Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | GSK3A | P49840 | 1/20 | 0.43 |
| ▸ | GSK3B | P49841 | 1/20 | 0.43 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.42 |
| ▸ | CYP2A6 | P11509 | 1/20 | 0.41 |
| ▸ | MAOA | P21397 | 3/20 | 0.40 |
| ▸ | MAOB | P27338 | 2/20 | 0.40 |
| ▸ | PARP1 | P09874 | 1/20 | 0.38 |
| ▸ | CA1 | P00915 | 1/20 | 0.37 |
| ▸ | CA2 | P00918 | 1/20 | 0.37 |
| ▸ | TRPA1 | O75762 | 1/20 | 0.36 |
| ▸ | CES1 | P23141 | 3/20 | 0.35 |
| ▸ | BCHE | P06276 | 2/20 | 0.35 |
| ▸ | MEN1 | O00255 | 2/20 | 0.35 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.35 |
| ▸ | MAPT | P10636 | 2/20 | 0.35 |
| ▸ | THRB | P10828 | 2/20 | 0.35 |
| ▸ | ALOX15 | P16050 | 2/20 | 0.35 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.35 |
| ▸ | HSD17B10 | Q99714 | 2/20 | 0.35 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.35 |
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 | |
|---|---|---|---|---|
| SCHEMBL461295 | 0.98 | GSK3A (0.46) | GSK3AGSK3BCYP1A2CYP2A6MAOA | |
| SCHEMBL29421729 | 0.98 | GSK3A (0.46) | GSK3AGSK3BCYP1A2CYP2A6MAOA | |
| SCHEMBL3102143 | 0.95 | GSK3A (0.43) | GSK3AGSK3BCYP1A2CYP2A6MAOA | |
| SCHEMBL3106328 | 0.95 | GSK3A (0.43) | GSK3AGSK3BCYP1A2CYP2A6MAOA | |
| SCHEMBL30579936 | 0.95 | GSK3A (0.43) | GSK3AGSK3BCYP1A2CYP2A6MAOA | |
| Hydrochloric Acid SCHEMBL8917627 | 0.95 | GSK3A (0.43) | GSK3AGSK3BCYP1A2CYP2A6MAOA | |
| SCHEMBL28090476 | 0.95 | GSK3A (0.43) | GSK3AGSK3BCYP1A2CYP2A6MAOA | |
| SCHEMBL6517663 | 0.91 | GSK3A (0.40) | GSK3AGSK3BCYP1A2CYP2A6MAOA | |
| SCHEMBL1793601 | 0.90 | MAOA (0.41) | GSK3AGSK3BCYP1A2CYP2A6MAOA | |
| SCHEMBL283346 | 0.80 | TRPA1 (0.50) | CYP1A2MAOAMAOBPARP1CA1 |
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 43 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-5955609-A | Trimer catalyst system for aliphatic and aromatic isocyanates | BAYER CORPORATION (US) | 1999-09-21 | — | — | US | claimed |
| US-9587060-B2 | Functionalized rubbery polymers | THE GOODYEAR TIRE & RUBBER COMPANY (US) | 2017-03-07 | — | — | US | disclosed |
| US-8344171-B2 | Process for making dihydrocarbyl hydrocarbonphosphonates | ALBEMARLE CORPORATION (US) | 2013-01-01 | — | — | US | disclosed |
| US-20100179342-A1 | PROCESS FOR MAKING DIHYDROCARBYL HYDROCARBONPHOSPHONATES | ALBEMARLE CORPORATION (US) | 2010-07-15 | — | — | US | disclosed |
| US-7714089-B2 | Functionalized monomers and functionalized rubbery polymers made therewith | THE GOODYEAR TIRE & RUBBER COMPANY (US) | 2010-05-11 | — | — | US | disclosed |
| EP-2164853-A1 | PROCESS FOR MAKING DIHYDROCARBYL HYDROCARBONPHOSPHONATES | Albermarle Corporation (US) | 2010-03-24 | — | — | EP | disclosed |
| US-7572303-B2 | A symmetrical dialkyl carbonate, a metal, borong, silicon, or group 7 compound, a hydrogen or hydrocarbon-based fuel, an oxidizer, and a metallic cocatalyst; minimized hydrolysis; improved combustion and storage stability | OCTANE INTERNATIONAL, LTD. (US) | 2009-08-11 | — | — | US | disclosed |
| US-7553963-B2 | Liquid partially trimerized and allophanized polyisocyanates based on toluene diisocyanate and diphenylmethane diisocyanate | BAYER MATERIALSCIENCE LLC (US) | 2009-06-30 | — | — | US | disclosed |
| US-20090156769-A1 | FUNCTIONALIZED MONOMERS AND FUNCTIONALIZED RUBBERY POLYMERS MADE THEREWITH | THE GOODYEAR TIRE & RUBBER COMPANY | 2009-06-18 | — | — | US | disclosed |
| WO-2008154268-A1 | PROCESS FOR MAKING DIHYDROCARBYL HYDROCARBONPHOSPHONATES | ALBEMARLE CORPORATION (US) | 2008-12-18 | — | — | WO | disclosed |
| US-6028158-A | Freeze-stable allophanate-modified toluene diisocyanate trimers | BAYER CORPORATION (US) | 2000-02-22 | — | — | US | disclosed |
| WO-1999066009-A2 | FUEL COMPOSITIONS EMPLOYING CATALYST COMBUSTION STRUCTURE | ORR WILLIAM C (US) | 1999-12-23 | — | — | WO | disclosed |
| US-5955609-A | Trimer catalyst system for aliphatic and aromatic isocyanates | BAYER CORPORATION (US) | 1999-09-21 | — | — | US | disclosed |
| US-5905151-A | LITHIUM SALT AND ALCOHOL; CATALYTIC CYCLIZATION TO ISOCYANURIC ACID DERIVATIVES | BAYER CORPORATION (US) | 1999-05-18 | — | — | US | disclosed |
| US-5241104-A | Reacting acid anhydride with arylacetic acid derivatives; for preparing optically active prostaglandins | SHIONOGI & CO., LTD. (JP) | 1993-08-31 | — | — | US | disclosed |
| EP-0373949-B1 | MONO ESTERS OF DICARBOXYLIC ACIDS, THEIR PREPARATION AND USE | SHIONOGI & CO (JP) | 1993-08-25 | — | — | EP | disclosed |
| US-5183909-A | Useful as intermediate for production of prostaglandins, terpenes, aminosugars, nucleotides and alkaloids | SHIONOGI & COMPANY, LTD. (JP) | 1993-02-02 | — | — | US | disclosed |
| US-5175341-A | Bicyclo 2.2.2!heptanedicarboxylic acid derivatives | SHIONOGI & CO., LTD. (JP) | 1992-12-29 | — | — | US | disclosed |
| US-5047574-A | CHEMICAL INTERMEDIATES FOR OPTICALLY ACTIVE PRODUCTS, MEDICINES | SHIONOGI & CO., LTD. (JP) | 1991-09-10 | — | — | US | disclosed |
| EP-0373949-A1 | Mono esters of dicarboxylic acids, their preparation and use | SHIONOGI SEIYAKU KABUSHIKI KAISHA trading under the name of SHIONOGI & CO. LTD. (JP) | 1990-06-20 | — | — | EP | disclosed |