Predicted protein targets (top 18)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | SLC6A2 | P23975 | 2/20 | 0.58 |
| ▸ | SLC6A3 | Q01959 | 2/20 | 0.58 |
| ▸ | ADRA1A | P35348 | 1/20 | 0.58 |
| ▸ | HTR2B | P41595 | 1/20 | 0.58 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.50 |
| ▸ | TSHR | P16473 | 1/20 | 0.43 |
| ▸ | CHRNA7 | P36544 | 1/20 | 0.41 |
| ▸ | TACR1 | P25103 | 8/20 | 0.40 |
| ▸ | SLC18A3 | Q16572 | 1/20 | 0.39 |
| ▸ | SIGMAR1 | Q99720 | 1/20 | 0.39 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.38 |
| ▸ | SLC6A4 | P31645 | 1/20 | 0.38 |
| ▸ | KCNH2 | Q12809 | 1/20 | 0.38 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.38 |
| ▸ | MEN1 | O00255 | 1/20 | 0.38 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.38 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.38 |
| ▸ | PRCP | P42785 | 1/20 | 0.37 |
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 | |
|---|---|---|---|---|
| SCHEMBL2257666 | 1.00 | SLC6A2 (0.58) | SLC6A2SLC6A3ADRA1AHTR2BALDH1A1 | |
| SCHEMBL1023795 | 0.89 | ALDH1A1 (0.59) | SLC6A2SLC6A3ADRA1AHTR2BALDH1A1 | |
| SCHEMBL4518432 | 0.86 | SLC6A2 (0.44) | SLC6A2SLC6A3ADRA1AHTR2BALDH1A1 | |
| SCHEMBL594796 | 0.85 | ALDH1A1 (0.57) | SLC6A2SLC6A3ADRA1AHTR2BALDH1A1 | |
| SCHEMBL16884713 | 0.84 | ALDH1A1 (0.45) | SLC6A2SLC6A3ADRA1AHTR2BALDH1A1 | |
| SCHEMBL218212 | 0.80 | SLC6A2 (0.46) | SLC6A2SLC6A3ADRA1AHTR2BALDH1A1 | |
| SCHEMBL16884718 | 0.80 | ALDH1A1 (0.46) | SLC6A2SLC6A3ADRA1AHTR2BALDH1A1 | |
| SCHEMBL3655086 | 0.79 | ALDH1A1 (0.51) | SLC6A2SLC6A3ADRA1AHTR2BALDH1A1 | |
| SCHEMBL10795916 | 0.79 | CHRNA7 (0.59) | SLC6A2SLC6A3ADRA1AHTR2BALDH1A1 | |
| SCHEMBL8117490 | 0.79 | ALDH1A1 (0.47) | SLC6A2SLC6A3ADRA1AHTR2BALDH1A1 |
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 405 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| WO-2025216834-A1 | AQUEOUS DISPERSION OF POLYMER PARTICLES AND ORGANIC OPACIFYING PIGMENT PARTICLES | ROHM AND HAAS COMPANY (US) | 2025-10-16 | — | — | WO | claimed |
| CN-116332710-B | Preparation method of metal-catalyzed benzyl ether and prepared benzyl ether | 合肥工业大学 | 2024-11-26 | — | — | CN | claimed |
| CN-116332710-A | Preparation method of metal-catalyzed benzyl ether and prepared benzyl ether | 合肥工业大学 | 2023-06-27 | — | — | CN | claimed |
| EP-3635062-B1 | A METHOD FOR PREVENTING HARDENER COMPOUNDS TO BE FORMED FROM HARDENER PRECURSORS AND EXTENDING SHELF LIFE OF THE DISPERSION | WISESPRAY INT OY (FI) | 2022-03-02 | — | — | EP | claimed |
| EP-2604619-A2 | Mannose derivatives as antagonists of bacterial adhesion | University of Basel (CH) | 2013-06-19 | — | — | EP | claimed |
| WO-2012164074-A1 | MANNOSE PHOSPHATE DERIVATIVES AS ANTAGONISTS OF BACTERIAL ADHESION | UNIVERSITY OF BASEL (CH) | 2012-12-06 | — | — | WO | claimed |
| US-20120270824-A1 | MANNOSE DERIVATIVES AS ANTAGONISTS OF BACTERIAL ADHESION | UNIVERSITY OF BASEL (CH) | 2012-10-25 | — | — | US | claimed |
| EP-2513128-A2 | MANNOSE DERIVATIVES AS ANTAGONISTS OF BACTERIAL ADHESION | University of Basel (CH) | 2012-10-24 | — | — | EP | claimed |
| WO-2011073112-A2 | MANNOSE DERIVATIVES AS ANTAGONISTS OF BACTERIAL ADHESION | UNIVERSITY OF BASEL (CH) | 2011-06-23 | — | — | WO | claimed |
| US-6632813-B1 | 6-subtituted-7-heteroquinoxalinecarboxylic acid derivatives and addition salts thereof and processes for the preparation of both | KYORIN PHARMACEUTICAL CO., LTD. (JP) | 2003-10-14 | — | — | US | claimed |
| EP-1341761-A1 | SUBSTITUTED INDOLES, PHARMACEUTICAL COMPOSITIONS CONTAINING SUCH INDOLES AND THEIR USE AS PPAR-$g(g) BINDING AGENTS | SMITHKLINE BEECHAM CORPORATION (US) | 2003-09-10 | — | — | EP | claimed |
| US-20030087902-A1 | Substituted indoles, pharmaceutical compounds containing such indoles and their use as PPAR-gamma binding agents | SMITHKLINE BEECHAM CORPORATION | 2003-05-08 | — | — | US | claimed |
| WO-2002030895-A1 | SUBSTITUTED INDOLES, PHARMACEUTICAL COMPOSITIONS CONTAINING SUCH INDOLES AND THEIR USE AS PPAR-η BINDING AGENTS | SMITHKLINE BEECHAM CORPORATION (US) | 2002-04-18 | — | — | WO | claimed |
| JP-57130969-A | — | — | None | — | — | JP | disclosed |
| JP-54125663-A | — | — | None | — | — | JP | disclosed |
| WO-2025216834-A1 | AQUEOUS DISPERSION OF POLYMER PARTICLES AND ORGANIC OPACIFYING PIGMENT PARTICLES | ROHM AND HAAS COMPANY (US) | 2025-10-16 | — | — | WO | disclosed |
| US-4008244-A | VULCANIZATION ACCELERATORS | PENNWALT CORPORATION (US) | 1977-02-15 | — | — | US | disclosed |
| US-3987017-A | OXAZOLIDINE- OR THIAZOLIDINE-CARBODI-THIOATES AS CURE ACCELERATORS | PENNWALT CORPORATION (US) | 1976-10-19 | — | — | US | disclosed |
| US-3976648-A | VULCANIZATION ACCELERATORS | PENNWALT CORPORATION (US) | 1976-08-24 | — | — | US | disclosed |
| US-3943143-A | Oxazolidine and thiazolidine derived carbodithioate compositions useful as vulcanization accelerators | PENNWALT CORPORATION (US) | 1976-03-09 | — | — | 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 (2 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-20030087902-A1 | Substituted indoles, pharmaceutical compounds containing such indoles and their use as PPAR-gamma binding agents | PPARG, PPARA, PPARD | SLC6A2 3098/4885SLC6A3 1963/4885ADRA1A 49/4885 |
| US-20120270824-A1 | MANNOSE DERIVATIVES AS ANTAGONISTS OF BACTERIAL ADHESION | MAN2A1, MANBA, M6PR | SLC6A2 2156/4885SLC6A3 1541/4885ADRA1A 427/4885 |
“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.