Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ALDH1A1 | P00352 | 6/20 | 0.41 |
| ▸ | ALOX15 | P16050 | 2/20 | 0.41 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.41 |
| ▸ | DAO | P14920 | 1/20 | 0.41 |
| ▸ | CA1 | P00915 | 5/20 | 0.37 |
| ▸ | CA2 | P00918 | 5/20 | 0.37 |
| ▸ | CA12 | O43570 | 4/20 | 0.37 |
| ▸ | CA7 | P43166 | 4/20 | 0.37 |
| ▸ | CA9 | Q16790 | 4/20 | 0.37 |
| ▸ | CA14 | Q9ULX7 | 4/20 | 0.37 |
| ▸ | TSHR | P16473 | 3/20 | 0.37 |
| ▸ | PTGS2 | P35354 | 2/20 | 0.37 |
| ▸ | ALOX5 | P09917 | 1/20 | 0.37 |
| ▸ | HSD17B10 | Q99714 | 3/20 | 0.37 |
| ▸ | CDC25A | P30304 | 1/20 | 0.37 |
| ▸ | CDC25B | P30305 | 1/20 | 0.37 |
| ▸ | KMT2A | Q03164 | 4/20 | 0.36 |
| ▸ | KDM4E | B2RXH2 | 3/20 | 0.36 |
| ▸ | SMN1; SMN2 | Q16637 | 2/20 | 0.36 |
| ▸ | CASP1 | P29466 | 2/20 | 0.36 |
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 | |
|---|---|---|---|---|
| SCHEMBL9698398 | 0.83 | ALDH1A1 (0.48) | ALDH1A1DAOCA1CA2CA12 | |
| SCHEMBL9699600 | 0.83 | ALDH1A1 (0.48) | ALDH1A1DAOCA1CA2CA12 | |
| SCHEMBL27839223 | 0.81 | ALDH1A1 (0.35) | ALDH1A1ALOX15CYP1A2DAOCA1 | |
| SCHEMBL9479377 | 0.81 | SMN1; SMN2 (0.35) | ALDH1A1ALOX15CYP1A2DAOCA1 | |
| SCHEMBL7016790 | 0.78 | HSD17B10 (0.37) | ALDH1A1ALOX15CYP1A2CA1CA2 | |
| Pyromellitic Acid SCHEMBL22443 | 0.77 | ALDH1A1 (0.53) | ALDH1A1ALOX15CYP1A2DAOCA1 | |
| Pyromellitic Acid SCHEMBL22127 | 0.77 | ALDH1A1 (0.53) | ALDH1A1ALOX15CYP1A2DAOCA1 | |
| SCHEMBL14413336 | 0.75 | ALDH1A1 (0.45) | ALDH1A1ALOX15CYP1A2DAOCA1 | |
| Pyromellitic Acid SCHEMBL11316481 | 0.74 | ALDH1A1 (0.50) | ALDH1A1ALOX15CYP1A2DAOCA1 | |
| Pyromellitic Acid SCHEMBL692530 | 0.74 | ALDH1A1 (0.50) | ALDH1A1ALOX15CYP1A2DAOCA1 |
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 15 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-0314766-B1 | METHOD FOR MAKING THIANTHRENE DIANHYDRIDE AND POLYIMIDES OBTAINED THEREFROM | GEN ELECTRIC (US) | 1993-11-03 | — | — | EP | disclosed |
| US-5185451-A | Bis-imides of dioxydiphthalic acid | OCCIDENTAL CHEMICAL CORPORATION (US) | 1993-02-09 | — | — | US | disclosed |
| US-5166404-A | Dioxydiphthalic acid esters | OCCIDENTAL CHEMICAL CORPORATION (US) | 1992-11-24 | — | — | US | disclosed |
| US-5089631-A | Intermediate for polyimides | OCCIDENTAL CHEMICAL CORPORATION (US) | 1992-02-18 | — | — | US | disclosed |
| US-5003086-A | Etherification, dehalogenation, cyclization of dihalophthalic anhydride to form monomers for polyimides | OCCIDENTAL CHEMICAL CORPORATION (US) | 1991-03-26 | — | — | US | disclosed |
| EP-0398206-A1 | Dioxydiphthalic anhydride | OCCIDENTAL CHEMICAL CORPORATION (US) | 1990-11-22 | — | — | EP | disclosed |
| US-4943642-A | POLYMER INTERMEDIATES, CURING AGENTS | OCCIDENTAL CHEMICAL CORPORATION (US) | 1990-07-24 | — | — | US | disclosed |
| US-4864015-A | OXIDATION RESISTANT COMPOSITES | GENERAL ELECTRIC COMPANY (US) | 1989-09-05 | — | — | US | disclosed |
| US-4864015-A | OXIDATION RESISTANT COMPOSITES | GENERAL ELECTRIC COMPANY (US) | 1989-09-05 | — | — | US | disclosed |
| EP-0314766-A1 | METHOD FOR MAKING THIANTHRENE DIANHYDRIDE AND POLYIMIDES OBTAINED THEREFROM. | GEN ELECTRIC (US) | 1989-05-10 | — | — | EP | disclosed |
| EP-0314766-A1 | METHOD FOR MAKING THIANTHRENE DIANHYDRIDE AND POLYIMIDES OBTAINED THEREFROM. | GEN ELECTRIC (US) | 1989-05-10 | — | — | EP | disclosed |
| US-4814466-A | FORMING A BISIMIDE FROM AN ALKALI SULFIDE AND AN N-ORGANO-4,5-DIHALOPHTHALIMIDE; HYDROLYSIS AND DEHYDRATION | GENERAL ELECTRIC COMPANY (US) | 1989-03-21 | — | — | US | disclosed |
| US-4814466-A | FORMING A BISIMIDE FROM AN ALKALI SULFIDE AND AN N-ORGANO-4,5-DIHALOPHTHALIMIDE; HYDROLYSIS AND DEHYDRATION | GENERAL ELECTRIC COMPANY (US) | 1989-03-21 | — | — | US | disclosed |
| WO-1988009353-A1 | METHOD FOR MAKING THIANTHRENE DIANHYDRIDE AND POLYIMIDES OBTAINED THEREFROM | GENERAL ELECTRIC COMPANY (US) | 1988-12-01 | — | — | WO | disclosed |
| WO-1988009353-A1 | METHOD FOR MAKING THIANTHRENE DIANHYDRIDE AND POLYIMIDES OBTAINED THEREFROM | GENERAL ELECTRIC COMPANY (US) | 1988-12-01 | — | — | WO | disclosed |