Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CALM1 | P0DP23 | 1/20 | 0.43 |
| ▸ | TSHR | P16473 | 4/20 | 0.39 |
| ▸ | ALDH1A1 | P00352 | 4/20 | 0.39 |
| ▸ | IDO1 | P14902 | 3/20 | 0.39 |
| ▸ | LOXL2 | Q9Y4K0 | 2/20 | 0.39 |
| ▸ | TP53 | P04637 | 1/20 | 0.39 |
| ▸ | TRPA1 | O75762 | 1/20 | 0.39 |
| ▸ | MAOB | P27338 | 1/20 | 0.38 |
| ▸ | HPGD | P15428 | 1/20 | 0.38 |
| ▸ | ALOX15 | P16050 | 1/20 | 0.38 |
| ▸ | ALOX12 | P18054 | 1/20 | 0.38 |
| ▸ | CASP1 | P29466 | 1/20 | 0.38 |
| ▸ | HSD17B10 | Q99714 | 1/20 | 0.38 |
| ▸ | TDP1 | Q9NUW8 | 2/20 | 0.36 |
| ▸ | CYP2A6 | P11509 | 1/20 | 0.36 |
| ▸ | HTR2A | P28223 | 1/20 | 0.36 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.36 |
| ▸ | TAAR1 | Q96RJ0 | 1/20 | 0.36 |
| ▸ | THRB | P10828 | 1/20 | 0.35 |
| ▸ | EPHX2 | P34913 | 1/20 | 0.35 |
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 | |
|---|---|---|---|---|
| Lithium Ion SCHEMBL8757501 | 0.97 | CALM1 (0.41) | CALM1TSHRALDH1A1IDO1LOXL2 | |
| SCHEMBL17417857 | 0.97 | CALM1 (0.41) | CALM1TSHRALDH1A1IDO1LOXL2 | |
| Ammonia Solution, Strong SCHEMBL15569691 | 0.97 | CALM1 (0.41) | CALM1TSHRALDH1A1IDO1LOXL2 | |
| Tetramethylammonium Ion SCHEMBL5079963 | 0.91 | ALDH1A1 (0.43) | CALM1TSHRALDH1A1IDO1LOXL2 | |
| Tetrylammonium SCHEMBL7555245 | 0.85 | TP53 (0.39) | CALM1TSHRALDH1A1TP53TDP1 | |
| SCHEMBL8521849 | 0.84 | PLA2G1B (0.40) | ALDH1A1IDO1LOXL2MAOBTAAR1 | |
| SCHEMBL6536703 | 0.84 | CYP1A2 (0.46) | TSHRIDO1MAOBHPGDALOX12 | |
| SCHEMBL4386780 | 0.83 | SIGMAR1 (0.41) | TRPA1CYP2A6HTR2ATAAR1 | |
| SCHEMBL8772340 | 0.82 | SMN1; SMN2 (0.37) | TP53SMN1; SMN2EPHX2 | |
| Tetrabuthylammonium SCHEMBL3362614 | 0.79 | DNM1 (0.45) | TP53SMN1; SMN2EPHX2 |
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 |
|---|---|---|---|---|---|---|---|
| EP-0435594-B1 | Photoinitiators | CYCOLOR INC (US) | 1997-05-02 | — | — | EP | claimed |
| US-5100755-A | Photosensitive materials | THE MEAD CORPORATION (US) | 1992-03-31 | — | — | US | claimed |
| EP-0435594-A2 | Photoinitiators | THE MEAD CORPORATION (US) | 1991-07-03 | — | — | EP | claimed |
| CN-108700785-B | Display element sealing agent, liquid crystal sealing agent, cured product of liquid crystal sealing agent, liquid crystal display panel, and method for producing liquid crystal display panel | 三井化学株式会社 | 2021-05-28 | — | — | CN | disclosed |
| US-10175174-B2 | Photoactivated chemical bleaching of dyes | GE HEALTHCARE BIO-SCIENCES CORP. (US) | 2019-01-08 | — | — | US | disclosed |
| EP-2932270-B1 | PHOTOACTIVATED CHEMICAL BLEACHING OF DYES | GE HEALTHCARE BIO SCIENCES CORP (US) | 2018-10-24 | — | — | EP | disclosed |
| US-9915592-B2 | Methods of analyzing an H and E stained biological sample | GENERAL ELECTRIC COMPANY (US) | 2018-03-13 | — | — | US | disclosed |
| US-9915592-B2 | Methods of analyzing an H and E stained biological sample | GENERAL ELECTRIC COMPANY (US) | 2018-03-13 | — | — | US | disclosed |
| US-20150316482-A1 | PHOTOACTIVATED CHEMICAL BLEACHING OF DYES | LEICA MICROSYSTEMS CMS GMBH (DE) | 2015-11-05 | — | — | US | disclosed |
| EP-2932270-A1 | PHOTOACTIVATED CHEMICAL BLEACHING OF DYES | Clarient Diagnostic Services, Inc. (US) | 2015-10-21 | — | — | EP | disclosed |
| WO-2014093455-A1 | PHOTOACTIVATED CHEMICAL BLEACHING OF DYES | CLARIENT DIAGNOSTIC SERVICES, INC. (US) | 2014-06-19 | — | — | WO | disclosed |
| EP-0353030-B1 | Photopolymerization initiator and photosensitive composition employing the same | CANON KK (JP) | 1995-03-15 | — | — | EP | disclosed |
| EP-0587338-A2 | Silver halide imaging materials | MINNESOTA MINING AND MANUFACTURING COMPANY (US) | 1994-03-16 | — | — | EP | disclosed |
| US-5260180-A | Photothermographic imaging media employing silver salts of tetrahydrocarbyl borate anions | MINNESOTA MINING AND MANUFACTURING COMPANY (US) | 1993-11-09 | — | — | US | disclosed |
| EP-0555058-A1 | (Oxo)sulfonium complex, polymerizable composition containing the complex, and method of polymerizing composition | TOYO INK MANUFACTURING CO., LTD. (JP) | 1993-08-11 | — | — | EP | disclosed |
| US-5124235-A | Photopolymerization initiator and photosensitive composition employing the same | CANON KABUSHIKI KAISHA (JP) | 1992-06-23 | — | — | US | disclosed |
| US-5100755-A | Photosensitive materials | THE MEAD CORPORATION (US) | 1992-03-31 | — | — | US | disclosed |
| EP-0435594-A2 | Photoinitiators | THE MEAD CORPORATION (US) | 1991-07-03 | — | — | EP | disclosed |
| EP-0408227-A1 | Photohardenable or photosoftenable compositions | THE MEAD CORPORATION (US) | 1991-01-16 | — | — | EP | disclosed |
| EP-0353030-A2 | Photopolymerization initiator and photosensitive composition employing the same | CANON KABUSHIKI KAISHA (JP) | 1990-01-31 | — | — | EP | disclosed |