Predicted protein targets (top 7)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CYP3A4 | P08684 | 1/20 | 0.57 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.57 |
| ▸ | ESR1 | P03372 | 2/20 | 0.44 |
| ▸ | ESR2 | Q92731 | 2/20 | 0.44 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.35 |
| ▸ | GAA | P10253 | 1/20 | 0.35 |
| ▸ | DRD1 | P21728 | 2/20 | 0.32 |
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 | |
|---|---|---|---|---|
| SCHEMBL1577689 | 1.00 | CYP3A4 (0.57) | CYP3A4TDP1ESR1ESR2KDM4E | |
| SCHEMBL4846594 | 0.85 | CYP3A4 (0.71) | CYP3A4TDP1ESR1ESR2KDM4E | |
| SCHEMBL1314228 | 0.82 | TDP1 (0.75) | CYP3A4TDP1ESR1ESR2KDM4E | |
| SCHEMBL15698273 | 0.82 | TDP1 (0.75) | CYP3A4TDP1ESR1ESR2KDM4E | |
| Ammonia Solution, Strong SCHEMBL27462603 | 0.79 | TDP1 (0.92) | CYP3A4TDP1ESR1ESR2KDM4E | |
| SCHEMBL8598884 | 0.77 | CYP3A4 (0.67) | CYP3A4TDP1ESR1ESR2KDM4E | |
| SCHEMBL18832826 | 0.77 | CYP3A4 (0.67) | CYP3A4TDP1ESR1ESR2KDM4E | |
| Hydrochloric Acid SCHEMBL2257990 | 0.76 | TDP1 (0.86) | CYP3A4TDP1ESR1ESR2KDM4E | |
| Hydrochloric Acid SCHEMBL15105546 | 0.76 | TDP1 (0.86) | CYP3A4TDP1ESR1ESR2KDM4E | |
| SCHEMBL2387556 | 0.76 | TDP1 (0.86) | CYP3A4TDP1ESR1ESR2KDM4E |
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 9 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-9166073-B2 | Method for producing conjugated polymer, conjugated polymer, photoelectric conversion element, solar cell, and solar cell module | MITSUBISHI CHEMICAL CORPORATION (JP) | 2015-10-20 | — | — | US | disclosed |
| EP-2774940-A1 | METHOD FOR PRODUCING CONJUGATED POLYMER, CONJUGATED POLYMER, PHOTOELECTRIC CONVERSION ELEMENT, SOLAR CELL, AND SOLAR CELL MODULE | Mitsubishi Chemical Corporation (JP) | 2014-09-10 | — | — | EP | disclosed |
| US-20140243488-A1 | METHOD FOR PRODUCING CONJUGATED POLYMER, CONJUGATED POLYMER, PHOTOELECTRIC CONVERSION ELEMENT, SOLAR CELL, AND SOLAR CELL MODULE | MITSUBISHI CHEMICAL CORPORATION (JP) | 2014-08-28 | — | — | US | disclosed |
| US-20130109858-A1 | METHOD OF SYNTHESIZING CORE-EXPANDED PERYLENE DIIMIDE DYE AND NOVEL CORE-EXPANDED PERYLENE DIIMIDE DYE | NITTO DENKO CORPORATION (JP) | 2013-05-02 | — | — | US | disclosed |
| EP-1753768-A1 | POLYMERISABLE THIENO¬3,2-b|THIOPHENES | Merck Patent GmbH (DE) | 2007-02-21 | — | — | EP | disclosed |
| EP-1720553-A1 | PYRIMIDINE COMPOUNDS AS PURINE RECEPTOR ANTAGONIST | VERNALIS (R&D) LTD (GB) | 2006-11-15 | — | — | EP | disclosed |
| WO-2005121150-A1 | POLYMERISABLE THIENO[3,2-b]THIOPHENES | MERCK PATENT GMBH (DE) | 2005-12-22 | — | — | WO | disclosed |
| WO-2005079801-A1 | PYRIMIDINE COMPOUNDS AS PURINE RECEPTOR ANTAGONIST | VERNALIS (R & D) LTD (GB) | 2005-09-01 | — | — | WO | disclosed |
| US-6150526-A | Piperidine derivative having renin inhibiting activity | HOFFMANN-LA ROCHE INC. (US) | 2000-11-21 | — | — | US | disclosed |