SCHEMBL497345

SCHEMBL497345

CCN(CC)c1cc(-c2ccc([N+](=O)[O-])cc2)c2cc(Cl)ccc2n1

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTT P42858 4/20 0.49
SMN1; SMN2 Q16637 3/20 0.49
ALDH1A1 P00352 2/20 0.49
MAPT P10636 2/20 0.49
KDM4E B2RXH2 2/20 0.49
NLRP3 Q96P20 1/20 0.49
RXFP1 Q9HBX9 1/20 0.49
NPC1 O15118 2/20 0.47
PGR P06401 1/20 0.45
ELANE P08246 1/20 0.43
NPBWR1 P48145 4/20 0.43
KMT2A Q03164 3/20 0.43
MEN1 O00255 2/20 0.43
RAB9A P51151 2/20 0.43
LMNA P02545 1/20 0.43
HPGD P15428 1/20 0.43
APEX1 P27695 1/20 0.41
TP53 P04637 1/20 0.40
PSD A5PKW4 1/20 0.40
AURKA O14965 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
SCHEMBL497373 0.87 ALDH1A1 (0.48) HTTSMN1; SMN2ALDH1A1MAPTKDM4E
SCHEMBL497205 0.82 AURKA (0.43) SMN1; SMN2ALDH1A1MAPTKDM4ENPC1
SCHEMBL497346 0.80 MAPT (0.49) HTTSMN1; SMN2ALDH1A1MAPTKDM4E
SCHEMBL4658394 0.79 PGR (0.42) HTTSMN1; SMN2ALDH1A1MAPTRXFP1
SCHEMBL497310 0.75 KDM4E (0.52) HTTSMN1; SMN2ALDH1A1MAPTKDM4E
SCHEMBL628610 0.73 KMT2A (0.46) HTTALDH1A1MAPTKDM4ENPC1
SCHEMBL4657403 0.68 MEN1 (0.40) ALDH1A1RXFP1PGRELANEKMT2A
SCHEMBL5911053 0.67 TP53 (0.43) HTTALDH1A1MAPTKDM4ERXFP1
SCHEMBL11822863 0.66 ELANE (0.64) SMN1; SMN2ALDH1A1MAPTNPC1ELANE
SCHEMBL16573977 0.66 ALDH1A1 (0.50) HTTSMN1; SMN2ALDH1A1MAPTKDM4E

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 HTT 1048/4885SMN1; SMN2 655/4885ALDH1A1 662/4885

“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.