Predicted protein targets (top 13)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CES1 | P23141 | 7/20 | 0.46 |
| ▸ | CES2 | O00748 | 5/20 | 0.46 |
| ▸ | KIF11 | P52732 | 1/20 | 0.42 |
| ▸ | LMNA | P02545 | 1/20 | 0.40 |
| ▸ | NAAA | Q02083 | 1/20 | 0.40 |
| ▸ | SRC | P12931 | 1/20 | 0.39 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.37 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.37 |
| ▸ | L3MBTL1 | Q9Y468 | 1/20 | 0.37 |
| ▸ | PRSS1 | P07477 | 1/20 | 0.37 |
| ▸ | CTSG | P08311 | 1/20 | 0.37 |
| ▸ | CTRB1 | P17538 | 1/20 | 0.37 |
| ▸ | CMA1 | P23946 | 1/20 | 0.37 |
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 | |
|---|---|---|---|---|
| SCHEMBL3251384 | 0.90 | CES1 (0.49) | CES1CES2LMNASRCKMT2A | |
| SCHEMBL7914713 | 0.88 | CES1 (0.44) | CES1CES2KIF11LMNANAAA | |
| SCHEMBL868096 | 0.83 | CES1 (0.51) | CES1CES2LMNASRC | |
| SCHEMBL8234137 | 0.83 | CES1 (0.40) | CES1CES2KIF11LMNANAAA | |
| SCHEMBL10880596 | 0.81 | CES1 (0.45) | CES1CES2LMNASRCKMT2A | |
| SCHEMBL4929013 | 0.79 | CES1 (0.46) | CES1CES2KIF11LMNANAAA | |
| SCHEMBL7945147 | 0.78 | CES1 (0.49) | CES1CES2LMNASRCKMT2A | |
| SCHEMBL1255415 | 0.78 | LMNA (0.50) | CES1CES2LMNASRCKMT2A | |
| SCHEMBL28163593 | 0.76 | CES1 (0.50) | CES1CES2KIF11LMNANAAA | |
| SCHEMBL476563 | 0.76 | CES1 (0.47) | CES1CES2LMNASRCL3MBTL1 |
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 46 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| WO-2012050951-A2 | VINYL ETHER FUNCTIONAL OLIGOMERS AND METHODS FOR MAKING AND USING SAME | RENSSELAER POLYTECHNIC UNIVERSITY (US) | 2012-04-19 | — | — | WO | claimed |
| CN-114729210-B | Laminate with wear layer containing inorganic nanoparticles and radiation curable ink containing inorganic nanoparticles having low viscosity | 3M创新有限公司 | 2024-03-12 | — | — | CN | disclosed |
| CN-115368844-B | Pressure-sensitive adhesive tape for mica-based composite material and preparation method thereof | 苏州赛伍应用技术股份有限公司 | 2024-02-13 | — | — | CN | disclosed |
| CN-116554814-A | Structural color binder, preparation method and application | 华中科技大学 | 2023-08-08 | — | — | CN | disclosed |
| CN-114901761-A | Laminates having inorganic nanoparticle-containing surface layer exhibiting low gloss appearance and inorganic nanoparticle-containing radiation curable inks | 3M创新有限公司 | 2022-08-12 | — | — | CN | disclosed |
| US-9822204-B2 | Vinyl ether functional oligomers and methods for making and using same | RENSSELAER POLYTECHNIC INSTITUTE (US) | 2017-11-21 | — | — | US | disclosed |
| US-20170240782-A1 | OPTICALLY CLEAR ADHESIVE AND OPTICAL LAMINATE | 3M INNOVATIVE PROPERTIES COMPANY | 2017-08-24 | — | — | US | disclosed |
| EP-3186327-A2 | OPTICALLY CLEAR ADHESIVE AND OPTICAL LAMINATE | 3M Innovative Properties Company (US) | 2017-07-05 | — | — | EP | disclosed |
| US-9410043-B2 | Reactive mixture for coating molded objects by means of reaction injection molding and coated molded object | EVONIK ROEHM GMBH (DE) | 2016-08-09 | — | — | US | disclosed |
| WO-2016069097-A2 | OPTICALLY CLEAR ADHESIVE AND OPTICAL LAMINATE | 3M INNOVATIVE PROPERTIES COMPANY (US) | 2016-05-06 | — | — | WO | disclosed |
| US-20050147859-A1 | proton-conducting polymer membrane has a crosslinked addition-condensation copolymers, containing monomers of a vinyl-containing phosphonic acid, polybenzimidazoles or polysulfones; permselectivity; not permeable to reactive fuels such as hydrogen gas or methanol and gaseous oxygen | BASF FUEL CELL GMBH (DE) | 2005-07-07 | — | — | US | disclosed |
| US-6747088-B1 | COATING HEAT-STABLE SUBSTRATES SUCH AS METAL SUBSTRATES AND MAY BE USED WITH ADVANTAGE FOR AUTOMOTIVE CLEARCOATS. | BASF AKTIENGESELLSCHAFT (DE) | 2004-06-08 | — | — | US | disclosed |
| US-20030153673-A1 | Curable aqueous polyurethane dispersions | BASF AKTIENGESELLSCHAFT (DE) | 2003-08-14 | — | — | US | disclosed |
| US-6177535-B1 | HYDROXY AND POLYHYDROXYALKYL (METH)ACRYLATE BLOCKED BIURETS AND ISOCYANURATES OF HEXAMETHYLENE DIISOCYANATE AND ISOPHORONE DIISOCYANATE, PHOTORESISTS | BASF AKTIENGESELLCHAFT (DE) | 2001-01-23 | — | — | US | disclosed |
| EP-0938689-A1 | UV-CURED OPTICAL ELEMENTS | Akzo Nobel N.V. (NL) | 1999-09-01 | — | — | EP | disclosed |
| WO-1998020373-A1 | UV-CURED OPTICAL ELEMENTS | AKZO NOBEL N.V. (NL) | 1998-05-14 | — | — | WO | disclosed |
| US-4610952-A | Photoresist compositions and method | GENERAL ELECTRIC COMPANY (US) | 1986-09-09 | — | — | US | disclosed |
| US-4609705-A | AROMATIC VONYL ETHER AND A MALEIMIDE | GENERAL ELECTRIC COMPANY (US) | 1986-09-02 | — | — | US | disclosed |
| US-4537854-A | Photoresist compositions and method | GENERAL ELECTRIC COMPANY (US) | 1985-08-27 | — | — | US | disclosed |
| US-4423136-A | Free radical curable resin compositions containing triarylsulfonium salt | GENERAL ELECTRIC COMPANY (US) | 1983-12-27 | — | — | US | disclosed |