SCHEMBL333767

SCHEMBL333767

COc1cc2c(cc1OC)CC(=O)N(CCC=O)CC2

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GAA P10253 1/20 0.61
SMN1; SMN2 Q16637 1/20 0.61
HCN4 Q9Y3Q4 2/20 0.55
MAPT P10636 1/20 0.55
SLC6A4 P31645 2/20 0.54
DRD3 P35462 2/20 0.54
CYP3A4 P08684 1/20 0.54
ALOX15 P16050 1/20 0.54
CHRM2 P08172 1/20 0.54
HTR1A P08908 1/20 0.54
KCNH2 Q12809 1/20 0.54
PDE4D Q08499 3/20 0.47
DRD1 P21728 2/20 0.46
DRD4 P21917 2/20 0.46
DRD5 P21918 2/20 0.46
MAOA P21397 2/20 0.44
MAOB P27338 2/20 0.44
MEN1 O00255 1/20 0.43
KMT2A Q03164 1/20 0.43
LMNA P02545 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
SCHEMBL15047160 0.92 HCN4 (0.58) GAASMN1; SMN2HCN4MAPTSLC6A4
SCHEMBL14696925 0.86 GAA (0.68) GAASMN1; SMN2HCN4MAPTSLC6A4
SCHEMBL14685767 0.85 GAA (0.66) GAASMN1; SMN2HCN4MAPTSLC6A4
SCHEMBL9665585 0.84 MEN1 (0.61) GAASMN1; SMN2MAPTDRD3HTR1A
SCHEMBL22738846 0.83 GAA (0.64) GAASMN1; SMN2HCN4MAPTSLC6A4
SCHEMBL20261656 0.83 GAA (0.64) GAASMN1; SMN2HCN4MAPTSLC6A4
SCHEMBL15980993 0.82 GAA (0.62) GAASMN1; SMN2HCN4MAPTSLC6A4
SCHEMBL8277872 0.82 ACHE (0.43) GAASMN1; SMN2HCN4MAPTSLC6A4
SCHEMBL10667822 0.81 GAA (0.53) GAASMN1; SMN2HCN4MAPTSLC6A4
SCHEMBL9032662 0.81 GAA (0.61) GAASMN1; SMN2HCN4MAPTSLC6A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2135861-B2 Process for the synthesis of the 7,8-dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one, and its application to the synthesis of ivabradine as well as its addition salts with a pharmaceutically acceptable acid SERVIER LAB (FR) 2020-12-16 EP disclosed
EP-2607353-B1 New method for synthesising ivabradine and its added salts with a pharmaceutically acceptable acid. SERVIER LAB (FR) 2014-08-27 EP disclosed
US-8513410-B2 Process for the synthesis of ivabradine and addition salts thereof with a pharmaceutically acceptable acid LES LABORATOIRES SERVIER (FR) 2013-08-20 US disclosed
US-8507668-B2 Process for the synthesis of ivabradine and addition salts thereof with a pharmaceutically acceptable acid LES LABORATOIRES SERVIER (FR) 2013-08-13 US disclosed
US-8507668-B2 Process for the synthesis of ivabradine and addition salts thereof with a pharmaceutically acceptable acid LES LABORATOIRES SERVIER (FR) 2013-08-13 US disclosed
WO-2013093220-A1 METHOD FOR SYNTHESISING IVABRADINE AND THE PHARMACEUTICALLY ACCEPTABLE ACID ADDITION SALTS THEREOF LES LABORATOIRES SERVIER (FR) 2013-06-27 WO disclosed
EP-2607354-A1 Process for the synthesis of ivabradine and addition salts thereof and its pharmaceutically acceptable acid Les Laboratoires Servier (FR) 2013-06-26 EP disclosed
EP-2607353-A1 New method for synthesising ivabradine and its added salts with a pharmaceutically acceptable acid. Les Laboratoires Servier (FR) 2013-06-26 EP disclosed
US-20130158257-A1 PROCESS FOR THE SYNTHESIS OF IVABRADINE AND ADDITION SALTS THEREOF WITH A PHARMACEUTICALLY ACCEPTABLE ACID LES LABORATOIRES SERVIER (FR) 2013-06-20 US disclosed
US-20130158257-A1 PROCESS FOR THE SYNTHESIS OF IVABRADINE AND ADDITION SALTS THEREOF WITH A PHARMACEUTICALLY ACCEPTABLE ACID LES LABORATOIRES SERVIER (FR) 2013-06-20 US disclosed
US-20110294999-A1 PROCESS FOR THE SYNTHESIS OF IVABRADINE AND ADDITION SALTS THEREOF WITH A PHARMACEUTICALLY ACCEPTABLE ACID LES LABORATOIRES SERVIER (FR) 2011-12-01 US disclosed
WO-2010089475-A1 NOVEL METHOD FOR THE SYNTHESIS OF IVABRADINE AND THE PHARMACEUTICALLY ACCEPTABLE ACID ADDITION SALTS THEREOF LES LABORATOIRES SERVIER (FR) 2010-08-12 WO disclosed
WO-2010072930-A1 NOVEL METHOD FOR THE SYNTHESIS OF IVABRADINE LES LABORATOIRES SERVIER (FR) 2010-07-01 WO disclosed
EP-2202225-A1 New method for synthesising ivabradine and its added salts with a pharmaceutically acceptable acid. Les Laboratoires Servier (FR) 2010-06-30 EP disclosed
US-20100160628-A1 Process for the synthesis of ivabradine and addition salts thereof with a pharmaceutically acceptable acid LES LABORATOIRES SERVIER (FR) 2010-06-24 US disclosed
US-4737495-A ANTIALLERGENS, ANTISCHEMIC, HYPOTENSIVE AGENTS DR. KARL TOMAE, GMBH (DE) 1988-04-12 US disclosed
EP-0204349-A2 Heteroaromatic amine derivatives, medicaments containing them and process for their preparation Dr. Karl Thomae GmbH (DE) 1986-12-10 EP disclosed
EP-0065229-B1 BENZAZEPINES, PROCESS FOR THEIR PREPARATION AND THEIR APPLICATION AS PHARMACEUTICAL PREPARATIONS Dr. Karl Thomae GmbH (DE) 1985-08-07 EP disclosed
US-4490369-A HYPOTENSIVE, BRRADYCARDIAL DR. KARL THOMAE GESELLSCHAFT MIT BESCHRANKTER HAFTUNG (DE) 1984-12-25 US disclosed
EP-0065229-A1 Benzazepines, process for their preparation and their application as pharmaceutical preparations Dr. Karl Thomae GmbH (DE) 1982-11-24 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 (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-20110294999-A1 PROCESS FOR THE SYNTHESIS OF IVABRADINE AND ADDITION SALTS THEREOF WITH A PHARMACEUTICALLY ACCEPTABLE ACID CYP4F2, CYP2F1, CYP2D6 GAA 885/4885SMN1; SMN2 2145/4885HCN4 37/4885
US-20100160628-A1 Process for the synthesis of ivabradine and addition salts thereof with a pharmaceutically acceptable acid CYP4F2, CYP2F1, CYP2D6 GAA 885/4885SMN1; SMN2 2145/4885HCN4 37/4885
US-20130158257-A1 PROCESS FOR THE SYNTHESIS OF IVABRADINE AND ADDITION SALTS THEREOF WITH A PHARMACEUTICALLY ACCEPTABLE ACID CYP4F2, CYP2F1, CYP2D6 GAA 995/4885SMN1; SMN2 2482/4885HCN4 16/4885

“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.