SCHEMBL1723183

SCHEMBL1723183

FC(F)(F)c1cccc(CCCCl)c1

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TAAR1 Q96RJ0 1/20 0.62
MIF P14174 2/20 0.53
HDAC1 Q13547 1/20 0.52
HDAC8 Q9BY41 1/20 0.52
IDO1 P14902 2/20 0.51
HTR2C P28335 2/20 0.50
HTR2B P41595 2/20 0.50
HTR2A P28223 1/20 0.50
ACP3 P15309 1/20 0.49
CYP2D6 P10635 2/20 0.48
TP53 P04637 1/20 0.48
CYP1A2 P05177 1/20 0.48
CYP3A4 P08684 1/20 0.48
TSHR P16473 1/20 0.48
CYP2C19 P33261 1/20 0.48
SIGMAR1 Q99720 1/20 0.48
DAO P14920 1/20 0.48
MAOB P27338 4/20 0.47
DPP4 P27487 1/20 0.47
KDM4E B2RXH2 1/20 0.46

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
SCHEMBL3119866 0.89 TAAR1 (0.67) TAAR1MIFHDAC1HDAC8IDO1
SCHEMBL11383498 0.83 TAAR1 (0.65) TAAR1MIFHDAC1HDAC8IDO1
SCHEMBL27956999 0.82 TAAR1 (0.48) TAAR1HDAC1HDAC8HTR2CHTR2B
SCHEMBL1046263 0.81 TAAR1 (0.62) TAAR1MIFHDAC1HDAC8IDO1
SCHEMBL21913967 0.81 TAAR1 (0.62) TAAR1MIFHDAC1HDAC8IDO1
SCHEMBL386982 0.81 TAAR1 (0.62) TAAR1MIFHDAC1HDAC8IDO1
SCHEMBL81245 0.81 TAAR1 (0.62) TAAR1MIFHDAC1HDAC8IDO1
SCHEMBL2090576 0.81 TAAR1 (0.62) TAAR1MIFHDAC1HDAC8IDO1
SCHEMBL1045499 0.81 TAAR1 (0.62) TAAR1MIFHDAC1HDAC8IDO1
SCHEMBL4664652 0.81 TAAR1 (0.62) TAAR1MIFHDAC1HDAC8IDO1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8969623-B2 Method for the preparation of cinacalcet and intermediates and impurities thereof Amneal Pharmaceuticals, LLC (US) 2015-03-03 US claimed
EP-2406211-A2 A NEW METHOD FOR THE PREPARATION OF CINACALCET AND NEW INTERMEDIATES THEREOF Megafine Pharma (P) Ltd. (IN) 2012-01-18 EP claimed
WO-2010103531-A2 A NEW METHOD FOR THE PREPARATION OF CINACALCET AND NEW INTERMEDIATES THEREOF MEGAFINE PHARMA (P) LTD. (IN) 2010-09-16 WO claimed
EP-2406211-B1 A NEW METHOD FOR THE PREPARATION OF CINACALCET AND NEW INTERMEDIATES THEREOF MEGAFINE PHARMA P LTD (IN) 2018-06-27 EP disclosed
WO-2017033134-A1 ENZYMATIC PROCESS FOR THE FOR PREPARATION OF (R)-1-(1-NAPHTHYL) ETHYLAMINE, AN INTERMEDIATE OF CINACALCET HYDROCHLORIDE LUPIN LIMITED (IN) 2017-03-02 WO disclosed
US-9469593-B2 Process for preparing cinacalcet hydrochloride SHANGHAI JINGXIN BIOMEDICAL CO., LTD. (CN) 2016-10-18 US disclosed
US-20150152040-A1 Method For The Preparation Of Cinacalcet And Intermediates And Impurities Thereof AMNEAL PHARMACEUTICALS LLC (US) 2015-06-04 US disclosed
US-20150080608-A1 PROCESS FOR PREPARING CINACALCET HYDROCHLORIDE SHANGHAI JINGXIN BIOMEDICAL CO., LTD. (CN) 2015-03-19 US disclosed
US-8969623-B2 Method for the preparation of cinacalcet and intermediates and impurities thereof Amneal Pharmaceuticals, LLC (US) 2015-03-03 US disclosed
US-20140081048-A1 Method For The Preparation Of Cinacalcet And Intermediates And Impurities Thereof MEGAFINE PHARMA (P) LTD. (IN) 2014-03-20 US disclosed
US-8575395-B2 Method for the preparation of cinacalcet and intermediates and impurities thereof Amneal Pharmaceuticals, LLC (US) 2013-11-05 US disclosed
WO-2010103531-A2 A NEW METHOD FOR THE PREPARATION OF CINACALCET AND NEW INTERMEDIATES THEREOF MEGAFINE PHARMA (P) LTD. (IN) 2010-09-16 WO disclosed
EP-2017263-A1 HETEROARYLAMIDE LOWER CARBOXYLIC ACID DERIVATIVE Daiichi Sankyo Company, Limited (JP) 2009-01-21 EP disclosed
US-RE37303-E1 Imidazole compounds and their therapeutic applications INSTITUT NATIONAL DEL LA SANTE ET DE LA RECHERCHE MEDICALE (FR) 2001-07-31 US disclosed
US-5708171-A HISTAMINE H3-RECEPTOR ANTAGONIST INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (FR) 1998-01-13 US disclosed
US-5559113-A ANTAGONISTS TO HISTAMINE H3 RECEPTORS, SEDATIVES, ANTICONVULSANTS, ANTIULCER AGENTS INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE 1996-09-24 US disclosed
EP-0046590-B1 PHEN(ALK)OXY-SUBSTITUTED OXIRANE-CARBOXYLIC ACIDS, PROCESS FOR THEIR PREPARATION, THEIR USE AND DRUGS CONTAINING THEM Byk Gulden Lomberg Chemische Fabrik GmbH (DE) 1985-05-22 EP disclosed
US-4337267-A HYPOKETONEMIC, HYPOGLYCEMIC, ANTIDIABETIC BYK GULDEN LOMBERG CHEMISCHE FABRIK GMBH (DE) 1982-06-29 US disclosed
WO-1982000643-A1 SUBSTITUTED OXIRANECARBONIC ACIDS,PREPARATION AND PHARMACEUTICAL UTILISATION THEREOF BYK GULDEN LOMBERG CHEM FAB (DE) 1982-03-04 WO disclosed
EP-0046590-A2 Phen(alk)oxy-substituted oxirane-carboxylic acids, process for their preparation, their use and drugs containing them Byk Gulden Lomberg Chemische Fabrik GmbH (DE) 1982-03-03 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-20150080608-A1 PROCESS FOR PREPARING CINACALCET HYDROCHLORIDE OTC, SI, CMA1 TAAR1 2402/4885MIF 2444/4885HDAC1 3384/4885
US-20140081048-A1 Method For The Preparation Of Cinacalcet And Intermediates And Impurities Thereof CMA1, SI, ALDH1A1 TAAR1 1331/4885MIF 2084/4885HDAC1 1038/4885
US-20150152040-A1 Method For The Preparation Of Cinacalcet And Intermediates And Impurities Thereof CMA1, SI, ALDH1A1 TAAR1 1331/4885MIF 2084/4885HDAC1 1038/4885

“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.