Predicted protein targets (top 13)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | NR1I2 | O75469 | 1/20 | 0.31 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.31 |
| ▸ | LMNA | P02545 | 1/20 | 0.31 |
| ▸ | CYP2C9 | P11712 | 1/20 | 0.31 |
| ▸ | MIF | P14174 | 1/20 | 0.31 |
| ▸ | TYR | P14679 | 1/20 | 0.31 |
| ▸ | ALOX15 | P16050 | 1/20 | 0.31 |
| ▸ | HTT | P42858 | 1/20 | 0.31 |
| ▸ | NFE2L2 | Q16236 | 1/20 | 0.31 |
| ▸ | HSD17B10 | Q99714 | 1/20 | 0.31 |
| ▸ | GABRA1 | P14867 | 1/20 | 0.30 |
| ▸ | GABRB2 | P47870 | 1/20 | 0.30 |
| ▸ | CA2 | P00918 | 1/20 | 0.30 |
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 | |
|---|---|---|---|---|
| SCHEMBL855717 | 0.77 | CA2 (0.30) | CA2 | |
| SCHEMBL2541721 | 0.76 | CA2 (0.38) | NR1I2ALDH1A1LMNACYP2C9MIF | |
| SCHEMBL2139327 | 0.76 | PTGS1 (0.31) | — | |
| SCHEMBL10670576 | 0.76 | ALDH1A1 (0.32) | NR1I2ALDH1A1LMNACYP2C9MIF | |
| SCHEMBL3236808 | 0.76 | CA2 (0.48) | NR1I2ALDH1A1LMNACYP2C9MIF | |
| SCHEMBL11568827 | 0.76 | — | — | |
| SCHEMBL12817698 | 0.72 | — | — | |
| SCHEMBL12817356 | 0.72 | — | — | |
| SCHEMBL12817631 | 0.72 | CA1 (0.31) | CA2 | |
| SCHEMBL3030633 | 0.71 | HSD11B1 (0.34) | — |
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 65 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-2484685-B1 | TRANSITION METAL COMPLEX, PREPARATION METHOD FOR SAID TRANSITION METAL COMPLEX, TRIMERIZATION CATALYST, PREPARATION METHOD FOR 1-HEXENE, PREPARATION METHOD FOR ETHYLENE POLYMER, SUBSTITUTED CYCLOPENTADIENE COMPOUND, AND PREPARATION METHOD FOR SAID SUBSTITUTED CYCLOPENTADIENE COMPOUND | SUMITOMO CHEMICAL CO (JP) | 2017-11-01 | — | — | EP | claimed |
| EP-2484685-A1 | TRANSITION METAL COMPLEX, PREPARATION METHOD FOR SAID TRANSITION METAL COMPLEX, TRIMERIZATION CATALYST, PREPARATION METHOD FOR 1-HEXENE, PREPARATION METHOD FOR ETHYLENE POLYMER, SUBSTITUTED CYCLOPENTADIENE COMPOUND, AND PREPARATION METHOD FOR SAID SUBSTITUTED CYCLOPENTADIENE COMPOUND | Sumitomo Chemical Co., Ltd (JP) | 2012-08-08 | — | — | EP | claimed |
| US-20120184431-A1 | TRANSITION METAL COMPLEX, PREPARATION METHOD FOR SAID TRANSITION METAL COMPLEX, TRIMERIZATION CATALYST, PREPARATION METHOD FOR 1-HEXENE, PREPARATION METHOD FOR ETHYLENE POLYMER, SUBSTITUTED CYCLOPENTADIENE COMPOUND, AND PREPARATION METHOD FOR SAID SUBSTITUTED CYCLOPENTADIENE COMPOUND | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2012-07-19 | — | — | US | claimed |
| US-10124326-B2 | Modified solid polyalkylaluminoxane and catalyst for olefin oligomerization reaction | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2018-11-13 | — | — | US | disclosed |
| US-9919300-B2 | 1-hexene production process | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2018-03-20 | — | — | US | disclosed |
| EP-2484685-B1 | TRANSITION METAL COMPLEX, PREPARATION METHOD FOR SAID TRANSITION METAL COMPLEX, TRIMERIZATION CATALYST, PREPARATION METHOD FOR 1-HEXENE, PREPARATION METHOD FOR ETHYLENE POLYMER, SUBSTITUTED CYCLOPENTADIENE COMPOUND, AND PREPARATION METHOD FOR SAID SUBSTITUTED CYCLOPENTADIENE COMPOUND | SUMITOMO CHEMICAL CO (JP) | 2017-11-01 | — | — | EP | disclosed |
| US-20170225155-A1 | MODIFIED SOLID POLYALKYLALUMINOXANE AND CATALYST FOR OLEFIN OLIOGOMERIZATION REACTION | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2017-08-10 | — | — | US | disclosed |
| EP-3202822-A1 | MODIFIED SOLID POLYALKYLALUMINOXANE AND CATALYST FOR OLEFIN OLIGOMERIZATION REACTION | Sumitomo Chemical Company Limited (JP) | 2017-08-09 | — | — | EP | disclosed |
| US-20170036200-A1 | 1-HEXENE PRODUCTION PROCESS | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2017-02-09 | — | — | US | disclosed |
| US-20150105572-A1 | TRANSITION METAL COMPLEX | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2015-04-16 | — | — | US | disclosed |
| US-20150105237-A1 | CATALYTIC COMPONENT FOR TRIMERIZATION AND TRIMERIZATION CATALYST | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2015-04-16 | — | — | US | disclosed |
| EP-0546998-A1 | Process for preparing N,N'-bis(hydrocarbyloxycarbonyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)diamines | CIBA-GEIGY AG (CH) | 1993-06-16 | — | — | EP | disclosed |
| US-5206414-A | Process for the preparation of hydroxyphenylpropionic acid esters | CIBA-GEIGY CORPORATION (US) | 1993-04-27 | — | — | US | disclosed |
| EP-0366040-B1 | COMPOUNDS CONTAINING PHENOL GROUPS AS ANTIOXIDANTS IN ORGANIC MATERIALS | CIBA-GEIGY AG (CH) | 1993-03-17 | — | — | EP | disclosed |
| EP-0524145-A1 | Multifunctional additives for lubricants | CIBA-GEIGY AG (CH) | 1993-01-20 | — | — | EP | disclosed |
| EP-0514332-A1 | Bis-phosphites | CIBA-GEIGY AG (CH) | 1992-11-19 | — | — | EP | disclosed |
| EP-0511156-A2 | Non symmetric aryl phosphites | CIBA-GEIGY AG (CH) | 1992-10-28 | — | — | EP | disclosed |
| EP-0474589-A1 | Orthophenolacetamides | CIBA-GEIGY AG (CH) | 1992-03-11 | — | — | EP | disclosed |
| EP-0437187-A2 | Process for the preparation of esters of hydroxyphenylpropanoic acid | CIBA-GEIGY AG (CH) | 1991-07-17 | — | — | EP | disclosed |
| EP-0366040-A1 | Compounds containing phenol groups as antioxidants in organic materials | CIBA-GEIGY AG (CH) | 1990-05-02 | — | — | EP | 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 (6 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-20170036200-A1 | 1-HEXENE PRODUCTION PROCESS | AP1M1, HK1, CYC1 | NR1I2 564/4885ALDH1A1 1321/4885LMNA 4214/4885 |
| US-20170225155-A1 | MODIFIED SOLID POLYALKYLALUMINOXANE AND CATALYST FOR OLEFIN OLIOGOMERIZATION REACTION | OGFR, GFER, ITGB7 | NR1I2 2932/4885ALDH1A1 1064/4885LMNA 3578/4885 |
| US-20150105572-A1 | TRANSITION METAL COMPLEX | AP1M1, AP3M1, EMC1 | NR1I2 513/4885ALDH1A1 2292/4885LMNA 3476/4885 |
| US-20150105237-A1 | CATALYTIC COMPONENT FOR TRIMERIZATION AND TRIMERIZATION CATALYST | AP1M1, AMY1A, AP3M1 | NR1I2 768/4885ALDH1A1 2399/4885LMNA 3976/4885 |
| US-20120184431-A1 | TRANSITION METAL COMPLEX, PREPARATION METHOD FOR SAID TRANSITION METAL COMPLEX, TRIMERIZATION CATALYST, PREPARATION METHOD FOR 1-HEXENE, PREPARATION METHOD FOR ETHYLENE POLYMER, SUBSTITUTED CYCLOPENTADIENE COMPOUND, AND PREPARATION METHOD FOR SAID SUBSTITUTED CYCLOPENTADIENE COMPOUND | EMC1, CYC1, AP1M1 | NR1I2 1137/4885ALDH1A1 2139/4885LMNA 2944/4885 |
| US-10124326-B2 | Modified solid polyalkylaluminoxane and catalyst for olefin oligomerization reaction | GFER, OGFR, TECR | NR1I2 3252/4885ALDH1A1 1567/4885LMNA 3364/4885 |
“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.