Predicted protein targets (top 9)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | TSHR | P16473 | 2/20 | 0.64 |
| ▸ | ALDH1A1 | P00352 | 4/20 | 0.53 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.53 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.52 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.36 |
| ▸ | MEN1 | O00255 | 1/20 | 0.35 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.35 |
| ▸ | SPHK2 | Q9NRA0 | 4/20 | 0.33 |
| ▸ | SPHK1 | Q9NYA1 | 4/20 | 0.33 |
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 | |
|---|---|---|---|---|
| SCHEMBL15962173 | 0.89 | TSHR (0.82) | TSHRALDH1A1TDP1SMN1; SMN2MAPK1 | |
| SCHEMBL19051883 | 0.87 | TSHR (0.78) | TSHRALDH1A1TDP1SMN1; SMN2MAPK1 | |
| SCHEMBL9885961 | 0.82 | TSHR (0.77) | TSHRALDH1A1TDP1SMN1; SMN2MAPK1 | |
| SCHEMBL10337390 | 0.81 | ALDH1A1 (0.77) | TSHRALDH1A1TDP1SMN1; SMN2MEN1 | |
| SCHEMBL3371973 | 0.80 | TSHR (0.52) | TSHRALDH1A1TDP1SMN1; SMN2MAPK1 | |
| SCHEMBL13974192 | 0.80 | TSHR (1.00) | TSHRALDH1A1TDP1SMN1; SMN2MAPK1 | |
| SCHEMBL17549553 | 0.80 | TSHR (1.00) | TSHRALDH1A1TDP1SMN1; SMN2MAPK1 | |
| SCHEMBL17549551 | 0.80 | TSHR (1.00) | TSHRALDH1A1TDP1SMN1; SMN2MAPK1 | |
| SCHEMBL21272 | 0.80 | TSHR (1.00) | TSHRALDH1A1TDP1SMN1; SMN2MAPK1 | |
| SCHEMBL17549552 | 0.80 | TSHR (1.00) | TSHRALDH1A1TDP1SMN1; SMN2MAPK1 |
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 19 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-8754138-B2 | Polymers obtained from monomers allowing a sequential polymerization, and their use for preparing ionic conductors | HYDRO-QUEBEC (CA) | 2014-06-17 | — | — | US | disclosed |
| US-8754138-B2 | Polymers obtained from monomers allowing a sequential polymerization, and their use for preparing ionic conductors | HYDRO-QUEBEC (CA) | 2014-06-17 | — | — | US | disclosed |
| US-8754138-B2 | Polymers obtained from monomers allowing a sequential polymerization, and their use for preparing ionic conductors | HYDRO-QUEBEC (CA) | 2014-06-17 | — | — | US | disclosed |
| US-20130277599-A1 | POLYMERS OBTAINED FROM MONOMERS ALLOWING A SEQUENTIAL POLYMERIZATION, AND THEIR USE FOR PREPARING IONIC CONDUCTORS | HYDRO-QUEBEC (CA) | 2013-10-24 | — | — | US | disclosed |
| US-20130277599-A1 | POLYMERS OBTAINED FROM MONOMERS ALLOWING A SEQUENTIAL POLYMERIZATION, AND THEIR USE FOR PREPARING IONIC CONDUCTORS | HYDRO-QUEBEC (CA) | 2013-10-24 | — | — | US | disclosed |
| US-20130277599-A1 | POLYMERS OBTAINED FROM MONOMERS ALLOWING A SEQUENTIAL POLYMERIZATION, AND THEIR USE FOR PREPARING IONIC CONDUCTORS | HYDRO-QUEBEC (CA) | 2013-10-24 | — | — | US | disclosed |
| US-8512899-B2 | Lithium batteries; polyethers from monomers having acrylic or vinyl ethylene double bonds or perfluorosulfonate at one end of the compound and a glycidyl, dioxolyl or dioxyl group at the other; controllable molecular weight range and crosslinking density; dissolving ionic compounds; solid electrolytes | HYDRO-QUEBEC (CA) | 2013-08-20 | — | — | US | disclosed |
| US-8512899-B2 | Lithium batteries; polyethers from monomers having acrylic or vinyl ethylene double bonds or perfluorosulfonate at one end of the compound and a glycidyl, dioxolyl or dioxyl group at the other; controllable molecular weight range and crosslinking density; dissolving ionic compounds; solid electrolytes | HYDRO-QUEBEC (CA) | 2013-08-20 | — | — | US | disclosed |
| US-8512899-B2 | Lithium batteries; polyethers from monomers having acrylic or vinyl ethylene double bonds or perfluorosulfonate at one end of the compound and a glycidyl, dioxolyl or dioxyl group at the other; controllable molecular weight range and crosslinking density; dissolving ionic compounds; solid electrolytes | HYDRO-QUEBEC (CA) | 2013-08-20 | — | — | US | disclosed |
| EP-1693390-B1 | Polymers from block copolymerisable monomers and their use e.g. for the preparation of ionic conductors | HYDRO QUEBEC (CA) | 2010-10-13 | — | — | EP | disclosed |
| US-20080213661-A1 | Polymers Obtained From Monomers Allowing A Sequential Polymerization, And Their Use For Preparing Ionic Conductors | HYDRO-QUEBEC (CA) | 2008-09-04 | — | — | US | disclosed |
| US-20080213661-A1 | Polymers Obtained From Monomers Allowing A Sequential Polymerization, And Their Use For Preparing Ionic Conductors | HYDRO-QUEBEC (CA) | 2008-09-04 | — | — | US | disclosed |
| EP-1693390-A1 | Polymers from block copolymerisable monomers and their use e.g. for the preparation of ionic conductors | HYDRO-QUEBEC (CA) | 2006-08-23 | — | — | EP | disclosed |
| EP-0967233-B1 | Ion conductive material | HYDRO QUEBEC (CA) | 2006-03-01 | — | — | EP | disclosed |
| US-20040220348-A1 | Polymers obtained from monomers allowing a sequential polymerization, and their use for preparing ionic conductors | MICHOT CHRISTOPHE (FR) | 2004-11-04 | — | — | US | disclosed |
| US-20030125437-A1 | Polymers obtained from monomers allowing a sequential polymerization, and their use for preparing ionic conductors | MICHOT CHRISTOPHE (FR) | 2003-07-03 | — | — | US | disclosed |
| US-6492449-B2 | POLYMERS OBTAINED BY ANIONIC INITIATION AND BEARING FUNCTIONS THAT CAN BE ACTIVATED BY CATIONIC INITIATIONS THAT ARE NOT REACTIVE IN THE PRESENCE OF ANIONIC POLYMERIZATION INITIATORS. | HYDRO-QUEBEC (CA) | 2002-12-10 | — | — | US | disclosed |
| US-20020128364-A1 | POLYMERS OBTAINED FROM MONOMERS ALLOWING A SEQUENTIAL POLYMERIZATION, AND THEIR USE FOR PREPARING IONIC CONDUCTORS | HYDRO-QUEBEC (CA) | 2002-09-12 | — | — | US | disclosed |
| EP-0967233-A1 | Polymers from block copolymerisable monomers and their use e.g. for the preparation of ionic conductors | HYDRO-QUEBEC (CA) | 1999-12-29 | — | — | EP | disclosed |
Patent text — is the patent's own abstract consistent with the prediction?
For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20130277599-A1 | POLYMERS OBTAINED FROM MONOMERS ALLOWING A SEQUENTIAL POLYMERIZATION, AND THEIR USE FOR PREPARING IONIC CONDUCTORS | KCNN4, PUF60, HCN4 | TSHR 4851/4885ALDH1A1 3267/4885TDP1 2208/4885 |
“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.