Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ALDH1A1 | P00352 | 9/20 | 0.63 |
| ▸ | MAPT | P10636 | 7/20 | 0.63 |
| ▸ | RAB9A | P51151 | 5/20 | 0.63 |
| ▸ | L3MBTL1 | Q9Y468 | 2/20 | 0.63 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.63 |
| ▸ | KMT2A | Q03164 | 7/20 | 0.59 |
| ▸ | LMNA | P02545 | 1/20 | 0.59 |
| ▸ | GAA | P10253 | 1/20 | 0.59 |
| ▸ | RELA | Q04206 | 1/20 | 0.57 |
| ▸ | MEN1 | O00255 | 4/20 | 0.56 |
| ▸ | PTGS2 | P35354 | 2/20 | 0.54 |
| ▸ | NPC1 | O15118 | 3/20 | 0.53 |
| ▸ | HPGD | P15428 | 2/20 | 0.53 |
| ▸ | CYP19A1 | P11511 | 1/20 | 0.53 |
| ▸ | CYP11B2 | P19099 | 1/20 | 0.53 |
| ▸ | SMN1; SMN2 | Q16637 | 2/20 | 0.53 |
| ▸ | PKM | P14618 | 1/20 | 0.50 |
| ▸ | ESR1 | P03372 | 1/20 | 0.50 |
| ▸ | GFER | P55789 | 1/20 | 0.50 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.49 |
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 | |
|---|---|---|---|---|
| SCHEMBL13980016 | 0.93 | ALDH1A1 (0.56) | ALDH1A1MAPTRAB9AL3MBTL1MAPK1 | |
| SCHEMBL9718468 | 0.92 | ESR1 (0.60) | ALDH1A1MAPTRAB9AL3MBTL1MAPK1 | |
| SCHEMBL13569445 | 0.87 | PTGS2 (0.53) | ALDH1A1MAPTRAB9AL3MBTL1MAPK1 | |
| SCHEMBL16946576 | 0.87 | CYP19A1 (0.72) | ALDH1A1MAPTRAB9AL3MBTL1MAPK1 | |
| SCHEMBL13930392 | 0.85 | MAPT (0.50) | ALDH1A1MAPTRAB9AL3MBTL1MAPK1 | |
| SCHEMBL13930398 | 0.85 | MAPT (0.50) | ALDH1A1MAPTRAB9AL3MBTL1MAPK1 | |
| SCHEMBL2210133 | 0.84 | CYP19A1 (0.57) | ALDH1A1MAPTRAB9AL3MBTL1MAPK1 | |
| SCHEMBL2121142 | 0.83 | CYP19A1 (0.71) | ALDH1A1MAPTPTGS2HPGDCYP19A1 | |
| SCHEMBL14570726 | 0.83 | PTGS1 (0.65) | ALDH1A1MAPTRAB9AL3MBTL1MAPK1 | |
| SCHEMBL25909565 | 0.83 | PTGS1 (0.65) | ALDH1A1MAPTRAB9AL3MBTL1MAPK1 |
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 25 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| JP-58198425-A | — | — | None | — | — | JP | disclosed |
| US-8017807-B2 | Tetrahydroxy compound, method for preparing the tetrahydroxy compound, and photoreceptor using the tetrahydroxy compound | RICOH COMPANY LIMITED (JP) | 2011-09-13 | — | — | US | disclosed |
| EP-1898262-B1 | Electrophotographic photoconductor and method for producing the same, image forming apparatus, and process cartridge | RICOH KK (JP) | 2009-12-30 | — | — | EP | disclosed |
| EP-1898262-A1 | Electrophotographic photoconductor and method for producing the same, image forming apparatus, and process cartridge | Ricoh Company, Ltd. (JP) | 2008-03-12 | — | — | EP | disclosed |
| US-20070128530-A1 | TETRAHYDROXY COMPOUND, METHOD FOR PREPARING THE TETRAHYDROXY COMPOUND, AND PHOTORECEPTOR USING THE TETRAHYDROXY COMPOUND | RICOH COMPANY, LTD. (JP) | 2007-06-07 | — | — | US | disclosed |
| US-5292602-A | Charge generating layer | FUGI ELECTRIC CO., LTD. (JP) | 1994-03-08 | — | — | US | disclosed |
| US-5292608-A | Charge generating layer | FUGI ELECTRIC CO., LTD. (JP) | 1994-03-08 | — | — | US | disclosed |
| US-5286590-A | Bisazo photoconductor for electrophotography | FUJI ELECTRIC CO., LTD. (JP) | 1994-02-15 | — | — | US | disclosed |
| US-5275898-A | Contains thiophene ring | FUJI ELECTRIC CO., LTD. (JP) | 1994-01-04 | — | — | US | disclosed |
| US-5266430-A | Bisazo gharge generating agent | FUJI ELECTRIC CO., LTD. (JP) | 1993-11-30 | — | — | US | disclosed |
| US-4971876-A | TETRAKISAZO COMPOUNDS | FUJI ELECTRIC CO., LTD. (JP) | 1990-11-20 | — | — | US | disclosed |
| US-4956250-A | MULTILAYER CHARGE GENERATING AZULENIUM COMPOUND FOR LIGHT SENSITIVE ELEMENTS | FUJI ELECTRIC CO., LTD. (JP) | 1990-09-11 | — | — | US | disclosed |
| US-4935323-A | THIOPHENE OR THIAZOLE-CONTAINING BISAZO CHARGE GENERATING COMPOUND | FUJI ELECTRIC CO., LTD. (JP) | 1990-06-19 | — | — | US | disclosed |
| US-4929525-A | SENSITIVE, DURABLE | FUJI ELECTRIC CO., LTD. | 1990-05-29 | — | — | US | disclosed |
| US-4917981-A | Photosensitive member for electrophotography | FUJI ELECTRIC CO., LTD. (JP) | 1990-04-17 | — | — | US | disclosed |
| US-4892949-A | ORGANIC PHOTOCONDUCTORS | RICOH COMPANY, LTD. (JP) | 1990-01-09 | — | — | US | disclosed |
| US-4877703-A | Photoconductor for electrophotography having a squarylium charge generating dye | FUJI ELECTRIC CO., LTD. (JP) | 1989-10-31 | — | — | US | disclosed |
| US-4871636-A | CHARGE GENERATING COMPOUND | FUJI ELECTRIC CO., LTD. (JP) | 1989-10-03 | — | — | US | disclosed |
| US-4859556-A | MULTILAYER; ELECTROCONDUCTIVE SUPPORT WITH PHOTOSENSITIVE MATERIAL | RICOH COMPANY, LTD. (JP) | 1989-08-22 | — | — | US | disclosed |
| JP-S58198425-A | ALPHA-PHENYLSTILBENE DERIVATIVE AND PREPARATION THEREOF | RICOH CO LTD | 1983-11-18 | — | — | JP | 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-20070128530-A1 | TETRAHYDROXY COMPOUND, METHOD FOR PREPARING THE TETRAHYDROXY COMPOUND, AND PHOTORECEPTOR USING THE TETRAHYDROXY COMPOUND | ALDH1A2, SLC9B2, SLC18A2 | ALDH1A1 485/4885MAPT 2694/4885RAB9A 394/4885 |
“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.