Predicted protein targets (top 15)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | TSHR | P16473 | 2/20 | 0.40 |
| ▸ | RECQL | P46063 | 2/20 | 0.40 |
| ▸ | CA1 | P00915 | 1/20 | 0.40 |
| ▸ | CA2 | P00918 | 1/20 | 0.40 |
| ▸ | GLA | P06280 | 1/20 | 0.40 |
| ▸ | HPGD | P15428 | 1/20 | 0.40 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.40 |
| ▸ | EPHX2 | P34913 | 1/20 | 0.40 |
| ▸ | NFKB1 | P19838 | 1/20 | 0.40 |
| ▸ | KCNA1 | Q09470 | 1/20 | 0.40 |
| ▸ | BLM | P54132 | 1/20 | 0.40 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.38 |
| ▸ | PMP22 | Q01453 | 1/20 | 0.38 |
| ▸ | ATM | Q13315 | 1/20 | 0.38 |
| ▸ | BBOX1 | O75936 | 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 | |
|---|---|---|---|---|
| SCHEMBL11287773 | 0.87 | RECQL (0.39) | TSHRRECQLCA1CA2GLA | |
| SCHEMBL10346546 | 0.85 | RECQL (0.40) | TSHRRECQLCA1CA2GLA | |
| Tetramethylammonium Ion SCHEMBL26929089 | 0.84 | CA1 (0.43) | TSHRRECQLCA1CA2GLA | |
| SCHEMBL884529 | 0.84 | — | — | |
| SCHEMBL17456590 | 0.84 | CA1 (0.48) | TSHRRECQLCA1CA2GLA | |
| SCHEMBL7587945 | 0.84 | CA1 (0.48) | TSHRRECQLCA1CA2GLA | |
| SCHEMBL11427865 | 0.84 | CA1 (0.48) | TSHRRECQLCA1CA2GLA | |
| SCHEMBL20637762 | 0.84 | CA1 (0.48) | TSHRRECQLCA1CA2GLA | |
| SCHEMBL11882830 | 0.84 | CA1 (0.48) | TSHRRECQLCA1CA2GLA | |
| SCHEMBL7126341 | 0.84 | — | — |
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 54 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-8801998-B2 | Method for producing a polyamide nanofiber product by electrospinning | MANN+HUMMEL GMBH (DE) | 2014-08-12 | — | — | US | claimed |
| US-20130206683-A1 | Method for Producing a Polyamide Nanofiber Product by Electrospinning, Polyamide Nanofiber Product, a Filter Medium with Polyamide Nanofiber Product, as well as a Filter Element with such a Filter Medium | MANN+HUMMEL GMBH (DE) | 2013-08-15 | — | — | US | claimed |
| US-8293673-B2 | Process for preparing 4-aminodiphenylamine | JIANGSU SINORGCHEM TECHNOLOGY CO., LTD. (CN) | 2012-10-23 | — | — | US | claimed |
| EP-1645555-B1 | A METHOD FOR PRODUCING 4-AMINODIPHENYLAMINE | JIANGSU SINORGCHEM TECH CO LTD (CN) | 2011-09-28 | — | — | EP | claimed |
| EP-1591438-B1 | A PROCESS FOR PREPARING 4-AMINODIPHENYLAMINE | SINORGCHEM CO SHANDONG (CN) | 2007-11-21 | — | — | EP | claimed |
| US-20070232832-A1 | PROCESS FOR PREPARING 4-AMINODIPHENYLAMINE | SINORGCHEM CO. | 2007-10-04 | — | — | US | claimed |
| US-7235694-B2 | Reacting nitrobenzene and aniline in presence of a powdery complex base catalyst to perform condensation, hydrogenation, separation and refining; reuse the catalyst; tetraalkyl ammonium hydroxide and a tetraalkyl ammonium salt | SINORGCHEM CO., SHANDONG (CN) | 2007-06-26 | — | — | US | claimed |
| US-7176333-B2 | Process for preparing 4-aminodiphenylamine | SINORGCHEM COMPANY, SHANDONG (CN) | 2007-02-13 | — | — | US | claimed |
| US-7084302-B2 | reacting nitrobenzene and aniline in presence of condensation basic catalyst to form mixtures of 4-nitrodiphenylamine and 4-nitrosodiphenylamine, then reacting with hydrogen in the presence of hydrogenation catalysts, separation and refining | SINORGCHEM SHANDONG CO., LTD. (CN) | 2006-08-01 | — | — | US | claimed |
| EP-1645555-A1 | A METHOD FOR PRODUCING 4-AMINODIPHENYLAMINE | Shi, Guangqiang (CN) | 2006-04-12 | — | — | EP | claimed |
| EP-1591438-A1 | A PROCESS FOR PREPARING 4-AMINODIPHENYLAMINE | Wang, Nongyue (CN) | 2005-11-02 | — | — | EP | claimed |
| US-20050240058-A1 | reacting nitrobenzene and aniline in presence of condensation basic catalyst to form mixtures of 4-nitrodiphenylamine and 4-nitrosodiphenylamine, then reacting with hydrogen in the presence of hydrogenation catalysts, separation and refining | NONGYUE WANG AND GUANGQIANG SHI (CN) | 2005-10-27 | — | — | US | claimed |
| US-20050065376-A1 | Process for preparing 4-aminodiphenylamine | GUANGQIANG SHI AND NONGYUE WANG (CN) | 2005-03-24 | — | — | US | claimed |
| EP-1753711-B1 | METHOD FOR PRODUCING QUATERNARY AMMONIUM COMPOUNDS | BASF SE (DE) | 2015-07-08 | — | — | EP | disclosed |
| US-9029603-B2 | Process for preparing alkylated p-phenylenediamines | JIANGSU SINORGCHEM TECHNOLOGY CO., LTD. (CN) | 2015-05-12 | — | — | US | disclosed |
| US-20130066113-A1 | PROCESS FOR PREPARING ALKYLATED P-PHENYLENEDIAMINES | JIANGSU SINORGCHEM TECHNOLOGY CO., LTD. (CN) | 2013-03-14 | — | — | US | disclosed |
| EP-0019226-A1 | Process for preparing N-(alpha-alkoxyethyl)-carboxylic acid amides | HOECHST AKTIENGESELLSCHAFT (DE) | 1980-11-26 | — | — | EP | disclosed |
| US-4145264-A | AROMATIC O-DICARBOXYLIC ACID NITRILES ELECTROLYZED IN AN ORGANIC LIQUID WITH AN ALKALINE ACTIVATOR | BASF AKTIENGESELLSCHAFT (DE) | 1979-03-20 | — | — | US | disclosed |
| US-4028201-A | Electrolytic monocarboxylation of activated olefins | MONSANTO COMPANY (US) | 1977-06-07 | — | — | US | disclosed |
| US-3984294-A | ELECTROLYTIC HYDRODIMERIZATION OF ACETONE | BASF AKTIENGESELLSCHAFT (DT) | 1976-10-05 | — | — | US | disclosed |