SCHEMBL497346

SCHEMBL497346

CCNc1cc(-c2ccc([N+](=O)[O-])cc2)c2cc(Cl)ccc2n1

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 4/20 0.49
HTT P42858 3/20 0.49
SMN1; SMN2 Q16637 3/20 0.49
ALDH1A1 P00352 3/20 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
HRH4 Q9H3N8 1/20 0.43
ELANE P08246 1/20 0.43
AGPAT2 O15120 1/20 0.42
APEX1 P27695 1/20 0.41
MEN1 O00255 2/20 0.40
KMT2A Q03164 2/20 0.40
LMNA P02545 2/20 0.40
NPBWR1 P48145 2/20 0.40
HPGD P15428 1/20 0.40
RAB9A P51151 1/20 0.40
MMP13 P45452 1/20 0.40
NPSR1 Q6W5P4 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
SCHEMBL497310 0.86 KDM4E (0.52) MAPTHTTSMN1; SMN2ALDH1A1KDM4E
SCHEMBL9881006 0.83 MAPK1 (0.53) MAPTHTTSMN1; SMN2ALDH1A1KDM4E
SCHEMBL4658374 0.82 ALDH1A1 (0.44) MAPTSMN1; SMN2ALDH1A1KDM4ENPC1
SCHEMBL497345 0.80 HTT (0.49) MAPTHTTSMN1; SMN2ALDH1A1KDM4E
SCHEMBL497373 0.76 ALDH1A1 (0.48) MAPTHTTSMN1; SMN2ALDH1A1KDM4E
SCHEMBL9881008 0.71 ALDH1A1 (0.47) MAPTSMN1; SMN2ALDH1A1KDM4ERXFP1
SCHEMBL7097532 0.70 HTR1A (0.50) MAPTHTTSMN1; SMN2ALDH1A1KDM4E
SCHEMBL497654 0.69 MAPK1 (0.52) MAPTALDH1A1KDM4EELANEMEN1
SCHEMBL9881003 0.69 ALDH1A1 (0.44) MAPTSMN1; SMN2ALDH1A1KDM4EMEN1
SCHEMBL7694158 0.69 KMT2A (0.55) MAPTHTTALDH1A1KDM4EHRH4

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 MAPT 4685/4885HTT 1048/4885SMN1; SMN2 655/4885

“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.