Predicted protein targets (top 17)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | LPAR3 | Q9UBY5 | 2/20 | 0.41 |
| ▸ | LPAR2 | Q9HBW0 | 1/20 | 0.41 |
| ▸ | TSHR | P16473 | 2/20 | 0.37 |
| ▸ | ALDH1A1 | P00352 | 4/20 | 0.35 |
| ▸ | ADORA1 | P30542 | 1/20 | 0.33 |
| ▸ | CDK1 | P06493 | 1/20 | 0.33 |
| ▸ | CCNB1 | P14635 | 1/20 | 0.33 |
| ▸ | CCNA2 | P20248 | 1/20 | 0.33 |
| ▸ | CDK2 | P24941 | 1/20 | 0.33 |
| ▸ | CCNA1 | P78396 | 1/20 | 0.33 |
| ▸ | LMNA | P02545 | 1/20 | 0.32 |
| ▸ | ABCC4 | O15439 | 1/20 | 0.32 |
| ▸ | MAPT | P10636 | 1/20 | 0.32 |
| ▸ | CA2 | P00918 | 1/20 | 0.32 |
| ▸ | CA9 | Q16790 | 1/20 | 0.32 |
| ▸ | TRPA1 | O75762 | 1/20 | 0.31 |
| ▸ | SLC2A1 | P11166 | 1/20 | 0.31 |
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 | |
|---|---|---|---|---|
| SCHEMBL25113324 | 0.98 | LPAR3 (0.44) | LPAR3LPAR2TSHRALDH1A1ADORA1 | |
| SCHEMBL3786970 | 0.96 | LPAR3 (0.42) | LPAR3LPAR2TSHRALDH1A1ADORA1 | |
| SCHEMBL19619508 | 0.91 | ALDH1A1 (0.35) | LPAR3LPAR2TSHRALDH1A1ADORA1 | |
| SCHEMBL37316 | 0.87 | LPAR3 (0.48) | LPAR3LPAR2TSHRALDH1A1ADORA1 | |
| SCHEMBL22268773 | 0.87 | TSHR (0.37) | LPAR3LPAR2TSHRALDH1A1LMNA | |
| SCHEMBL22268682 | 0.87 | LPAR3 (0.37) | LPAR3LPAR2TSHRALDH1A1ADORA1 | |
| SCHEMBL891891 | 0.85 | LPAR3 (0.52) | LPAR3LPAR2TSHRALDH1A1ADORA1 | |
| SCHEMBL2027305 | 0.85 | LPAR3 (0.52) | LPAR3LPAR2TSHRALDH1A1ADORA1 | |
| SCHEMBL2026655 | 0.85 | LPAR3 (0.52) | LPAR3LPAR2TSHRALDH1A1ADORA1 | |
| SCHEMBL16581541 | 0.85 | LPAR3 (0.46) | LPAR3LPAR2TSHRALDH1A1ADORA1 |
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 49 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-115895064-A | Three-in-one full-plant nourishing antibacterial insole containing ginseng and carex meyeriana latex and manufacturing process of insole | 吉林省天佑乌拉草新型材料科技有限公司 | 2023-04-04 | — | — | CN | disclosed |
| CN-105198793-B | Oxime ester photoinitiators | 巴斯夫欧洲公司 | 2019-08-13 | — | — | CN | disclosed |
| CN-105531260-B | Oxime ester photoinitiator | 巴斯夫欧洲公司 | 2019-05-31 | — | — | CN | disclosed |
| CN-105358527-B | Oxime ester photoinitiator | 巴斯夫欧洲公司 | 2018-09-25 | — | — | CN | disclosed |
| CN-105175315-B | Photo-corrosion-resisting agent composition | 巴斯夫欧洲公司 | 2018-08-28 | — | — | CN | disclosed |
| CN-107652222-A | Oxime ester photoinitiators | 巴斯夫欧洲公司 | 2018-02-02 | — | — | CN | disclosed |
| CN-104284888-B | Oxime ester photoinitiators | 巴斯夫欧洲公司 | 2017-10-27 | — | — | CN | disclosed |
| CN-106604912-A | Oxime sulfonate derivatives | 巴斯夫欧洲公司 | 2017-04-26 | — | — | CN | disclosed |
| CN-103153952-B | The oxime ester derivative of benzo carbazole compound and in photopolymerisable compositions as the purposes of photoinitiator | 巴斯夫欧洲公司 | 2016-07-13 | — | — | CN | disclosed |
| CN-103443072-B | Polymerizable composition comprising oxime sulfonate as thermal curing agent | BASF SE (DE) | 2016-05-18 | — | — | CN | disclosed |
| US-20100113504-A1 | AMIDE COMPOUNDS AND THEIR USE AS ANTITUMOR AGENTS | SIGMA-TAU INDUSTRIE FARMACEUTICHE RIUNITE S.P.A. (IT) | 2010-05-06 | — | — | US | disclosed |
| CN-101687846-A | oxime ester photoinitiators | BASF SE | 2010-03-31 | — | — | CN | disclosed |
| CN-101687794-A | oxime ester photoinitiators | BASF SE | 2010-03-31 | — | — | CN | disclosed |
| CN-101679394-A | oxime ester photoinitiators | BASF SE | 2010-03-24 | — | — | CN | disclosed |
| CN-101636453-A | Transparent tinting material, coloured composition and uses thereof | BASF SE | 2010-01-27 | — | — | CN | disclosed |
| CN-101384672-A | Blue colour filters with enhanced contrast | CIBA HOLDING INC (CH) | 2009-03-11 | — | — | CN | disclosed |
| CN-101321727-A | Oxime ester photoinitiators | CIBA SC HOLDING AG (CH) | 2008-12-10 | — | — | CN | disclosed |
| CN-101023084-A | Compositions containing phthalocyanine dyes | CIBA SC HOLDING AG (CH) | 2007-08-22 | — | — | CN | disclosed |
| CN-101018829-A | Cyanopyridine-based azo dyes | HUNTSMAN ADV MAT SWITZERLAND (CH) | 2007-08-15 | — | — | CN | disclosed |
| CN-101014569-A | Oxime ester photoinitiators | CIBA SC HOLDING AG (CH) | 2007-08-08 | — | — | CN | 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-20100113504-A1 | AMIDE COMPOUNDS AND THEIR USE AS ANTITUMOR AGENTS | HDAC3, HCCS, CCNH | LPAR3 651/4885LPAR2 3102/4885TSHR 2522/4885 |
“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.