Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | SLC6A2 | P23975 | 2/20 | 0.52 |
| ▸ | TAAR1 | Q96RJ0 | 2/20 | 0.52 |
| ▸ | MAOA | P21397 | 1/20 | 0.52 |
| ▸ | SLC6A4 | P31645 | 1/20 | 0.52 |
| ▸ | SLC6A3 | Q01959 | 1/20 | 0.52 |
| ▸ | SIGMAR1 | Q99720 | 1/20 | 0.52 |
| ▸ | CYP2A6 | P11509 | 1/20 | 0.52 |
| ▸ | ADORA2A | P29274 | 1/20 | 0.52 |
| ▸ | ADORA1 | P30542 | 1/20 | 0.52 |
| ▸ | CYP2D6 | P10635 | 2/20 | 0.52 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.52 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.52 |
| ▸ | EPHX1 | P07099 | 1/20 | 0.50 |
| ▸ | TACR1 | P25103 | 2/20 | 0.45 |
| ▸ | LMNA | P02545 | 1/20 | 0.44 |
| ▸ | POLB | P06746 | 1/20 | 0.44 |
| ▸ | ANPEP | P15144 | 1/20 | 0.44 |
| ▸ | CNR1 | P21554 | 1/20 | 0.44 |
| ▸ | CNR2 | P34972 | 1/20 | 0.44 |
| ▸ | PRKACA | P17612 | 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 | |
|---|---|---|---|---|
| SCHEMBL2785511 | 0.92 | CYP2D6 (0.52) | SLC6A2TAAR1MAOASLC6A4SLC6A3 | |
| SCHEMBL924299 | 0.92 | CYP2D6 (0.52) | SLC6A2TAAR1MAOASLC6A4SLC6A3 | |
| SCHEMBL2333573 | 0.92 | CYP2D6 (0.52) | SLC6A2TAAR1MAOASLC6A4SLC6A3 | |
| SCHEMBL248882 | 0.92 | CYP2D6 (0.52) | SLC6A2TAAR1MAOASLC6A4SLC6A3 | |
| SCHEMBL10804153 | 0.90 | CYP1A2 (0.62) | SLC6A2TAAR1SLC6A4SLC6A3CYP2A6 | |
| SCHEMBL12706002 | 0.90 | CYP1A2 (0.62) | SLC6A2TAAR1SLC6A4SLC6A3CYP2A6 | |
| SCHEMBL468022 | 0.85 | EPHX1 (0.61) | SLC6A2TAAR1MAOASLC6A4SLC6A3 | |
| SCHEMBL3451169 | 0.85 | EPHX1 (0.61) | SLC6A2TAAR1MAOASLC6A4SLC6A3 | |
| SCHEMBL272604 | 0.85 | EPHX1 (0.61) | SLC6A2TAAR1MAOASLC6A4SLC6A3 | |
| Hydrochloric Acid SCHEMBL28839661 | 0.83 | EPHX1 (0.58) | SLC6A2TAAR1MAOASLC6A4SLC6A3 |
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 21 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-0092194-B1 | METHOD OF OBTAINING OPTICALLY ACTIVE HALF ESTERS | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1987-07-08 | — | — | EP | claimed |
| EP-0093511-B1 | METHOD FOR PRODUCING AND OPTICALLY ACTIVE 2,2-DIMETHYLCYCLOPROPANECARBOXYLIC ACID | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1986-09-24 | — | — | EP | claimed |
| US-4542235-A | Method for producing an optically active 2,2-dimethylcyclopropanecarboxylic acid | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1985-09-17 | — | — | US | claimed |
| EP-0093511-A1 | Method for producing and optically active 2,2-dimethylcyclopropanecarboxylic acid | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1983-11-09 | — | — | EP | claimed |
| EP-0092194-A1 | Method of obtaining optically active half esters | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1983-10-26 | — | — | EP | claimed |
| US-3970700-A | Racemization of optically active amines | SUMITOMO CHEMICAL COMPANY, LIMITED (JA) | 1976-07-20 | — | — | US | claimed |
| US-3954870-A | RANEY NICKEL CATALYST | SUMITOMO CHEMICAL COMPANY, LIMITED (JA) | 1976-05-04 | — | — | US | claimed |
| JP-55092343-A | — | — | None | — | — | JP | disclosed |
| EP-2018364-B1 | THERAPEUTIC FLUOROETHYL UREAS | ALLERGAN INC (US) | 2013-08-21 | — | — | EP | disclosed |
| US-7709507-B2 | Therapeutic fluoroethyl ureas | ALLERGAN, INC. (US) | 2010-05-04 | — | — | US | disclosed |
| US-20070270498-A1 | THERAPEUTIC FLUOROETHYL UREAS | ALLERGAN, INC. | 2007-11-22 | — | — | US | disclosed |
| EP-0092194-B1 | METHOD OF OBTAINING OPTICALLY ACTIVE HALF ESTERS | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1987-07-08 | — | — | EP | disclosed |
| EP-0093511-B1 | METHOD FOR PRODUCING AND OPTICALLY ACTIVE 2,2-DIMETHYLCYCLOPROPANECARBOXYLIC ACID | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1986-09-24 | — | — | EP | disclosed |
| EP-0093511-A1 | Method for producing and optically active 2,2-dimethylcyclopropanecarboxylic acid | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1983-11-09 | — | — | EP | disclosed |
| EP-0092194-A1 | Method of obtaining optically active half esters | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1983-10-26 | — | — | EP | disclosed |
| US-4246424-A | IN PRESENCE OF ALKALI METAL AND POLYCYCLIC AROMATIC HYDROCARBON | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1981-01-20 | — | — | US | disclosed |
| JP-S5592343-A | PREPARATION OF OPTICALLY ACTIVE SUBSTITUTED ISOVALERIC ACID | KATSUTA YOSHIO | 1980-07-12 | — | — | JP | disclosed |
| US-4158016-A | CONTACTING WITH AN ALKALI METAL POLYCYCLIC AROMATIC HYDROCARBON CATALYST | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1979-06-12 | — | — | US | disclosed |
| US-3970700-A | Racemization of optically active amines | SUMITOMO CHEMICAL COMPANY, LIMITED (JA) | 1976-07-20 | — | — | US | disclosed |
| US-3954870-A | RANEY NICKEL CATALYST | SUMITOMO CHEMICAL COMPANY, LIMITED (JA) | 1976-05-04 | — | — | US | disclosed |
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-20070270498-A1 | THERAPEUTIC FLUOROETHYL UREAS | SLC14A1, MAPT, UTS2R | SLC6A2 716/4885TAAR1 2600/4885MAOA 3805/4885 |
“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.