Predicted protein targets (top 12)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | NAAA | Q02083 | 1/20 | 0.67 |
| ▸ | EPHX1 | P07099 | 1/20 | 0.61 |
| ▸ | TSHR | P16473 | 3/20 | 0.59 |
| ▸ | HCAR2 | Q8TDS4 | 1/20 | 0.55 |
| ▸ | RAD52 | P43351 | 1/20 | 0.55 |
| ▸ | NPSR1 | Q6W5P4 | 1/20 | 0.55 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.54 |
| ▸ | DGKA | P23743 | 1/20 | 0.54 |
| ▸ | ACHE | P22303 | 6/20 | 0.54 |
| ▸ | FAAH | O00519 | 1/20 | 0.53 |
| ▸ | LMNA | P02545 | 1/20 | 0.53 |
| ▸ | CES2 | O00748 | 1/20 | 0.52 |
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 | |
|---|---|---|---|---|
| SCHEMBL1835881 | 1.00 | NAAA (0.67) | NAAAEPHX1TSHRHCAR2RAD52 | |
| SCHEMBL1839030 | 1.00 | NAAA (0.67) | NAAAEPHX1TSHRHCAR2RAD52 | |
| SCHEMBL119774 | 1.00 | NAAA (0.67) | NAAAEPHX1TSHRHCAR2RAD52 | |
| SCHEMBL1834574 | 1.00 | NAAA (0.67) | NAAAEPHX1TSHRHCAR2RAD52 | |
| SCHEMBL1839498 | 1.00 | NAAA (0.67) | NAAAEPHX1TSHRHCAR2RAD52 | |
| SCHEMBL1837444 | 1.00 | NAAA (0.67) | NAAAEPHX1TSHRHCAR2RAD52 | |
| SCHEMBL1841329 | 1.00 | NAAA (0.67) | NAAAEPHX1TSHRHCAR2RAD52 | |
| SCHEMBL4934658 | 1.00 | NAAA (0.67) | NAAAEPHX1TSHRHCAR2RAD52 | |
| SCHEMBL1838958 | 1.00 | NAAA (0.67) | NAAAEPHX1TSHRHCAR2RAD52 | |
| SCHEMBL1839798 | 1.00 | NAAA (0.67) | NAAAEPHX1TSHRHCAR2RAD52 |
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 49 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-4446310-A1 | METHOD FOR PRODUCING BLOCKED ISOCYANATE COMPOUND AND METHOD FOR PRODUCING ISOCYANATE COMPOUND | Asahi Kasei Kabushiki Kaisha (JP) | 2024-10-16 | — | — | EP | disclosed |
| CN-118382612-A | Method for producing blocked isocyanate compound and method for producing isocyanate compound | 旭化成株式会社 | 2024-07-23 | — | — | CN | disclosed |
| EP-3838892-B1 | METHOD FOR PRODUCING ISOCYANATE | ASAHI CHEMICAL IND (JP) | 2022-10-12 | — | — | EP | disclosed |
| EP-3293173-B1 | METHOD FOR PRODUCING ISOCYANATE | ASAHI CHEMICAL IND (JP) | 2021-07-28 | — | — | EP | disclosed |
| EP-3838892-A1 | METHOD FOR PRODUCING ISOCYANATE | Asahi Kasei Kabushiki Kaisha (JP) | 2021-06-23 | — | — | EP | disclosed |
| EP-2980066-B1 | METHOD FOR PRODUCING ISOCYANATE | ASAHI CHEMICAL IND (JP) | 2021-04-21 | — | — | EP | disclosed |
| EP-3153499-B1 | METHOD FOR PRODUCING N-SUBSTITUTED CARBAMIC ACID ESTER | ASAHI CHEMICAL IND (JP) | 2018-09-19 | — | — | EP | disclosed |
| EP-3293173-A1 | METHOD FOR PRODUCING ISOCYANATE | Asahi Kasei Kabushiki Kaisha (JP) | 2018-03-14 | — | — | EP | disclosed |
| EP-2322504-B9 | PROCESS FOR THE PREPARATION OF N-SUBSTITUTED CARBAMIC ACID ESTER AND PROCESS FOR THE PREPARATION OF ISOCYANATE USING THE N-SUBSTITUTED CARBAMIC ACID ESTER | ASAHI CHEMICAL IND (JP) | 2017-09-06 | — | — | EP | disclosed |
| US-9714215-B2 | Method for producing isocyanate | ASAHI KASEI CHEMICALS CORPORATION (JP) | 2017-07-25 | — | — | US | disclosed |
| US-20040266974-A1 | METHOD AND APPARATUS FOR PRODUCTION OF ALKYL ARYL ETHER AND DIARYL CARBONATE | GENERAL ELECTRIC COMPANY | 2004-12-30 | — | — | US | disclosed |
| WO-2004113264-A2 | METHOD AND APPARATUS FOR WASTE STREAM RECOVERY | GENERAL ELECTRIC COMPANY (US) | 2004-12-29 | — | — | WO | disclosed |
| EP-1337503-A2 | METHOD FOR THE CONTINUOUS PRODUCTION OF AROMATIC CARBONATES | GENERAL ELECTRIC COMPANY (US) | 2003-08-27 | — | — | EP | disclosed |
| US-6600061-B1 | Method for making aromatic carbonates. In this method, an aryl alcohol is reacted with a dialkyl carbonate in a reactor (e.g., a distillation column) to produce an arylalkyl carbonate and diaryl carbonate. The total yield is 40% | GENERAL ELECTRIC COMPANY | 2003-07-29 | — | — | US | disclosed |
| US-6596895-B2 | Diphenyl carbonate is made by reacting an aryl alcohol with a dialkyl carbonate to produce aryl alkylcarbonate and diaryl carbonate and reacting the diphenyl carbonate with a dihydric phenol to produce an aromatic polycarbonate | GENERAL ELECTRIC COMPANY | 2003-07-22 | — | — | US | disclosed |
| US-6596894-B2 | Feeding the top section of a distillation column an aryl alcohol and a titanium alkyl or aryl oxide catalyst and the bottom that has a temperature of 220-240 degrees C a dialkyl carbonate | GENERAL ELECTRIC COMPANY | 2003-07-22 | — | — | US | disclosed |
| US-20020156312-A1 | Feeding the top section of a distillation column an aryl alcohol and a titanium alkyl or aryl oxide catalyst and the bottom that has a temperature of 220-240 degrees C a dialkyl carbonate | SABIC GLOBAL TECHNOLOGIES B.V. (NL) | 2002-10-24 | — | — | US | disclosed |
| US-20020107355-A1 | Method for the continuous production of aromatic carbonates | SABIC GLOBAL TECHNOLOGIES B.V. (NL) | 2002-08-08 | — | — | US | disclosed |
| WO-2002040439-A2 | METHOD FOR THE CONTINUOUS PRODUCTION OF AROMATIC CARBONATES | GENERAL ELECTRIC COMPANY (US) | 2002-05-23 | — | — | WO | disclosed |
| US-3992453-A | Hydroformylation process | UNIVERSAL OIL PRODUCTS COMPANY (US) | 1976-11-16 | — | — | US | disclosed |