SCHEMBL4171815

SCHEMBL4171815

CNc1ncnc2ccc(-c3cccc(CN(Cc4ccccn4)C(=O)c4ccc(OC)c(OC)c4)c3)cc12

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 12/20 0.47
CYP3A4 P08684 12/20 0.47
HSD17B10 Q99714 11/20 0.47
CYP1A2 P05177 11/20 0.47
CYP2C19 P33261 10/20 0.47
CYP2D6 P10635 10/20 0.47
MAPK1 P28482 10/20 0.47
USP2 O75604 8/20 0.47
CLK4 Q9HAZ1 8/20 0.47
TSHR P16473 4/20 0.47
LMNA P02545 9/20 0.46
CYP2C9 P11712 4/20 0.46
HPGD P15428 4/20 0.45
KDM4E B2RXH2 3/20 0.45
TDP1 Q9NUW8 1/20 0.45
RAF1 P04049 3/20 0.45
MAP2K1 Q02750 2/20 0.45
ALOX12 P18054 1/20 0.43
MEN1 O00255 2/20 0.43
KMT2A Q03164 2/20 0.43

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
SCHEMBL4180400 0.90 CYP1A2 (0.52) ALDH1A1CYP3A4HSD17B10CYP1A2CYP2C19
SCHEMBL4184475 0.88 CYP1A2 (0.48) ALDH1A1CYP3A4HSD17B10CYP1A2CYP2C19
SCHEMBL4183059 0.87 CLK4 (0.45) ALDH1A1CYP3A4HSD17B10CYP1A2CYP2C19
SCHEMBL4176479 0.86 MAP4K4 (0.50) ALDH1A1CYP3A4HSD17B10CYP1A2CYP2C19
SCHEMBL4184452 0.85 CYP1A2 (0.47) ALDH1A1CYP3A4HSD17B10CYP1A2CYP2C19
SCHEMBL4178480 0.85 CYP3A4 (0.52) ALDH1A1CYP3A4HSD17B10CYP1A2CYP2C19
SCHEMBL4174209 0.85 CYP1A2 (0.44) ALDH1A1CYP3A4HSD17B10CYP1A2CYP2C19
SCHEMBL4180095 0.84 MAP4K4 (0.48) ALDH1A1CYP3A4HSD17B10CYP1A2CYP2C19
SCHEMBL4178303 0.84 CYP3A4 (0.48) ALDH1A1CYP3A4HSD17B10CYP1A2CYP2C19
SCHEMBL4177316 0.83 ALDH1A1 (0.49) ALDH1A1CYP3A4HSD17B10CYP1A2CYP2C19

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
US-20090069320-A1 Substituted 4-Amino-Quinazoline Compounds with Metabotropic Glutamate Receptor Regulating Activity and Uses Thereof GRUENENTHAL GMBH (DE) 2009-03-12 US claimed
EP-1996562-A1 SUBSTITUTED 4-AMINO-QUINAZOLINE DERIVATIVES AS REGULATORS OF METABOTROPIC GLUTAMATE RECEPTORS AND THEIR USE FOR PRODUCING DRUGS Grünenthal GmbH (DE) 2008-12-03 EP claimed
WO-2007104560-A1 SUBSTITUTED 4-AMINO-QUINAZOLINE DERIVATIVES AS REGULATORS OF METABOTROPIC GLUTAMATE RECEPTORS AND THEIR USE FOR PRODUCING DRUGS Grünenthal GmbH (DE) 2007-09-20 WO claimed
US-20090069320-A1 Substituted 4-Amino-Quinazoline Compounds with Metabotropic Glutamate Receptor Regulating Activity and Uses Thereof GRUENENTHAL GMBH (DE) 2009-03-12 US disclosed
EP-1996562-A1 SUBSTITUTED 4-AMINO-QUINAZOLINE DERIVATIVES AS REGULATORS OF METABOTROPIC GLUTAMATE RECEPTORS AND THEIR USE FOR PRODUCING DRUGS Grünenthal GmbH (DE) 2008-12-03 EP disclosed
WO-2007104560-A1 SUBSTITUTED 4-AMINO-QUINAZOLINE DERIVATIVES AS REGULATORS OF METABOTROPIC GLUTAMATE RECEPTORS AND THEIR USE FOR PRODUCING DRUGS Grünenthal GmbH (DE) 2007-09-20 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-20090069320-A1 Substituted 4-Amino-Quinazoline Compounds with Metabotropic Glutamate Receptor Regulating Activity and Uses Thereof GRM1, GRIN1, GRM2 ALDH1A1 2269/4885CYP3A4 4173/4885HSD17B10 3489/4885

“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.