Predicted protein targets (top 9)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ALDH1A1 | P00352 | 3/20 | 0.41 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.39 |
| ▸ | TSHR | P16473 | 3/20 | 0.37 |
| ▸ | LMNA | P02545 | 2/20 | 0.37 |
| ▸ | HSD17B10 | Q99714 | 1/20 | 0.37 |
| ▸ | MEN1 | O00255 | 1/20 | 0.37 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.37 |
| ▸ | CES2 | O00748 | 1/20 | 0.32 |
| ▸ | CES1 | P23141 | 1/20 | 0.32 |
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 | |
|---|---|---|---|---|
| Propanol SCHEMBL16762189 | 0.96 | ALDH1A1 (0.39) | ALDH1A1SMN1; SMN2TSHRLMNAHSD17B10 | |
| Propanol SCHEMBL28112461 | 0.92 | — | — | |
| Propanol SCHEMBL28292919 | 0.92 | — | — | |
| Propanol SCHEMBL11326667 | 0.89 | ALDH1A1 (0.39) | ALDH1A1SMN1; SMN2TSHRLMNAHSD17B10 | |
| Propanol SCHEMBL29968655 | 0.89 | ALDH1A1 (0.39) | ALDH1A1SMN1; SMN2TSHRLMNAHSD17B10 | |
| Butyl Alcohol SCHEMBL8815824 | 0.83 | ALDH1A1 (0.69) | ALDH1A1SMN1; SMN2TSHRLMNAHSD17B10 | |
| SCHEMBL133782 | 0.83 | TSHR (0.33) | TSHRLMNACES2CES1 | |
| SCHEMBL30740491 | 0.83 | TSHR (0.33) | TSHRLMNACES2CES1 | |
| SCHEMBL30740424 | 0.83 | — | — | |
| Propanol SCHEMBL6348995 | 0.83 | ALDH1A1 (0.38) | ALDH1A1TSHRMEN1KMT2A |
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 28 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-2537828-A1 | METHOD FOR PRODUCING CYANOALKENYLCYCLOPROPANECARBOXYLIC ACID SALT | Sumitomo Chemical Company, Limited (JP) | 2012-12-26 | — | — | EP | disclosed |
| US-20120310003-A1 | METHOD FOR PRODUCING CYANOALKENYLCYCLOPROPANECARBOXYLIC ACID SALT | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2012-12-06 | — | — | US | disclosed |
| EP-1731509-B1 | PROCESS FOR PRODUCING NITROGENOUS 5-MEMBERED CYCLIC COMPOUND | JAPAN SCIENCE & TECH AGENCY (JP) | 2011-10-19 | — | — | EP | disclosed |
| EP-2208525-A2 | Process for steam reforming of a hydrocarbon | Battelle Memorial Institute (US) | 2010-07-21 | — | — | EP | disclosed |
| US-7705161-B2 | Process for producing nitrogenous 5-membered cyclic compound | JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) | 2010-04-27 | — | — | US | disclosed |
| EP-1251949-B1 | METHOD AND APPARATUS FOR OBTAINING ENHANCED PRODUCTION RATE OF THERMAL CHEMICAL REACTIONS | BATTELLE MEMORIAL INSTITUTE (US) | 2010-04-14 | — | — | EP | disclosed |
| US-20090220770-A1 | POLYMERIZABLE COMPOSITION, HIGH-REFRACTIVE-INDEX RESIN COMPOSITION, AND OPTICAL MEMBER MADE OF THE SAME | MITSUBISHI CHEMICAL CORPORATION (JP) | 2009-09-03 | — | — | US | disclosed |
| US-20070191614-A1 | Process for producing nitrogenous 5-membered cyclic compound | JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) | 2007-08-16 | — | — | US | disclosed |
| EP-1731509-A1 | PROCESS FOR PRODUCING NITROGENOUS 5-MEMBERED CYCLIC COMPOUND | Japan Science and Technology Agency (JP) | 2006-12-13 | — | — | EP | disclosed |
| EP-1102628-B1 | METHOD AND APPARATUS FOR OBTAINING ENHANCED PRODUCTION RATE OF THERMAL CHEMICAL REACTIONS | BATTELLE MEMORIAL INSTITUTE (US) | 2006-11-29 | — | — | EP | disclosed |
| EP-1251949-A1 | METHOD AND APPARATUS FOR OBTAINING ENHANCED PRODUCTION RATE OF THERMAL CHEMICAL REACTIONS | BATTELLE MEMORIAL INSTITUTE (US) | 2002-10-30 | — | — | EP | disclosed |
| US-20020031471-A1 | METHOD AND APPARATUS FOR OBTAINING ENHANCED PRODUCTION RATE OF THERMAL CHEMICAL REACTIONS | ENERGY, U.S. DEPARTMENT OF | 2002-03-14 | — | — | US | disclosed |
| WO-2001054807-A1 | METHOD AND APPARATUS FOR OBTAINING ENHANCED PRODUCTION RATE OF THERMAL CHEMICAL REACTIONS | BATTELLE MEMORIAL INSTITUTE (US) | 2001-08-02 | — | — | WO | disclosed |
| EP-1102628-A1 | METHOD AND APPARATUS FOR OBTAINING ENHANCED PRODUCTION RATE OF THERMAL CHEMICAL REACTIONS | BATTELLE MEMORIAL INSTITUTE (US) | 2001-05-30 | — | — | EP | disclosed |
| WO-2000006295-A1 | METHOD AND APPARATUS FOR OBTAINING ENHANCED PRODUCTION RATE OF THERMAL CHEMICAL REACTIONS | BATTELLE MEMORIAL INSTITUTE (US) | 2000-02-10 | — | — | WO | disclosed |
| EP-0330697-A4 | PREPARATION OF ABO 3? COMPOUNDS FROM MIXED METAL AROMATIC COORDINATION COMPLEXES | — | 1991-06-05 | — | — | EP | disclosed |
| US-4946810-A | Preparation of ABO3 compounds from mixed metal aromatic coordination complexes | THE DOW CHEMICAL COMPANY (US) | 1990-08-07 | — | — | US | disclosed |
| US-4880758-A | FORMING A POWDER BY DECOMPOSING A COMPLEX OF A METAL A COMPOUND, A METAL B COMPOUND, A SOLVATE, AN ALCOHOL AND A DISUBSTITUTED AROMATIC COMPOUND | THE DOW CHEMICAL COMPANY (US) | 1989-11-14 | — | — | US | disclosed |
| EP-0330697-A1 | PREPARATION OF ABO 3? COMPOUNDS FROM MIXED METAL AROMATIC COORDINATION COMPLEXES | THE DOW CHEMICAL COMPANY (US) | 1989-09-06 | — | — | EP | disclosed |
| WO-1989001922-A1 | PREPARATION OF ABO3 COMPOUNDS FROM MIXED METAL AROMATIC COORDINATION COMPLEXES | THE DOW CHEMICAL COMPANY (US) | 1989-03-09 | — | — | WO | 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 (2 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-20120310003-A1 | METHOD FOR PRODUCING CYANOALKENYLCYCLOPROPANECARBOXYLIC ACID SALT | MCCC2, AOC2, DDC | ALDH1A1 809/4885SMN1; SMN2 3861/4885TSHR 1331/4885 |
| US-20070191614-A1 | Process for producing nitrogenous 5-membered cyclic compound | HRH4, HRH2, HRH1 | ALDH1A1 605/4885SMN1; SMN2 4424/4885TSHR 897/4885 |
“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.