Predicted protein targets (top 18)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CYP3A4 | P08684 | 2/20 | 1.00 |
| ▸ | TSHR | P16473 | 1/20 | 1.00 |
| ▸ | NFE2L2 | Q16236 | 5/20 | 0.39 |
| ▸ | GAA | P10253 | 2/20 | 0.38 |
| ▸ | ALDH1A1 | P00352 | 4/20 | 0.37 |
| ▸ | MAPT | P10636 | 1/20 | 0.35 |
| ▸ | HPGD | P15428 | 1/20 | 0.35 |
| ▸ | AGTR1 | P30556 | 1/20 | 0.35 |
| ▸ | SLC40A1 | Q9NP59 | 1/20 | 0.35 |
| ▸ | PGK1 | P00558 | 1/20 | 0.34 |
| ▸ | PGK2 | P07205 | 1/20 | 0.34 |
| ▸ | HTR3E | A5X5Y0 | 2/20 | 0.34 |
| ▸ | HTR3B | O95264 | 2/20 | 0.34 |
| ▸ | HTR3A | P46098 | 2/20 | 0.34 |
| ▸ | HTR3D | Q70Z44 | 2/20 | 0.34 |
| ▸ | HTR3C | Q8WXA8 | 2/20 | 0.34 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.34 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.34 |
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 | |
|---|---|---|---|---|
| Nitrapyrin SCHEMBL4115039 | 1.00 | CYP3A4 (1.00) | CYP3A4TSHRNFE2L2GAAALDH1A1 | |
| Nitrapyrin SCHEMBL29349488 | 1.00 | CYP3A4 (1.00) | CYP3A4TSHRNFE2L2GAAALDH1A1 | |
| Nitrapyrin SCHEMBL21758631 | 0.98 | CYP3A4 (0.95) | CYP3A4TSHRNFE2L2GAAALDH1A1 | |
| Nitrapyrin SCHEMBL9644890 | 0.88 | CYP3A4 (0.77) | CYP3A4TSHRNFE2L2GAAALDH1A1 | |
| Nitrapyrin SCHEMBL18065800 | 0.88 | TSHR (0.77) | CYP3A4TSHRNFE2L2GAAALDH1A1 | |
| Nitrapyrin SCHEMBL30415064 | 0.84 | TSHR (0.71) | CYP3A4TSHRNFE2L2GAAALDH1A1 | |
| SCHEMBL3297356 | 0.84 | TSHR (0.71) | CYP3A4TSHRALDH1A1PGK1PGK2 | |
| SCHEMBL17141418 | 0.81 | CYP3A4 (0.68) | CYP3A4TSHRNFE2L2ALDH1A1PGK1 | |
| SCHEMBL17141411 | 0.81 | CYP3A4 (0.68) | CYP3A4TSHRNFE2L2ALDH1A1PGK1 | |
| SCHEMBL11391263 | 0.79 | CYP3A4 (0.64) | CYP3A4TSHRNFE2L2GAAALDH1A1 |
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 13299 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-4747215-A1 | PYRAZOLE DERIVATIVES AS DUAL FUNCTION UREASE AND NITRIFICATION INHIBITOR | Sabic Agri-Nutrients Company (SA) | 2026-05-27 | — | — | EP | claimed |
| US-20260137082-A1 | FUNGICIDAL COMPOSITIONS COMPRISING FLUDIOXONIL | SYNGENTA CROP PROTECTION AG (CH) | 2026-05-21 | — | — | US | claimed |
| WO-2026099762-A1 | AMINODITHIOCARBAMATE DERIVATIVES AS DUAL FUNCTION UREASE AND NITRIFICATION INHIBITOR | SABIC Agri-Nutrients Company (SA) | 2026-05-15 | — | — | WO | claimed |
| US-12623979-B2 | Nitrification inhibitors to improve fertilizer efficiency | SOILGENIC TECHNOLOGIES, LLC (US) | 2026-05-12 | — | — | US | claimed |
| US-12582116-B2 | Agricultural formulations | DOW GLOBAL TECHNOLOGIES LLC (US) | 2026-03-24 | — | — | US | claimed |
| EP-4710766-A1 | MIXTURES OF AMBRUTICIN WITH AT LEAST ONE FURTHER PESTICIDE | BASF SE (DE) | 2026-03-18 | — | — | EP | claimed |
| US-20260068884-A1 | COMPOSITION USED FOR KILLING FUNGI AND METHOD FOR APPLYING COMPOSITION | JIANGSU FLAG CHEMICAL INDUSTRY CO., LTD. (CN) | 2026-03-12 | — | — | US | claimed |
| EP-4682136-A2 | INHIBITORS OF SOIL NITRIFICATION AND PROCESSES TO PREVENT SAME | Tessenderlo Group NV (BE) | 2026-01-21 | — | — | EP | claimed |
| EP-3294058-B1 | AGROCHEMICAL EMULSIONS | CRODA INC (US) | 2025-12-24 | — | — | EP | claimed |
| US-12497341-B2 | Reaction methods for producing nitrogenous phosphoryl compounds that are in situ fluid compositions | SOILGENIC TECHNOLOGIES, LLC (US) | 2025-12-16 | — | — | US | claimed |
| US-4487935-A | GOOD MIXING, MULTISTAGE | KALAMA CHEMICAL, INC. (US) | 1984-12-11 | — | — | US | claimed |
| US-4474789-A | (Trichloromethyl)pyridine compounds useful for promoting growth and/or improving feed utilization efficiency in ruminants | THE DOW CHEMICAL COMPANY (US) | 1984-10-02 | — | — | US | claimed |
| EP-0030101-B1 | PREPARATION OF (DICHLOROMETHYL) PYRIDINES BY REDUCTIVE DECHLORINATION | THE DOW CHEMICAL COMPANY (US) | 1983-06-08 | — | — | EP | claimed |
| US-4327220-A | Process for reducing picoline derivatives using copper catalyst | THE DOW CHEMICAL COMPANY (US) | 1982-04-27 | — | — | US | claimed |
| EP-0030101-A1 | Preparation of (dichloromethyl) pyridines by reductive dechlorination | THE DOW CHEMICAL COMPANY (US) | 1981-06-10 | — | — | EP | claimed |
| US-4266964-A | SAID ANTIDOTES BEING CHLOROPYRIDINE COMPOUNDS | THE DOW CHEMICAL COMPANY (US) | 1981-05-12 | — | — | US | claimed |
| US-4260766-A | Preparation of (dichloromethyl) pyridines by reductive dechlorination | THE DOW CHEMICAL COMPANY (US) | 1981-04-07 | — | — | US | claimed |
| US-4256894-A | REACTING LIQUID CHLORO-SUBSTITUTED (TRICHLOROMETHYL) PYRIDINE WITH CHLORINE IN THE PRESENCE OF A LEWIS ACID CATALYST | THE DOW CHEMICAL COMPANY (US) | 1981-03-17 | — | — | US | claimed |
| EP-0006348-A1 | Surfactant compositions and biologically active formulations prepared therewith | ICI AMERICAS INC. (US) | 1980-01-09 | — | — | EP | claimed |
| EP-0005064-A1 | Process for preparing 2,3,5,6-tetrachloropyridine | THE DOW CHEMICAL COMPANY (US) | 1979-10-31 | — | — | EP | claimed |