Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ESR1 | P03372 | 5/20 | 0.48 |
| ▸ | ESR2 | Q92731 | 4/20 | 0.48 |
| ▸ | MEN1 | O00255 | 4/20 | 0.48 |
| ▸ | KMT2A | Q03164 | 4/20 | 0.48 |
| ▸ | CA9 | Q16790 | 4/20 | 0.46 |
| ▸ | HSD17B1 | P14061 | 1/20 | 0.44 |
| ▸ | LMNA | P02545 | 4/20 | 0.44 |
| ▸ | CYP3A4 | P08684 | 4/20 | 0.44 |
| ▸ | MAPT | P10636 | 4/20 | 0.44 |
| ▸ | CYP1A2 | P05177 | 3/20 | 0.44 |
| ▸ | CYP2C19 | P33261 | 3/20 | 0.44 |
| ▸ | ALOX15 | P16050 | 3/20 | 0.44 |
| ▸ | HIF1A | Q16665 | 3/20 | 0.44 |
| ▸ | HSD17B10 | Q99714 | 3/20 | 0.44 |
| ▸ | GAA | P10253 | 2/20 | 0.44 |
| ▸ | NR3C1 | P04150 | 2/20 | 0.44 |
| ▸ | TP53 | P04637 | 2/20 | 0.44 |
| ▸ | ADORA3 | P0DMS8 | 2/20 | 0.44 |
| ▸ | CYP2D6 | P10635 | 2/20 | 0.44 |
| ▸ | CYP2C9 | P11712 | 2/20 | 0.44 |
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 | |
|---|---|---|---|---|
| SCHEMBL17548938 | 1.00 | ESR1 (0.48) | ESR1ESR2MEN1KMT2ACA9 | |
| SCHEMBL14626976 | 1.00 | ESR1 (0.48) | ESR1ESR2MEN1KMT2ACA9 | |
| SCHEMBL14298196 | 0.89 | CA9 (0.52) | MEN1KMT2ACA9LMNACYP3A4 | |
| SCHEMBL12360950 | 0.89 | CA9 (0.52) | MEN1KMT2ACA9LMNACYP3A4 | |
| SCHEMBL12260084 | 0.81 | FURIN (0.61) | ESR1ESR2MEN1KMT2ACA9 | |
| SCHEMBL13645704 | 0.81 | CA9 (0.47) | ESR1ESR2KMT2ACA9HSD17B1 | |
| SCHEMBL4364091 | 0.81 | FURIN (0.61) | ESR1ESR2MEN1KMT2ACA9 | |
| SCHEMBL12741076 | 0.79 | CA9 (0.56) | CA9LMNACYP3A4MAPTCYP1A2 | |
| SCHEMBL514858 | 0.79 | CA9 (0.56) | CA9LMNACYP3A4MAPTCYP1A2 | |
| SCHEMBL514859 | 0.79 | CA9 (0.56) | CA9LMNACYP3A4MAPTCYP1A2 |
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 282 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-118725243-A | 3D printable water-reinforced polymer material and preparation method and application thereof | 东华大学 | 2024-10-01 | — | — | CN | claimed |
| CN-117861720-A | Layered aluminophosphates as catalysts for Beckmann rearrangement | 艾德凡斯化学公司 | 2024-04-12 | — | — | CN | claimed |
| CN-116496174-A | Refining method of p-hydroxyacetophenone ammoximation reaction product | 江苏新瀚新材料股份有限公司 | 2023-07-28 | — | — | CN | claimed |
| CN-111607055-B | High molecular weight polyurethane based on dynamic reversible covalent bond and preparation method and application thereof | 中国科学院化学研究所 | 2021-07-16 | — | — | CN | claimed |
| CN-112251164-A | Electromagnetic shielding adhesive tape and preparation method thereof | 深圳日高胶带新材料有限公司 | 2021-01-22 | — | — | CN | claimed |
| EP-2771317-B1 | LIQUID PHASE CATALYTIC BECKMANN REARRANGEMENT OF OXIMES TO PRODUCE LACTAMS | ADVANSIX RESINS & CHEMICALS LLC (US) | 2020-12-09 | — | — | EP | claimed |
| CN-108355709-B | Application of bismuth trifluoromethanesulfonate as Beckmann rearrangement reaction catalyst | 嘉兴学院 | 2020-12-08 | — | — | CN | claimed |
| CN-111607055-A | High molecular weight polyurethane based on dynamic reversible covalent bond and preparation method and application thereof | 中国科学院化学研究所 | 2020-09-01 | — | — | CN | claimed |
| CN-110714213-A | Cyanide-free alkaline cuprous copper electroplating complexing agent | 武汉奥邦表面技术有限公司 | 2020-01-21 | — | — | CN | claimed |
| EP-3233804-B1 | BECKMANN REARRANGEMENT USING HIERARCHICAL ALUMINOPHOSPHATES AS CATALYSTS | ADVANSIX RESINS & CHEMICALS LLC (US) | 2019-09-04 | — | — | EP | claimed |
| US-4855499-A | Novel process to prevent formation of chlorinated by-products in APAP production | HOECHST CELANESE CORPORATION (US) | 1989-08-08 | — | — | US | claimed |
| EP-0326397-A2 | A process for producing an aqueous 4-hydroxyacetophenone (4-hap) which is stable at room temperature | HOECHST CELANESE CORPORATION (US) | 1989-08-02 | — | — | EP | claimed |
| EP-0168908-B1 | PROCESS FOR PRODUCING N-ACYL-ACYLOXY AROMATIC AMINES | CELANESE CORPORATION (US) | 1988-12-07 | — | — | EP | claimed |
| US-4665216-A | Process for producing n-acyl-acyloxy aromatic amines | CELANESE CORPORATION (US) | 1987-05-12 | — | — | US | claimed |
| CN-85101149-A | The preparation method of N-acyl group-hydroxyl and N-acyl group-acyloxy aromatic amine | — | 1987-01-17 | — | — | CN | claimed |
| EP-0194849-A2 | Improved process for producing N-acyl-acyloxy aromatic amines | CELANESE CORPORATION (US) | 1986-09-17 | — | — | EP | claimed |
| US-4568763-A | Process for producing N-acyl-acyloxy aromatic amines | CELANESE CORPORATION (US) | 1986-02-04 | — | — | US | claimed |
| EP-0168908-A1 | Process for producing N-acyl-acyloxy aromatic amines | CELANESE CORPORATION (US) | 1986-01-22 | — | — | EP | claimed |
| US-4560789-A | Process for producing 4-acetoxyacetanilide | CELANESE CORPORATION (US) | 1985-12-24 | — | — | US | claimed |
| US-4524217-A | Process for producing N-acyl-hydroxy aromatic amines | CELANESE CORPORATION (US) | 1985-06-18 | — | — | US | claimed |