Predicted protein targets (top 15)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | MEN1 | O00255 | 2/20 | 0.56 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.56 |
| ▸ | LMNA | P02545 | 2/20 | 0.49 |
| ▸ | ALDH1A1 | P00352 | 4/20 | 0.47 |
| ▸ | TSHR | P16473 | 1/20 | 0.47 |
| ▸ | AKR1C3 | P42330 | 1/20 | 0.47 |
| ▸ | KDM4E | B2RXH2 | 2/20 | 0.45 |
| ▸ | HPGD | P15428 | 2/20 | 0.45 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.45 |
| ▸ | RECQL | P46063 | 1/20 | 0.45 |
| ▸ | MTNR1A | P48039 | 2/20 | 0.44 |
| ▸ | MTNR1B | P49286 | 2/20 | 0.44 |
| ▸ | NPSR1 | Q6W5P4 | 1/20 | 0.43 |
| ▸ | GLA | P06280 | 1/20 | 0.43 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.43 |
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 | |
|---|---|---|---|---|
| SCHEMBL187458 | 1.00 | MEN1 (0.56) | MEN1KMT2ALMNAALDH1A1TSHR | |
| SCHEMBL3682708 | 1.00 | MEN1 (0.56) | MEN1KMT2ALMNAALDH1A1TSHR | |
| SCHEMBL8430294 | 0.91 | MEN1 (0.47) | MEN1KMT2ALMNAALDH1A1KDM4E | |
| SCHEMBL8430296 | 0.91 | MEN1 (0.47) | MEN1KMT2ALMNAALDH1A1KDM4E | |
| SCHEMBL16516485 | 0.91 | MEN1 (0.49) | MEN1KMT2ALMNAALDH1A1KDM4E | |
| SCHEMBL16516487 | 0.91 | MEN1 (0.49) | MEN1KMT2ALMNAALDH1A1KDM4E | |
| SCHEMBL16516488 | 0.91 | MEN1 (0.49) | MEN1KMT2ALMNAALDH1A1KDM4E | |
| SCHEMBL25669721 | 0.88 | EPHX1 (0.49) | MEN1KMT2ALMNAALDH1A1KDM4E | |
| SCHEMBL12394376 | 0.86 | LMNA (0.49) | MEN1KMT2ALMNAALDH1A1AKR1C3 | |
| SCHEMBL7522147 | 0.85 | MEN1 (0.47) | MEN1KMT2ALMNAALDH1A1AKR1C3 |
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 145 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122036790-A | Chiral phosphine-acyclic phosphoramidite ligand, preparation method and application thereof | 中国科学院大连化学物理研究所 | 2026-05-15 | — | — | CN | disclosed |
| CN-118307428-B | Chiral alpha unnatural amino acid and preparation method thereof by rare noble metal complex | 北京元延医药科技股份有限公司 | 2025-01-10 | — | — | CN | disclosed |
| CN-118307428-A | Chiral alpha unnatural amino acid and preparation method thereof by rare noble metal complex | 北京元延医药科技股份有限公司 | 2024-07-09 | — | — | CN | disclosed |
| CN-115043787-B | Preparation method of 2,4, 5-trisubstituted oxazole compound | 西安交通大学 | 2023-10-24 | — | — | CN | disclosed |
| CN-116655691-A | Synthesis and application of chiral spiro [ chromane-4, 1' -indan ] phosphite monophosphorus ligand | 南开大学 | 2023-08-29 | — | — | CN | disclosed |
| CN-113373466-B | Electrochemical synthesis method of beta-acetaminocarbonyl compound | 安徽科技学院 | 2023-07-21 | — | — | CN | disclosed |
| CN-113121615-B | Ferrocene boracic chiral diphosphine ligand and preparation method and application thereof | 南方科技大学 | 2023-02-17 | — | — | CN | disclosed |
| CN-112824422-B | Chiral ferrocene-indole diphosphine ligand as well as preparation method and application thereof | 中国科学院大连化学物理研究所（CN） | 2023-01-13 | — | — | CN | disclosed |
| CN-115043787-A | Preparation method of 2,4, 5-trisubstituted oxazole compound | 西安交通大学 | 2022-09-13 | — | — | CN | disclosed |
| CN-113121615-A | Ferrocene boracic chiral diphosphine ligand and preparation method and application thereof | 南方科技大学 | 2021-07-16 | — | — | CN | disclosed |
| EP-0528865-A1 | CHIRAL PHOSPHOLANE TRANSITION METAL CATALYSTS. | DU PONT (US) | 1993-03-03 | — | — | EP | disclosed |
| EP-0198397-B1 | METHOD OF PRODUCING L-PHENYLALANINE | KURARAY CO., LTD. (JP) | 1993-01-07 | — | — | EP | disclosed |
| US-5171892-A | Chiral phospholanes via chiral 1,4-diol cyclic sulfates | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 1992-12-15 | — | — | US | disclosed |
| WO-1991017998-A1 | CHIRAL PHOSPHOLANE TRANSITION METAL CATALYSTS | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 1991-11-28 | — | — | WO | disclosed |
| US-4743547-A | PURITY, ENZYME HYDROLYSIS | KURARAY CO., LTD. (JP) | 1988-05-10 | — | — | US | disclosed |
| US-4654176-A | Sulphonated chiral phosphines, their preparation and their use | RHONE-POULENC SANTE (FR) | 1987-03-31 | — | — | US | disclosed |
| EP-0198397-A2 | Method of producing L-phenylalanine | KURARAY CO., LTD. (JP) | 1986-10-22 | — | — | EP | disclosed |
| EP-0000403-B1 | BISPHOSPHINIC METAL COMPLEXES, PROCESS FOR THEIR PREPARATION, HYDROGENATION CATALYSTS FROM THESE COMPOUNDS, AND A HYDROGENATION PROCESS EMPLOYING THESE CATALYSTS | F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) | 1981-06-17 | — | — | EP | disclosed |
| US-4187241-A | BIS(DIARYLPHOSPHINOMETHYL)CYCLOBUTANE, ENANTIOSELECTIVE HYDROGENATION CATALYSTS | HOFFMAN-LA ROCHE INC. (US) | 1980-02-05 | — | — | US | disclosed |
| US-4120870-A | Metal phosphine complex | HOFFMANN-LA ROCHE INC. (US) | 1978-10-17 | — | — | US | disclosed |