SCHEMBL1763291

SCHEMBL1763291

c1ccc([C@@H]2CC[C@@H](c3ccccc3)N2)cc1

nearest known ligand 0.54

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.50
KMT2A Q03164 1/20 0.50
SLC18A3 Q16572 1/20 0.46
SIGMAR1 Q99720 1/20 0.46
PRCP P42785 1/20 0.45
KCNH2 Q12809 1/20 0.43
SCN3A Q9NY46 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.42
DPP4 P27487 1/20 0.41

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
SCHEMBL23393883 1.00 MEN1 (0.50) MEN1KMT2ASLC18A3SIGMAR1PRCP
SCHEMBL1763293 1.00 MEN1 (0.50) MEN1KMT2ASLC18A3SIGMAR1PRCP
SCHEMBL13363848 1.00 MEN1 (0.50) MEN1KMT2ASLC18A3SIGMAR1PRCP
SCHEMBL1763221 1.00 MEN1 (0.50) MEN1KMT2ASLC18A3SIGMAR1PRCP
SCHEMBL13436114 1.00 MEN1 (0.50) MEN1KMT2ASLC18A3SIGMAR1PRCP
SCHEMBL14065400 0.90 MEN1 (0.47) MEN1KMT2ASLC18A3SIGMAR1PRCP
SCHEMBL4865057 0.90 MEN1 (0.47) MEN1KMT2ASLC18A3SIGMAR1PRCP
SCHEMBL6924404 0.90 MEN1 (0.47) MEN1KMT2ASLC18A3SIGMAR1PRCP
SCHEMBL11468464 0.87 MEN1 (0.45) MEN1KMT2ASLC18A3SIGMAR1PRCP
SCHEMBL19283462 0.86 MEN1 (0.64) MEN1KMT2APRCPKCNH2SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1845078-B1 PROCESS FOR PRODUCING LARGE CYCLIC KETONE AND INTERMEDIATE THEREFOR TAKASAGO PERFUMERY CO LTD (JP) 2017-06-07 EP disclosed
US-9233920-B2 Process for the preparation of dihydropyrrole derivatives SYNGENTA PARTICIPATIONS AG (CH) 2016-01-12 US disclosed
US-9233920-B2 Process for the preparation of dihydropyrrole derivatives SYNGENTA PARTICIPATIONS AG (CH) 2016-01-12 US disclosed
EP-2580211-B1 PROCESS FOR THE PREPARATION OF DIHYDROPYRROLE DERIVATIVES SYNGENTA PARTICIPATIONS AG (CH) 2015-08-19 EP disclosed
US-8759541-B2 Chiral acyclic diaminocarbene ligands, precursors therefore and their use in organic synthesis reactions THADANI AVINASH N (CA) 2014-06-24 US disclosed
US-20130237583-A1 PROCESS FOR THE PREPARATION OF DIHYDROPYRROLE DERIVATIVES SYNGENTA CROP PROTECTION LLC (US) 2013-09-12 US disclosed
US-20130237583-A1 PROCESS FOR THE PREPARATION OF DIHYDROPYRROLE DERIVATIVES SYNGENTA CROP PROTECTION LLC (US) 2013-09-12 US disclosed
WO-2011154555-A1 PROCESS FOR THE PREPARATION OF DIHYDROPYRROLE DERIVATIVES SYNGENTA PARTICIPATIONS AG (CH) 2011-12-15 WO disclosed
US-20110118475-A1 CHIRAL ACYCLIC DIAMINOCARBENE LIGANDS, PRECURSORS THEREFORE AND THEIR USE IN ORGANIC SYNTHESIS REACTIONS THADANI AVINASH N 2011-05-19 US disclosed
US-7683191-B2 Organic salts and method for producing chiral organic compounds Studiangesellschaft Kohle mbH (DE) 2010-03-23 US disclosed
US-7683191-B2 Organic salts and method for producing chiral organic compounds Studiangesellschaft Kohle mbH (DE) 2010-03-23 US disclosed
WO-2010003226-A1 CHIRAL ACYCLIC DIAMINOCARBENE LIGANDS, PRECURSORS THEREFORE AND THEIR USE IN ORGANIC SYNTHESIS REACTIONS THADANI AVINASH N (CA) 2010-01-14 WO disclosed
US-20090281346-A1 METHOD FOR THE PRODUCTION OF CHIRAL AMINOCARBONYL COMPOUNDS STUDIENGESELLSCHAFT KOHLE MBH (DE) 2009-11-12 US disclosed
US-20090281346-A1 METHOD FOR THE PRODUCTION OF CHIRAL AMINOCARBONYL COMPOUNDS STUDIENGESELLSCHAFT KOHLE MBH (DE) 2009-11-12 US disclosed
US-20090030216-A1 ORGANIC SALTS AND METHOD FOR PRODUCING CHIRAL ORGANIC COMPOUNDS STUDIENGESELLSCHAFT KOHLE MBH (DE) 2009-01-29 US disclosed
US-20090030216-A1 ORGANIC SALTS AND METHOD FOR PRODUCING CHIRAL ORGANIC COMPOUNDS STUDIENGESELLSCHAFT KOHLE MBH (DE) 2009-01-29 US disclosed
US-7479574-B2 Method of producing macrocyclic ketone, and intermediate thereof TAKASAGO INTERNATIONAL CORPORATION (JP) 2009-01-20 US disclosed
WO-2008009275-A1 METHOD FOR THE PRODUCTION OF CHIRAL AMINOCARBONYL COMPOUNDS STUDIENGESELLSCHAFT KOHLE MBH (DE) 2008-01-24 WO disclosed
US-20070287870-A1 Method of Producing Macrocyclic Ketone, and Intermediate Thereof TAKASAGO INTERNATIONAL CORPORATION (JP) 2007-12-13 US disclosed
EP-1845078-A1 PROCESS FOR PRODUCING LARGE CYCLIC KETONE AND INTERMEDIATE THEREFOR Takasago International Corporation (JP) 2007-10-17 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 (5 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-20070287870-A1 Method of Producing Macrocyclic Ketone, and Intermediate Thereof MSMO1, CYP17A1, DNMT1 MEN1 57/4885KMT2A 553/4885SLC18A3 598/4885
US-20090030216-A1 ORGANIC SALTS AND METHOD FOR PRODUCING CHIRAL ORGANIC COMPOUNDS ICMT, OTC, PNPO MEN1 2400/4885KMT2A 2501/4885SLC18A3 1574/4885
US-20110118475-A1 CHIRAL ACYCLIC DIAMINOCARBENE LIGANDS, PRECURSORS THEREFORE AND THEIR USE IN ORGANIC SYNTHESIS REACTIONS AOC1, ODC1, AMD1 MEN1 267/4885KMT2A 1109/4885SLC18A3 911/4885
US-20090281346-A1 METHOD FOR THE PRODUCTION OF CHIRAL AMINOCARBONYL COMPOUNDS AOC3, AOC2, AOC1 MEN1 2676/4885KMT2A 4040/4885SLC18A3 3666/4885
US-20130237583-A1 PROCESS FOR THE PREPARATION OF DIHYDROPYRROLE DERIVATIVES CYP1A1, CYP1B1, CYP1A2 MEN1 1740/4885KMT2A 2160/4885SLC18A3 4313/4885

“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.