SCHEMBL2846166

SCHEMBL2846166

COc1ccc(CCOCCc2ccc(OC)cc2)cc1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TAAR1 Q96RJ0 1/20 0.61
MAOB P27338 2/20 0.55
CALM1 P0DP23 2/20 0.55
IDO1 P14902 2/20 0.54
AOC3 Q16853 2/20 0.53
SIGMAR1 Q99720 1/20 0.53
CA12 O43570 1/20 0.52
CA1 P00915 1/20 0.52
CA2 P00918 1/20 0.52
CA7 P43166 1/20 0.52
CA9 Q16790 1/20 0.52
CA14 Q9ULX7 1/20 0.52
F2RL1 P55085 1/20 0.52
TUBB4A P04350 1/20 0.52
TUBB P07437 1/20 0.52
TUBA3C P0DPH7 1/20 0.52
TUBA1B P68363 1/20 0.52
TUBA4A P68366 1/20 0.52
TUBB4B P68371 1/20 0.52
TUBB3 Q13509 1/20 0.52

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
SCHEMBL17230504 0.92 TAAR1 (0.53) TAAR1MAOBCALM1IDO1AOC3
SCHEMBL4027553 0.90 TAAR1 (0.52) TAAR1MAOBCALM1IDO1AOC3
SCHEMBL6123807 0.90 TAAR1 (0.52) TAAR1MAOBCALM1IDO1AOC3
SCHEMBL3163847 0.90 TAAR1 (0.52) TAAR1MAOBCALM1IDO1AOC3
SCHEMBL9021362 0.90 TAAR1 (0.52) TAAR1MAOBCALM1IDO1AOC3
SCHEMBL10793001 0.89 TAAR1 (0.55) TAAR1MAOBCALM1IDO1AOC3
SCHEMBL24175834 0.88 TAAR1 (0.50) TAAR1MAOBCALM1IDO1AOC3
SCHEMBL6541809 0.87 TAAR1 (0.53) TAAR1MAOBCALM1IDO1AOC3
SCHEMBL27756949 0.87 TAAR1 (0.53) TAAR1MAOBCALM1IDO1AOC3
SCHEMBL9021185 0.87 TAAR1 (0.53) TAAR1MAOBCALM1IDO1AOC3

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 18 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118354670-A Biodegradable insect trap 丹尼米尔知识产权有限责任公司 2024-07-16 CN disclosed
US-9242955-B2 Synthesis of cyclic carbonates UNIVERSITY OF YORK (GB) 2016-01-26 US disclosed
CN-101679343-B Synthesis of cyclic carbonates in the presence of dimeric aluminium (salen) catalysts UNIV NEWCASTLE 2014-06-18 CN disclosed
EP-2146977-B1 SYNTHESIS OF CYCLIC CARBONATES IN THE PRESENCE OF DIMERIC ALUMINIUM (SALEN) CATALYSTS UNIV NEWCASTLE (GB) 2012-11-14 EP disclosed
US-20100130752-A1 SYNTHESIS OF CYCLIC CARBONATES UNIVERSITY OF NEWCASTLE UPON TYNE (GB) 2010-05-27 US disclosed
CN-101679343-A Synthesis of cyclic carbonates in the presence of dimeric aluminium (salen) catalysts UNIV NEWCASTLE 2010-03-24 CN disclosed
EP-2146977-A1 SYNTHESIS OF CYCLIC CARBONATES IN THE PRESENCE OF DIMERIC ALUMINIUM (SALEN) CATALYSTS University Of Newcastle-Upon Tyne (GB) 2010-01-27 EP disclosed
WO-2009059941-A1 METHOD FOR TEH REGIOSELECTIVE ALKOXYALKYLATION OF SUBSTITUTED BENZENES BASF SE (DE) 2009-05-14 WO disclosed
WO-2008132474-A1 SYNTHESIS OF CYCLIC CARBONATES IN THE PRESENCE OF DIMERIC ALUMINIUM (SALEN) CATALYSTS UNIVERSITY OF NEWCASTLE UPON TYNE (GB) 2008-11-06 WO disclosed
EP-0965658-A1 Process for electrochemical preparation of organic compounds using solid polymer electrolyte technology at temperatures near the boiling point of the electrolyzed solution BASF AKTIENGESELLSCHAFT (DE) 1999-12-22 EP disclosed
EP-0965660-A1 Process for producing methoxylated benzyl, benzal or benzoyl compounds by anodic methoxylation BASF AKTIENGESELLSCHAFT (DE) 1999-12-22 EP disclosed
EP-0638665-B1 Process for the preparation of benzaldehyde dialkyl acetals BASF AG (DE) 1996-10-30 EP disclosed
EP-0638665-A1 Process for the preparation of benzaldehyde dialkyl acetals BASF Aktiengesellschaft (DE) 1995-02-15 EP disclosed
EP-0393667-B1 PROCESS FOR THE PRODUCTION OF BENZYL METHYL ESTERS BASF Aktiengesellschaft (DE) 1993-06-23 EP disclosed
EP-0393667-A1 Process for the production of benzyl methyl esters BASF Aktiengesellschaft (DE) 1990-10-24 EP disclosed
EP-0059373-B1 PROCESS FOR THE PREPARATION OF BENZYL ALCOHOLS BASF Aktiengesellschaft (DE) 1984-05-23 EP disclosed
EP-0054699-B1 METHOD FOR THE CATALYTIC HYDROGENOLYSIS OF PARA-SUBSTITUTED BENZALDEHYDE-DIMETHYL ACETALS INTO THE CORRESPONDING BENZYLMETHYL ETHERS HOECHST AKTIENGESELLSCHAFT (DE) 1984-03-14 EP disclosed
EP-0054699-A2 Method for the catalytic hydrogenolysis of para-substituted benzaldehyde-dimethyl acetals into the corresponding benzylmethyl ethers HOECHST AKTIENGESELLSCHAFT (DE) 1982-06-30 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-20100130752-A1 SYNTHESIS OF CYCLIC CARBONATES CA2, SCO2, CA7 TAAR1 3397/4885MAOB 1272/4885CALM1 521/4885

“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.