Predicted protein targets (top 19)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | PARP10 | Q53GL7 | 1/20 | 0.61 |
| ▸ | LTA4H | P09960 | 2/20 | 0.56 |
| ▸ | NR1H2 | P55055 | 1/20 | 0.56 |
| ▸ | BAX | Q07812 | 1/20 | 0.56 |
| ▸ | MEN1 | O00255 | 1/20 | 0.52 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.52 |
| ▸ | ESR1 | P03372 | 1/20 | 0.52 |
| ▸ | ESR2 | Q92731 | 1/20 | 0.52 |
| ▸ | LPAR1 | Q92633 | 2/20 | 0.46 |
| ▸ | LPAR5 | Q9H1C0 | 2/20 | 0.46 |
| ▸ | FAAH | O00519 | 1/20 | 0.45 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.43 |
| ▸ | L3MBTL1 | Q9Y468 | 2/20 | 0.43 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.43 |
| ▸ | HTT | P42858 | 1/20 | 0.43 |
| ▸ | LMNA | P02545 | 1/20 | 0.43 |
| ▸ | CXCL8 | P10145 | 1/20 | 0.43 |
| ▸ | DAO | P14920 | 1/20 | 0.42 |
| ▸ | FFAR1 | O14842 | 1/20 | 0.42 |
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 | |
|---|---|---|---|---|
| SCHEMBL6293051 | 0.89 | PARP10 (0.66) | PARP10MEN1KMT2AESR1LPAR1 | |
| SCHEMBL6289863 | 0.87 | PARP10 (0.63) | PARP10MEN1KMT2AESR1LPAR1 | |
| SCHEMBL6293904 | 0.85 | PARP10 (0.61) | PARP10MEN1KMT2AESR1LPAR1 | |
| SCHEMBL6293879 | 0.85 | PARP10 (0.61) | PARP10MEN1KMT2AESR1LPAR1 | |
| SCHEMBL2458461 | 0.85 | PARP10 (0.61) | PARP10MEN1KMT2AESR1LPAR1 | |
| SCHEMBL6290343 | 0.85 | PARP10 (0.61) | PARP10MEN1KMT2AESR1LPAR1 | |
| SCHEMBL4211500 | 0.84 | LTA4H (0.68) | PARP10LTA4HNR1H2BAXMEN1 | |
| SCHEMBL6290371 | 0.83 | PARP10 (0.59) | PARP10LTA4HMEN1KMT2AESR1 | |
| SCHEMBL6290746 | 0.83 | PARP10 (0.59) | PARP10LTA4HMEN1KMT2AESR1 | |
| SCHEMBL702582 | 0.82 | PARP10 (0.58) | PARP10LTA4HMEN1KMT2AESR1 |
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 13 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| WO-2017093351-A1 | CPLA2 INHIBITORS | Westfälische Wilhelms-Universität Münster (DE) | 2017-06-08 | — | — | WO | disclosed |
| EP-1380342-B1 | COMPLEX CATALYST, PROCESS FOR PRODUCING THE COMPLEX CATALYST, AND PROCESS FOR PRODUCING ALCOHOL DERIVATIVE WITH THE COMPLEX CATALYST | SUMITOMO CHEMICAL CO (JP) | 2009-07-01 | — | — | EP | disclosed |
| CN-1281320-C | Complex catalyst process for producing the complex catalyst and process for producing alcohol derivative with the complex catalyst | SUMITOMO CHEMICAL CO (JP) | 2006-10-25 | — | — | CN | disclosed |
| US-6995110-B2 | Complex catalyst, process for producing the complex catalyst, and process for producing alcohol derivative with the complex catalyst | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2006-02-07 | — | — | US | disclosed |
| CN-1503696-A | Complex catalyst, process for producing the complex catalyst, and process for producing alcohol derivative using the complex catalyst | ס�ѻ�ѧ��ҵ��ʽ���� | 2004-06-09 | — | — | CN | disclosed |
| US-20040077487-A1 | Complex catalyst, process for producing the complex catalyst, and process for producing alchohol derivative with the complex catalyst | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2004-04-22 | — | — | US | disclosed |
| EP-1380342-A1 | COMPLEX CATALYST, PROCESS FOR PRODUCING THE COMPLEX CATALYST, AND PROCESS FOR PRODUCING ALCOHOL DERIVATIVE WITH THE COMPLEX CATALYST | SUMITOMO CHEMICAL COMPANY LIMITED (JP) | 2004-01-14 | — | — | EP | disclosed |
| US-5012017-A | Peroxide oxidation of halogenated phenoxyphenones to phenoxyophenyl esters, then conversions to phenoxyphenols | DOWELANCO (US) | 1991-04-30 | — | — | US | disclosed |
| WO-1990009979-A1 | METHODS FOR THE PREPARATION OF BROMINATED INTERMEDIATES | THE DOW CHEMICAL COMPANY (US) | 1990-09-07 | — | — | WO | disclosed |
| CN-1045094-A | The method for preparing the bromination intermediate | DOW CHEMICAL CO (US) | 1990-09-05 | — | — | CN | disclosed |
| EP-0384043-A2 | Methods for the preparation of brominated intermediates | THE DOW CHEMICAL COMPANY (US) | 1990-08-29 | — | — | EP | disclosed |
| US-4607051-A | Carbamic acid compound and use as a pesticide | HOFFMANN-LA ROCHE INC. (US) | 1986-08-19 | — | — | US | disclosed |
| US-4413010-A | Carbamic acid esters and use as pesticides | HOFFMANN-LA ROCHE INC. (US) | 1983-11-01 | — | — | US | disclosed |