Predicted protein targets (top 9)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.68 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.68 |
| ▸ | LMNA | P02545 | 1/20 | 0.54 |
| ▸ | DNM1 | Q05193 | 10/20 | 0.48 |
| ▸ | OPRM1 | P35372 | 1/20 | 0.46 |
| ▸ | MEN1 | O00255 | 1/20 | 0.46 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.46 |
| ▸ | TSHR | P16473 | 1/20 | 0.46 |
| ▸ | EPHX1 | P07099 | 1/20 | 0.46 |
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 | |
|---|---|---|---|---|
| SCHEMBL13627232 | 1.00 | ALDH1A1 (0.68) | ALDH1A1TDP1LMNADNM1OPRM1 | |
| SCHEMBL5074318 | 1.00 | ALDH1A1 (0.68) | ALDH1A1TDP1LMNADNM1OPRM1 | |
| SCHEMBL3797556 | 1.00 | ALDH1A1 (0.68) | ALDH1A1TDP1LMNADNM1OPRM1 | |
| SCHEMBL3628105 | 1.00 | ALDH1A1 (0.68) | ALDH1A1TDP1LMNADNM1OPRM1 | |
| SCHEMBL1164854 | 1.00 | ALDH1A1 (0.68) | ALDH1A1TDP1LMNADNM1OPRM1 | |
| SCHEMBL3625440 | 1.00 | ALDH1A1 (0.68) | ALDH1A1TDP1LMNADNM1OPRM1 | |
| Water SCHEMBL9435613 | 0.97 | ALDH1A1 (0.65) | ALDH1A1TDP1LMNADNM1OPRM1 | |
| SCHEMBL24200454 | 0.97 | ALDH1A1 (0.64) | ALDH1A1TDP1LMNADNM1OPRM1 | |
| SCHEMBL20495959 | 0.97 | ALDH1A1 (0.64) | ALDH1A1TDP1LMNADNM1OPRM1 | |
| SCHEMBL22658086 | 0.97 | ALDH1A1 (0.64) | ALDH1A1TDP1LMNADNM1OPRM1 |
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 29 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20250304543-A1 | PROCESS FOR MAKING A SUBSTANTIALLY NITROSAMINE-FREE, SUBSTANTIALLY PEROXIDE-FREE, SUBSTANTIALLY COLORLESS AMINE OXIDE | BASF SE (DE) | 2025-10-02 | — | — | US | disclosed |
| EP-4536645-A1 | PROCESS FOR MAKING A SUBSTANTIALLY NITROSAMINE-FREE, SUBSTANTIALLY PEROXIDE-FREE, SUBSTANTIALLY COLORLESS AMINE OXIDE | BASF SE (DE) | 2025-04-16 | — | — | EP | disclosed |
| WO-2023237729-A1 | PROCESS FOR MAKING A SUBSTANTIALLY NITROSAMINE-FREE, SUBSTANTIALLY PEROXIDE-FREE, SUBSTANTIALLY COLORLESS AMINE OXIDE | BASF SE (DE) | 2023-12-14 | — | — | WO | disclosed |
| CN-104119505-B | Containing pyrroles's indoles 1,4-Dithiapentalene-two thieno-benzodiazole conjugated polymer material and its preparation method and application | Haiyangwang Lighting Technology Co., Ltd. (CN) | 2016-06-01 | — | — | CN | disclosed |
| CN-104119510-B | Containing pyrroles's indoles 1,4-Dithiapentalene-bis-thieno benzotriazole conjugated polymer and preparation method thereof and application | Haiyangwang Lighting Technology Co., Ltd. (CN) | 2016-05-11 | — | — | CN | disclosed |
| CN-104211910-A | Conjugated polymer, preparation method and applications thereof | OCEANS KING LIGHTING SCIENCE | 2014-12-17 | — | — | CN | disclosed |
| CN-104211914-A | Conjugated polymer, preparation method, and applications thereof | OCEANS KING LIGHTING SCIENCE | 2014-12-17 | — | — | CN | disclosed |
| CN-104211920-A | Conjugated polymer, preparation method and applications thereof | OCEANS KING LIGHTING SCIENCE | 2014-12-17 | — | — | CN | disclosed |
| CN-104211919-A | Conjugated polymer, preparation method, and applications thereof | OCEANS KING LIGHTING SCIENCE | 2014-12-17 | — | — | CN | disclosed |
| CN-104211911-A | Conjugated polymer, preparation method, and applications thereof | OCEANS KING LIGHTING SCIENCE | 2014-12-17 | — | — | CN | disclosed |
| US-5023376-A | Using alkyleneaminopoly(methylene phosphonic acid) compounds | INTEROX AMERICA (US) | 1991-06-11 | — | — | US | disclosed |
| EP-0424965-A1 | Amine oxide process | ETHYL CORPORATION (US) | 1991-05-02 | — | — | EP | disclosed |
| US-4994614-A | Reacting tertiary amines with aqueous hydrogen peroxide in presence of synergistic combination of ascorbic acid and carbon dioxide; purity | ETHYL CORPORATION (US) | 1991-02-19 | — | — | US | disclosed |
| EP-0409043-A1 | Reduction of nitrosamine formation | SOLVAY INTEROX (US) | 1991-01-23 | — | — | EP | disclosed |
| US-4960934-A | Amine oxide process | ETHYL CORPORATION (US) | 1990-10-02 | — | — | US | disclosed |
| US-4942260-A | REACTION OF A TERT-AMINE WITH HYDROGEN PEROXIDE IN THE PRESENCE OF CATALYTIC CARBON DIOXIDE | ETHYL CORPORATION (US) | 1990-07-17 | — | — | US | disclosed |
| EP-0356918-A1 | Amine oxide process | ETHYL CORPORATION (US) | 1990-03-07 | — | — | EP | disclosed |
| US-4889954-A | DIALKYLCARBONATE CATALYST | ETHYL CORPORATION (US) | 1989-12-26 | — | — | US | disclosed |
| EP-0320694-A2 | Amine oxide process | ETHYL CORPORATION (US) | 1989-06-21 | — | — | EP | disclosed |
| EP-0307184-A2 | Preparation of Amine Oxides | ETHYL CORPORATION (US) | 1989-03-15 | — | — | EP | disclosed |