Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | PTGS2 | P35354 | 3/20 | 0.46 |
| ▸ | ESR1 | P03372 | 2/20 | 0.46 |
| ▸ | ADRA2A | P08913 | 2/20 | 0.46 |
| ▸ | ADORA3 | P0DMS8 | 2/20 | 0.46 |
| ▸ | TACR2 | P21452 | 2/20 | 0.46 |
| ▸ | SLC6A2 | P23975 | 2/20 | 0.46 |
| ▸ | SLC6A4 | P31645 | 2/20 | 0.46 |
| ▸ | SLC6A3 | Q01959 | 2/20 | 0.46 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.46 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.46 |
| ▸ | LMNA | P02545 | 1/20 | 0.46 |
| ▸ | SHBG | P04278 | 1/20 | 0.46 |
| ▸ | TP53 | P04637 | 1/20 | 0.46 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.46 |
| ▸ | HSPD1 | P10809 | 1/20 | 0.46 |
| ▸ | ADRB3 | P13945 | 1/20 | 0.46 |
| ▸ | HTR2C | P28335 | 1/20 | 0.46 |
| ▸ | HSPE1 | P61604 | 1/20 | 0.46 |
| ▸ | HIF1A | Q16665 | 1/20 | 0.46 |
| ▸ | TST | Q16762 | 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 | |
|---|---|---|---|---|
| SCHEMBL7765522 | 1.00 | PTGS2 (0.46) | PTGS2ESR1ADRA2AADORA3TACR2 | |
| SCHEMBL29640428 | 1.00 | PTGS2 (0.46) | PTGS2ESR1ADRA2AADORA3TACR2 | |
| SCHEMBL29399785 | 1.00 | PTGS2 (0.46) | PTGS2ESR1ADRA2AADORA3TACR2 | |
| SCHEMBL8142919 | 1.00 | PTGS2 (0.46) | PTGS2ESR1ADRA2AADORA3TACR2 | |
| SCHEMBL227244 | 0.93 | SNCA (0.46) | PTGS2ADORA3SLC6A2SLC6A3ALDH1A1 | |
| SCHEMBL29640461 | 0.93 | SNCA (0.46) | PTGS2ADORA3SLC6A2SLC6A3ALDH1A1 | |
| SCHEMBL8150371 | 0.92 | NOX1 (0.50) | PTGS2ADORA3SLC6A2SLC6A3LMNA | |
| SCHEMBL8156091 | 0.92 | NOX1 (0.50) | PTGS2ADORA3SLC6A2SLC6A3LMNA | |
| SCHEMBL223661 | 0.92 | NOX1 (0.50) | PTGS2ADORA3SLC6A2SLC6A3LMNA | |
| SCHEMBL7771194 | 0.86 | PTGS2 (0.46) | PTGS2ESR1ADRA2AADORA3TACR2 |
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 1239 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-12247165-B2 | Anti-syneresis agents for fracturing operations | HALLIBURTON ENERGY SERVICES, INC. (US) | 2025-03-11 | — | — | US | claimed |
| US-20250051634-A1 | ANTI-SYNERESIS AGENTS FOR FRACTURING OPERATIONS | HALLIBURTON ENERGY SERVICES, INC. (US) | 2025-02-13 | — | — | US | claimed |
| EP-2814922-B1 | WORKING FLUIDS COMPRISING DIFLUOROMETHANE AND DI-PENTAERYTHRITOL ESTER | LANXESS CORP (US) | 2021-01-13 | — | — | EP | claimed |
| US-10072164-B2 | Active energy ray-curable inkjet ink composition and printed product | DNP FINE CHEMICALS CO., LTD. (JP) | 2018-09-11 | — | — | US | claimed |
| EP-2247687-B1 | COMPOSITIONS AND METHODS OF TREATING HIGH TEMPERATURE SUBTERRANEAN FORMATIONS | BAKER HUGHES A GE CO LLC (US) | 2018-07-25 | — | — | EP | claimed |
| US-9902786-B2 | Method for immediately terminating radical polymerizations, inhibitor solution, and use thereof | ALLESSA GMBH (DE) | 2018-02-27 | — | — | US | claimed |
| EP-2941443-B1 | METHOD FOR IMMEDIATELY TERMINATING RADICAL POLYMERIZATIONS, INHIBITOR SOLUTION, AND USE THEREOF | ALLESSA GMBH (DE) | 2017-02-15 | — | — | EP | claimed |
| US-20170009089-A1 | ACTIVE ENERGY RAY-CURABLE INKJET INK COMPOSITION AND PRINTED PRODUCT | DNP FINE CHEMICALS CO LTD (JP) | 2017-01-12 | — | — | US | claimed |
| EP-2166060-B1 | Stabilized aqueous polymer compositions | TOUGAS OILFIELD SOLUTIONS GMBH (DE) | 2016-08-10 | — | — | EP | claimed |
| EP-2085424-B2 | Stabilized aqueous polymer compositions | TOUGAS OILFIELD SOLUTIONS GMBH (DE) | 2016-01-13 | — | — | EP | claimed |
| EP-0334500-A1 | Vinyl aromatic compositons stabilized against polymerization | UNIROYAL CHEMICAL COMPANY, Inc. (US) | 1989-09-27 | — | — | EP | claimed |
| EP-0325059-A2 | Polymerization inhibitor composition for vinyl aromatic compounds | UNIROYAL CHEMICAL COMPANY, Inc. (US) | 1989-07-26 | — | — | EP | claimed |
| EP-0216029-A2 | Method of indirect liquid-phase heat transfer | UNION CARBIDE CORPORATION (US) | 1987-04-01 | — | — | EP | claimed |
| EP-0212150-A2 | Method of indirect liquid-phase heat transfer | UNION CARBIDE CORPORATION (US) | 1987-03-04 | — | — | EP | claimed |
| US-4624299-A | THERMAL STABILITY | UNION CARBIDE CORPORATION (US) | 1986-11-25 | — | — | US | claimed |
| US-4617984-A | USING A LOW MOLECULAR WEIGHT POLYETHER FLUID | UNION CARBIDE CORPORATION (US) | 1986-10-21 | — | — | US | claimed |
| US-4363745-A | STERICALLY HINDERED PHENOL, BIS(A,A-DIMETHYLBENZYL) DIPHENYLAMINE AND A PHENOTHIAZINE COMPOUND STABILIZERS | THE DOW CHEMICAL COMPANY (US) | 1982-12-14 | — | — | US | claimed |
| US-4275173-A | SYNERGISTIC COMBINATION OF A STERICALLY HINDERED PHENOL AND 4,4*-BIS/A,A-DIMETHYLBENZYL/DIPHENYL AMINE AND A PHENOTHIAZINE PROVIDE OXIDATION RESISTANCE | THE DOW CHEMICAL COMPANY (US) | 1981-06-23 | — | — | US | claimed |
| US-4265783-A | SYNERGISTIC COMBINATION OF STERIC HINDERED PHENOL, 4,4*-BIS/A,A-DIMETHYL BENZYL/DIPHENYLAMINE AND A PHENOTHIAZINE | THE DOW CHEMICAL COMPANY (US) | 1981-05-05 | — | — | US | claimed |
| US-4010211-A | 2,6-DI-TERT-BUTYL-P-CRESOL, DISUBSTITUTED DIPHENYLAMINE, PHENOTHIAZINE COMPOUND | OLIN CORPORATION (US) | 1977-03-01 | — | — | US | claimed |