SCHEMBL1724427

SCHEMBL1724427

CC(N)CNc1ccccc1

nearest known ligand 0.48

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
MAPT P10636 3/20 0.48
FNTA P49354 1/20 0.47
FNTB P49356 1/20 0.47
MAOA P21397 4/20 0.46
SLC6A2 P23975 2/20 0.46
TAAR1 Q96RJ0 2/20 0.46
SLC6A4 P31645 1/20 0.46
SLC6A3 Q01959 1/20 0.46
SIGMAR1 Q99720 1/20 0.46
CYP2A6 P11509 1/20 0.46
ADORA2A P29274 1/20 0.46
ADORA1 P30542 1/20 0.46
ALDH1A1 P00352 1/20 0.44
TDP1 Q9NUW8 1/20 0.44
HTT P42858 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.43
AOC3 Q16853 1/20 0.42
MAOB P27338 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.

Compoundsimilaritytop predictedshared targets
SCHEMBL13258280 1.00 MAPT (0.48) MAPTFNTAFNTBMAOASLC6A2
SCHEMBL13257889 1.00 MAPT (0.48) MAPTFNTAFNTBMAOASLC6A2
Hydrochloric Acid SCHEMBL6449887 0.98 MAPT (0.47) MAPTFNTAFNTBMAOASLC6A2
Hydrochloric Acid SCHEMBL12006787 0.98 MAPT (0.47) MAPTFNTAFNTBMAOASLC6A2
SCHEMBL1751240 0.88 FNTA (0.64) FNTAFNTBMAOASLC6A2TAAR1
SCHEMBL14511191 0.83 MAPT (0.46) MAPTFNTAFNTBMAOASLC6A2
SCHEMBL182877 0.81 MAPT (0.52) MAPTALDH1A1TDP1HTTSMN1; SMN2
SCHEMBL3634927 0.80 MAPT (0.39) MAPTFNTAFNTBALDH1A1HTT
SCHEMBL8898926 0.80 MAPT (0.54) MAPTFNTAFNTBMAOAALDH1A1
Iodide SCHEMBL29028129 0.79 MAPT (0.50) MAPTALDH1A1TDP1HTTSMN1; SMN2

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 41 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117777960-A Low-conductivity high-cooling-efficiency electric vehicle cooling liquid and preparation method thereof 深圳市艾德化学品科技有限公司 2024-03-29 CN claimed
CN-114507164-B Gemini surfactant, preparation method, composition and application thereof 中国石油天然气股份有限公司 2023-10-24 CN claimed
CN-116410101-A Asymmetric Gemini surfactant, preparation method and application thereof 中国石油天然气股份有限公司 2023-07-11 CN claimed
JP-8253456-A None JP disclosed
EP-4559964-A1 AMINE DERIVATIVES AS ADDITIVES IN RUBBERS BASF SE (DE) 2025-05-28 EP disclosed
CN-116410101-B Asymmetric Gemini surfactant, preparation method and application thereof 中国石油天然气股份有限公司 2025-02-28 CN disclosed
CN-117777960-A Low-conductivity high-cooling-efficiency electric vehicle cooling liquid and preparation method thereof 深圳市艾德化学品科技有限公司 2024-03-29 CN disclosed
EP-4326813-A1 POLYISOBUTENE DERIVATIVES AS AN ADDITIVE IN RUBBERS BASF SE (DE) 2024-02-28 EP disclosed
US-11866547-B2 Method for producing functionalized polyesters HENKEL AG & CO. KGAA (DE) 2024-01-09 US disclosed
EP-3551626-B1 BENZENESULFONAMIDE COMPOUNDS AND THEIR USE AS THERAPEUTIC AGENTS XENON PHARMACEUTICALS INC (CA) 2023-10-25 EP disclosed
CN-114507164-B Gemini surfactant, preparation method, composition and application thereof 中国石油天然气股份有限公司 2023-10-24 CN disclosed
WO-2006040179-A1 AMINOETHYLAROMATIC COMPOUNDS SUITABLE FOR TREATING DISORDERS THAT RESPOND TO MODULATION OF THE DOPAMINE D3 RECEPTOR ABBOTT GMBH & CO. KG (DE) 2006-04-20 WO disclosed
JP-H08253456-A 2-PERHYDROPYRIMIDINONE DERIVATIVE, HERBICIDE COMPRISING THE SAME AS ACTIVE INGREDIENT AND INTERMEDIATE FOR PRODUCING THE SAME MITSUBISHI CHEM CORP 1996-10-01 JP disclosed
US-5059391-A USE OF POLYARALKYLAMINES AS CORROSION INHIBITORS BAYER AKTIENGESELLSCHAFT (DE) 1991-10-22 US disclosed
EP-0306831-B1 USE OF POLYARALKYL AMINES AS CORROSION INHIBITORS BAYER AG (DE) 1991-07-03 EP disclosed
EP-0114374-B1 SUBSTITUTED 4-AMINOMETHYLENE CHROMANS OR CHROMENES, PROCESS FOR THEIR PREPARATION AND THEIR USE IN MEDICINES BAYER AG (DE) 1986-07-23 EP disclosed
US-4563458-A CIRCULATORY SYSTEM DISORDERS BAYER AKTIENGESELLSCHAFT (DE) 1986-01-07 US disclosed
EP-0114374-A1 Substituted 4-aminomethylene chromans or chromenes, process for their preparation and their use in medicines BAYER AG (DE) 1984-08-01 EP disclosed
US-4264494-A Chromium complex dyestuffs for natural polyamides and synthetic nylons BASF AKTIENGESELLSCHAFT (DE) 1981-04-28 US disclosed
US-4212801-A Unsymmetrical 1:2-chromium complexes containing an azo and an azomethine bond BASF AKTIENGESELLSCHAFT (DE) 1980-07-15 US disclosed