Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CA1 | P00915 | 4/20 | 0.52 |
| ▸ | CA2 | P00918 | 4/20 | 0.52 |
| ▸ | CA7 | P43166 | 2/20 | 0.52 |
| ▸ | CA9 | Q16790 | 2/20 | 0.52 |
| ▸ | CA12 | O43570 | 1/20 | 0.52 |
| ▸ | CA14 | Q9ULX7 | 1/20 | 0.52 |
| ▸ | ACHE | P22303 | 1/20 | 0.44 |
| ▸ | LTA4H | P09960 | 1/20 | 0.43 |
| ▸ | ESR2 | Q92731 | 1/20 | 0.43 |
| ▸ | CES2 | O00748 | 1/20 | 0.43 |
| ▸ | CES1 | P23141 | 1/20 | 0.43 |
| ▸ | ENPP2 | Q13822 | 1/20 | 0.43 |
| ▸ | TDP1 | Q9NUW8 | 3/20 | 0.42 |
| ▸ | MAPK1 | P28482 | 2/20 | 0.42 |
| ▸ | GAA | P10253 | 2/20 | 0.41 |
| ▸ | MAPT | P10636 | 2/20 | 0.41 |
| ▸ | SMN1; SMN2 | Q16637 | 2/20 | 0.41 |
| ▸ | LMNA | P02545 | 1/20 | 0.41 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.41 |
| ▸ | CYP2C9 | P11712 | 1/20 | 0.41 |
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 | |
|---|---|---|---|---|
| SCHEMBL9006669 | 0.88 | NFE2L2 (0.58) | SMN1; SMN2LMNACYP1A2CYP2C9CYP2C19 | |
| SCHEMBL9006667 | 0.88 | NFE2L2 (0.58) | SMN1; SMN2LMNACYP1A2CYP2C9CYP2C19 | |
| SCHEMBL4530562 | 0.87 | RAB9A (0.35) | ESR2TDP1MAPTSMN1; SMN2LMNA | |
| SCHEMBL12834526 | 0.87 | HSD11B1 (0.43) | CA1CA2CA7CA9CA12 | |
| SCHEMBL13455409 | 0.81 | LMNA (0.55) | CA1CA2CES2CES1GAA | |
| SCHEMBL9909122 | 0.81 | LMNA (0.52) | ACHETDP1GAAMAPTLMNA | |
| SCHEMBL1505815 | 0.80 | KIF11 (0.39) | ESR2MAPK1GAASMN1; SMN2LMNA | |
| SCHEMBL12833375 | 0.80 | KIF11 (0.39) | ESR2MAPK1GAASMN1; SMN2LMNA | |
| SCHEMBL12833374 | 0.80 | KMT2A (0.43) | CA1CA2LTA4HESR2TDP1 | |
| SCHEMBL8934991 | 0.80 | KIF11 (0.39) | ESR2MAPK1GAASMN1; SMN2LMNA |
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 14 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-3613810-A1 | ARTICLES AND COMPOSITIONS COMPRISING HOST POLYMERS AND CHROMOPHORES AND METHODS OF PRODUCING THE SAME | General Dynamics Mission Systems, Inc. (US) | 2020-02-26 | — | — | EP | disclosed |
| US-20200048428-A1 | ARTICLES AND COMPOSITIONS COMPRISING HOST POLYMERS AND CHROMOPHORES AND METHODS OF PRODUCING THE SAME | GENERAL DYNAMICS MISSION SYSTEMS, INC. | 2020-02-13 | — | — | US | disclosed |
| US-9370750-B2 | Polyolefin-PFCB ionomer | GM Global Technology Operations LLC (US) | 2016-06-21 | — | — | US | disclosed |
| US-20140065514-A1 | Polyolefin-PFCB Ionomer | GM Global Technology Operations LLC (US) | 2014-03-06 | — | — | US | disclosed |
| US-20110245429-A1 | Cross Linked Organic Conductive Layer | GOUGH, NEIL (GB) | 2011-10-06 | — | — | US | disclosed |
| EP-0428709-B1 | REACTIVE COMPOUNDS CONTAINING PERFLUOROVINYL GROUPS | DOW CHEMICAL CO (US) | 1995-05-24 | — | — | EP | disclosed |
| US-5210265-A | Multistage reaction to form monomers for polymers such as polyesters by dimerization of trifluorovinyl compounds by dehalogenation and cyclization | THE DOW CHEMICAL COMPANY (US) | 1993-05-11 | — | — | US | disclosed |
| US-5198513-A | Compounds for engineering thermoplastics or dimers | THE DOW CHEMICAL COMPANY (US) | 1993-03-30 | — | — | US | disclosed |
| US-5037919-A | Endcapper for polyesters, polycarbonates, polyamides and polyethers | THE DOW CHEMICAL COMPANY (US) | 1991-08-06 | — | — | US | disclosed |
| EP-0429618-A1 | REACTIVE COMPOUNDS CONTAINING PERFLUOROCYCLOBUTANE RINGS | THE DOW CHEMICAL COMPANY (US) | 1991-06-05 | — | — | EP | disclosed |
| US-5021602-A | Monomers for condensation polymers | THE DOW CHEMICAL COMPANY (US) | 1991-06-04 | — | — | US | disclosed |
| EP-0428709-A1 | REACTIVE COMPOUNDS CONTAINING PERFLUOROVINYL GROUPS. | DOW CHEMICAL CO (US) | 1991-05-29 | — | — | EP | disclosed |
| WO-1990015044-A2 | REACTIVE COMPOUNDS CONTAINING PERFLUOROCYCLOBUTANE RINGS | THE DOW CHEMICAL COMPANY (US) | 1990-12-13 | — | — | WO | disclosed |
| WO-1990015042-A2 | REACTIVE COMPOUNDS CONTAINING PERFLUOROVINYL GROUPS | THE DOW CHEMICAL COMPANY (US) | 1990-12-13 | — | — | 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.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20110245429-A1 | Cross Linked Organic Conductive Layer | GJB2, GJA1, KCNH3 | CA1 2557/4885CA2 2055/4885CA7 1930/4885 |
“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.