Predicted protein targets (top 5)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | MAPT | P10636 | 3/20 | 0.38 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.38 |
| ▸ | LMNA | P02545 | 1/20 | 0.34 |
| ▸ | HPGD | P15428 | 1/20 | 0.32 |
| ▸ | CHKA | P35790 | 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 | |
|---|---|---|---|---|
| SCHEMBL23661070 | 0.97 | MAPT (0.37) | MAPTALDH1A1LMNAHPGDCHKA | |
| SCHEMBL497686 | 0.97 | MAPT (0.37) | MAPTALDH1A1LMNAHPGDCHKA | |
| SCHEMBL368150 | 0.92 | MAPT (0.37) | MAPTALDH1A1LMNAHPGDCHKA | |
| SCHEMBL497034 | 0.92 | MAPT (0.37) | MAPTALDH1A1LMNAHPGDCHKA | |
| SCHEMBL11814787 | 0.92 | MAPT (0.44) | MAPTALDH1A1LMNA | |
| SCHEMBL497507 | 0.90 | ALDH1A1 (0.35) | MAPTALDH1A1LMNAHPGD | |
| SCHEMBL23486255 | 0.90 | ALDH1A1 (0.35) | MAPTALDH1A1LMNAHPGD | |
| SCHEMBL6699994 | 0.90 | ALDH1A1 (0.35) | MAPTALDH1A1LMNAHPGD | |
| SCHEMBL8992014 | 0.90 | ALDH1A1 (0.35) | MAPTALDH1A1LMNAHPGD | |
| SCHEMBL23661069 | 0.90 | ALDH1A1 (0.35) | MAPTALDH1A1LMNAHPGD |
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 621 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-4479487-A1 | SOLUBLE WATER SCAVENGER MOLECULES FOR USE WITH DIELECTRIC FLUIDS | General Electric Technology GmbH (CH) | 2024-12-25 | — | — | EP | claimed |
| CN-117069574-A | Preparation method of loxoprofen acid | 常州瑞明药业有限公司 | 2023-11-17 | — | — | CN | claimed |
| CN-116947623-A | Method for preparing loxoprofen acid and loxoprofen sodium | 常州瑞明药业有限公司 | 2023-10-27 | — | — | CN | claimed |
| WO-2023156969-A1 | SOLUBLE WATER SCAVENGER MOLECULES FOR USE WITH DIELECTRIC FLUIDS | GENERAL ELECTRIC TECHNOLOGY GMBH (CH) | 2023-08-24 | — | — | WO | claimed |
| US-20230265349-A1 | SOLUBLE WATER SCAVENGER MOLECULES FOR USE WITH DIELECTRIC FLUIDS | GENERAL ELECTRIC TECHNOLOGY GMBH (CH) | 2023-08-24 | — | — | US | claimed |
| US-20220119569-A1 | Curable and Solvent Soluble Formulations and Methods of Making and Using Therof | POLY6 TECHNOLOGIES, INC. | 2022-04-21 | — | — | US | claimed |
| US-20200062877-A1 | Curable and Solvent Soluble Formulations and Methods of Making and Using Therof | POLY6 TECHNOLOGIES, INC. | 2020-02-27 | — | — | US | claimed |
| WO-2018156766-A2 | CURABLE AND SOLVENT SOLUBLE FORMULATIONS AND METHODS OF MAKING AND USING THEREOF | POLY6 TECHNOLOGIES, INC. (US) | 2018-08-30 | — | — | WO | claimed |
| US-9080068-B2 | Gallium formulated ink and methods of making and using same | ROHM AND HAAS ELECTRONIC MATERIALS LLC (US) | 2015-07-14 | — | — | US | claimed |
| EP-2284203-B1 | Method for preparation of polyolefins containing exo-olefin chain ends | CHEVRON ORONITE CO (US) | 2015-03-04 | — | — | EP | claimed |
| EP-1778747-A2 | METHOD FOR PREPARING POLYOLEFINS CONTAINING A HIGH PERCENTAGE OF EXO-OLEFIN CHAIN ENDS | Chevron Oronite Company LLC (US) | 2007-05-02 | — | — | EP | claimed |
| WO-2006033739-A9 | METHOD FOR PREPARING POLYOLEFINS CONTAINING A HIGH PERCENTAGE OF EXO-OLEFIN CHAIN ENDS | CHEVRON ORONITE CO (US) | 2006-05-26 | — | — | WO | claimed |
| WO-2006033739-A2 | METHOD FOR PREPARING POLYOLEFINS CONTAINING A HIGH PERCENTAGE OF EXO-OLEFIN CHAIN ENDS | CHEVRON ORONITE COMPANY LLC (US) | 2006-03-30 | — | — | WO | claimed |
| US-20060041084-A1 | Quenching a cationic quasi-living polyolefin polymer system with one or more hindered secondary or tertiary amines | CHEVRON ORONITE COMPANY LLC | 2006-02-23 | — | — | US | claimed |
| US-20060041081-A1 | ionizing, in presence of lewis acid, polyolefin containing tert-chloride chain ends and reacting the ionized polyolefin with pyrrole, imidazole compounds | CHEVRON ORONITE COMPANY LLC | 2006-02-23 | — | — | US | claimed |
| WO-2005049568-A1 | A PROCESS FOR INDUSTRIALLY VIABLE PREPARATION OF (S,S,S) PHENYLMETHYL-2-AZABICYCLO-[3.3.0]-OCTANE-3-CARBOXYLATE TOSYLATE | BABU POTLURI RAMESH (IN) | 2005-06-02 | — | — | WO | claimed |
| US-20040261198-A1 | Restructuring and finishing of keratin fibers | HENKEL KOMMANDITGESELLSCHAFT AUF AKTIEN (HENKEL KGAA) (DE) | 2004-12-30 | — | — | US | claimed |
| EP-1455736-A1 | RESTRUCTURING AND FINISHING OF KERATIN FIBERS | Henkel Kommanditgesellschaft auf Aktien (DE) | 2004-09-15 | — | — | EP | claimed |
| WO-2003053375-A1 | RESTRUCTURING AND FINISHING OF KERATIN FIBERS | HENKEL KOMMANDITGESELLSCHAFT AUF AKTIEN (DE) | 2003-07-03 | — | — | WO | claimed |
| US-6153783-A | REACTING A CYCLOALKANONE WITH A 2-SUBSTITUTED-1-ALKENE USING AN ENAMINE CATALYST TO PRODUCE A CORRESPONDINGLY SUBSTITUTED INTERMEDIATE; RING OPENING BY ULTRAVIOLET RADIATION AND USING A REACTING SOLVENT | COGNIS CORPORATION (US) | 2000-11-28 | — | — | US | claimed |