SCHEMBL427062

SCHEMBL427062

N[C@H]1CN2CCC1CC2

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL47241 1.00 — —
SCHEMBL17203543 1.00 — —
SCHEMBL9431600 1.00 — —
SCHEMBL260640 1.00 — —
Bromide SCHEMBL19834621 0.97 CHRNA7 (0.94) —
Hydrochloric Acid SCHEMBL348634 0.97 CHRNA7 (0.94) —
Hydrochloric Acid SCHEMBL260467 0.97 CHRNA7 (0.94) —
Hydrochloric Acid SCHEMBL2183739 0.97 CHRNA7 (0.94) —
Hydrochloric Acid SCHEMBL492194 0.97 CHRNA7 (0.94) —
Bromide SCHEMBL7114503 0.97 CHRNA7 (0.94) —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107531689-B Acid addition salts of 3-aminoquinuclidine without deliquescence 有机合成药品工业株式会社 2021-04-13 — — CN claimed
EP-3279199-B1 NON-DELIQUESCENT ACID ADDITION SALT OF 3-AMINOQUINUCLIDINE YUKI GOSEI YAKUHIN KOGYO KK (JP) 2020-06-03 — — EP claimed
US-20180118736-A1 NON-DELIQUESCENT ACID ADDITION SALT OF 3-AMINOQUINUCLIDINE YUKI GOSEI KOGYO CO. LTD. (JP) 2018-05-03 — — US claimed
EP-3279199-A1 NON-DELIQUESCENT ACID ADDITION SALT OF 3-AMINOQUINUCLIDINE YUKI GOSEI KOGYO CO., LTD. (JP) 2018-02-07 — — EP claimed
WO-2017060287-A1 PROCESS FOR THE PREPARATION OF ENCENICLINE FROM 7-CHLORO-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID CHLORIDE AND (R)-QUINUCLIDIN-3-AMINE IN THE PRESENCE OF IMIDAZOLE SANDOZ AG (CH) 2017-04-13 — — WO claimed
EP-2771340-B1 6-(4-HYDROXY-PHENYL)-1H-PYRAZOLO[3,4-B]PYRIDINE-4-CARBOXYLIC ACID AMIDE DERIVATIVES AS KINASE INHIBITORS SANOFI SA (FR) 2016-04-13 — — EP claimed
US-8178672-B2 Synthesis of imidazooxazole and imidazothiazole inhibitors of p38 MAP kinase ARQULE, INC. (US) 2012-05-15 — — US claimed
EP-2258704-A1 Synthesis of imidazooxazole and imidazothiazole inhibitors of p38 map kinase ArQule, Inc. (US) 2010-12-08 — — EP claimed
EP-1633752-B1 ISOQUINOLINE-3-CARBOXYLIC ACID AMIDES AND PHARMACEUTICAL USES THEREOF NOVARTIS AG (CH) 2010-10-06 — — EP claimed
US-20090111985-A1 Synthesis of imidazooxazole and imidazothiazole inhibitors of p38 map kinase ARQULE, INC. 2009-04-30 — — US claimed
EP-1809636-A1 SYNTHESIS OF IMIDAZOOXAZOLE AND IMIDAZOTHIAZOLE INHIBITORS OF P38 MAP KINASE ARQULE, INC. (US) 2007-07-25 — — EP claimed
WO-2006044869-A1 SYNTHESIS OF IMIDAZOOXAZOLE AND IMIDAZOTHIAZOLE INHIBITORS OF P38 MAP KINASE ARQULE, INC. (US) 2006-04-27 — — WO claimed
US-20050113574-A1 Methods and compositions comprising diamines as new anti-tubercular therapeutics SEQUELLA, INC. 2005-05-26 — — US claimed
EP-0594569-A1 PREPARATION OF S-(-)- AND R-(+)-N-(QUINUCLIDINYL-3)-AMIDE CHIRON LABORATORIES A/S (NO) 1994-05-04 — — EP claimed
US-5290938-A Preparation of S-(-)- and R-(+)-N-(quinuclidinyl-3)-amide CHIRON LABORATORIES A.S. (NO) 1994-03-01 — — US claimed
WO-1991004253-A1 PREPARATION OF S-(-)- AND R-(+)-N-(QUINUCLIDINYL-3)-AMIDE CHIRON LABORATORIES A.S (NO) 1991-04-04 — — WO claimed
EP-0311724-A1 Anxiolytic-R-N-(1-azabicyclo[2.2.2]oct-3-yl) benzamides and thiobenzamides SYNTHELABO (FR) 1989-04-19 — — EP claimed
JP-1199969-A — — None — — JP disclosed
EP-0312157-A2 Tetrapeptide renin inhibitors having a novel c-terminal amino acid MERCK & CO. INC. (US) 1989-04-19 — — EP disclosed
EP-0311724-A1 Anxiolytic-R-N-(1-azabicyclo[2.2.2]oct-3-yl) benzamides and thiobenzamides SYNTHELABO (FR) 1989-04-19 — — EP disclosed
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