Predicted protein targets (top 11)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | GCGR | P47871 | 3/20 | 0.51 |
| ▸ | DHFR | P00374 | 1/20 | 0.46 |
| ▸ | TYR | P14679 | 1/20 | 0.43 |
| ▸ | CNR2 | P34972 | 1/20 | 0.41 |
| ▸ | MGLL | Q99685 | 1/20 | 0.40 |
| ▸ | RARB | P10826 | 1/20 | 0.40 |
| ▸ | SOAT1 | P35610 | 2/20 | 0.40 |
| ▸ | ELANE | P08246 | 1/20 | 0.39 |
| ▸ | CTSG | P08311 | 1/20 | 0.39 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.39 |
| ▸ | MAPT | P10636 | 1/20 | 0.39 |
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 | |
|---|---|---|---|---|
| SCHEMBL2201817 | 1.00 | GCGR (0.51) | GCGRDHFRTYRCNR2MGLL | |
| SCHEMBL2202192 | 1.00 | GCGR (0.51) | GCGRDHFRTYRCNR2MGLL | |
| SCHEMBL2199195 | 1.00 | GCGR (0.51) | GCGRDHFRTYRCNR2MGLL | |
| SCHEMBL2202743 | 1.00 | GCGR (0.51) | GCGRDHFRTYRCNR2MGLL | |
| SCHEMBL2203973 | 1.00 | GCGR (0.51) | GCGRDHFRTYRCNR2MGLL | |
| SCHEMBL2204801 | 0.98 | GCGR (0.52) | GCGRDHFRTYRCNR2KDM4E | |
| SCHEMBL2203886 | 0.94 | GCGR (0.47) | GCGRDHFRCNR2KDM4E | |
| SCHEMBL2855337 | 0.89 | GCGR (0.49) | GCGRTYRMGLLRARBSOAT1 | |
| SCHEMBL2864086 | 0.88 | GCGR (0.50) | GCGRTYRELANECTSGKDM4E | |
| SCHEMBL2201210 | 0.87 | ESR2 (0.43) | GCGRCNR2KDM4E |
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 15 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-2792673-B1 | Carbamic acid ester derivatives for the production of isocyanate and aromatic hydroxy compounds | ASAHI CHEMICAL IND (JP) | 2018-07-25 | — | — | EP | disclosed |
| CN-103467730-B | Carbamate compounds | Asahi Kasei Chemical K. K. (JP) | 2015-12-23 | — | — | CN | disclosed |
| EP-2213658-B1 | METHOD FOR PRODUCTION OF ISOCYANATE AND AROMATIC HYDROXY COMPOUND | ASAHI KASEI CHEMICALS CORP (JP) | 2015-09-09 | — | — | EP | disclosed |
| EP-2792673-A1 | Carbamic acid ester derivatives for the production of isocyanate and aromatic hydroxy compounds | Asahi Kasei Chemicals Corporation (JP) | 2014-10-22 | — | — | EP | disclosed |
| CN-101868445-B | Method for producing isocyanate and aromatic hydroxy compound | ASAHI CHEMICAL CORP | 2014-06-18 | — | — | CN | disclosed |
| CN-101652344-B | Method for production of isocyanate using composition comprising carbamic acid ester and aromatic hydroxy compound, and composition for transport or storage of carbamic acid ester | ASAHI CHEMICAL CORP JP | 2014-06-04 | — | — | CN | disclosed |
| US-8703989-B2 | Isocyanates and aromatic hydroxy compounds | ASAHI KASEI CHEMICALS CORPORATION (JP) | 2014-04-22 | — | — | US | disclosed |
| CN-102026965-B | Method for producing isocyanate | ASAHI KASEI CHEMICALS CORP | 2014-02-26 | — | — | CN | disclosed |
| CN-103467730-A | Carbamate compound | ASAHI KASEI CHEMICAL CORP | 2013-12-25 | — | — | CN | disclosed |
| US-20130178643-A1 | Isocyanates and Aromatic Hydroxy Compounds | ASAHI KASEI CHEMICAL CORPORATION (JP) | 2013-07-11 | — | — | US | disclosed |
| US-8293934-B2 | Isocyanates and aromatic hydroxy compounds | ASAHI KASEI CHEMICALS CORPORATION (JP) | 2012-10-23 | — | — | US | disclosed |
| US-20110319648-A1 | Isocyanates and Aromatic Hydroxy Compounds | SHINOHATA MASAAKI (JP) | 2011-12-29 | — | — | US | disclosed |
| US-7977504-B2 | Process for producing isocyanates and aromatic hydroxy compounds | ASAHI KASEI CHEMICALS CORPORATION (JP) | 2011-07-12 | — | — | US | disclosed |
| US-20100274047-A1 | PROCESS FOR PRODUCING OF ISOCYANATES AND AROMATIC HYDROXY COMPOUNDS | ASAHI KASEI CHEMICALS CORPORATION (JP) | 2010-10-28 | — | — | US | disclosed |
| EP-2213658-A1 | METHOD FOR PRODUCTION OF ISOCYANATE AND AROMATIC HYDROXY COMPOUND | Asahi Kasei Chemicals Corporation (JP) | 2010-08-04 | — | — | 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 (3 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-20110319648-A1 | Isocyanates and Aromatic Hydroxy Compounds | PAH, APEH, HPD | GCGR 1946/4885DHFR 1761/4885TYR 85/4885 |
| US-20130178643-A1 | Isocyanates and Aromatic Hydroxy Compounds | PAH, APEH, HPD | GCGR 1946/4885DHFR 1761/4885TYR 85/4885 |
| US-20100274047-A1 | PROCESS FOR PRODUCING OF ISOCYANATES AND AROMATIC HYDROXY COMPOUNDS | PAH, APEH, HPD | GCGR 1943/4885DHFR 1282/4885TYR 138/4885 |
“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.