SCHEMBL571886

SCHEMBL571886

CCCN(CCC)c1ccncc1

nearest known ligand 0.53

Predicted protein targets (top 5)

geneUniProtsupporting neighboursconfidence
SLC6A2 P23975 10/20 0.49
CHRM5 P08912 1/20 0.48
CHKA P35790 1/20 0.48
NR1H2 P55055 1/20 0.39
NR1H3 Q13133 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.

Compoundsimilaritytop predictedshared targets
SCHEMBL21078065 0.92 NR1H2 (0.48) SLC6A2CHRM5CHKANR1H2NR1H3
SCHEMBL8021770 0.91 SLC6A2 (0.46) SLC6A2CHRM5CHKANR1H2NR1H3
SCHEMBL20751838 0.87 SLC6A2 (0.41) SLC6A2CHRM5CHKA
SCHEMBL811561 0.86 NR1H2 (0.50) SLC6A2CHRM5CHKANR1H2NR1H3
SCHEMBL18029423 0.85 SLC6A2 (0.40) SLC6A2CHRM5CHKA
SCHEMBL8590762 0.85 NR1H2 (0.46) SLC6A2CHRM5CHKANR1H2NR1H3
Hydrochloric Acid SCHEMBL10636513 0.85 NR1H2 (0.49) SLC6A2CHRM5CHKANR1H2NR1H3
SCHEMBL25385537 0.83 NR1H2 (0.44) SLC6A2CHRM5CHKANR1H2NR1H3
SCHEMBL8011634 0.83 NR1H2 (0.44) SLC6A2CHRM5CHKANR1H2NR1H3
SCHEMBL18590690 0.83 NR1H2 (0.44) SLC6A2CHRM5CHKANR1H2NR1H3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119944058-A Lithium ion battery electrolyte and lithium ion battery 西安金沙江电池有限公司 2025-05-06 CN claimed
CN-113857473-A Copper nanowire material and preparation method and application thereof 南方电网电力科技股份有限公司 2021-12-31 CN claimed
US-5162522-A Method for producing cephem compounds TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1992-11-10 US claimed
US-4402843-A Viscosity index improvers with dispersant properties prepared by reaction of lithiated hydrogenated copolymers with 4-substituted aminopyridines PHILLIPS PETROLEUM COMPANY (US) 1983-09-06 US claimed
US-4192820-A Preparation of 3-methyl-2-buten-1-al BASF AKTIENGESELLSCHAFT (DE) 1980-03-11 US claimed
US-4192949-A FROM CORRESPONDING PHENOLS BY ETHERIFICATION WITH DIALKYL CARBONATE IN TERTIARY AMINE OR PHOSPHINE BASF AKTIENGESELLSCHAFT (DE) 1980-03-11 US claimed
CN-119944058-A Lithium ion battery electrolyte and lithium ion battery 西安金沙江电池有限公司 2025-05-06 CN disclosed
CN-119529236-A Epoxy resin composition, epoxy resin composition containing reinforcing fibers, prepreg, thermoplastic resin, and fiber-reinforced plastic 日铁化学材料株式会社 2025-02-28 CN disclosed
CN-117069652-B Double-onium salt catalyst and application thereof in polyether sulfone synthesis 富海(东营)新材料科技有限公司 2024-01-12 CN disclosed
CN-117069652-A Double-onium salt catalyst and application thereof in polyether sulfone synthesis 富海(东营)新材料科技有限公司 2023-11-17 CN disclosed
WO-2023167049-A1 EPOXY RESIN COMPOSITION, REINFORCING FIBER-CONTAINING EPOXY RESIN COMPOSITION, PREPREG, FIBER REINFORCED PLASTIC EMPLOYING SAME, AND THERMOPLASTIC EPOXY RESIN 日鉄ケミカル&マテリアル株式会社 2023-09-07 WO disclosed
CN-113857473-A Copper nanowire material and preparation method and application thereof 南方电网电力科技股份有限公司 2021-12-31 CN disclosed
CN-113857473-A Copper nanowire material and preparation method and application thereof 南方电网电力科技股份有限公司 2021-12-31 CN disclosed
EP-0007439-A1 Sulphamic acid halides and method for their preparation BASF Aktiengesellschaft (DE) 1980-02-06 EP disclosed
EP-0006990-A1 N,N-bis-halogenomethyl-carbamic acid esters and process for their preparation BASF Aktiengesellschaft (DE) 1980-01-23 EP disclosed
EP-0006463-A1 Process for the production of 2-substituted 1-alkyl-nitroimidazoles BASF Aktiengesellschaft (DE) 1980-01-09 EP disclosed
US-4165342-A BY OXIDATIVE DEHYDROGENATION OF THE ALCOHOL, LAYERS OF SILVER AND COPPER CATALYST CRYSTALS BASF AKTIENGESELLSCHAFT (DE) 1979-08-21 US disclosed
EP-0002807-A1 Process for the preparation of alpha-hydroxy-beta,beta-dimethyl-gamma-butyrolactone BASF Aktiengesellschaft (DE) 1979-07-11 EP disclosed
EP-0000162-A1 Method for preparing aralkyl and alkyl phenol ethers BASF Aktiengesellschaft (DE) 1979-01-10 EP disclosed
US-4131620-A ETHERIFICATION OF N-(2-HALOALKYL)-SULFAMIC ACID HALIDES BASF AKTIENGESELLSCHAFT (DE) 1978-12-26 US disclosed