Predicted protein targets (top 9)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | PDE4A | P27815 | 1/20 | 0.54 |
| ▸ | LMNA | P02545 | 2/20 | 0.52 |
| ▸ | L3MBTL1 | Q9Y468 | 1/20 | 0.52 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.50 |
| ▸ | KDM4E | B2RXH2 | 2/20 | 0.43 |
| ▸ | USP2 | O75604 | 1/20 | 0.40 |
| ▸ | SLCO1B1 | Q9Y6L6 | 1/20 | 0.40 |
| ▸ | TOP1 | P11387 | 1/20 | 0.32 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.30 |
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 | |
|---|---|---|---|---|
| SCHEMBL8718317 | 1.00 | PDE4A (0.54) | PDE4ALMNAL3MBTL1TDP1KDM4E | |
| SCHEMBL8722914 | 1.00 | PDE4A (0.54) | PDE4ALMNAL3MBTL1TDP1KDM4E | |
| SCHEMBL4001566 | 1.00 | PDE4A (0.54) | PDE4ALMNAL3MBTL1TDP1KDM4E | |
| SCHEMBL27579718 | 1.00 | PDE4A (0.54) | PDE4ALMNAL3MBTL1TDP1KDM4E | |
| SCHEMBL28131184 | 0.98 | TDP1 (0.55) | PDE4ALMNAL3MBTL1TDP1KDM4E | |
| SCHEMBL4744871 | 0.93 | LMNA (0.48) | PDE4ALMNAL3MBTL1TDP1KDM4E | |
| SCHEMBL8718440 | 0.93 | LMNA (0.48) | PDE4ALMNAL3MBTL1TDP1KDM4E | |
| SCHEMBL28231713 | 0.93 | LMNA (0.48) | PDE4ALMNAL3MBTL1TDP1KDM4E | |
| SCHEMBL7525631 | 0.93 | LMNA (0.48) | PDE4ALMNAL3MBTL1TDP1KDM4E | |
| SCHEMBL13604627 | 0.86 | PDE4A (0.54) | PDE4ALMNAL3MBTL1TDP1KDM4E |
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 |
|---|---|---|---|---|---|---|---|
| WO-2025121420-A1 | POLYCARBONATE AND METHOD FOR PRODUCING THE SAME | ＡＧＣ株式会社 | 2025-06-12 | — | — | WO | disclosed |
| WO-2007088559-A1 | PROCESS FOR PRODUCING SUBSTITUTED SULPHOXIDES | JUBILANT ORGANOSYS LIMITED (IN) | 2007-08-09 | — | — | WO | disclosed |
| EP-1467968-A1 | N-(4-SUBSTITUTED PHENYL)-ANTHRANILIC ACID HYDROXAMATE ESTERS | Warner-Lambert Company LLC (US) | 2004-10-20 | — | — | EP | disclosed |
| WO-2003062191-A1 | N-(4-SUBSTITUTED PHENYL)-ANTHRANILIC ACID HYDROXAMATE ESTERS | WARNER-LAMBERT COMPANY LLC (US) | 2003-07-31 | — | — | WO | disclosed |
| EP-1175385-A1 | D-MANNITOL DERIVATIVES AS HIV ASPARTYL PROTEASE INHIBITORS | Pharmacor Inc. (CA) | 2002-01-30 | — | — | EP | disclosed |
| EP-1082328-A1 | PRODUCTION OF OPTICALLY ACTIVE PHOSPHOLANES | BASF AKTIENGESELLSCHAFT (DE) | 2001-03-14 | — | — | EP | disclosed |
| WO-2000066524-A1 | D-MANNITOL DERIVATIVES AS HIV ASPARTYL PROTEASE INHIBITORS | PHARMACOR INC. (CA) | 2000-11-09 | — | — | WO | disclosed |
| EP-0971925-A1 | PYRIMIDOPYRIMIDINE COMPOUNDS | NEWCASTLE UNIVERSITY VENTURES LIMITED (GB) | 2000-01-19 | — | — | EP | disclosed |
| WO-1999062917-A1 | PRODUCTION OF OPTICALLY ACTIVE PHOSPHOLANES | BASF AKTIENGESELLSCHAFT (DE) | 1999-12-09 | — | — | WO | disclosed |
| WO-1998043974-A1 | PYRIMIDOPYRIMIDINE COMPOUNDS | NEWCASTLE UNIVERSITY VENTURES LIMITED (GB) | 1998-10-08 | — | — | WO | disclosed |
| WO-1998007653-A1 | CHIRAL HYDRIDE COMPLEXES | ZEELAND CHEMICALS, INC. (US) | 1998-02-26 | — | — | WO | disclosed |
| US-4588824-A | (S)-GLYCEROL-1,2-ACETONIDE FROM 1,2:5,6-DI-O-ISOPROPYLIDENE-D-MANNITOL, LEAD TETRAACETATE, ALKALI BOROHYDRIDE | MERCK & CO., INC. (US) | 1986-05-13 | — | — | US | disclosed |
| US-4408063-A | FROM A SULFONYLOXY HALOALCOHOL | MERCK & CO., INC. (US) | 1983-10-04 | — | — | US | disclosed |
| US-4346042-A | Preparation of epihalohydrin enantiomers | MERCK & CO., INC. (US) | 1982-08-24 | — | — | US | disclosed |
| EP-0006615-A1 | Process for preparing epihalohydrin enantiomers | MERCK & CO. INC. (US) | 1980-01-09 | — | — | EP | disclosed |