Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | DHFR | P00374 | 1/20 | 0.46 |
| ▸ | PIK3CG | P48736 | 1/20 | 0.46 |
| ▸ | NQO2 | P16083 | 2/20 | 0.45 |
| ▸ | LMNA | P02545 | 5/20 | 0.45 |
| ▸ | MEN1 | O00255 | 3/20 | 0.45 |
| ▸ | KMT2A | Q03164 | 3/20 | 0.45 |
| ▸ | TDP1 | Q9NUW8 | 3/20 | 0.45 |
| ▸ | L3MBTL1 | Q9Y468 | 3/20 | 0.45 |
| ▸ | MAPK1 | P28482 | 3/20 | 0.45 |
| ▸ | HTT | P42858 | 2/20 | 0.45 |
| ▸ | TP53 | P04637 | 2/20 | 0.45 |
| ▸ | ADORA2A | P29274 | 1/20 | 0.43 |
| ▸ | ADORA1 | P30542 | 1/20 | 0.43 |
| ▸ | KDM4E | B2RXH2 | 7/20 | 0.42 |
| ▸ | GAA | P10253 | 4/20 | 0.42 |
| ▸ | ALDH1A1 | P00352 | 9/20 | 0.42 |
| ▸ | HPGD | P15428 | 3/20 | 0.42 |
| ▸ | TSHR | P16473 | 2/20 | 0.42 |
| ▸ | HSD17B10 | Q99714 | 2/20 | 0.42 |
| ▸ | ALOX15 | P16050 | 1/20 | 0.41 |
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 | |
|---|---|---|---|---|
| SCHEMBL29423330 | 1.00 | DHFR (0.46) | DHFRPIK3CGNQO2LMNAMEN1 | |
| SCHEMBL12131349 | 0.96 | ALDH1A1 (0.46) | DHFRPIK3CGNQO2LMNAMEN1 | |
| SCHEMBL14789192 | 0.88 | TDP1 (0.43) | DHFRPIK3CGNQO2LMNAMEN1 | |
| SCHEMBL16702152 | 0.83 | DHFR (0.47) | DHFRPIK3CGLMNAMEN1KMT2A | |
| SCHEMBL13197741 | 0.82 | LMNA (0.54) | DHFRPIK3CGLMNAMEN1KMT2A | |
| SCHEMBL20798675 | 0.81 | KMT2A (0.54) | DHFRPIK3CGNQO2LMNAMEN1 | |
| SCHEMBL30860100 | 0.81 | KMT2A (0.54) | DHFRPIK3CGNQO2LMNAMEN1 | |
| SCHEMBL20212684 | 0.80 | CKS1B (0.40) | DHFRPIK3CGLMNAMEN1KMT2A | |
| SCHEMBL24311024 | 0.79 | KDM4E (0.37) | DHFRPIK3CGNQO2LMNAMEN1 | |
| SCHEMBL14819242 | 0.78 | ATP4A (0.49) | L3MBTL1HTTTP53KDM4EALDH1A1 |
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 99 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-106892908-B | Synthetic method of 5- (8-bromo-2, 3-diphenyl quinoxaline-5-yl) thiophene-2-formaldehyde | 西安瑞联新材料股份有限公司 | 2021-04-06 | — | — | CN | claimed |
| CN-117050324-A | Quinoxaline bridged terpyridine iron coordination polymer electrochromic material | 南京林业大学 | 2023-11-14 | — | — | CN | disclosed |
| CN-101492529-B | Soluble polythiophene derivative and application thereof in photoelectric component | 财团法人工业技术研究院 | 2022-10-11 | — | — | CN | disclosed |
| WO-2022062597-A1 | THERMALLY ACTIVATED DELAYED FLUORESCENCE MATERIAL AND USE THEREOF | 浙江百可半导体材料有限公司 | 2022-03-31 | — | — | WO | disclosed |
| WO-2022062597-A1 | THERMALLY ACTIVATED DELAYED FLUORESCENCE MATERIAL AND USE THEREOF | 浙江百可半导体材料有限公司 | 2022-03-31 | — | — | WO | disclosed |
| CN-112142717-B | Thermal activation delayed fluorescent material and application thereof | 浙江百可半导体材料有限公司 | 2022-02-11 | — | — | CN | disclosed |
| CN-108530423-B | Water-soluble aggregation-induced emission quinoxaline compound and preparation method and application thereof | 华南理工大学 | 2021-07-20 | — | — | CN | disclosed |
| CN-106892908-B | Synthetic method of 5- (8-bromo-2, 3-diphenyl quinoxaline-5-yl) thiophene-2-formaldehyde | 西安瑞联新材料股份有限公司 | 2021-04-06 | — | — | CN | disclosed |
| CN-112142717-A | Thermal activation delayed fluorescent material and application thereof | 浙江百可半导体材料有限公司 | 2020-12-29 | — | — | CN | disclosed |
| EP-3512848-B1 | COMPOUNDS WITH CARBAZOLE STRUCTURES | MERCK PATENT GMBH (DE) | 2020-11-18 | — | — | EP | disclosed |
| US-20030208032-A1 | Fluorene-containing polymers and compounds useful in the preparation thereof | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2003-11-06 | — | — | US | disclosed |
| WO-2003020790-A2 | CONJUGATED POLYMERS CONTAINING SPIROBIFLUORENE UNITS AND THE USE THEREOF | COVION ORGANIC SEMICONDUCTORS GMBH (DE) | 2003-03-13 | — | — | WO | disclosed |
| US-6514632-B1 | Electroluminescent films and coatings for light emitting diodes; efficiency | DOW GLOBAL TECHNOLOGIES INC. | 2003-02-04 | — | — | US | disclosed |
| US-6512083-B1 | Film prepared from the polymers of this invention. this invention is a light-emitting diode comprised of one or more layers of polymer films, at least one of which is derived from the oligomers and polymers of the invention. | DOW GLOBAL TECHNOLOGIES INC. | 2003-01-28 | — | — | US | disclosed |
| US-6362310-B1 | LIGHT EMITTING POLYMER | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2002-03-26 | — | — | US | disclosed |
| US-6353083-B1 | CONJUGATED COPOLYMER COMPRISING UNITS DERIVED FROM 9-SUBSTITUTED FLUORENE MONOMERS AND/OR 9,9-DISUBSTITUTED FLUORENE MONOMERS AND TWO DISTINCT RESIDUAL MONOMERIC UNITS THAT HAVE HOLE TRANSPORTING PROPERTIES | THE DOW CHEMICAL COMPANY | 2002-03-05 | — | — | US | disclosed |
| EP-1155096-A1 | FLUORENE COPOLYMERS AND DEVICES MADE THEREFROM | THE DOW CHEMICAL COMPANY (US) | 2001-11-21 | — | — | EP | disclosed |
| US-6255449-B1 | PROCESS FOR PREPARING POLYMERS HAVING AT LEAST THREE FLUORENE GROUPS IN BACKBONE, WHICH COMPRISES HEATING 2,7-DIHALO-9-SUBSTITUTED FLUORENES UNDER REACTION CONDITIONS SUFFICIENT TO FORM SAID POLYMERS | THE DOW CHEMICAL COMPANY | 2001-07-03 | — | — | US | disclosed |
| US-6169163-B1 | NOVEL 2,7-DIHALOFLUORENES SUBSTITUTED AT 9-POSITION | THE DOW CHEMICAL COMPANY | 2001-01-02 | — | — | US | disclosed |
| WO-2000046321-A1 | FLUORENE COPOLYMERS AND DEVICES MADE THEREFROM | THE DOW CHEMICAL COMPANY (US) | 2000-08-10 | — | — | WO | disclosed |