SCHEMBL14065415

SCHEMBL14065415

Cc1ccc2cccc(CCN)c2c1

nearest known ligand 0.53

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
CYP2A6 P11509 3/20 0.53
CYP1A2 P05177 3/20 0.53
TAAR1 Q96RJ0 4/20 0.52
HTR2A P28223 3/20 0.50
HTR1D P28221 1/20 0.50
MTNR1A P48039 7/20 0.42
MTNR1B P49286 4/20 0.41
TDP1 Q9NUW8 1/20 0.41
MAOA P21397 1/20 0.41
NQO2 P16083 1/20 0.40

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
SCHEMBL8033115 0.90 CYP2A6 (0.50) CYP2A6CYP1A2TAAR1HTR2AHTR1D
SCHEMBL15345396 0.85 CYP2A6 (0.57) CYP2A6CYP1A2TAAR1HTR2AHTR1D
SCHEMBL7838287 0.84 CYP2A6 (0.55) CYP2A6CYP1A2HTR2AMTNR1AMTNR1B
SCHEMBL19518945 0.80 CYP2A6 (0.47) CYP2A6CYP1A2HTR2AMTNR1AMTNR1B
SCHEMBL7752840 0.79 CYP2A6 (0.59) CYP2A6CYP1A2HTR2AMTNR1AMTNR1B
Ammonia Solution, Strong SCHEMBL27919153 0.79 CYP1A2 (0.50) CYP2A6CYP1A2HTR2AMTNR1A
SCHEMBL19392617 0.79 HTR1A (0.53) CYP2A6CYP1A2TAAR1HTR2AHTR1D
SCHEMBL17187823 0.79 MPO (0.50) CYP2A6CYP1A2TAAR1HTR2AMTNR1A
SCHEMBL7103988 0.79 MTNR1A (0.57) CYP1A2TAAR1HTR2AHTR1DMTNR1A
SCHEMBL17187827 0.79 HTR2A (0.50) CYP2A6TAAR1HTR2AMTNR1AMTNR1B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3016931-B1 A NOVEL PROCESS FOR THE PREPARATION OF TETRALIN AND NAPHTHALENE DERIVATIVES PHARMATHEN SA (GR) 2021-02-24 EP disclosed
EP-2921473-B1 1-CYAN-1-(7-METHOXYL-1-NAPHTYL) METHANOL ESTER COMPOUND AND PREPARATION METHOD AND USE THEREOF JIANGXI SYNERGY PHARMACEUTICAL CO LTD (CN) 2017-09-27 EP disclosed
US-RE46218-E1 Process for the synthesis of agomelatine LES LABORATOIRES SERVIER (FR) 2016-11-29 US disclosed
US-8853449-B2 Process for the synthesis of agomelatine LES LABORATOIRES SERVIER (FR) 2014-10-07 US disclosed
US-8779199-B2 Agomelatine intermediates and preparation method thereof LES LABORATOIRES SERVIER (FR) 2014-07-15 US disclosed
US-20130289307-A1 PROCESS FOR THE SYNTHESIS OF AGOMELATINE LES LABORATOIRES SERVIER (FR) 2013-10-31 US disclosed
US-20130267738-A1 AGOMELATINE INTERMEDIATES AND PREPARATION METHOD THEREOF LES LABORATORIES SERVIER (FR) 2013-10-10 US disclosed
EP-1564202-B1 Novel process for synthesizing and a novel crystal form of agomelatin as well as pharmaceutical preparations containing these SERVIER LAB (FR) 2008-09-10 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 (2 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-20130267738-A1 AGOMELATINE INTERMEDIATES AND PREPARATION METHOD THEREOF COMT, AGO2, MC5R CYP2A6 130/4885CYP1A2 40/4885TAAR1 296/4885
US-20130289307-A1 PROCESS FOR THE SYNTHESIS OF AGOMELATINE COMT, PNMT, TPH1 CYP2A6 90/4885CYP1A2 45/4885TAAR1 703/4885

“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.