SCHEMBL4670484

SCHEMBL4670484

CNc1ccc2cc(O)ccc2c1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
APP P05067 8/20 0.50
CYP1A2 P05177 2/20 0.50
CYP3A4 P08684 3/20 0.48
ALOX15 P16050 2/20 0.48
HIF1A Q16665 2/20 0.48
HSD17B10 Q99714 2/20 0.48
ALDH1A1 P00352 1/20 0.48
TP53 P04637 1/20 0.48
THRB P10828 1/20 0.48
HPGD P15428 1/20 0.48
CASP1 P29466 1/20 0.48
RECQL P46063 1/20 0.48
ESR1 P03372 4/20 0.46
ESR2 Q92731 4/20 0.46
TSHR P16473 1/20 0.46
TDP1 Q9NUW8 1/20 0.46
MAPT P10636 1/20 0.44
SULT1A1 P50225 1/20 0.44
ABL1 P00519 2/20 0.43
ABCB1 P08183 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
SCHEMBL27937998 0.93 APP (0.49) APPCYP1A2CYP3A4ALOX15HIF1A
SCHEMBL8156941 0.85 EGFR (0.48) APPCYP1A2CYP3A4ALOX15HIF1A
SCHEMBL4948579 0.84 SNCA (0.56) APPCYP3A4ALOX15HIF1AHSD17B10
Dimethylamine SCHEMBL28406614 0.83 CYP1A2 (0.62) CYP1A2CYP3A4ALOX15HIF1AHSD17B10
SCHEMBL28101043 0.83 CYP3A4 (0.45) APPCYP3A4ALOX15HIF1AHSD17B10
SCHEMBL25973229 0.78 EGFR (0.47) APPCYP1A2CYP3A4ALOX15HIF1A
SCHEMBL9702097 0.77 CYP3A4 (0.54) APPCYP1A2CYP3A4ALOX15HIF1A
SCHEMBL69484 0.77 CYP1A2 (0.77) CYP1A2CYP3A4ALOX15HIF1AHSD17B10
SCHEMBL627219 0.77 CYP1A2 (0.77) CYP1A2CYP3A4ALOX15HIF1AHSD17B10
SCHEMBL29364786 0.77 CYP1A2 (0.77) CYP1A2CYP3A4ALOX15HIF1AHSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-103298772-B Method for producing aromatic alcohol or heterocyclic aromatic alcohol MITSUBISHI GAS CHEMICAL CO 2015-06-24 CN disclosed
CN-103298772-A Method for producing aromatic alcohol or heterocyclic aromatic alcohol MITSUBISHI GAS CHEMICAL CO 2013-09-11 CN disclosed
EP-1397341-B1 6-(ARYL-AMIDO OR ARYL-AMIDOMETHYL)-NAPHTHALEN-2-YLOXY-ACIDIC DERIVATIVES AS INHIBITORS OF PLASMINOGEN ACTIVATOR INHIBITOR TYPE-1 (PAI-1) WYETH CORP (US) 2008-08-06 EP disclosed
EP-1397341-A1 6-(ARYL-AMIDO OR ARYL-AMIDOMETHYL)-NAPHTHALEN-2-YLOXY-ACIDIC DERIVATIVES AS INHIBITORS OF PLASMINOGEN ACTIVATOR INHIBITOR TYPE-1 (PAI-1) Wyeth (US) 2004-03-17 EP disclosed
US-6589970-B2 This invention provides novel compounds, pharmaceutical compositions and methods of treating thrombotic disorders in mammals, the compounds having the formula: WYETH 2003-07-08 US disclosed
US-20030045560-A1 6-(Aryl-amido or aryl-amidomethyl)-naphthalen-2-yloxy-acidic derivatives as inhibitors of plasminogen activator inhibitor type-1 (PAI-1) WYETH 2003-03-06 US disclosed
WO-2003000649-A1 6-(ARYL-AMIDO OR ARYL-AMIDOMETHYL)-NAPHTHALEN-2-YLOXY-ACIDIC DERIVATIVES AS INHIBITORS OF PLASMINOGEN ACTIVATOR INHIBITOR TYPE-1 (PAI-1) WYETH (US) 2003-01-03 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-20030045560-A1 6-(Aryl-amido or aryl-amidomethyl)-naphthalen-2-yloxy-acidic derivatives as inhibitors of plasminogen activator inhibitor type-1 (PAI-1) SERPINC1, F11, SERPINE1 APP 3225/4885CYP1A2 766/4885CYP3A4 1173/4885

“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.