Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | LMNA | P02545 | 3/20 | 0.59 |
| ▸ | ALDH1A1 | P00352 | 3/20 | 0.59 |
| ▸ | HPGD | P15428 | 2/20 | 0.59 |
| ▸ | HSD17B10 | Q99714 | 2/20 | 0.59 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.59 |
| ▸ | GAA | P10253 | 1/20 | 0.59 |
| ▸ | CYP1A2 | P05177 | 7/20 | 0.52 |
| ▸ | CYP2A6 | P11509 | 5/20 | 0.50 |
| ▸ | TDP1 | Q9NUW8 | 3/20 | 0.43 |
| ▸ | ESR1 | P03372 | 3/20 | 0.39 |
| ▸ | ESR2 | Q92731 | 3/20 | 0.39 |
| ▸ | BCL2L1 | Q07817 | 1/20 | 0.36 |
| ▸ | MCL1 | Q07820 | 1/20 | 0.36 |
| ▸ | PDE3B | Q13370 | 1/20 | 0.36 |
| ▸ | PDE3A | Q14432 | 1/20 | 0.36 |
| ▸ | NCK1 | P16333 | 1/20 | 0.35 |
| ▸ | BACE1 | P56817 | 1/20 | 0.35 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.34 |
| ▸ | TSHR | P16473 | 1/20 | 0.34 |
| ▸ | L3MBTL1 | Q9Y468 | 1/20 | 0.34 |
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL14444114 | 0.83 | CYP1A2 (0.50) | LMNAALDH1A1HPGDHSD17B10KDM4E | |
| SCHEMBL11057827 | 0.83 | POLB (0.46) | LMNAALDH1A1HPGDHSD17B10KDM4E | |
| SCHEMBL13288386 | 0.79 | NCEH1 (0.49) | LMNAALDH1A1HPGDHSD17B10KDM4E | |
| SCHEMBL27286459 | 0.79 | CYP1A2 (0.46) | LMNAALDH1A1HPGDHSD17B10KDM4E | |
| SCHEMBL15976515 | 0.79 | ESR1 (0.58) | LMNAALDH1A1HPGDHSD17B10KDM4E | |
| SCHEMBL607927 | 0.78 | CYP1A2 (0.71) | LMNAALDH1A1HPGDHSD17B10KDM4E | |
| SCHEMBL599166 | 0.77 | ALDH1A1 (0.63) | LMNAALDH1A1HPGDHSD17B10KDM4E | |
| SCHEMBL806512 | 0.76 | CYP19A1 (0.52) | LMNAALDH1A1HPGDHSD17B10KDM4E | |
| SCHEMBL597341 | 0.76 | CYP1A2 (0.67) | LMNAALDH1A1HPGDHSD17B10KDM4E | |
| SCHEMBL2723074 | 0.76 | CYP2A6 (0.52) | LMNAALDH1A1HPGDHSD17B10KDM4E |
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 31 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| WO-2021141507-A1 | AROMATIC SULPHONAMIDES DERIVATIVES THAT INHIBITS PDI A3, THEIR SYNTHESIS AND USE | Uniwersytet Jagielloński (PL) | 2021-07-15 | — | — | WO | disclosed |
| EP-3453697-A1 | COMPOUND HAVING NAPHTHALENE RING, LIQUID CRYSTAL COMPOSITION, AND LIQUID CRYSTAL DISPLAY ELEMENT | JNC Corporation (JP) | 2019-03-13 | — | — | EP | disclosed |
| EP-2302015-B1 | OPTICALLY ISOTROPIC LIQUID CRYSTALLINE MEDIUM, AND OPTICAL ELEMENT | JNC CORP (JP) | 2016-10-05 | — | — | EP | disclosed |
| US-8475887-B2 | Optically isotropic liquid crystal medium, and optical device | JNC CORPORATION (JP) | 2013-07-02 | — | — | US | disclosed |
| US-8475887-B2 | Optically isotropic liquid crystal medium, and optical device | JNC CORPORATION (JP) | 2013-07-02 | — | — | US | disclosed |
| EP-2098583-B1 | Optically isotropic liquid crystal medium and optical device | JNC CORP (JP) | 2012-03-21 | — | — | EP | disclosed |
| EP-2302015-A1 | OPTICALLY ISOTROPIC LIQUID CRYSTALLINE MEDIUM, AND OPTICAL ELEMENT | Chisso Corporation (JP) | 2011-03-30 | — | — | EP | disclosed |
| US-20110069245-A1 | OPTICALLY ISOTROPIC LIQUID CRYSTALLINE MEDIUM, AND OPTICAL ELEMENT | CHISSO PETROCHEMICAL CORPORATION (JP) | 2011-03-24 | — | — | US | disclosed |
| US-20110069245-A1 | OPTICALLY ISOTROPIC LIQUID CRYSTALLINE MEDIUM, AND OPTICAL ELEMENT | CHISSO PETROCHEMICAL CORPORATION (JP) | 2011-03-24 | — | — | US | disclosed |
| EP-2028252-B1 | Liquid crystal compound having chloronaphthalene moiety, liquid crystal composition, and optical device | CHISSO CORP (JP) | 2010-10-27 | — | — | EP | disclosed |
| EP-2028252-A1 | Liquid crystal compound having chloronaphthalene moiety, liquid crystal composition, and optical device | Chisso Corporation (JP) | 2009-02-25 | — | — | EP | disclosed |
| EP-1762605-A1 | Naphthalene compound with terminal hydrogen, liquid crystal composition including the compound, and LCD device including the liquid crystal composition | Chisso Petrochemial Corporation (JP) | 2007-03-14 | — | — | EP | disclosed |
| US-20070051919-A1 | NAPHTHALENE COMPOUND WITH TERMINAL HYDROGEN, LIQUID CRYSTAL COMPOSITION INCLUDING THE COMPOUND, AND LCD DEVICE INCLUDING THE LIQUID CRYSTAL COMPOSITION | CHISSO PETROCHEMICAL CORPORATION (JP) | 2007-03-08 | — | — | US | disclosed |
| US-20070051919-A1 | NAPHTHALENE COMPOUND WITH TERMINAL HYDROGEN, LIQUID CRYSTAL COMPOSITION INCLUDING THE COMPOUND, AND LCD DEVICE INCLUDING THE LIQUID CRYSTAL COMPOSITION | CHISSO PETROCHEMICAL CORPORATION (JP) | 2007-03-08 | — | — | US | disclosed |
| US-4161607-A | Thermally stable, rigid bisphenols | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 1979-07-17 | — | — | US | disclosed |
| US-4107444-A | INTERMEDIATES FOR POLYESTERS | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 1978-08-15 | — | — | US | disclosed |
| US-4096341-A | MONOMERS FOR POLYESTERS | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 1978-06-20 | — | — | US | disclosed |
| US-4085091-A | Thermally stable, rigid polyesters from thermally stable, rigid dibasic acids and aromatic dihydroxy compounds | E. I. DUPONT DE NEMOURS AND COMPANY (US) | 1978-04-18 | — | — | US | disclosed |
| US-4065432-A | Thermally stable, rigid polyesters from aromatic dibasic acids and thermally stable, rigid bisphenols | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 1977-12-27 | — | — | US | disclosed |
| US-4065431-A | Thermally stable, rigid polyesters from aromatic dibasic acids and thermally stable, rigid diols | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 1977-12-27 | — | — | US | 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.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20070051919-A1 | NAPHTHALENE COMPOUND WITH TERMINAL HYDROGEN, LIQUID CRYSTAL COMPOSITION INCLUDING THE COMPOUND, AND LCD DEVICE INCLUDING THE LIQUID CRYSTAL COMPOSITION | LEF1, CFD, FOXO1 | LMNA 941/4885ALDH1A1 2679/4885HPGD 1344/4885 |
“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.