Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | GSK3B | P49841 | 4/20 | 0.57 |
| ▸ | MEN1 | O00255 | 5/20 | 0.56 |
| ▸ | KMT2A | Q03164 | 5/20 | 0.56 |
| ▸ | RAB9A | P51151 | 3/20 | 0.56 |
| ▸ | NPC1 | O15118 | 2/20 | 0.56 |
| ▸ | HTR3E | A5X5Y0 | 1/20 | 0.56 |
| ▸ | HTR3B | O95264 | 1/20 | 0.56 |
| ▸ | HTR3A | P46098 | 1/20 | 0.56 |
| ▸ | HTR3D | Q70Z44 | 1/20 | 0.56 |
| ▸ | HTR3C | Q8WXA8 | 1/20 | 0.56 |
| ▸ | TAAR1 | Q96RJ0 | 1/20 | 0.55 |
| ▸ | MAPT | P10636 | 2/20 | 0.54 |
| ▸ | LMNA | P02545 | 1/20 | 0.54 |
| ▸ | GAA | P10253 | 1/20 | 0.54 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.54 |
| ▸ | L3MBTL1 | Q9Y468 | 1/20 | 0.54 |
| ▸ | CA4 | P22748 | 1/20 | 0.52 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.50 |
| ▸ | CDK2 | P24941 | 1/20 | 0.50 |
| ▸ | KDR | P35968 | 1/20 | 0.50 |
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 | |
|---|---|---|---|---|
| SCHEMBL1405164 | 1.00 | GSK3B (0.57) | GSK3BMEN1KMT2ARAB9ANPC1 | |
| SCHEMBL17707284 | 0.94 | HTR3E (0.62) | GSK3BMEN1KMT2ARAB9ANPC1 | |
| SCHEMBL10818541 | 0.94 | HTR3E (0.62) | GSK3BMEN1KMT2ARAB9ANPC1 | |
| SCHEMBL10534869 | 0.91 | GSK3B (0.55) | GSK3BMEN1KMT2ARAB9ANPC1 | |
| SCHEMBL14006059 | 0.83 | HTR3E (0.56) | GSK3BMEN1KMT2ARAB9ANPC1 | |
| SCHEMBL8441056 | 0.83 | HTR3E (0.56) | GSK3BMEN1KMT2ARAB9ANPC1 | |
| SCHEMBL3940471 | 0.83 | NPC1 (0.56) | GSK3BMEN1KMT2ARAB9ANPC1 | |
| SCHEMBL3940476 | 0.83 | NPC1 (0.56) | GSK3BMEN1KMT2ARAB9ANPC1 | |
| SCHEMBL18643913 | 0.82 | MEN1 (0.56) | GSK3BMEN1KMT2ARAB9ANPC1 | |
| SCHEMBL2681633 | 0.82 | KMT2A (0.63) | GSK3BMEN1KMT2ARAB9ANPC1 |
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 31 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-113754558-B | Method for synthesizing azobenzene through copper salt catalyzed C-N coupling reaction | 桂林理工大学 | 2023-06-23 | — | — | CN | disclosed |
| CN-113754558-A | Method for synthesizing azobenzene by catalyzing C-N coupling reaction through copper salt | 桂林理工大学 | 2021-12-07 | — | — | CN | disclosed |
| WO-2021074275-A1 | EFFECTIVE PHOTOMODULATION OF LANTHANIDE (III) ION LUMINESCENCE IN THE VISIBLE OR NEAR-INFRARED RANGE | UNIVERSITE DE RENNES 1 (FR) | 2021-04-22 | — | — | WO | disclosed |
| US-9868873-B2 | Photochromic security enabled ink for digital offset printing applications | XEROX CORPORATION (US) | 2018-01-16 | — | — | US | disclosed |
| US-9404001-B2 | Photochromic latex ink | XEROX CORPORATION (US) | 2016-08-02 | — | — | US | disclosed |
| US-20150153479-A1 | PHOTOCHROMIC LATEX INK | XEROX CORPORATION (US) | 2015-06-04 | — | — | US | disclosed |
| US-20130305947-A1 | PHOTOCHROMIC SECURITY ENABLED INK FOR DIGITAL OFFSET PRINTING APPLICATIONS | XEROX CORPORATION (US) | 2013-11-21 | — | — | US | disclosed |
| EP-1591830-B1 | Reimageable medium | XEROX CORP (US) | 2011-03-09 | — | — | EP | disclosed |
| US-7708396-B2 | Photochromic phase change inks | XEROX CORPORATION (US) | 2010-05-04 | — | — | US | disclosed |
| US-7521159-B2 | Multicolor electronic paper | XEROX CORPORATION (US) | 2009-04-21 | — | — | US | disclosed |
| US-20050244742-A1 | Reimageable medium with light absorbing material | XEROX CORPORATION | 2005-11-03 | — | — | US | disclosed |
| US-20050244743-A1 | Reimageable medium | XEROX CORPORATION. | 2005-11-03 | — | — | US | disclosed |
| EP-1591830-A2 | Reimageable medium | Xerox Corporation (US) | 2005-11-02 | — | — | EP | disclosed |
| EP-1591831-A2 | Reimageable medium with light absorbing material | Xerox Corporation (US) | 2005-11-02 | — | — | EP | disclosed |
| EP-1591829-A1 | Method for forming temporary image | Xerox Corporation (US) | 2005-11-02 | — | — | EP | disclosed |
| US-5759729-A | A DRY TONER COMPRISING A RESIN, PHOTOCHROMATIC SPIROPYRAN, -OXAZINE OR -THIOPYRAN DYE AND A CHARGE CONTROL AGENT;ELECTROGRAPHY; XEROGRAPHY | XEROX CORPORATION (US) | 1998-06-02 | — | — | US | disclosed |
| US-5710420-A | Method for embedding and recovering machine-readable information | XEROX CORPORATION (US) | 1998-01-20 | — | — | US | disclosed |
| US-5633109-A | Ink compositions with liposomes containing photochromic compounds | XEROX CORPORATION (US) | 1997-05-27 | — | — | US | disclosed |
| US-5593486-A | Photochromic hot melt ink compositions | XEROX CORPORATION (US) | 1997-01-14 | — | — | US | disclosed |
| US-5551973-A | LIQUID CRYSTAL GEL PHASE, MICROEMULSION PHASE | XEROX CORPORATION (US) | 1996-09-03 | — | — | US | disclosed |