Predicted protein targets (top 17)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CYP3A4 | P08684 | 1/20 | 0.39 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.39 |
| ▸ | ESR1 | P03372 | 4/20 | 0.38 |
| ▸ | ESR2 | Q92731 | 4/20 | 0.38 |
| ▸ | TP53 | P04637 | 1/20 | 0.36 |
| ▸ | KCNN4 | O15554 | 1/20 | 0.33 |
| ▸ | SIGMAR1 | Q99720 | 1/20 | 0.32 |
| ▸ | PSIP1 | O75475 | 1/20 | 0.31 |
| ▸ | CES2 | O00748 | 1/20 | 0.30 |
| ▸ | CES1 | P23141 | 1/20 | 0.30 |
| ▸ | PCSK9 | Q8NBP7 | 1/20 | 0.30 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.30 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.30 |
| ▸ | GAA | P10253 | 1/20 | 0.30 |
| ▸ | HPGD | P15428 | 1/20 | 0.30 |
| ▸ | LTA4H | P09960 | 1/20 | 0.30 |
| ▸ | LMNA | P02545 | 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 | |
|---|---|---|---|---|
| SCHEMBL13391635 | 0.87 | CYP3A4 (0.45) | CYP3A4TDP1ESR1ESR2TP53 | |
| SCHEMBL9441831 | 0.87 | CYP3A4 (0.45) | CYP3A4TDP1ESR1ESR2TP53 | |
| SCHEMBL30145249 | 0.87 | HPGD (0.40) | CYP3A4TDP1ESR1ESR2KDM4E | |
| SCHEMBL4750482 | 0.86 | LTA4H (0.36) | CYP3A4TDP1ESR1ESR2TP53 | |
| SCHEMBL11115959 | 0.84 | LTA4H (0.37) | CYP3A4TDP1ESR1ESR2TP53 | |
| SCHEMBL15659608 | 0.82 | DNM1 (0.39) | TP53SIGMAR1CES2CES1LTA4H | |
| Iodide SCHEMBL491999 | 0.82 | CYP3A4 (0.41) | CYP3A4TDP1ESR1ESR2TP53 | |
| SCHEMBL9492996 | 0.82 | CYP3A4 (0.41) | CYP3A4TDP1ESR1ESR2TP53 | |
| Bromide SCHEMBL493074 | 0.82 | CYP3A4 (0.41) | CYP3A4TDP1ESR1ESR2TP53 | |
| Hydrochloric Acid SCHEMBL493348 | 0.82 | TDP1 (0.41) | CYP3A4TDP1ESR1ESR2TP53 |
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 30 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-3527639-B1 | A METHOD FOR BONDING A THERMOPLASTIC MATERIAL BY MICROWAVE-IRRADIATION | PROIONIC GMBH (AT) | 2021-09-08 | — | — | EP | claimed |
| CN-112209967-B | Chiral spiro monophosphine-oxazoline ligand and preparation method thereof | 浙江九洲药业股份有限公司 | 2025-03-04 | — | — | CN | disclosed |
| EP-3527639-B1 | A METHOD FOR BONDING A THERMOPLASTIC MATERIAL BY MICROWAVE-IRRADIATION | PROIONIC GMBH (AT) | 2021-09-08 | — | — | EP | disclosed |
| CN-112209967-A | Chiral spiro monophosphine-oxazoline ligand and preparation method thereof | 瑞博(杭州)医药科技有限公司 | 2021-01-12 | — | — | CN | disclosed |
| CN-111909206-A | Chiral spiro monophosphine ligand and preparation method thereof | 浙江瑞博制药有限公司 | 2020-11-10 | — | — | CN | disclosed |
| US-6492532-B2 | Method for producing carbonyl compound by dehydrogenating alcohol | MITSUBISHI CHEMICAL CORPORATION (JP) | 2002-12-10 | — | — | US | disclosed |
| US-20020002289-A1 | Method for producing carbonyl compound by dehydrogenating alcohol | MITSUBISHI CHEMICAL CORPORATION (JP) | 2002-01-03 | — | — | US | disclosed |
| EP-1160245-A1 | PROCESS FOR PRODUCING CARBONYL COMPOUNDS BY DEHYDROGENATION OF ALCOHOLS | MITSUBISHI CHEMICAL CORPORATION (JP) | 2001-12-05 | — | — | EP | disclosed |
| EP-0531174-B1 | Oligomerization catalyst for alpha-olefins and process for oligomerizing alpha-olefins | MITSUI PETROCHEMICAL IND (JP) | 1995-06-21 | — | — | EP | disclosed |
| US-5286695-A | Oligomerization catalyst for α-olefins and process for oligomerizing α-olefins | MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) | 1994-02-15 | — | — | US | disclosed |
| US-4265827-A | METHYLCYCOHEXYL-O-ANISYLARSINE OPTICALLY ACTIVE CATALYST | MONSANTO COMPANY (US) | 1981-05-05 | — | — | US | disclosed |
| US-4261919-A | OF BETA-SUBSTITUTED-ALPHA-ACYLAMIDO-ACRYLIC ACIDS TO YIELD OPTICALLY ACTIVE MIXTURE | MONSANTO COMPANY (US) | 1981-04-14 | — | — | US | disclosed |
| US-4255595-A | Optically active cyclooctenyl ethyl alcohol | STUDIENGESELLSCHAFT KOHLE MBH (DE) | 1981-03-10 | — | — | US | disclosed |
| US-4155946-A | CATALYST CONSISTS OF A NICKEL COMPOUND, A TRIALKYL ALUMINUM COMPOUND; PHOSPHOROUS COMPOUND AND A HALOGENATED PHENOL | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1979-05-22 | — | — | US | disclosed |
| US-4152366-A | POLYMERIZABLE TO OPTICALLY ACTIVE POLYMERS | STUDIENGESELLSCHAFT KOHLE MBH (DE) | 1979-05-01 | — | — | US | disclosed |
| US-4124533-A | HYDROGENATION CATALYSTS | MONSANTO COMPANY (US) | 1978-11-07 | — | — | US | disclosed |
| US-4119652-A | HYDROGENATION CATALYSTS; COORDINATION COMPOUNDS OF IRIDIUM, RHODIUM OR RUTHENIUM WITH PHOSPHINE OR ARSINE LIGANDS; OPTICALLY ACTIVE | MONSANTO COMPANY (US) | 1978-10-10 | — | — | US | disclosed |
| US-4098834-A | Optically active 3-substituted cyclooctene bicyclo-[6.0.3.]-undecene-3 and exo-2-vinyl norbornane | STUDIENGESELLSCHAFT KOHLE MBH (DE) | 1978-07-04 | — | — | US | disclosed |
| US-4096250-A | ANTI-ARTHRITIC | SMITHKLINE CORPORATION (US) | 1978-06-20 | — | — | US | disclosed |
| US-3978147-A | NI, LEWIS ACID, PHOSPHINE | STUDIENGESELLSCHAFT KOHLE M.B.H (DT) | 1976-08-31 | — | — | US | disclosed |