Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | KCNN4 | O15554 | 3/20 | 0.41 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.39 |
| ▸ | CYP2D6 | P10635 | 3/20 | 0.39 |
| ▸ | SIGMAR1 | Q99720 | 2/20 | 0.39 |
| ▸ | LMNA | P02545 | 2/20 | 0.39 |
| ▸ | CYP1A2 | P05177 | 2/20 | 0.39 |
| ▸ | CYP3A4 | P08684 | 2/20 | 0.39 |
| ▸ | CYP2C9 | P11712 | 2/20 | 0.39 |
| ▸ | CYP2C19 | P33261 | 2/20 | 0.39 |
| ▸ | TSHR | P16473 | 1/20 | 0.39 |
| ▸ | NFKB1 | P19838 | 1/20 | 0.39 |
| ▸ | SCN1A | P35498 | 1/20 | 0.39 |
| ▸ | MTOR | P42345 | 1/20 | 0.39 |
| ▸ | RAB9A | P51151 | 1/20 | 0.39 |
| ▸ | SCN2A | Q99250 | 1/20 | 0.39 |
| ▸ | SCN3A | Q9NY46 | 1/20 | 0.39 |
| ▸ | DRD2 | P14416 | 2/20 | 0.39 |
| ▸ | OPRM1 | P35372 | 2/20 | 0.39 |
| ▸ | DRD3 | P35462 | 2/20 | 0.39 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.38 |
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 | |
|---|---|---|---|---|
| SCHEMBL5070186 | 0.86 | KIF11 (0.41) | KCNN4SIGMAR1MEN1KMT2ATAAR1 | |
| SCHEMBL8860222 | 0.85 | SIGMAR1 (0.40) | KCNN4SIGMAR1MEN1KMT2AKIF11 | |
| SCHEMBL23581511 | 0.83 | SIGMAR1 (0.40) | SMN1; SMN2SIGMAR1MEN1KMT2AMAPK1 | |
| SCHEMBL17529778 | 0.83 | SIGMAR1 (0.40) | SMN1; SMN2SIGMAR1MEN1KMT2AMAPK1 | |
| SCHEMBL1415754 | 0.83 | SIGMAR1 (0.40) | SMN1; SMN2SIGMAR1MEN1KMT2AMAPK1 | |
| SCHEMBL647077 | 0.83 | SIGMAR1 (0.40) | SMN1; SMN2SIGMAR1MEN1KMT2AMAPK1 | |
| SCHEMBL739411 | 0.80 | KCNN4 (0.44) | KCNN4CYP3A4CYP2C19TSHRTAAR1 | |
| SCHEMBL4749821 | 0.79 | TSHR (0.42) | TSHRRAB9AKIF11ESR1ESR2 | |
| SCHEMBL28240935 | 0.78 | KCNN4 (0.37) | KCNN4SMN1; SMN2CYP1A2CYP2C9CYP2C19 | |
| SCHEMBL8780444 | 0.78 | KCNN4 (0.43) | KCNN4CYP2C19TSHRTAAR1CHRM3 |
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 481 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119529260-A | Polycaprolactone-poly (2-vinyl) ethylene glycol copolymer and preparation method thereof | 上海交通大学 | 2025-02-28 | — | — | CN | claimed |
| CN-117510826-A | Vinyl functional polyether polyol and preparation method thereof | 上海交通大学 | 2024-02-06 | — | — | CN | claimed |
| US-20230167144-A1 | PREPARATION AND ITS APPLICATION OF A CYANIDE-BRIDGED METAL ORGANIC COMPOUND WITH INTRAMOLECULAR MAGNETIC TRANSFORMATION | Hubei Jingmen Industrial Technology Research Institute Co., Ltd. (CN) | 2023-06-01 | — | — | US | claimed |
| US-20200385570-A1 | POLYCARBONATE COMPOSITIONS | BASF SE (DE) | 2020-12-10 | — | — | US | claimed |
| CN-105826596-B | Preparation method of ionic liquid and secondary battery | 微宏动力系统（湖州）有限公司 | 2020-11-06 | — | — | CN | claimed |
| EP-3710145-A1 | POLYCARBONATE COMPOSITIONS | BASF SE (DE) | 2020-09-23 | — | — | EP | claimed |
| CN-111518145-A | Cyanide-bridged metal organic compound with intramolecular magnetic transformation, and preparation method and application thereof | 荆楚理工学院 | 2020-08-11 | — | — | CN | claimed |
| CN-111328293-A | Polycarbonate compositions | 巴斯夫欧洲公司 | 2020-06-23 | — | — | CN | claimed |
| CN-107021941-B | Ionic liquid and preparation method thereof | 微宏动力系统（湖州）有限公司 | 2020-06-19 | — | — | CN | claimed |
| US-10411301-B2 | Ionic liquids and preparation method thereof | MICROVAST POWER SYSTEMS CO., LTD. (CN) | 2019-09-10 | — | — | US | claimed |
| US-4939309-A | REACTING ARYL HALIDE WITH NICKEL-ORGANOPHOSPHINE-ORGANOMETAL-LIC-BIDENTATE LIGAND CATALYST | EASTMAN KODAK COMPANY (US) | 1990-07-03 | — | — | US | claimed |
| EP-0174174-B1 | A METHOD OF STABILISING HYDROXY-CONTAINING POLYMERS OF BUTADIENE OR SUBSTITUTED DERIVATIVES THEREOF | ELF ATOCHEM S.A. (FR) | 1990-05-23 | — | — | EP | claimed |
| US-4670577-A | Novel process | ROUSSEL UCLAF (FR) | 1987-06-02 | — | — | US | claimed |
| US-4593128-A | Using a di- or triphenylphosphine compound | ATLANTIC RICHFIELD COMPANY (US) | 1986-06-03 | — | — | US | claimed |
| EP-0174174-A2 | A method of stabilising hydroxy-containing polymers of butadiene or substituted derivatives thereof | ELF ATOCHEM S.A. (FR) | 1986-03-12 | — | — | EP | claimed |
| EP-0119899-B1 | PROCESS FOR THE PREPARATION OF 4-PENTENOIC ACID DERIVATIVES | ROUSSEL-UCLAF (FR) | 1986-03-05 | — | — | EP | claimed |
| EP-0119899-A1 | Process for the preparation of 4-pentenoic acid derivatives | ROUSSEL-UCLAF (FR) | 1984-09-26 | — | — | EP | claimed |
| US-4351969-A | Preparation of chlorophenols | RHONE-POULENC INDUSTRIES (FR) | 1982-09-28 | — | — | US | claimed |
| US-4151171-A | CARBONYLATION, HYDROLYSIS, DECARBONYLATION, CYCLIZATION | CHEVRON RESEARCH COMPANY (US) | 1979-04-24 | — | — | US | claimed |
| US-4113735-A | Process for the production of N-acetyl-2-pyrrolidone | CHEVRON RESEARCH COMPANY (US) | 1978-09-12 | — | — | US | claimed |
Patent text — is the patent's own abstract consistent with the prediction?
For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-10411301-B2 | Ionic liquids and preparation method thereof | DNMT3A, SOD1, CLK2 | KCNN4 831/4885SMN1; SMN2 2272/4885CYP2D6 2533/4885 |
“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.