057438 1.00 L3MBTL1 (0.58) L3MBTL1TDP1TSHRCETPLTA4H
SCHEMBL14526009 1.00 L3MBTL1 (0.58) L3MBTL1TDP1TSHRCETPLTA4H
SCHEMBL2886385 1.00 L3MBTL1 (0.58) L3MBTL1TDP1TSHRCETPLTA4H
SCHEMBL1923328 1.00 L3MBTL1 (0.58) L3MBTL1TDP1TSHRCETPLTA4H
SCHEMBL11995970 1.00 L3MBTL1 (0.58) L3MBTL1TDP1TSHRCETPLTA4H
SCHEMBL21081916 1.00 L3MBTL1 (0.58) L3MBTL1TDP1TSHRCETPLTA4H
SCHEMBL2231686 1.00 L3MBTL1 (0.58) L3MBTL1TDP1TSHRCETPLTA4H

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122080034-A Polycyclic aromatic compound and organic electroluminescent element 2026-05-26 CN disclosed
CN-120157693-A Polycyclic aromatic compound and organic electroluminescent element 爱思开新材料捷恩智株式会社 2025-06-17 CN disclosed
CN-120118107-A Polycyclic aromatic compound and organic electroluminescent element 爱思开新材料捷恩智株式会社 2025-06-10 CN disclosed
CN-120040479-A Polycyclic aromatic compound and organic electroluminescent element 爱思开新材料捷恩智株式会社 2025-05-27 CN disclosed
CN-119823157-A Compound, material for organic element, ink composition, organic electroluminescent element, display device, and lighting device 学校法人关西学院 2025-04-15 CN disclosed
CN-119823158-A Compound, material for organic element, ink composition, organic electroluminescent element, display device, and lighting device 学校法人关西学院 2025-04-15 CN disclosed
CN-113454093-B Compound, material for organic element, ink composition, organic electroluminescent element, display device, and lighting device 学校法人关西学院 2025-02-07 CN disclosed
CN-119219683-A Polycyclic aromatic compound, polymer compound, material for organic device, organic electroluminescent element, display device, and lighting device 国立大学法人京都大学 2024-12-31 CN disclosed
CN-119219684-A Polycyclic aromatic compound, polymer compound, material for organic device, organic electroluminescent element, display device, and lighting device 国立大学法人京都大学 2024-12-31 CN disclosed
CN-119219682-A Polycyclic aromatic compound, polymer compound, material for organic device, organic electroluminescent element, display device, and lighting device 国立大学法人京都大学 2024-12-31 CN disclosed
US-6566538-B1 Preparation of 5-(aryloxymethyl)-g-butyrolactone derivatives MILLENNIUM PHARMACEUTICALS, INC. 2003-05-20 US disclosed
US-6462248-B1 THROUGH CONVERSION, ISOMERIZATION AND/OR ADSORPTIVE SEPARATION OF AROMATIC COMPOUNDS TORAY INDUSTRIES, INC. (JP) 2002-10-08 US disclosed
EP-1094805-A4 SUBSTITUTED OXYGEN ALICYCLIC COMPOUNDS, INCLUDING METHODS FOR SYNTHESIS THEREOF MILLENNIUM PHARM INC (US) 2002-08-28 EP disclosed
US-6433197-B1 REACTING ARYLHYDROXY COMPOUND AND AN EPOXY COMPOUND TO FORM AN EPOXY-ARYL ETHER; REACTING EPOXY-ARYL ETHER WITH ACTIVE METHYLENE COMPOUND TO FORM A LACTONE; REDUCING TO PROVIDE HYDROXY-SUBSTITUTED TETRAHYDROFURAN MILLENNIUM PHARMACEUTICALS, INC. 2002-08-13 US disclosed
US-20020040154-A1 Substituted oxygen alicyclic compounds, including methods for synthesis thereof MILLENNIUM PHARMACEUTICALS, INC. 2002-04-04 US disclosed
US-6306895-B1 PREPARATION OF CYCLIC OXYGEN COMPOUNDS, INCLUDING 2,5-DISUBSTITUTED TETAHYDROFURANS, 2,6-DISUBSTITUTED TETRAHYDROPYRANS, 2,7-DISUBSTITUTED OXEPANES AND 2,8-OXOCANES. THE INVENTION ALSO PROVIDES NEW CYCLIC OXYGEN COMPOUNDS AND MILLENIUM PHARMACEUTICALS, INC. 2001-10-23 US disclosed
EP-1094805-A1 SUBSTITUTED OXYGEN ALICYCLIC COMPOUNDS, INCLUDING METHODS FOR SYNTHESIS THEREOF Millennium Pharmaceuticals, Inc. (US) 2001-05-02 EP disclosed
EP-0985649-A2 Method for producing an aromatic compound having an alkyl group with at least three carbon atoms TORAY INDUSTRIES, INC. (JP) 2000-03-15 EP disclosed
WO-2000001381-A1 SUBSTITUTED OXYGEN ALICYCLIC COMPOUNDS, INCLUDING METHODS FOR SYNTHESIS THEREOF LEUKOSITE, INC. (US) 2000-01-13 WO disclosed
EP-0664316-A1 Polycarbonate composition having improved resistance to gamma-ray radiation TEIJIN LIMITED (JP) 1995-07-26 EP 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 (1 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-20020040154-A1 Substituted oxygen alicyclic compounds, including methods for synthesis thereof OXER1, COX6C, MT-CO2 L3MBTL1 4653/4885TDP1 3528/4885TSHR 4332/4885

“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.