Predicted protein targets (top 11)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.39 |
| ▸ | TSHR | P16473 | 2/20 | 0.36 |
| ▸ | THRB | P10828 | 1/20 | 0.35 |
| ▸ | LMNA | P02545 | 1/20 | 0.33 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.32 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.32 |
| ▸ | AOX1 | Q06278 | 1/20 | 0.32 |
| ▸ | MAPT | P10636 | 1/20 | 0.31 |
| ▸ | HIF1A | Q16665 | 1/20 | 0.30 |
| ▸ | FAAH | O00519 | 2/20 | 0.30 |
| ▸ | TRPV1 | Q8NER1 | 1/20 | 0.30 |
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 | |
|---|---|---|---|---|
| SCHEMBL2853062 | 0.86 | TSHR (0.44) | ALDH1A1TSHRTHRBLMNAMAPT | |
| SCHEMBL2847082 | 0.84 | TSHR (0.44) | ALDH1A1TSHRTHRBMAPTHIF1A | |
| SCHEMBL11124880 | 0.82 | MAPT (0.33) | ALDH1A1TSHRLMNATDP1MAPT | |
| SCHEMBL2854282 | 0.81 | ALDH1A1 (0.42) | ALDH1A1TSHRFAAHTRPV1 | |
| SCHEMBL26743670 | 0.79 | ALDH1A1 (0.31) | ALDH1A1 | |
| SCHEMBL745664 | 0.78 | — | — | |
| SCHEMBL2849253 | 0.78 | TSHR (0.46) | ALDH1A1TSHRFAAHTRPV1 | |
| SCHEMBL21862159 | 0.78 | CA12 (0.39) | ALDH1A1TSHRFAAHTRPV1 | |
| SCHEMBL4965746 | 0.76 | ALDH1A1 (0.36) | ALDH1A1TSHRTHRBLMNAAOX1 | |
| SCHEMBL9848753 | 0.76 | ALDH1A1 (0.36) | ALDH1A1TSHRTHRBLMNAAOX1 |
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 40 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| 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 |
| 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 |
| EP-0229884-B1 | METHOD FOR THE PREPARATION OF 2,5 DIMETHOXY- AND 2,5 DIETHOXY-TETRAHYDROFURANE | Degussa Aktiengesellschaft (DE) | 1989-05-03 | — | — | EP | claimed |
| EP-0229884-A1 | Method for the preparation of 2,5 dimethoxy- and 2,5 diethoxy-tetrahydrofurane | Degussa Aktiengesellschaft (DE) | 1987-07-29 | — | — | EP | claimed |
| US-4680420-A | Process for the producing 2,5-dimethoxytetrahydrofuran and 2,5-diethoxytetrahydrofuran | DEGUSSA AKTIENGESELLSCHAFT (DE) | 1987-07-14 | — | — | US | claimed |
| CN-103172503-B | Preparation method of lycopene intermediate 3-methyl-4, 4-dialkoxy-1-butyraldehyde | NANJING UNIVERSITY OF TECHNOLOGY | 2015-03-11 | — | — | CN | disclosed |
| CN-103172503-A | Preparation method of lycopene intermediate 3-methyl-4, 4-dialkoxy-1-butyraldehyde | NANJING UNIVERSITY OF TECHNOLOGY | 2013-06-26 | — | — | CN | disclosed |
| CN-102199078-B | Method for preparing lycopene intermediate 3-methyl-4, 4-dialkoxyl-1-butyraldehyde | ZHEJIANG MED XINCHANG PHARM | 2013-04-03 | — | — | CN | disclosed |
| CN-101679282-B | Process for producing N-substituted (3-dihalomethyl-1-methylpyrazol-4-yl) carboxamides | BASF SE | 2012-11-28 | — | — | CN | disclosed |
| CN-102199078-A | Method for preparing lycopene intermediate 3-methyl-4, 4-dialkoxyl-1-butyraldehyde | ZHEJIANG MED XINCHANG PHARM | 2011-09-28 | — | — | CN | disclosed |
| EP-0151241-A1 | Process for the preparation of 1,4-butane-dialdehyde | Degussa Aktiengesellschaft (DE) | 1985-08-14 | — | — | EP | disclosed |
| US-4348539-A | Heteronuclear-bridged rhodium clusters | UNION CARBIDE CORPORATION (US) | 1982-09-07 | — | — | US | disclosed |
| US-4336206-A | Process for the manufacture of cyanohydrin acylates of aldehydes | HOECHST AKTIENGESELLSCHAFT (DE) | 1982-06-22 | — | — | US | disclosed |
| US-4288380-A | Heteronuclear-bridged rhodium clusters | UNION CARBIDE CORPORATION (US) | 1981-09-08 | — | — | US | disclosed |
| EP-0028892-A1 | A heteronuclear-bridged rhodium cluster and its application as catalyst for hydroformylation of olefins | UNION CARBIDE CORPORATION (US) | 1981-05-20 | — | — | EP | disclosed |
| US-4176190-A | Diuretic and saliuretic sulphamoylbenzoic acids | CIBA-GEIGY CORPORATION (US) | 1979-11-27 | — | — | US | disclosed |