Predicted protein targets (top 1)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | TSHR | P16473 | 1/20 | 0.40 |
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 | |
|---|---|---|---|---|
| SCHEMBL10870807 | 1.00 | TSHR (0.40) | TSHR | |
| SCHEMBL6904916 | 1.00 | TSHR (0.40) | TSHR | |
| SCHEMBL10868788 | 1.00 | TSHR (0.40) | TSHR | |
| SCHEMBL10870784 | 1.00 | TSHR (0.40) | TSHR | |
| SCHEMBL10869461 | 1.00 | TSHR (0.40) | TSHR | |
| SCHEMBL10870055 | 1.00 | TSHR (0.40) | TSHR | |
| SCHEMBL10870835 | 1.00 | TSHR (0.40) | TSHR | |
| SCHEMBL10869939 | 1.00 | TSHR (0.40) | TSHR | |
| SCHEMBL6472048 | 1.00 | TSHR (0.40) | TSHR | |
| SCHEMBL6903468 | 1.00 | TSHR (0.40) | TSHR |
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 23 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-113874341-B | Process for preparing derivatives of 1, 1-dialkylethane-1, 2-diols useful as intermediates | 科学与工业研究委员会 | 2024-05-31 | — | — | CN | disclosed |
| CN-110003432-A | A kind of preparation method of fluorochemical urethane | 苏州大学 | 2019-07-12 | — | — | CN | disclosed |
| CN-108707227-A | A kind of preparation method of the copolyether containing fluoroalkyl | 苏州大学 | 2018-10-26 | — | — | CN | disclosed |
| US-7880038-B2 | complexing a tungsten boride and molybdenum boride, a phosphate compound, Mo and W metal, hydrogen peroxide and an amine oxide to form a catalyst, reacting an olefin with H2O2 in the pH 0 to 2 or more, in presence of above catalyst to produce carbonyl compounds by oxidative breaking of C-C bond of olefin | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2011-02-01 | — | — | US | disclosed |
| EP-1618953-B1 | USE OF A METAL CATALYST | SUMITOMO CHEMICAL CO (JP) | 2010-12-08 | — | — | EP | disclosed |
| US-20060211891-A1 | Metal catalyst and its use | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2006-09-21 | — | — | US | disclosed |
| US-7074947-B2 | Process for producing epoxide compound | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2006-07-11 | — | — | US | disclosed |
| EP-1618953-A1 | METAL CATALYST AND ITS USE | Sumitomo Chemical Company, Limited (JP) | 2006-01-25 | — | — | EP | disclosed |
| US-20050020841-A1 | Process for producing expoxide compound | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2005-01-27 | — | — | US | disclosed |
| EP-1473290-A1 | PROCESS FOR PRODUCING EPOXIDE COMPOUND | Sumitomo Chemical Company, Limited (JP) | 2004-11-03 | — | — | EP | disclosed |
| EP-1304321-A2 | Process for preparing 3-Hydroxyesters from epoxide derivatives | SAMSUNG ELECTRONICS CO., LTD. (KR) | 2003-04-23 | — | — | EP | disclosed |
| US-6541414-B2 | For preparing an 1,3-alkanediol through carbonylation of an epoxide derivative | SAMSUNG ELECTRONICS CO., LTD. (KR) | 2003-04-01 | — | — | US | disclosed |
| US-6521801-B2 | Catalytic carbonylation of epoxide derivative includes reacting with alcohol and carbon monoxide to form hydroxyester which is hydrogenated to form diol | SAMSUNG ELECTRONICS CO., LTD. (KR) | 2003-02-18 | — | — | US | disclosed |
| US-6465680-B2 | USING COBALT CATALYST AND PROMOTER | SAMSUNG ELECTRONICS CO., LTD. (KR) | 2002-10-15 | — | — | US | disclosed |
| US-20020099245-A1 | For preparing an 1,3-alkanediol through carbonylation of an epoxide derivative | SAMSUNG ELECTRONICS CO., LTD (KR) | 2002-07-25 | — | — | US | disclosed |
| US-20020065439-A1 | Catalytic carbonylation of epoxide derivative includes reacting with alcohol and carbon monoxide to form hydroxyester which is hydrogenated to form diol | DAVY PROCESS TECHNOLOGY LIMITED (GB) | 2002-05-30 | — | — | US | disclosed |
| US-20020035290-A1 | Process for preparing malonate derivatives or beta -keto esters from epoxide derivatives | SAMSUNG ELECTRONICS CO., LTD. | 2002-03-21 | — | — | US | disclosed |
| US-6348632-B1 | Process for preparing 1,3-alkanediol from epoxide derivative | SAMSUNG ELECTRONICS CO. LTD. (KR) | 2002-02-19 | — | — | US | disclosed |
| EP-1122235-A2 | Process for preparing 1,3-alkanediol from epoxide derivative | SAMSUNG ELECTRONICS CO., LTD. (KR) | 2001-08-08 | — | — | EP | disclosed |
| US-3935152-A | THERMOPLASTIC, EPOXY COMPOUND | DAICEL LTD. (JA) | 1976-01-27 | — | — | US | 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 (4 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-20020099245-A1 | For preparing an 1,3-alkanediol through carbonylation of an epoxide derivative | CYP2E1, ADH1C, OR51E2 | TSHR 4684/4885 |
| US-20060211891-A1 | Metal catalyst and its use | SOD1, NOX4, MVD | TSHR 2499/4885 |
| US-20020035290-A1 | Process for preparing malonate derivatives or beta -keto esters from epoxide derivatives | CYP4A11, ME1, CYP2E1 | TSHR 4610/4885 |
| US-20020065439-A1 | Catalytic carbonylation of epoxide derivative includes reacting with alcohol and carbon monoxide to form hydroxyester which is hydrogenated to form diol | CYP2E1, ADH1C, ADH1A | TSHR 4712/4885 |
“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.