Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | AOC3 | Q16853 | 1/20 | 0.53 |
| ▸ | LMNA | P02545 | 3/20 | 0.43 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.43 |
| ▸ | TSHR | P16473 | 3/20 | 0.42 |
| ▸ | MAPK1 | P28482 | 2/20 | 0.42 |
| ▸ | HIF1A | Q16665 | 2/20 | 0.42 |
| ▸ | TDP1 | Q9NUW8 | 2/20 | 0.42 |
| ▸ | ALOX15 | P16050 | 1/20 | 0.41 |
| ▸ | APEX1 | P27695 | 1/20 | 0.41 |
| ▸ | GABBR2 | O75899 | 1/20 | 0.41 |
| ▸ | GABBR1 | Q9UBS5 | 1/20 | 0.41 |
| ▸ | GAA | P10253 | 1/20 | 0.41 |
| ▸ | TP53 | P04637 | 1/20 | 0.41 |
| ▸ | HPGD | P15428 | 1/20 | 0.41 |
| ▸ | ADRB2 | P07550 | 1/20 | 0.41 |
| ▸ | CYP2A6 | P11509 | 1/20 | 0.40 |
| ▸ | IDO1 | P14902 | 2/20 | 0.39 |
| ▸ | HSD17B10 | Q99714 | 1/20 | 0.39 |
| ▸ | BRD4 | O60885 | 1/20 | 0.39 |
| ▸ | HDAC4 | P56524 | 1/20 | 0.39 |
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 | |
|---|---|---|---|---|
| SCHEMBL2306502 | 1.00 | AOC3 (0.53) | AOC3LMNASMN1; SMN2TSHRMAPK1 | |
| SCHEMBL3924289 | 1.00 | AOC3 (0.53) | AOC3LMNASMN1; SMN2TSHRMAPK1 | |
| SCHEMBL29700206 | 0.82 | AOC3 (0.55) | AOC3LMNASMN1; SMN2TSHRMAPK1 | |
| SCHEMBL10799093 | 0.82 | TAAR1 (0.39) | AOC3LMNASMN1; SMN2TSHRHIF1A | |
| SCHEMBL3917589 | 0.81 | AOC3 (0.50) | AOC3LMNASMN1; SMN2TSHRMAPK1 | |
| SCHEMBL3917591 | 0.81 | AOC3 (0.50) | AOC3LMNASMN1; SMN2TSHRMAPK1 | |
| SCHEMBL27504475 | 0.80 | TAAR1 (0.60) | LMNASMN1; SMN2TSHRHIF1ATDP1 | |
| SCHEMBL6715483 | 0.80 | TAAR1 (0.60) | LMNASMN1; SMN2TSHRHIF1ATDP1 | |
| SCHEMBL1155443 | 0.80 | AOC3 (0.53) | AOC3LMNASMN1; SMN2TSHRMAPK1 | |
| SCHEMBL4297797 | 0.80 | AOC3 (0.53) | AOC3LMNASMN1; SMN2TSHRMAPK1 |
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 45 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-0718407-B1 | Intermediates for the synthesis of eliprodil enantiomers and process for their preparation | SANOFI SYNTHELABO (FR) | 2002-02-13 | — | — | EP | claimed |
| US-5677168-A | Enantiomeric separation of (RS)1-(4-chlorophenyl)-2-chloroethanol by lipase catalyzed hydrolysis of its acetate | SYNTHELABO (FR) | 1997-10-14 | — | — | US | claimed |
| EP-0718407-A1 | Intermediates for the synthesis of eliprodil enantiomers and process for their preparation | SYNTHELABO (FR) | 1996-06-26 | — | — | EP | claimed |
| JP-8252097-A | — | — | None | — | — | JP | disclosed |
| CN-119614529-A | Short-chain dehydrogenase, engineering bacteria and application thereof in asymmetric reduction of potential chiral carbonyl compounds | 杭州文德阶生物科技有限公司 | 2025-03-14 | — | — | CN | disclosed |
| CN-110016444-B | Acinetobacter ZJPH1806 and application thereof in preparation of miconazole chiral intermediate | 浙江工业大学 | 2021-05-11 | — | — | CN | disclosed |
| CN-110016444-A | Acinetobacter calcoaceticus ZJPH1806 and its application for preparing Miconazole chiral intermediate | 浙江工业大学 | 2019-07-16 | — | — | CN | disclosed |
| WO-2017001733-A1 | BICYCLIC HETEROCYCLE DERIVATIVES AS BROMODOMAIN INHIBITORS | ORION CORPORATION (FI) | 2017-01-05 | — | — | WO | disclosed |
| CN-101243040-B | Synthesis method of mandipropamid and derivatives thereof | SYNGENTA PARTICIPATIONS AG | 2012-12-05 | — | — | CN | disclosed |
| US-7601667-B2 | Ruthenium/iridium complexes; hydrogenation catalysts | KANTO KAGAKU KABUSHIKI KAISHA (JP) | 2009-10-13 | — | — | US | disclosed |
| EP-1934159-B1 | METHOD FOR FRACTIONATING STEREOISOMERIC COMPOUNDS | BASF SE (DE) | 2009-03-25 | — | — | EP | disclosed |
| US-5677168-A | Enantiomeric separation of (RS)1-(4-chlorophenyl)-2-chloroethanol by lipase catalyzed hydrolysis of its acetate | SYNTHELABO (FR) | 1997-10-14 | — | — | US | disclosed |
| JP-H08252097-A | INTERMEDIATE IN SYNTHESIS OF ENANTIOMER OF ELIPRODIL AND ITS PRODUCTION | SYNTHELABO SA | 1996-10-01 | — | — | JP | disclosed |
| EP-0718407-A1 | Intermediates for the synthesis of eliprodil enantiomers and process for their preparation | SYNTHELABO (FR) | 1996-06-26 | — | — | EP | disclosed |
| EP-0718407-A1 | Intermediates for the synthesis of eliprodil enantiomers and process for their preparation | SYNTHELABO (FR) | 1996-06-26 | — | — | EP | disclosed |
| US-5266485-A | Biosynthesis | KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) | 1993-11-30 | — | — | US | disclosed |
| EP-0493617-A1 | PROCESS FOR PRODUCING OPTICALLY ACTIVE (-)-2-HALO-1-(SUBSTITUTED PHENYL)ETHANOL AND (-)-SUBSTITUTED STYRENE OXIDE | KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) | 1992-07-08 | — | — | EP | disclosed |
| EP-0390777-A1 | CYCLOCARBONATE COMPOUNDS | DAINIPPON INK AND CHEMICALS, INC. (JP) | 1990-10-10 | — | — | EP | disclosed |
| WO-1989000565-A1 | CYCLOCARBONATE COMPOUNDS | DAINIPPON INK & CHEMICALS, INC. (JP) | 1989-01-26 | — | — | WO | disclosed |
| US-4598085-A | Fungicidal 1-(2-aryl-2-R-ethyl)-1H-1,2,4-triazoles | JANSSEN PHARMACEUTICA N.V. (BE) | 1986-07-01 | — | — | US | disclosed |