Ivabradine

Ivabradine

SCHEMBL333200

COc1cc2c(cc1OC)CC(=O)N(CCCN(C)CC1Cc3cc(OC)c(OC)cc31)CC2

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

HCN4

The experimentally established mechanism targets of Ivabradine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
HCN4 known ✓ Q9Y3Q4 3/20 1.00
CHRM2 P08172 1/20 1.00
HTR1A P08908 1/20 1.00
SLC6A4 P31645 1/20 1.00
DRD3 P35462 1/20 1.00
KCNH2 Q12809 1/20 1.00
MAPT P10636 1/20 0.64
CYP3A4 P08684 1/20 0.63
ALOX15 P16050 1/20 0.63
GAA P10253 1/20 0.47
SMN1; SMN2 Q16637 1/20 0.47
ABCB1 P08183 1/20 0.39
KCNN2 Q9H2S1 4/20 0.39
KCNN3 Q9UGI6 4/20 0.39
BRD4 O60885 2/20 0.39
KCNN1 Q92952 2/20 0.39

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
Ivabradine SCHEMBL333201 1.00 HCN4 (1.00) HCN4CHRM2HTR1ASLC6A4DRD3
Ivabradine SCHEMBL23472 1.00 HCN4 (1.00) HCN4CHRM2HTR1ASLC6A4DRD3
Ivabradine SCHEMBL29687794 1.00 HCN4 (1.00) HCN4CHRM2HTR1ASLC6A4DRD3
Ivabradine SCHEMBL29387763 1.00 HCN4 (1.00) HCN4CHRM2HTR1ASLC6A4DRD3
Ivabradine SCHEMBL5163239 1.00 HCN4 (1.00) HCN4CHRM2HTR1ASLC6A4DRD3
Ivabradine SCHEMBL2589476 0.99 HCN4 (0.98) HCN4CHRM2HTR1ASLC6A4DRD3
Ivabradine SCHEMBL29465192 0.99 HCN4 (0.98) HCN4CHRM2HTR1ASLC6A4DRD3
Ivabradine SCHEMBL1032017 0.99 HCN4 (0.98) HCN4CHRM2HTR1ASLC6A4DRD3
Ivabradine SCHEMBL2821678 0.99 HCN4 (0.98) HCN4CHRM2HTR1ASLC6A4DRD3
Ivabradine SCHEMBL29561458 0.99 HCN4 (0.98) HCN4CHRM2HTR1ASLC6A4DRD3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2566850-A1 INDUSTRIAL PROCESS FOR THE SYNTHESIS OF IVABRADINE SALTS Richter Gedeon Nyrt. (HU) 2013-03-13 EP claimed
WO-2011138625-A1 INDUSTRIAL PROCESS FOR THE SYNTHESIS OF IVABRADINE SALTS RICHTER GEDEON NYRT. (HU) 2011-11-10 WO claimed
US-20230235290-A1 RECOMBINANT CARDIOMYOCYTES AND CARDIOMYOCYTE CELL LINES EXPRESSING HERG UNIV ALBERTA (CA) 2023-07-27 US disclosed
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
WO-2019202611-A1 AN IMPROVED PROCESS FOR THE SYNTHESIS OF IVABRADINE AND ITS PHARMACEUTICALLY ACCEPTABLE SALTS METROCHEM API PVT (IN) 2019-10-24 WO disclosed
EP-2566850-B1 INDUSTRIAL PROCESS FOR THE SYNTHESIS OF IVABRADINE HYDROBROMIDE SALT RICHTER GEDEON NYRT (HU) 2018-04-11 EP disclosed
US-9809554-B2 Process for preparing ivabradine OLON S.P.A. (IT) 2017-11-07 US disclosed
WO-2017138017-A1 PROCESS FOR THE PREPARATION OF BENZAZEPINE-2-ONE DERIVATIVE IND-SWIFT LABORATORIES LIMITED (IN) 2017-08-17 WO disclosed
EP-3156399-A1 POLYMORPHIC FORMS OF IVABRADINE HYDROCHLORIDE Cadila Healthcare Limited (IN) 2017-04-19 EP disclosed
US-20170100408-A1 IVABRADINE ADSORBATES LABORATORIO CHIMICO INTERNAZIONALE S.P.A. (IT) 2017-04-13 US disclosed
EP-2999693-B1 A PROCESS FOR PREPARING IVABRADINE OLON SPA (IT) 2017-04-12 EP disclosed
EP-2241554-A1 Process for the synthesis of ivabradine and its pharmaceutically acceptable acid addition salts Les Laboratoires Servier (FR) 2010-10-20 EP disclosed
EP-2241554-A1 Process for the synthesis of ivabradine and its pharmaceutically acceptable acid addition salts Les Laboratoires Servier (FR) 2010-10-20 EP disclosed
WO-2010112704-A1 NOVEL METHOD FOR THE SYNTHESIS OF IVABRADINE AND THE ADDITION SALTS THEREOF WITH A PHARMACEUTICALLY ACCEPTABLE ACID LES LABORATOIRES SERVIER (FR) 2010-10-07 WO disclosed
WO-2010112705-A1 NOVEL METHOD FOR THE SYNTHESIS OF IVABRADINE AND THE ADDITION SALTS THEREOF WITH A PHARMACEUTICALLY ACCEPTABLE ACID LES LABORATOIRES SERVIER (FR) 2010-10-07 WO disclosed
US-20100249398-A1 Process for the synthesis of ivabradine and addition salts thereof with a pharmaceutically acceptable acid LES LABORATOIRES SERVIER (FR) 2010-09-30 US disclosed
US-20100249397-A1 Process for the synthesis of ivabradine and addition salts thereof with a pharmaceutically acceptable acid LES LABORATOIRES SERVIER (FR) 2010-09-30 US 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-7361651-B2 γd-crystalline form of ivabradine hydrochloride, a process for its preparation and pharmaceutical compositions containing it LES LABORATOIRES SERVIER (FR) 2008-04-22 US disclosed
US-5296482-A (Benzocycloalkyl) alkylamines ADIR ET COMPAGNIE (FR) 1994-03-22 US 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-20230235290-A1 RECOMBINANT CARDIOMYOCYTES AND CARDIOMYOCYTE CELL LINES EXPRESSING HERG TNNI3, MYLK2, TNNT2 HCN4 55/4885CHRM2 3700/4885HTR1A 3633/4885
US-20100249398-A1 Process for the synthesis of ivabradine and addition salts thereof with a pharmaceutically acceptable acid CYP4F2, CYP2F1, CYP2D6 HCN4 37/4885CHRM2 2611/4885HTR1A 1678/4885
US-20170100408-A1 IVABRADINE ADSORBATES NISCH, SLC5A2, CYP4F2 HCN4 10/4885CHRM2 101/4885HTR1A 1142/4885
US-20100160628-A1 Process for the synthesis of ivabradine and addition salts thereof with a pharmaceutically acceptable acid CYP4F2, CYP2F1, CYP2D6 HCN4 37/4885CHRM2 2611/4885HTR1A 1678/4885
US-20100249397-A1 Process for the synthesis of ivabradine and addition salts thereof with a pharmaceutically acceptable acid CYP4F2, CYP2F1, CYP2D6 HCN4 37/4885CHRM2 2611/4885HTR1A 1678/4885

“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.