Predicted protein targets (top 3)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | EPHX1 | P07099 | 1/20 | 0.31 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.31 |
| ▸ | L3MBTL1 | Q9Y468 | 1/20 | 0.31 |
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 | |
|---|---|---|---|---|
| Sulfuric Acid SCHEMBL16910001 | 0.83 | TP53 (0.39) | — | |
| SCHEMBL5059323 | 0.80 | TP53 (0.33) | — | |
| SCHEMBL28476257 | 0.78 | — | — | |
| Trifluoromethanesulfonic Acid SCHEMBL27506904 | 0.78 | NPSR1 (0.35) | EPHX1ALDH1A1L3MBTL1 | |
| Trifluoromethanesulfonic Acid SCHEMBL611061 | 0.78 | ALDH1A1 (0.35) | EPHX1ALDH1A1L3MBTL1 | |
| Trifluoromethanesulfonic Acid SCHEMBL610462 | 0.78 | NPSR1 (0.35) | EPHX1ALDH1A1L3MBTL1 | |
| Trifluoroacetic Acid SCHEMBL5360197 | 0.77 | CHRM2 (0.34) | ALDH1A1L3MBTL1 | |
| Trifluoromethanesulfonic Acid SCHEMBL2285727 | 0.77 | ALDH1A1 (0.41) | EPHX1ALDH1A1L3MBTL1 | |
| Trifluoromethanesulfonic Acid SCHEMBL5551212 | 0.76 | ALDH1A1 (0.33) | EPHX1ALDH1A1L3MBTL1 | |
| Trifluoromethanesulfonic Acid SCHEMBL609215 | 0.76 | ALDH1A1 (0.33) | EPHX1ALDH1A1L3MBTL1 |
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.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-12305004-B2 | Cationically polymerizable composition | JNC CORPORATION (JP) | 2025-05-20 | — | — | US | disclosed |
| US-20230333474-A1 | RESIST UNDERLAYER FILM-FORMING COMPOSITION COMPRISING FLUOROALKYL GROUP-CONTAINING ORGANIC ACID OR SALT THEREOF | NISSAN CHEMICAL CORPORATION (JP) | 2023-10-19 | — | — | US | disclosed |
| CN-116235112-A | Composition for forming resist underlayer film comprising fluoroalkyl group-containing organic acid or salt thereof | 日产化学株式会社 | 2023-06-06 | — | — | CN | disclosed |
| WO-2022065374-A1 | RESIST UNDERLAYER FILM-FORMING COMPOSITION COMPRISING FLUOROALKYL GROUP-CONTAINING ORGANIC ACID OR SALT THEREOF | 日産化学株式会社 | 2022-03-31 | — | — | WO | disclosed |
| CN-107089915-B | Low-temperature liquid-phase preparation method of acrylic ester | 中国科学院过程工程研究所 | 2020-04-28 | — | — | CN | disclosed |
| EP-3327472-B1 | HOLOGRAPHIC OPTICAL ELEMENT AND PRODUCTION METHOD THEREFOR | KONICA MINOLTA INC (JP) | 2019-10-30 | — | — | EP | disclosed |
| US-20190185711-A1 | EPOXY RESIN COMPOSITION AND CURED RESIN FILM WITH LOW CURING SHRINKAGE AND EXCELLENT ADHESION | JNC CORPORATION (JP) | 2019-06-20 | — | — | US | disclosed |
| US-10308665-B2 | Method for the synthesis of rapamycin derivatives | SYNBIAS PHARMA AG (CH) | 2019-06-04 | — | — | US | disclosed |
| EP-3313853-B1 | METHOD FOR THE SYNTHESIS OF RAPAMYCIN DERIVATIVES | SYNBIAS PHARMA AG (CH) | 2019-05-08 | — | — | EP | disclosed |
| CN-109642069-A | Epoxy resin composition and low-curing-shrinkage resin cured film having excellent adhesion | 捷恩智株式会社 | 2019-04-16 | — | — | CN | disclosed |
| CN-1053627-A | WATER SOLUBLE CRAYON COMPOSITION | UNION CARBIDE CHEM PLASTIC (US) | 1991-08-07 | — | — | CN | disclosed |
| EP-0435386-A1 | Water soluble crayon compositions | UNION CARBIDE CHEMICALS AND PLASTICS COMPANY, INC. (US) | 1991-07-03 | — | — | EP | disclosed |
| US-4786705-A | HIGH SOLIDS COATING COMPOSITIONS | UNION CARBIDE CORPORATION (US) | 1988-11-22 | — | — | US | disclosed |
| US-4725653-A | Low viscosity adducts of a polycaprolactone polyol and a polyepoxide | UNION CARBIDE CORPORATION (US) | 1988-02-16 | — | — | US | disclosed |
| US-4707535-A | USING A FLUORINATED ALKYLSULFONIC ACID CATALYST | UNION CARBIDE CORPORATION (US) | 1987-11-17 | — | — | US | disclosed |
| US-4629779-A | Low viscosity adducts of a polycaprolactone polyol and a polyepoxide | UNION CARBIDE CORPORATION (US) | 1986-12-16 | — | — | US | disclosed |
| US-4599401-A | POLYETHERS, POLYESTERS, POLYLACTONES | UNION CARBIDE CORPORATION (US) | 1986-07-08 | — | — | US | disclosed |
| EP-0143120-A2 | Low viscosity adducts of poly (active hydrogen) organic compounds and a polyepoxide | UNION CARBIDE CORPORATION (US) | 1985-06-05 | — | — | EP | disclosed |
| EP-0143121-A2 | Low viscosity adducts of a polycaprolactone polyol and a polyepoxide | UNION CARBIDE CORPORATION (US) | 1985-06-05 | — | — | EP | disclosed |
| EP-0139042-A2 | Low viscosity adducts of a poly(active hydrogen) organic compound and a polyepoxide | UNION CARBIDE CORPORATION (US) | 1985-05-02 | — | — | 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.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-10308665-B2 | Method for the synthesis of rapamycin derivatives | RICTOR, MTOR, MLST8 | EPHX1 3750/4885ALDH1A1 4436/4885L3MBTL1 3100/4885 |
“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.