Known targets — ChEMBL curated mechanism
CHRM1CHRM2CHRM3CHRM4CHRM5SLC6A2dacAdacBdacCftsImrcAmrcBmrdA
The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | HTT | P42858 | 3/20 | 0.42 |
| ▸ | TERT | O14746 | 1/20 | 0.39 |
| ▸ | LMNA | P02545 | 3/20 | 0.39 |
| ▸ | SMN1; SMN2 | Q16637 | 3/20 | 0.39 |
| ▸ | MAPT | P10636 | 3/20 | 0.37 |
| ▸ | KDM4E | B2RXH2 | 3/20 | 0.37 |
| ▸ | HSD17B10 | Q99714 | 2/20 | 0.37 |
| ▸ | MAPK1 | P28482 | 2/20 | 0.36 |
| ▸ | CYP3A4 | P08684 | 2/20 | 0.36 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.36 |
| ▸ | THPO | P40225 | 1/20 | 0.36 |
| ▸ | MEN1 | O00255 | 2/20 | 0.36 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.36 |
| ▸ | APAF1 | O14727 | 1/20 | 0.36 |
| ▸ | NPC1 | O15118 | 1/20 | 0.36 |
| ▸ | PLA2G1B | P04054 | 1/20 | 0.36 |
| ▸ | HSP90AA1 | P07900 | 1/20 | 0.36 |
| ▸ | RAB9A | P51151 | 1/20 | 0.36 |
| ▸ | NPSR1 | Q6W5P4 | 1/20 | 0.36 |
| ▸ | ATG4B | Q9Y4P1 | 1/20 | 0.36 |
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 | |
|---|---|---|---|---|
| SCHEMBL2935751 | 0.88 | LMNA (0.41) | HTTLMNASMN1; SMN2MAPTKDM4E | |
| SCHEMBL2230708 | 0.86 | HTT (0.52) | HTTTERTLMNASMN1; SMN2MAPT | |
| SCHEMBL3108192 | 0.86 | SMN1; SMN2 (0.37) | HTTLMNASMN1; SMN2MAPTKDM4E | |
| SCHEMBL3100213 | 0.86 | SMN1; SMN2 (0.37) | HTTLMNASMN1; SMN2MAPTKDM4E | |
| Toluene SCHEMBL14859755 | 0.85 | LMNA (0.41) | HTTLMNASMN1; SMN2MAPTKDM4E | |
| Lithium SCHEMBL30985259 | 0.85 | HTT (0.51) | HTTTERTLMNASMN1; SMN2MAPT | |
| SCHEMBL2913208 | 0.85 | HTT (0.45) | HTTTERTLMNASMN1; SMN2MAPT | |
| SCHEMBL5546185 | 0.84 | HTT (0.39) | HTTTERTLMNASMN1; SMN2MAPT | |
| SCHEMBL14720371 | 0.84 | HTT (0.61) | HTTLMNASMN1; SMN2MAPTMAPK1 | |
| SCHEMBL7195915 | 0.84 | HTT (0.61) | HTTLMNASMN1; SMN2MAPTMAPK1 |
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 612 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20250382408-A1 | EPOXY-TERMINATED ISOCYANATE PREPOLYMERS, AND PROCESS FOR THE PREPARATION THEREOF | BASF SE (DE) | 2025-12-18 | — | — | US | claimed |
| US-12226215-B2 | Conductive polymeric composition and method for preparing the conductive polymeric composition | Giuseppe USAI (IT) | 2025-02-18 | — | — | US | claimed |
| CN-119403855-A | Epoxy blocked isocyanate prepolymer and method for producing same | 巴斯夫欧洲公司 | 2025-02-07 | — | — | CN | claimed |
| US-20240336833-A1 | POLYCANNABINOIDS FOR COMMODITY POLYMERS AND COMMODITY ELECTRONICS | UNIVERSITY OF CONNECTICUT | 2024-10-10 | — | — | US | claimed |
| EP-3986978-B1 | AQUEOUS DELAYED ACID SYSTEM FOR WELL STIMULATION | BAKER HUGHES HOLDINGS LLC (US) | 2024-05-15 | — | — | EP | claimed |
| CN-111117594-B | Electrochromic material and electrochromic device based on dynamic metal-ligand complexation | 吉林大学 | 2024-03-26 | — | — | CN | claimed |
| US-11932813-B2 | Electrochromic materials; preparation and use thereof | UNIVERSITY OF CONNECTICUT (US) | 2024-03-19 | — | — | US | claimed |
| WO-2023247278-A1 | EPOXY-TERMINATED ISOCYANATE PREPOLYMERS, AND PROCESS FOR THE PREPARATION THEREOF | BASF SE (DE) | 2023-12-28 | — | — | WO | claimed |
| CN-115010836-B | Electrochromic polymer, nano particle and device | 吉林大学 | 2023-09-08 | — | — | CN | claimed |
| US-11567385-B2 | Electrochromic device | THE BOEING COMPANY (US) | 2023-01-31 | — | — | US | claimed |
| WO-2006094052-A2 | GEL POLYMER ELECTROLYTES | TRITON SYSTEMS, INC. (US) | 2006-09-08 | — | — | WO | claimed |
| EP-1663921-A2 | METHOD FOR PRODUCING HALOALKANES FROM ALCOHOLS | BASF AKTIENGESELLSCHAFT (DE) | 2006-06-07 | — | — | EP | claimed |
| WO-2006048171-A1 | METHOD FOR PRODUCING POLYISOCYANATES | BASF AKTIENGESELLSCHAFT (DE) | 2006-05-11 | — | — | WO | claimed |
| WO-2006045518-A1 | METHOD FOR SEPARATING GAS | SOLVAY FLUOR GMBH (DE) | 2006-05-04 | — | — | WO | claimed |
| WO-2006029788-A1 | METHOD FOR SEPARATING HYDROGEN CHLORIDE AND PHOSGENE | BASF AKTIENGESELLSCHAFT (DE) | 2006-03-23 | — | — | WO | claimed |
| US-20060054511-A1 | Electrochemical deblocking using a hydrazine derivative | CUSTOMARRAY, INC. | 2006-03-16 | — | — | US | claimed |
| WO-2005083829-A2 | PROTECTED ACTIVE METAL ELECTRODE AND BATTERY CELL STRUCTURES WITH NON-AQUEOUS INTERLAYER ARCHITECTURE | POLYPLUS BATTERY COMPANY (US) | 2005-09-09 | — | — | WO | claimed |
| US-20050175894-A1 | Prevents the active metal from deleterious reaction with the environment on the other (cathode) side of the impervious layer, which may include aqueous or non-aqueous liquid electrolytes (catholytes) and/or a variety electrochemically active materials, including liquid, solid and gaseous oxidizers | POLYPLUS BATTERY COMPANY | 2005-08-11 | — | — | US | claimed |
| WO-2005026089-A2 | METHOD FOR PRODUCING HALOALKANES FROM ALCOHOLS | BASF AKTIENGESELLSCHAFT (DE) | 2005-03-24 | — | — | WO | claimed |
| US-20040191617-A1 | Chemical resistance; anodes, cathodes; protective membrane coating | POLYPLUS BATTERY COMPANY | 2004-09-30 | — | — | US | claimed |