Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ACHE | P22303 | 3/20 | 0.64 |
| ▸ | ALDH1A1 | P00352 | 4/20 | 0.57 |
| ▸ | TSHR | P16473 | 1/20 | 0.57 |
| ▸ | CYP3A4 | P08684 | 2/20 | 0.52 |
| ▸ | HSD17B1 | P14061 | 4/20 | 0.44 |
| ▸ | HSD17B2 | P37059 | 4/20 | 0.44 |
| ▸ | CYP2C19 | P33261 | 2/20 | 0.44 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.44 |
| ▸ | LMNA | P02545 | 2/20 | 0.44 |
| ▸ | HSD17B10 | Q99714 | 2/20 | 0.44 |
| ▸ | CA12 | O43570 | 1/20 | 0.44 |
| ▸ | CA2 | P00918 | 1/20 | 0.44 |
| ▸ | CA5A | P35218 | 1/20 | 0.44 |
| ▸ | CA9 | Q16790 | 1/20 | 0.44 |
| ▸ | CA14 | Q9ULX7 | 1/20 | 0.44 |
| ▸ | CA5B | Q9Y2D0 | 1/20 | 0.44 |
| ▸ | SIGMAR1 | Q99720 | 2/20 | 0.41 |
| ▸ | ADRA1A | P35348 | 4/20 | 0.39 |
| ▸ | ADRA2A | P08913 | 3/20 | 0.39 |
| ▸ | ADRA1D | P25100 | 3/20 | 0.39 |
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 | |
|---|---|---|---|---|
| SCHEMBL8499385 | 1.00 | ACHE (0.64) | ACHEALDH1A1TSHRCYP3A4HSD17B1 | |
| SCHEMBL7875127 | 0.94 | ACHE (0.57) | ACHEALDH1A1TSHRCYP3A4HSD17B1 | |
| SCHEMBL7654504 | 0.93 | ACHE (0.55) | ACHEALDH1A1TSHRCYP3A4HSD17B1 | |
| SCHEMBL19192998 | 0.91 | ACHE (0.53) | ACHEALDH1A1TSHRCYP3A4HSD17B1 | |
| SCHEMBL2609916 | 0.88 | ACHE (0.50) | ACHEALDH1A1TSHRCYP3A4HSD17B1 | |
| SCHEMBL2609917 | 0.88 | ACHE (0.50) | ACHEALDH1A1TSHRCYP3A4HSD17B1 | |
| SCHEMBL31256035 | 0.87 | ALDH1A1 (0.65) | ACHEALDH1A1TSHRCYP3A4HSD17B1 | |
| SCHEMBL2355267 | 0.87 | ALDH1A1 (0.65) | ACHEALDH1A1TSHRCYP3A4HSD17B1 | |
| SCHEMBL977663 | 0.87 | ACHE (0.58) | ACHEALDH1A1CYP3A4HSD17B1HSD17B2 | |
| SCHEMBL9436732 | 0.86 | ALDH1A1 (0.55) | ACHEALDH1A1TSHRCYP3A4HSD17B1 |
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 52 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-7799497-B2 | Silanol containing overcoated photoconductors | XEROX CORPORATION (US) | 2010-09-21 | — | — | US | claimed |
| US-7592110-B2 | Polyhydroxy siloxane photoconductors | XEROX CORPORATION (US) | 2009-09-22 | — | — | US | claimed |
| US-20080193866-A1 | Polyhydroxy siloxane photoconductors | XEROX CORPORATION | 2008-08-14 | — | — | US | claimed |
| US-20080107985-A1 | Silanol containing overcoated photoconductors | XEROX CORPORATION | 2008-05-08 | — | — | US | claimed |
| EP-3083881-B1 | MOLECULAR GLASS MIXTURES FOR ORGANIC ELECTRONICS APPLICATIONS | MOLECULAR GLASSES INC (US) | 2020-09-09 | — | — | EP | disclosed |
| US-10461269-B2 | Crosslinkable, /polymerizable and combinations thereof charge-transporting molecular glass mixtures, luminescent molecular glass mixtures, or combinations thereof for organic light emitting diodes and other organic electronics and photonics applications and method of making same | MOLECULAR GLASSES, INC. (US) | 2019-10-29 | — | — | US | disclosed |
| US-9859505-B2 | Charge-transporting molecular glass mixtures, luminescent molecular glass mixtures, or combinations thereof or organic light emitting diodes and other organic electronics and photonics applications | MOLECULAR GLASSES, INC. (US) | 2018-01-02 | — | — | US | disclosed |
| EP-3083881-A1 | MOLECULAR GLASS MIXTURES FOR ORGANIC ELECTRONICS APPLICATIONS | Molecular Glasses, Inc. (US) | 2016-10-26 | — | — | EP | disclosed |
| CN-105793779-A | Molecular glass mixtures for organic electronics applications | 分子玻璃公司 | 2016-07-20 | — | — | CN | disclosed |
| EP-3039487-A1 | MOLECULAR GLASS MIXTURES FOR ORGANIC ELECTRONICS APPLICATIONS | Molaire Consulting LLC (US) | 2016-07-06 | — | — | EP | disclosed |
| WO-2015095859-A1 | MOLECULAR GLASS MIXTURES FOR ORGANIC ELECTRONICS APPLICATIONS | MOLAIRE CONSULTING LLC (US) | 2015-06-25 | — | — | WO | disclosed |
| US-20150179714-A1 | Crosslinkable, /Polymerizable and Combinations Thereof Charge-transporting Molecular Glass Mixtures, Luminescent Molecular Glass Mixtures, or Combinations Thereof for Organic Light Emitting Diodes and other Organic Electronics and Photonics Applications and Mothod of Making Same. | Molaire Consulting | 2015-06-25 | — | — | US | disclosed |
| US-5436099-A | Photoreceptor with low surface energy overcoat | XEROX CORPORATION (US) | 1995-07-25 | — | — | US | disclosed |
| EP-0660191-A1 | Layered photoreceptor with overcoatings containing hydrogen bonded materials | XEROX CORPORATION (US) | 1995-06-28 | — | — | EP | disclosed |
| US-5368967-A | Layered photoreceptor with overcoat containing hydrogen bonded materials | XEROX CORPORATION (US) | 1994-11-29 | — | — | US | disclosed |
| EP-0295115-B1 | ARYLAMINE COMPOUNDS | XEROX CORPORATION (US) | 1992-06-24 | — | — | EP | disclosed |
| US-5011939-A | Hydroxy functionalized arylamine compounds | XEROX CORPORATION (US) | 1991-04-30 | — | — | US | disclosed |
| US-4895783-A | SOLVENT RESISTANCE, WEAR RESISTANCE | XEROX CORPORATION (US) | 1990-01-23 | — | — | US | disclosed |
| US-4871634-A | Electrophotographic elements using hydroxy functionalized arylamine compounds | XEROX CORPORATION (US) | 1989-10-03 | — | — | US | disclosed |
| EP-0295115-A2 | Arylamine compounds | XEROX CORPORATION (US) | 1988-12-14 | — | — | EP | disclosed |