Predicted protein targets (top 5)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | THRB | P10828 | 1/20 | 0.38 |
| ▸ | LMNA | P02545 | 1/20 | 0.36 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.35 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.35 |
| ▸ | TDP1 | Q9NUW8 | 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 | |
|---|---|---|---|---|
| SCHEMBL11451477 | 0.97 | THRB (0.36) | THRBLMNAALDH1A1MAPK1TDP1 | |
| SCHEMBL3822689 | 0.97 | THRB (0.36) | THRBLMNAALDH1A1MAPK1TDP1 | |
| SCHEMBL2855533 | 0.79 | ALDH1A1 (0.33) | ALDH1A1MAPK1TDP1 | |
| SCHEMBL28908691 | 0.78 | LMNA (0.43) | THRBLMNAALDH1A1MAPK1TDP1 | |
| SCHEMBL12442358 | 0.76 | — | — | |
| SCHEMBL4967277 | 0.76 | — | — | |
| SCHEMBL2850575 | 0.75 | TSHR (0.39) | ALDH1A1 | |
| SCHEMBL27700346 | 0.74 | THRB (0.40) | THRBLMNA | |
| SCHEMBL9644124 | 0.74 | — | — | |
| SCHEMBL7328517 | 0.74 | — | — |
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 122 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-105111214-A | Preparation method of pemetrexed disodium | UNIV JIANGXI AGRICULTURAL | 2015-12-02 | — | — | CN | claimed |
| CN-101376708-B | Method for synthesizing polyalkyl ether polymer with as propanal group as end group | INST PROCESS ENG CAS | 2010-12-08 | — | — | CN | claimed |
| CN-1973006-B | Single-component system based on co-reactive latex, preparation method and use in the field of formol-free coatings | ARKEMA | 2010-11-10 | — | — | CN | claimed |
| EP-1778804-B1 | SINGLE-COMPONENT SYSTEM BASED ON CO-REACTIVE LATEX, PREPARATION METHOD AND USE IN THE FIELD OF FORMOL-FREE COATINGS | ARKEMA FRANCE (FR) | 2010-01-20 | — | — | EP | claimed |
| CN-101376708-A | Method for synthesizing polyalkyl ether polymer with as propanal group as end group | INST PROCESS ENG CAS (CN) | 2009-03-04 | — | — | CN | claimed |
| US-20080028982-A1 | Single-Component System Based On Co-Reactive Latex, Preparation Method And Use In The Field Of Formol-Free Coatings | VERGE CHRISTOPHE | 2008-02-07 | — | — | US | claimed |
| CN-1973006-A | Single-component system based on co-reactive latex, preparation method and use in the field of formol-free coatings | ARKEMA (FR) | 2007-05-30 | — | — | CN | claimed |
| EP-1778804-A1 | SINGLE-COMPONENT SYSTEM BASED ON CO-REACTIVE LATEX, PREPARATION METHOD AND USE IN THE FIELD OF FORMOL-FREE COATINGS | Arkema France (FR) | 2007-05-02 | — | — | EP | claimed |
| WO-2006010804-A1 | SINGLE-COMPONENT SYSTEM BASED ON CO-REACTIVE LATEX, PREPARATION METHOD AND USE IN THE FIELD OF FORMOL-FREE COATINGS | ARKEMA FRANCE (FR) | 2006-02-02 | — | — | WO | claimed |
| WO-1992018640-A1 | ENZYMATIC METHOD FOR PREPARING ENANTIOMER- AND DIASTERIOMER-PURE KETOSES AND THEIR 1-ORTHOPHOSPHATE ESTERS | BOEHRINGER MANNHEIM GMBH (DE) | 1992-10-29 | — | — | WO | claimed |
| CN-109824591-A | A kind of synthetic method of chloro- 6,7- dihydro -5H- cyclopentano [b] pyridine -5- ketone of 3- | 药雅科技(上海)有限公司 | 2019-05-31 | — | — | CN | disclosed |
| EP-2690084-B1 | METHOD FOR PRODUCING HYDROXYL GROUP-CONTAINING ACETAL COMPOUND | NOF CORP (JP) | 2017-04-19 | — | — | EP | disclosed |
| EP-1538145-B1 | PROCESS FOR PRODUCTION OF PHENOXY-SUBSTITUTED 2-PYRIDONE COMPOUNDS | SUMITOMO CHEMICAL CO (JP) | 2016-02-17 | — | — | EP | disclosed |
| CN-105111214-A | Preparation method of pemetrexed disodium | UNIV JIANGXI AGRICULTURAL | 2015-12-02 | — | — | CN | disclosed |
| CN-103443063-B | For the production of the method for hydroxyl acetal compound | NOF CORP. (JP) | 2015-11-25 | — | — | CN | disclosed |
| WO-1991009016-A2 | HALOPHENYL SUBSTITUTED HETEROCYCLIC DERIVATIVES | MERCK PATENT GMBH (DE) | 1991-06-27 | — | — | WO | disclosed |
| EP-0223588-B1 | PROCESS FOR THE PREPARATION OF BETA-LACTAM COMPOUNDS | IMPERIAL CHEMICAL INDUSTRIES PLC (GB) | 1991-06-12 | — | — | EP | disclosed |
| US-4834772-A | Battery electrolyte | CAPE COD RESEARCH, INC. (US) | 1989-05-30 | — | — | US | disclosed |
| EP-0223588-A1 | Process for the preparation of beta-lactam compounds | IMPERIAL CHEMICAL INDUSTRIES PLC (GB) | 1987-05-27 | — | — | EP | disclosed |
| EP-0028892-B1 | A HETERONUCLEAR-BRIDGED RHODIUM CLUSTER AND ITS APPLICATION AS CATALYST FOR HYDROFORMYLATION OF OLEFINS | UNION CARBIDE CORPORATION (US) | 1986-03-19 | — | — | EP | disclosed |