Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | KDM4E | B2RXH2 | 2/20 | 0.62 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.62 |
| ▸ | AOC3 | Q16853 | 8/20 | 0.58 |
| ▸ | SLC6A2 | P23975 | 1/20 | 0.50 |
| ▸ | SLC6A4 | P31645 | 1/20 | 0.50 |
| ▸ | SLC6A3 | Q01959 | 1/20 | 0.50 |
| ▸ | GAA | P10253 | 1/20 | 0.47 |
| ▸ | ADRA2C | P18825 | 2/20 | 0.45 |
| ▸ | ADRA2A | P08913 | 1/20 | 0.45 |
| ▸ | LMNA | P02545 | 1/20 | 0.45 |
| ▸ | HIF1A | Q16665 | 1/20 | 0.45 |
| ▸ | CHRM2 | P08172 | 1/20 | 0.42 |
| ▸ | ADRA1A | P35348 | 1/20 | 0.42 |
| ▸ | RGS12 | O14924 | 1/20 | 0.42 |
| ▸ | GLA | P06280 | 1/20 | 0.42 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.42 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.42 |
| ▸ | CYP2C9 | P11712 | 1/20 | 0.42 |
| ▸ | PKM | P14618 | 1/20 | 0.42 |
| ▸ | ALOX15 | P16050 | 1/20 | 0.42 |
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 | |
|---|---|---|---|---|
| SCHEMBL5525965 | 1.00 | KDM4E (0.62) | KDM4EALDH1A1AOC3SLC6A2SLC6A4 | |
| SCHEMBL3252189 | 1.00 | KDM4E (0.62) | KDM4EALDH1A1AOC3SLC6A2SLC6A4 | |
| SCHEMBL5109281 | 1.00 | KDM4E (0.62) | KDM4EALDH1A1AOC3SLC6A2SLC6A4 | |
| SCHEMBL3251773 | 1.00 | KDM4E (0.62) | KDM4EALDH1A1AOC3SLC6A2SLC6A4 | |
| SCHEMBL6577786 | 0.84 | AOC3 (0.73) | KDM4EALDH1A1AOC3SLC6A2SLC6A4 | |
| SCHEMBL15743820 | 0.84 | AOC3 (0.73) | KDM4EALDH1A1AOC3SLC6A2SLC6A4 | |
| SCHEMBL864654 | 0.81 | AOC3 (0.42) | KDM4EALDH1A1AOC3SLC6A2SLC6A4 | |
| SCHEMBL6575401 | 0.81 | AOC3 (0.54) | KDM4EALDH1A1AOC3SLC6A2SLC6A4 | |
| SCHEMBL14003539 | 0.81 | AOC3 (0.42) | KDM4EALDH1A1AOC3SLC6A2SLC6A4 | |
| SCHEMBL3246862 | 0.78 | SLC6A4 (0.44) | KDM4EALDH1A1AOC3SLC6A2SLC6A4 |
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 24 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-1853545-B1 | PROCESS FOR OBTAINING ENANTIOMERS OF CHRYSANTHEMIC ACID | ENDURA SPA (IT) | 2010-05-26 | — | — | EP | claimed |
| EP-1853545-A2 | PROCESS FOR OBTAINING ENANTIOMERS OF CHRYSANTHEMIC ACID | ENDURA S.p.A. (IT) | 2007-11-14 | — | — | EP | claimed |
| WO-2006087357-A2 | PROCESS FOR OBTAINING ENANTIOMERS OF CHRYSANTHEMIC ACID | ENDURA S.P.A. (IT) | 2006-08-24 | — | — | WO | claimed |
| US-4337352-A | SALT FORMATION WITH OPTICALLY ACTIVE AMINE | BAYER AKTIENGESELLSCHAFT (DE) | 1982-06-29 | — | — | US | claimed |
| US-4285884-A | Process for resolution of racemic DL-α-aminocarboxylic acids | RIEDEL-DE HAEN AKTIENGESELLSCHAFT (DE) | 1981-08-25 | — | — | US | claimed |
| EP-0001821-B1 | RESOLUTION OF D,L-ALPHA-AMINO ACIDS AND SALTS USED THEREFOR | RIEDEL-DE HAEN AKTIENGESELLSCHAFT (DE) | 1981-04-29 | — | — | EP | claimed |
| EP-0001821-A1 | Resolution of D,L-alpha-amino acids and salts used therefor | RIEDEL-DE HAEN AKTIENGESELLSCHAFT (DE) | 1979-05-16 | — | — | EP | claimed |
| CN-101119960-B | Process for obtaining enantiomers of chrysanthemic acid | ENDURA SPA | 2011-08-17 | — | — | CN | disclosed |
| EP-1853545-B1 | PROCESS FOR OBTAINING ENANTIOMERS OF CHRYSANTHEMIC ACID | ENDURA SPA (IT) | 2010-05-26 | — | — | EP | disclosed |
| EP-1853545-B1 | PROCESS FOR OBTAINING ENANTIOMERS OF CHRYSANTHEMIC ACID | ENDURA SPA (IT) | 2010-05-26 | — | — | EP | disclosed |
| CN-101119960-A | Process for obtaining enantiomers of chrysanthemic acid | ENDURA SPA (IT) | 2008-02-06 | — | — | CN | disclosed |
| EP-1853545-A2 | PROCESS FOR OBTAINING ENANTIOMERS OF CHRYSANTHEMIC ACID | ENDURA S.p.A. (IT) | 2007-11-14 | — | — | EP | disclosed |
| EP-1853545-A2 | PROCESS FOR OBTAINING ENANTIOMERS OF CHRYSANTHEMIC ACID | ENDURA S.p.A. (IT) | 2007-11-14 | — | — | EP | disclosed |
| US-4337352-A | SALT FORMATION WITH OPTICALLY ACTIVE AMINE | BAYER AKTIENGESELLSCHAFT (DE) | 1982-06-29 | — | — | US | disclosed |
| US-4337352-A | SALT FORMATION WITH OPTICALLY ACTIVE AMINE | BAYER AKTIENGESELLSCHAFT (DE) | 1982-06-29 | — | — | US | disclosed |
| US-4285884-A | Process for resolution of racemic DL-α-aminocarboxylic acids | RIEDEL-DE HAEN AKTIENGESELLSCHAFT (DE) | 1981-08-25 | — | — | US | disclosed |
| EP-0001821-B1 | RESOLUTION OF D,L-ALPHA-AMINO ACIDS AND SALTS USED THEREFOR | RIEDEL-DE HAEN AKTIENGESELLSCHAFT (DE) | 1981-04-29 | — | — | EP | disclosed |
| EP-0006187-B1 | SEPARATION OF ENANTIOMERS OF CHIRAL CARBOXYLIC ACIDS | BAYER AG (DE) | 1980-12-10 | — | — | EP | disclosed |
| EP-0006187-A1 | Separation of enantiomers of chiral carboxylic acids | BAYER AG (DE) | 1980-01-09 | — | — | EP | disclosed |
| EP-0001821-A1 | Resolution of D,L-alpha-amino acids and salts used therefor | RIEDEL-DE HAEN AKTIENGESELLSCHAFT (DE) | 1979-05-16 | — | — | EP | disclosed |