Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | GABRA1 | P14867 | 2/20 | 0.34 |
| ▸ | GABRB2 | P47870 | 2/20 | 0.34 |
| ▸ | P4HB | P07237 | 1/20 | 0.32 |
| ▸ | TSHR | P16473 | 2/20 | 0.31 |
| ▸ | CYP1A2 | P05177 | 2/20 | 0.31 |
| ▸ | CYP3A4 | P08684 | 2/20 | 0.31 |
| ▸ | FAAH | O00519 | 1/20 | 0.31 |
| ▸ | CA1 | P00915 | 1/20 | 0.31 |
| ▸ | CA2 | P00918 | 1/20 | 0.31 |
| ▸ | LMNA | P02545 | 1/20 | 0.31 |
| ▸ | HPGD | P15428 | 1/20 | 0.31 |
| ▸ | GABRB1 | P18505 | 1/20 | 0.31 |
| ▸ | GABRG2 | P18507 | 1/20 | 0.31 |
| ▸ | PTGS1 | P23219 | 1/20 | 0.31 |
| ▸ | SLC6A2 | P23975 | 1/20 | 0.31 |
| ▸ | HTR2C | P28335 | 1/20 | 0.31 |
| ▸ | GABRB3 | P28472 | 1/20 | 0.31 |
| ▸ | GABRA5 | P31644 | 1/20 | 0.31 |
| ▸ | GABRA3 | P34903 | 1/20 | 0.31 |
| ▸ | HTR2B | P41595 | 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 | |
|---|---|---|---|---|
| SCHEMBL30389926 | 0.80 | GABRA1 (0.48) | GABRA1GABRB2TSHRCYP1A2CYP3A4 | |
| SCHEMBL3911665 | 0.80 | TSHR (0.38) | TSHR | |
| SCHEMBL4808650 | 0.80 | GABRA1 (0.48) | GABRA1GABRB2TSHRCYP1A2CYP3A4 | |
| SCHEMBL2865478 | 0.79 | GABRA1 (0.43) | GABRA1GABRB2TSHRCYP1A2CYP3A4 | |
| SCHEMBL1424464 | 0.79 | TSHR (0.35) | TSHRLMNAHPGDBLMMAOA | |
| SCHEMBL588784 | 0.76 | GABRA1 (0.39) | GABRA1GABRB2P4HBTSHRCYP1A2 | |
| SCHEMBL10621286 | 0.76 | — | — | |
| SCHEMBL5422503 | 0.76 | GABRA1 (0.34) | GABRA1GABRB2P4HBTSHRCYP1A2 | |
| SCHEMBL4143745 | 0.76 | P2RX7 (0.37) | GABRA1GABRB2P4HBTSHRCYP1A2 | |
| SCHEMBL6829698 | 0.75 | GABRA1 (0.37) | GABRA1GABRB2TSHRCYP1A2CYP3A4 |
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 48 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-4545625-A1 | REMOVING TOXIC CHEMICALS FROM CONTAMINATED SURFACES | Guild Associates, Inc. (US) | 2025-04-30 | — | — | EP | disclosed |
| US-20250121237-A1 | Removing Toxic Chemicals from Contaminated Surfaces | Guild Associates Inc. (US) | 2025-04-17 | — | — | US | disclosed |
| CN-115772103-B | Method for preparing sulfoxide compound by catalytic oxidation of thioether | 华东师范大学 | 2025-04-01 | — | — | CN | disclosed |
| CN-112533934-B | Polyoxometallate compounds exhibiting bright emissions and methods of making same | 纳米2D材料有限公司 | 2024-07-19 | — | — | CN | disclosed |
| WO-2024114161-A1 | METHOD FOR PREPARING SULFOXIDE COMPOUND BY CATALYTICALLY OXIDIZING SULFIDE | 华东师范大学 | 2024-06-06 | — | — | WO | disclosed |
| CN-115772103-A | Method for preparing sulfoxide compound by catalytic oxidation of thioether | 华东师范大学 | 2023-03-10 | — | — | CN | disclosed |
| CN-108623581-B | Method for preparing paninula compound | 中国海洋大学 | 2021-10-22 | — | — | CN | disclosed |
| CN-112533934-A | Polyoxometallate compounds exhibiting bright emission and methods of making the same | 纳米2D材料有限公司 | 2021-03-19 | — | — | CN | disclosed |
| US-10828873-B1 | Textile composite having sorptive and reactive properties against toxic agents | BATTELLE MEMORIAL INSTITUTE (US) | 2020-11-10 | — | — | US | disclosed |
| US-10773114-B1 | Zirconium hydroxide-based slurry for decontamination and detoxification | THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE ARMY (US) | 2020-09-15 | — | — | US | disclosed |
| US-6197965-B1 | POLYARYLALKYLAMINO-SUBSTITUED PYRIDINE DERIVATIVES; DRUGS, MEDICINE, DIAGNOSTICS | ISIS PHARMACEUTICALS, INC. | 2001-03-06 | — | — | US | disclosed |
| EP-0817787-A4 | NITROGENOUS MACROCYCLIC COMPOUNDS | ISIS PHARMACEUTICALS INC (US) | 2000-09-13 | — | — | EP | disclosed |
| CN-1241570-A | New process for preparation of organosilanes functionalised in the 3-position | DEGUSSA (DE) | 2000-01-19 | — | — | CN | disclosed |
| WO-1998010286-A1 | METHODS FOR PROCESSING CHEMICAL COMPOUNDS HAVING REACTIVE FUNCTIONAL GROUPS | ISIS PHARMACEUTICALS, INC. (US) | 1998-03-12 | — | — | WO | disclosed |
| WO-1998005961-A1 | COMPOUNDS HAVING A PLURALITY OF NITROGENOUS SUBSTITUENTS | ISIS PHARMACEUTICALS, INC. (US) | 1998-02-12 | — | — | WO | disclosed |
| EP-0817787-A1 | NITROGENOUS MACROCYCLIC COMPOUNDS | ISIS PHARMACEUTICALS, INC. (US) | 1998-01-14 | — | — | EP | disclosed |
| WO-1996030377-A1 | NITROGENOUS MACROCYCLIC COMPOUNDS | ISIS PHARMACEUTICALS, INC. (US) | 1996-10-03 | — | — | WO | disclosed |
| US-4524073-A | β-Lactam compounds | BEECHAM GROUP P.1.C. (GB) | 1985-06-18 | — | — | US | disclosed |
| US-4449005-A | REACTING A CHLOROETHYL SULFIDE AND QUATERNARY AMMONIUM OR QUATERNARY PHOSPHONIUM FLUORIDE TO PRODUCE A VINYL SULFIDE | THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE ARMY (US) | 1984-05-15 | — | — | US | disclosed |
| EP-0101199-A1 | Beta-lactam compounds | BEECHAM GROUP PLC (GB) | 1984-02-22 | — | — | EP | disclosed |