SCHEMBL2237855

SCHEMBL2237855

COC(=O)c1cccc2cc(OC)ccc12

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MTNR1A P48039 3/20 0.56
PDE4B Q07343 1/20 0.56
MTNR1B P49286 2/20 0.53
KDM4E B2RXH2 2/20 0.51
CDC25B P30305 2/20 0.51
ALDH1A1 P00352 1/20 0.51
HPGD P15428 1/20 0.51
NPSR1 Q6W5P4 1/20 0.51
AURKA O14965 1/20 0.51
MET P08581 1/20 0.51
KDR P35968 1/20 0.51
TEK Q02763 1/20 0.51
AURKB Q96GD4 1/20 0.51
CNR2 P34972 2/20 0.50
PLA2G2A P14555 2/20 0.50
NR4A2 P43354 1/20 0.50
CYP1A2 P05177 1/20 0.50
CYP2D6 P10635 1/20 0.50
CYP2C9 P11712 1/20 0.50
CYP2C19 P33261 1/20 0.50

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
SCHEMBL9039778 0.89 MTNR1A (0.52) MTNR1APDE4BMTNR1BKDM4ECDC25B
SCHEMBL16755706 0.87 SLC6A2 (0.56) MTNR1APDE4BMTNR1BKDM4ECDC25B
SCHEMBL9747620 0.85 MTNR1A (0.55) MTNR1AMTNR1BKDM4ECDC25BALDH1A1
SCHEMBL2510203 0.85 CDC25B (0.64) MTNR1AMTNR1BKDM4ECDC25BALDH1A1
SCHEMBL31613816 0.85 CDC25B (0.64) MTNR1AMTNR1BKDM4ECDC25BALDH1A1
SCHEMBL14465841 0.85 PDE4B (0.52) MTNR1APDE4BMTNR1BKDM4ECDC25B
SCHEMBL11272281 0.85 CDC25B (0.60) MTNR1AMTNR1BKDM4ECDC25BALDH1A1
SCHEMBL8661902 0.84 MTNR1A (0.78) MTNR1AMTNR1BKDM4ECDC25BALDH1A1
SCHEMBL31613069 0.84 KDR (0.67) MTNR1AMTNR1BKDM4ECDC25BALDH1A1
SCHEMBL2509951 0.84 MTNR1A (0.52) MTNR1AMTNR1BCDC25BAURKAMET

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 64 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5424479-A Reacting aromatic hydroxycarboxylic acids in a mixture with methoxycarboxylic acids with dimethyl sulfate in water CASSELLA AG (DE) 1995-06-13 US claimed
US-5412150-A Bromination in presence of oxidizer which can oxidize by-product hydrogen bromide to bromine CASSELLA AG (DE) 1995-05-02 US claimed
US-4590290-A REACTING DIMETHYL SULFATE WITH G-HYDROXY-1-NAPHTHOIC ACID AMERICAN CYANAMID COMPANY (US) 1986-05-20 US claimed
JP-7069993-A None JP disclosed
WO-2025118034-A1 COMPOUNDS ACTIVE AT THE SEROTONERGIC 5-HT2A RECEPTOR Psylo Pty Ltd (AU) 2025-06-12 WO disclosed
EP-1639058-B1 PHOTOCHROMIC COMPOUNDS TRANSITIONS OPTICAL INC (US) 2020-10-21 EP disclosed
CN-105838349-B photochromic compounds 光学转变公司 2019-12-06 CN disclosed
EP-2357217-B9 PHOTOCHROMIC COMPOUNDS TRANSITIONS OPTICAL INC (US) 2019-03-13 EP disclosed
US-10227343-B2 Isoquiniline and napthalene-substituted compounds as mGluR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction VANDERBILT UNIVERSITY (US) 2019-03-12 US disclosed
EP-2357217-B1 PHOTOCHROMIC COMPOUNDS TRANSITIONS OPTICAL INC (US) 2018-10-31 EP disclosed
EP-2360224-B1 Photochromic compounds TRANSITIONS OPTICAL INC (US) 2018-10-17 EP disclosed
US-4568693-A ANTIDIATBETIC AGENTS AYERST, MCKENNA & HARRISON, INC. (CA) 1986-02-04 US disclosed
US-4562286-A Process for preparing methoxytrifluoromethylnaphthoic acid from dimethylnaphthalene OCCIDENTAL CHEMICAL CORPORATION (US) 1985-12-31 US disclosed
US-4560794-A Process for preparing methoxytrifluoromethylnaphthoic acid from methylnaphthoic acid OCCIDENTAL CHEMICAL CORPORATION (US) 1985-12-24 US disclosed
EP-0059596-B1 N-NAPHTHOYLGLYCINE DERIVATIVES AYERST, MCKENNA AND HARRISON INC. (CA) 1985-04-24 EP disclosed
US-4499310-A 5-Methyl-1-(trifluoromethyl)-2-naphthalenol, process for its preparation and ethers thereof AYERST, MCKENNA & HARRISON, INC. (CA) 1985-02-12 US disclosed
US-4439617-A TREATING DIABETES, ENZYME INHIBITOR AYERST, MCKENNA & HARRISON INC. (CA) 1984-03-27 US disclosed
US-4408077-A 6-(Lower alkoxy)-5-(trifluoromethyl)-1-naphthalenecarboxaldehydes AYERST, MCKEENA & HARRISON, INC. (CA) 1983-10-04 US disclosed
US-4391825-A ALDOSE REDUCTASE INHIBITORS, FOR TREATING DIABETIC COMPLICATIONS AYERST, MCKENNA & HARRISON INC. (CA) 1983-07-05 US disclosed
EP-0059596-A1 N-Naphthoylglycine derivatives AYERST, MCKENNA AND HARRISON INC. (CA) 1982-09-08 EP 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-10227343-B2 Isoquiniline and napthalene-substituted compounds as mGluR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction GRIA4, GRM4, GRIK4 MTNR1A 329/4885PDE4B 396/4885MTNR1B 304/4885

“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.