SCHEMBL3308637

SCHEMBL3308637

CCCC(C)N1CCCCC1

nearest known ligand 0.55

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
SLC6A3 Q01959 13/20 0.37
SLC6A2 P23975 11/20 0.37
SLC6A4 P31645 8/20 0.36
CYP3A4 P08684 1/20 0.35
CYP2D6 P10635 1/20 0.35
CYP2C19 P33261 1/20 0.35
HRH3 Q9Y5N1 1/20 0.35

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
SCHEMBL27615511 1.00 SLC6A3 (0.37) SLC6A3SLC6A2SLC6A4CYP3A4CYP2D6
SCHEMBL19272636 1.00 SLC6A3 (0.37) SLC6A3SLC6A2SLC6A4CYP3A4CYP2D6
SCHEMBL20445553 1.00 SLC6A3 (0.37) SLC6A3SLC6A2SLC6A4CYP3A4CYP2D6
Hydrochloric Acid SCHEMBL11371719 0.98 SLC6A3 (0.36) SLC6A3SLC6A2SLC6A4CYP3A4CYP2D6
Iodide SCHEMBL10609626 0.98 SLC6A3 (0.36) SLC6A3SLC6A2SLC6A4CYP3A4CYP2D6
Bromide SCHEMBL10551499 0.98 SLC6A3 (0.36) SLC6A3SLC6A2SLC6A4CYP3A4CYP2D6
SCHEMBL28225794 0.97 SLC6A3 (0.38) SLC6A3SLC6A2SLC6A4
SCHEMBL302084 0.97 SLC6A3 (0.38) SLC6A3SLC6A2SLC6A4
SCHEMBL8737404 0.97 SLC6A3 (0.38) SLC6A3SLC6A2SLC6A4
Bromide SCHEMBL15941451 0.95 SLC6A3 (0.37) SLC6A3SLC6A2SLC6A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105826596-B Preparation method of ionic liquid and secondary battery 微宏动力系统(湖州)有限公司 2020-11-06 CN claimed
EP-3503268-B1 LIQUID ELECTROLYTE FORMULATION FOR LITHIUM METAL SECONDARY BATTERY AND LITHIUM METAL SECONDARY BATTERY COMPRISING THE SAME BELENOS CLEAN POWER HOLDING AG (CH) 2020-09-16 EP claimed
CN-102965082-B Working substance pair for absorptive thermal cycling system with heat source temperature ranging from 60 to 130 DEG C UNIV CHINA GEOSCIENCES WUHAN 2015-03-04 CN claimed
CN-102965082-A Working substance pair for absorptive thermal cycling system with heat source temperature ranging from 60 to 130 DEG C UNIV CHINA GEOSCIENCES WUHAN 2013-03-13 CN claimed
CN-101027395-A Biosynthetic gene clusters for the preparation of complex polyketides WYETH CORP (US) 2007-08-29 CN claimed
CN-1058399-A New piperidine ether and thioether as cholesteral biosynthesis inhibitor MERRELL DOW PHARMA (US) 1992-02-05 CN claimed
WO-2025079679-A1 POLYESTER FILM, METHOD FOR PRODUCING SAME, AND RESIN COMPOSITION 東洋紡株式会社 2025-04-17 WO disclosed
WO-2025079719-A1 COPOLYESTER FILM AND HEAT-SHRINKABLE POLYESTER FILM 東洋紡株式会社 2025-04-17 WO disclosed
WO-2025079681-A1 WHITE POLYESTER FILM 東洋紡株式会社 2025-04-17 WO disclosed
WO-2025079717-A1 POLYESTER FILM HAVING RESIN THIN FILM LAYER 東洋紡株式会社 2025-04-17 WO disclosed
WO-2025079674-A1 THERMOPLASTIC RESIN COMPOSITION 東洋紡株式会社 2025-04-17 WO disclosed
WO-2025079727-A1 LAMINATE HAVING POLYESTER FILM AND FUNCTIONAL LAYER 東洋紡株式会社 2025-04-17 WO disclosed
WO-2024115571-A1 POLYSILOXANE COMPOSITION MERCK PATENT GMBH (DE) 2024-06-06 WO disclosed
CN-1515259-A 4-aminosubstituted-2-substituted-1,2,3,4-tetrahydroquinoline used as CETP inhibitor �������Զ�˹�Ʒ� 2004-07-28 CN disclosed
CN-1318057-A 4-amino substituted-2-substituted-1, 2,3, 4-tetrahydroquinolines as CETP inhibitors PFIZER PROD INC (US) 2001-10-17 CN disclosed
CN-1318058-A 4-carboxyamino-2-substituted-1,2,3,4-tetrahydroquinolines as CRTP inhibitors PFIZER PROD INC (US) 2001-10-17 CN disclosed
CN-1306526-A Novel heterocyclically substituted amides with cysteine protease-inhibiting effect BASF AG (DE) 2001-08-01 CN disclosed
CN-1306505-A Substituted benzamides, their prodn. and use BASF AKTIENGESLLSESCHAFT (DE) 2001-08-01 CN disclosed
CN-1301255-A Heterocyclically substituted amides, their production and their use BASF AG (DE) 2001-06-27 CN disclosed
CN-1058399-A New piperidine ether and thioether as cholesteral biosynthesis inhibitor MERRELL DOW PHARMA (US) 1992-02-05 CN disclosed