Predicted protein targets (top 19)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | AOC3 | Q16853 | 2/20 | 0.36 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.36 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.36 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.35 |
| ▸ | FFAR1 | O14842 | 1/20 | 0.35 |
| ▸ | GPR84 | Q9NQS5 | 1/20 | 0.35 |
| ▸ | POLB | P06746 | 2/20 | 0.33 |
| ▸ | TP53 | P04637 | 1/20 | 0.33 |
| ▸ | LMNA | P02545 | 1/20 | 0.32 |
| ▸ | HIF1A | Q16665 | 1/20 | 0.32 |
| ▸ | SIGMAR1 | Q99720 | 2/20 | 0.32 |
| ▸ | PPARG | P37231 | 2/20 | 0.32 |
| ▸ | PPARA | Q07869 | 2/20 | 0.32 |
| ▸ | SLC6A2 | P23975 | 1/20 | 0.32 |
| ▸ | SLC6A3 | Q01959 | 1/20 | 0.32 |
| ▸ | NPC1 | O15118 | 1/20 | 0.32 |
| ▸ | RAB9A | P51151 | 1/20 | 0.32 |
| ▸ | ESR1 | P03372 | 1/20 | 0.31 |
| ▸ | ESR2 | Q92731 | 1/20 | 0.31 |
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 | |
|---|---|---|---|---|
| Benzene SCHEMBL28276839 | 1.00 | AOC3 (0.36) | AOC3CYP3A4TDP1SMN1; SMN2FFAR1 | |
| SCHEMBL26632197 | 0.98 | AOC3 (0.35) | AOC3CYP3A4TDP1SMN1; SMN2FFAR1 | |
| SCHEMBL5272440 | 0.98 | AOC3 (0.37) | AOC3CYP3A4TDP1SMN1; SMN2FFAR1 | |
| Hydrochloric Acid SCHEMBL8522468 | 0.96 | AOC3 (0.34) | AOC3CYP3A4TDP1SMN1; SMN2FFAR1 | |
| Hydrochloric Acid SCHEMBL5733614 | 0.96 | AOC3 (0.34) | AOC3CYP3A4TDP1SMN1; SMN2FFAR1 | |
| Hydrochloric Acid SCHEMBL6594318 | 0.96 | AOC3 (0.34) | AOC3CYP3A4TDP1SMN1; SMN2FFAR1 | |
| Hydrochloric Acid SCHEMBL5733618 | 0.96 | AOC3 (0.34) | AOC3CYP3A4TDP1SMN1; SMN2FFAR1 | |
| SCHEMBL1208471 | 0.92 | AOC3 (0.33) | AOC3CYP3A4TDP1SMN1; SMN2FFAR1 | |
| SCHEMBL1207844 | 0.92 | AOC3 (0.33) | AOC3CYP3A4TDP1SMN1; SMN2FFAR1 | |
| SCHEMBL19183386 | 0.90 | SMN1; SMN2 (0.36) | AOC3CYP3A4TDP1SMN1; SMN2FFAR1 |
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
Appears in 2035 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-4090654-B1 | METHODS, PROCESSES AND INTERMEDIATES FOR PREPARING CHROMAN COMPOUNDS | LUPIN LTD (IN) | 2025-07-09 | — | — | EP | claimed |
| US-12344592-B2 | Methods, processes and intermediates for preparing chroman compounds | LUPIN LIMITED (IN) | 2025-07-01 | — | — | US | claimed |
| WO-2025104433-A1 | CATALYST AND SYNTHESIS THEREOF | UNIVERSITY OF STRATHCLYDE (GB) | 2025-05-22 | — | — | WO | claimed |
| WO-2024038044-A1 | PROCESS FOR THE PREPARATION OF BIO-BASED OLEFINS FROM PRIMARY ALCOHOL | BASF SE (DE) | 2024-02-22 | — | — | WO | claimed |
| EP-4281436-A1 | SYNTHESIS OF POLYFLUORINATED ARYL AND HETEROARYL CARBOXAMIDES | BASF SE (DE) | 2023-11-29 | — | — | EP | claimed |
| CN-116655504-A | Preparation method of diaryl sulfide compound | 浙江扬帆新材料股份有限公司 | 2023-08-29 | — | — | CN | claimed |
| US-20230140054-A1 | METHODS, PROCESSES AND INTERMEDIATES FOR PREPARING CHROMAN COMPOUNDS | LUPIN LIMITED (IN) | 2023-05-04 | — | — | US | claimed |
| EP-4143158-A1 | PREPARATION OF AROMATIC CARBOXYAMIDES BY PALLADIUM-CATALYZED CARBONYLATION REACTION | BASF SE (DE) | 2023-03-08 | — | — | EP | claimed |
| EP-4132902-A1 | PD-CATALYZED AMINATION OF FLUORINATED ARYL CHLORIDES | BASF SE (DE) | 2023-02-15 | — | — | EP | claimed |
| CN-115557992-A | Thermochromic fluorescent material and preparation method and application thereof | 常州大学 | 2023-01-03 | — | — | CN | claimed |
| US-5290743-A | Process for regenerating a deactivated rhodium hydroformylation catalyst system | ARCO CHEMICAL TECHNOLOGY L.P. (US) | 1994-03-01 | — | — | US | claimed |
| US-5250731-A | Asymmetric hydrogenation of N-acylhydrazones to N-acylhydrazines in presence of chiral phospholane complex | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 1993-10-05 | — | — | US | claimed |
| WO-1993019040-A1 | PREPARATION OF OPTICALLY ACTIVE HYDRAZINES AND AMINES | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 1993-09-30 | — | — | WO | claimed |
| US-5216118-A | Preparation of aromatic polyimides from CO, primary diamine and bis (halo aromatic carboxylic acid ester) | EASTMAN KODAK COMPANY (US) | 1993-06-01 | — | — | US | claimed |
| EP-0293053-B1 | PROCESS FOR THE PREPARATION OF CYCLIC CARBOXYLIC ANHYDRIDES | SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) | 1992-03-04 | — | — | EP | claimed |
| EP-0189694-B1 | PROCESS FOR THE PREPARATION OF ISOCYANATES AND ISOCYANATE DERIVATIVES | SOCIETE NATIONALE DES POUDRES ET EXPLOSIFS (FR) | 1988-08-10 | — | — | EP | claimed |
| US-4709087-A | REACTING AN ORGANIC HALIDE WITH A METAL CYANATE IN THE PRESENCE OF A COMPLEX NICKEL CATALYST | SOCIETE NATIONALE DES POUDRES ET EXPLOSIFS (FR) | 1987-11-24 | — | — | US | claimed |
| US-4691069-A | Hydrogentation of unsaturated aliphatic hydrocarbons | SOUTH AFRICAN INVENTIONS DEVELOPMENT CORPORATION (ZA) | 1987-09-01 | — | — | US | claimed |
| US-4654176-A | Sulphonated chiral phosphines, their preparation and their use | RHONE-POULENC SANTE (FR) | 1987-03-31 | — | — | US | claimed |
| EP-0189694-A1 | Process for the preparation of isocyanates and isocyanate derivatives | SOCIETE NATIONALE DES POUDRES ET EXPLOSIFS (FR) | 1986-08-06 | — | — | EP | claimed |