SCHEMBL497205

SCHEMBL497205

CCN(CC)c1cc(-c2ccc(N)cc2)c2cc(Cl)ccc2n1

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AURKA O14965 1/20 0.43
AURKB Q96GD4 1/20 0.43
KDM4E B2RXH2 3/20 0.41
KMT2A Q03164 2/20 0.41
MAPK1 P28482 2/20 0.41
HSP90AB1 P08238 1/20 0.41
PDE10A Q9Y233 1/20 0.40
APP P05067 2/20 0.39
ELANE P08246 1/20 0.38
ALDH1A1 P00352 2/20 0.37
HPGD P15428 2/20 0.37
HSD17B10 Q99714 2/20 0.37
TP53 P04637 2/20 0.37
MAPT P10636 2/20 0.37
MEN1 O00255 1/20 0.37
NPC1 O15118 1/20 0.37
GAA P10253 1/20 0.37
NFKB1 P19838 1/20 0.37
SNCA P37840 1/20 0.37
RAB9A P51151 1/20 0.37

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
SCHEMBL497345 0.82 HTT (0.49) AURKAAURKBKDM4EKMT2AELANE
SCHEMBL497514 0.78 MAPK1 (0.49) AURKAAURKBKDM4EKMT2AMAPK1
SCHEMBL4658374 0.77 ALDH1A1 (0.44) AURKAAURKBKDM4EKMT2AMAPK1
SCHEMBL4658376 0.76 NR4A2 (0.42) KDM4EKMT2AMAPK1HSP90AB1ALDH1A1
Tert-Butyl Formate SCHEMBL28112713 0.71 FABP3 (0.44) AURKAAURKBKDM4EMAPK1PDE10A
SCHEMBL497373 0.69 ALDH1A1 (0.48) KDM4EKMT2AELANEALDH1A1HPGD
SCHEMBL23674305 0.68 LTB4R (0.48) AURKAAURKBKDM4EMAPK1PDE10A
SCHEMBL497480 0.67 MAPK1 (0.61) AURKAAURKBKDM4EKMT2AMAPK1
SCHEMBL8381530 0.66 ACP1 (0.42) KDM4EMAPK1PDE10AALDH1A1GAA
SCHEMBL8375411 0.66 RXFP1 (0.47) KDM4EKMT2AMAPK1ALDH1A1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1999112-B1 SUBSTITUTED 2-AMINO-4-PHENYL-DIHYDROQUINOLINES, METHOD FOR THE PRODUCTION THEREOF, USE THEREOF AS MEDICAMENTS, AND MEDICAMENTS CONTAINING THEM SANOFI SA (FR) 2015-04-22 EP disclosed
US-8106204-B2 Substituted 2-amino-4-phenyldihydroquinolines, processes for their preparation, pharmaceutical compositions and methods for their use SANOFI-AVENTIS (FR) 2012-01-31 US disclosed
US-20090118329-A1 Novel Substituted 2-Amino-4-Phenyldihydroquinolines, Processes for their Preparation, Pharmaceutical Compositions and Methods for Their Use SANOFI-AVENTIS (FR) 2009-05-07 US disclosed
CN-101395137-A Substituted 2-amino-4-phenyl-dhydroquinolines, method for the production thereof, use thereof as medicaments, and medicaments containing them SANOFI AVENTIS (FR) 2009-03-25 CN disclosed
EP-1999112-A2 SUBSTITUTED 2-AMINO-4-PHENYL-D HYDROQUINOLINES, METHOD FOR THE PRODUCTION THEREOF, USE THEREOF AS MEDICAMENTS, AND MEDICAMENTS CONTAINING THEM Sanofi-Aventis (FR) 2008-12-10 EP disclosed
WO-2007107246-A2 SUBSTITUTED 2-AMINO-4-PHENYL-DιHYDROQUINOLINES, METHOD FOR THE PRODUCTION THEREOF, USE THEREOF AS MEDICAMENTS, AND MEDICAMENTS CONTAINING THEM SANOFI-AVENTIS (DE) 2007-09-27 WO 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 (1 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-20090118329-A1 Novel Substituted 2-Amino-4-Phenyldihydroquinolines, Processes for their Preparation, Pharmaceutical Compositions and Methods for Their Use NHERF1, SLC10A1, SLC9A3 AURKA 3081/4885AURKB 3165/4885KDM4E 2068/4885

“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.