Predicted protein targets (top 18)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CYP3A4 | P08684 | 2/20 | 0.45 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.45 |
| ▸ | ESR1 | P03372 | 6/20 | 0.41 |
| ▸ | ESR2 | Q92731 | 6/20 | 0.41 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.36 |
| ▸ | TAAR1 | Q96RJ0 | 2/20 | 0.33 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.33 |
| ▸ | LMNA | P02545 | 1/20 | 0.33 |
| ▸ | TSHR | P16473 | 1/20 | 0.33 |
| ▸ | ALOX12 | P18054 | 1/20 | 0.33 |
| ▸ | ACHE | P22303 | 1/20 | 0.33 |
| ▸ | ALOX15 | P16050 | 1/20 | 0.33 |
| ▸ | SLC6A2 | P23975 | 1/20 | 0.33 |
| ▸ | KCNN4 | O15554 | 1/20 | 0.32 |
| ▸ | DRD1 | P21728 | 2/20 | 0.31 |
| ▸ | AOC3 | Q16853 | 1/20 | 0.31 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.31 |
| ▸ | GAA | P10253 | 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 | |
|---|---|---|---|---|
| SCHEMBL9661777 | 0.97 | CYP3A4 (0.43) | CYP3A4TDP1ESR1ESR2MAPK1 | |
| SCHEMBL31460412 | 0.90 | CYP3A4 (0.38) | CYP3A4TDP1ESR1ESR2MAPK1 | |
| SCHEMBL301240 | 0.82 | CYP3A4 (0.45) | CYP3A4TDP1ESR1ESR2MAPK1 | |
| SCHEMBL11649729 | 0.82 | CYP3A4 (0.45) | CYP3A4TDP1ESR1ESR2MAPK1 | |
| SCHEMBL2313918 | 0.82 | CYP3A4 (0.45) | CYP3A4TDP1ESR1ESR2MAPK1 | |
| Hydrochloric Acid SCHEMBL28963440 | 0.80 | CYP3A4 (0.43) | CYP3A4TDP1ESR1ESR2MAPK1 | |
| SCHEMBL10412404 | 0.80 | CYP3A4 (0.43) | CYP3A4TDP1ESR1ESR2MAPK1 | |
| SCHEMBL24363333 | 0.78 | CYP3A4 (0.41) | CYP3A4TDP1ESR1ESR2MAPK1 | |
| SCHEMBL9879421 | 0.78 | CYP3A4 (0.41) | CYP3A4TDP1ESR1ESR2MAPK1 | |
| Bromide SCHEMBL1582990 | 0.78 | CYP3A4 (0.41) | CYP3A4TDP1ESR1ESR2MAPK1 |
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 147 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-3856738-A1 | PROCESS FOR THE PREPARATION OF SPHINGOSINE-1-PHOSPHATE RECEPTOR AGONIST | Química Sintética, S.A. (ES) | 2021-08-04 | — | — | EP | claimed |
| WO-2020064818-A1 | PROCESS FOR THE PREPARATION OF SPHINGOSINE-1-PHOSPHATE RECEPTOR AGONIST | Química Sintética, S.A. (ES) | 2020-04-02 | — | — | WO | claimed |
| EP-2812310-A1 | METHOD FOR PRODUCING SUBSTITUTED ANTHRANILIC ACID DERIVATIVES | Bayer Intellectual Property GmbH (DE) | 2014-12-17 | — | — | EP | claimed |
| EP-2683686-A1 | METHOD FOR PRODUCING PRIMARY AMINES OBTAINED BY HOMOGENEOUSLY CATALYZED ALCOHOL AMINATION | BASF SE (DE) | 2014-01-15 | — | — | EP | claimed |
| WO-2013117601-A1 | METHOD FOR PRODUCING SUBSTITUTED ANTHRANILIC ACID DERIVATIVES | BAYER INTELLECTUAL PROPERTY GMBH (DE) | 2013-08-15 | — | — | WO | claimed |
| WO-2012119927-A1 | METHOD FOR PRODUCING PRIMARY AMINES OBTAINED BY HOMOGENEOUSLY CATALYZED ALCOHOL AMINATION | BASF SE (DE) | 2012-09-13 | — | — | WO | claimed |
| EP-2427468-A1 | PREPARATION OF A METAL COMPLEX | JOHNSON MATTHEY PUBLIC LIMITED COMPANY (GB) | 2012-03-14 | — | — | EP | claimed |
| WO-2010128316-A1 | PREPARATION OF A METAL COMPLEX | JOHNSON MATTHEY PUBLIC LIMITED COMPANY (GB) | 2010-11-11 | — | — | WO | claimed |
| WO-2007029031-A1 | METAL COMPOUND AND PREPARATION METHOD THEREFOR | JOHNSON MATTHEY PLC (GB) | 2007-03-15 | — | — | WO | claimed |
| WO-2023167321-A1 | MECHANOCHEMICAL REACTION ADDITIVE, MECHANOCHEMICAL METHOD, LIGAND COMPOUND, AND COMPLEX | 国立大学法人北海道大学 | 2023-09-07 | — | — | WO | disclosed |
| EP-3986552-A1 | ISOXAZOLE CARBOXYLIC ACIDS AS LPA ANTAGONISTS | Bristol-Myers Squibb Company (US) | 2022-04-27 | — | — | EP | disclosed |
| EP-3986553-A1 | CYCLOBUTYL CARBOXYLIC ACIDS AS LPA ANTAGONISTS | Bristol-Myers Squibb Company (US) | 2022-04-27 | — | — | EP | disclosed |
| EP-3877358-A1 | PROCESS FOR PRODUCING SUBSTITUTED AMINO ALCOHOLS | BASF SE (DE) | 2021-09-15 | — | — | EP | disclosed |
| EP-3873877-A1 | PROCESS FOR PRODUCING HYDROXYMETHYL-ALCOHOLS | BASF SE (DE) | 2021-09-08 | — | — | EP | disclosed |
| WO-2001027112-A1 | 5-(2-SUBSTITUTED-5-HETEROCYCLYLSULPHONYLPYRID-3-YL)-DIHYDROPYRAZOLO[4,3-D]PYRIMIDIN-7-ONES AS PHOSPHODIESTERASE INHIBITORS | PFIZER LIMITED (GB) | 2001-04-19 | — | — | WO | disclosed |
| EP-0954558-A1 | FUEL COMPOSITIONS EXHIBITING IMPROVED FUEL STABILITY | ORR, William C. (US) | 1999-11-10 | — | — | EP | disclosed |
| WO-1998026028-A1 | FUEL COMPOSITIONS EXHIBITING IMPROVED FUEL STABILITY | ORR WILLIAM C (US) | 1998-06-18 | — | — | WO | disclosed |
| WO-1995008526-A1 | HYDROGENATION | PFIZER RESEARCH AND DEVELOPMENT COMPANY, N.V./S.A. (IE) | 1995-03-30 | — | — | WO | disclosed |
| EP-0369528-B1 | CATALYST COMPOSITIONS | SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) | 1992-01-02 | — | — | EP | disclosed |
| EP-0369528-A1 | Catalyst compositions | SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) | 1990-05-23 | — | — | EP | disclosed |