Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | L3MBTL1 | Q9Y468 | 3/20 | 0.46 |
| ▸ | MAPT | P10636 | 2/20 | 0.46 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.46 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.46 |
| ▸ | LMNA | P02545 | 2/20 | 0.41 |
| ▸ | GAA | P10253 | 2/20 | 0.41 |
| ▸ | POLB | P06746 | 1/20 | 0.41 |
| ▸ | HTT | P42858 | 3/20 | 0.40 |
| ▸ | NPC1 | O15118 | 1/20 | 0.40 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.39 |
| ▸ | PTGS1 | P23219 | 1/20 | 0.39 |
| ▸ | SLC6A2 | P23975 | 1/20 | 0.39 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.39 |
| ▸ | PTGS2 | P35354 | 1/20 | 0.39 |
| ▸ | SLC6A3 | Q01959 | 1/20 | 0.39 |
| ▸ | HIF1A | Q16665 | 1/20 | 0.39 |
| ▸ | HDAC6 | Q9UBN7 | 1/20 | 0.39 |
| ▸ | TSHR | P16473 | 1/20 | 0.39 |
| ▸ | MAOB | P27338 | 2/20 | 0.39 |
| ▸ | LIPE | Q05469 | 1/20 | 0.39 |
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 | |
|---|---|---|---|---|
| SCHEMBL10414960 | 0.80 | LMNA (0.53) | L3MBTL1MAPTMAPK1TDP1LMNA | |
| SCHEMBL3070157 | 0.80 | LMNA (0.53) | L3MBTL1MAPTLMNAGAACYP1A2 | |
| SCHEMBL6201495 | 0.79 | MAOB (0.51) | L3MBTL1MAPTLMNAGAAHTT | |
| SCHEMBL28151052 | 0.79 | MAOB (0.55) | L3MBTL1MAPTMAPK1TDP1LMNA | |
| SCHEMBL3609423 | 0.79 | MAOB (0.46) | L3MBTL1MAPTMAPK1TDP1LMNA | |
| SCHEMBL27822827 | 0.79 | APP (0.50) | L3MBTL1MAPTMAPK1TDP1LMNA | |
| SCHEMBL11687714 | 0.79 | AGXT (0.44) | L3MBTL1MAPTMAPK1TDP1LMNA | |
| SCHEMBL511881 | 0.79 | BCHE (0.40) | L3MBTL1MAPTMAPK1TDP1LMNA | |
| SCHEMBL17698456 | 0.79 | MAPT (0.42) | L3MBTL1MAPTMAPK1TDP1LMNA | |
| SCHEMBL29167670 | 0.78 | BCHE (0.39) | L3MBTL1MAPTMAPK1TDP1GAA |
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 32 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-4029690-A | WITH 2,5-DIMETHYL-2,4-HEXADIENE AND AN ALKYL DIAZOACETATE WITH A COPPER COMPLEX CATALYST | SUMITOMO CHEMICAL COMPANY, LIMITED (JA) | 1977-06-14 | — | — | US | claimed |
| US-4029683-A | WITH A SCHIFF BASE, CHRYSANTHEMATE SYNTHESIS CATALYST | SUMITOMO CHEMICAL COMPANY, LIMITED (JA) | 1977-06-14 | — | — | US | claimed |
| CN-110372571-B | 2- (2, 2-diarylethyl) -cyclic amine derivative or salt, synthesis and application thereof, and composition | 中国科学院大连化学物理研究所 | 2022-11-15 | — | — | CN | disclosed |
| CN-113226464-A | N- (pyridin-2-ylsulfonyl) cyclopropanecarboxamide derivatives and their use in the treatment of CFTR mediated diseases | 诺华股份有限公司 | 2021-08-06 | — | — | CN | disclosed |
| CN-110372571-A | A kind of 2- (2,2- diaryl ethyl)-Cycloamine derivative or salt and synthesis and application and composition | 中国科学院大连化学物理研究所 | 2019-10-25 | — | — | CN | disclosed |
| EP-0641786-B1 | Process for producing optically active alcohol | SUMITOMO CHEMICAL CO (JP) | 1997-08-20 | — | — | EP | disclosed |
| EP-0381434-B1 | Process for producing optically active alcohol | SUMITOMO CHEMICAL CO (JP) | 1997-04-16 | — | — | EP | disclosed |
| EP-0435687-B1 | Process for isomerization of oxime ethers | SUMITOMO CHEMICAL CO (JP) | 1995-03-29 | — | — | EP | disclosed |
| EP-0641786-A1 | Process for producing optically active alcohol | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1995-03-08 | — | — | EP | disclosed |
| EP-0485069-B1 | Process for producing optically active amines | SUMITOMO CHEMICAL CO (JP) | 1995-02-15 | — | — | EP | disclosed |
| EP-0347766-B1 | 4,5,7,8-Tetrahydro-6H-thiazolo[5,4-d]azepines, their preparation and their use as medicaments | THOMAE GMBH DR K (DE) | 1994-05-25 | — | — | EP | disclosed |
| EP-0022608-B1 | PROCESS FOR THE PREPARATION OF CYCLOPROPANE CARBOXYLIC ACID ESTERS | IMPERIAL CHEMICAL INDUSTRIES PLC (GB) | 1983-07-06 | — | — | EP | disclosed |
| US-4344894-A | TRANSITION METAL COMPLEX OF SCHIFF BASES AS CATALYSTS | IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) | 1982-08-17 | — | — | US | disclosed |
| US-4343935-A | CATALYSTS FOR CYCLOPROPANIZATION OF OLEFINS BY DIAZOACETATES | IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) | 1982-08-10 | — | — | US | disclosed |
| US-4288387-A | REACTION OF A HALOGENOPENTENE OR HEXENE WITH A DIAZOACETIC ESTER IN THE PRESENCE OF CATALYST WHICH IS METALLIC COPPER, A COPPER SALT, A RHODIUM SALT, OR A TRANSITION METAL COMPLEX OF A CHIRAL SCHIFF BASE | IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) | 1981-09-08 | — | — | US | disclosed |
| EP-0023075-A1 | Process for the preparation of cyclopropane carboxylic acid esters | IMPERIAL CHEMICAL INDUSTRIES PLC (GB) | 1981-01-28 | — | — | EP | disclosed |
| EP-0022608-A1 | Process for the preparation of cyclopropane carboxylic acid esters | IMPERIAL CHEMICAL INDUSTRIES PLC (GB) | 1981-01-21 | — | — | EP | disclosed |
| US-4197408-A | COPPER COMPLEX CATALYST, 2,5-DIMETHYL-2,4-HEXADIEN) REACTED WITH DIAZOACETATE | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1980-04-08 | — | — | US | disclosed |
| US-4029690-A | WITH 2,5-DIMETHYL-2,4-HEXADIENE AND AN ALKYL DIAZOACETATE WITH A COPPER COMPLEX CATALYST | SUMITOMO CHEMICAL COMPANY, LIMITED (JA) | 1977-06-14 | — | — | US | disclosed |
| US-4029683-A | WITH A SCHIFF BASE, CHRYSANTHEMATE SYNTHESIS CATALYST | SUMITOMO CHEMICAL COMPANY, LIMITED (JA) | 1977-06-14 | — | — | US | disclosed |