SCHEMBL178418

SCHEMBL178418

CN1CCC(C#N)CC1

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
SCHEMBL9631219 0.91 KDM4E (0.35)
SCHEMBL12774143 0.87 L3MBTL3 (0.37)
SCHEMBL13613023 0.84
SCHEMBL2760279 0.84
SCHEMBL2760288 0.84
Hydrochloric Acid SCHEMBL31357021 0.82
SCHEMBL24894374 0.79 POLB (0.34)
SCHEMBL17285903 0.79 ALDH1A1 (0.41)
SCHEMBL17285970 0.77 ALDH1A1 (0.40)
SCHEMBL151431 0.77 IRAK4 (0.36)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107652289-A Substituted tricyclic compound as FGFR inhibitor 因塞特控股公司 2018-02-02 CN claimed
EP-3250290-A1 COMPOSITIONS AND METHODS FOR TREATING TOXOPLASMOSIS, CRYPTOSPORIDIOSIS AND OTHER APICOMPLEXAN PROTOZOAN RELATED DISEASES University of Washington (US) 2017-12-06 EP claimed
CN-107383009-A Substituted tricyclic compound as FGFR inhibitor 因塞特控股公司 2017-11-24 CN claimed
WO-2016123152-A1 COMPOSITIONS AND METHODS FOR TREATING TOXOPLASMOSIS, CRYPTOSPORIDIOSIS AND OTHER APICOMPLEXAN PROTOZOAN RELATED DISEASES UNIVERSITY OF WASHINGTON (US) 2016-08-04 WO claimed
EP-2403853-B1 PYRROLOPYRIMIDINES USED AS KINASE INHIBITORS MEDICAL RES COUNCIL TECHNOLOGY (GB) 2013-08-14 EP claimed
US-20120088753-A1 PYRROLOPYRIMIDINES AND USED AS KINASE INHIBITORS MEDICAL RESEARCH COUNCIL TECHNOLOGY (GB) 2012-04-12 US claimed
EP-2403853-A1 PYRROLOPYRIMIDINES USED AS KINASE INHIBITORS Medical Research Council Technology (GB) 2012-01-11 EP claimed
WO-2010100431-A1 PYRROLOPYRIMIDINES USED AS KINASE INHIBITORS MEDICAL RESEARCH COUNCIL TECHNOLOGY (GB) 2010-09-10 WO claimed
US-12570625-B2 3-(5-hydroxy-1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives and uses thereof NOVARTIS AG (CH) 2026-03-10 US disclosed
EP-4568959-A1 BICYCLIC TETRAHYDROTHIAZEPINE DERIVATIVES F. Hoffmann-La Roche AG (CH) 2025-06-18 EP disclosed
WO-2025098509-A1 PYRROLIDINE DERIVATIVE, PHARMACEUTICAL COMPOSITION AND USE THEREOF IN MEDICINE 康百达(四川)生物医药科技有限公司 2025-05-15 WO disclosed
WO-2024151833-A1 SPIRO DERIVATIVES AS M4 ACTIVATORS/MODULATORS AND USES THEREOF CEREVEL THERAPEUTICS, LLC (US) 2024-07-18 WO disclosed
US-20240228493-A1 LRRK2 INHIBITORS AND USES THEREOF NEURON23, INC. 2024-07-11 US disclosed
EP-4327886-A2 PYRIMIDO- PYRIDAZINONE COMPOUNDS AND USE THEREOF Libertas Bio, Inc. (US) 2024-02-28 EP disclosed
EP-0749966-A1 5-HT 3 RECEPTOR AGONIST, NOVEL THIAZOLE DERIVATIVE, AND INTERMEDIATE THEREFOR YAMANOUCHI PHARMACEUTICAL CO. LTD. (JP) 1996-12-27 EP disclosed
EP-0213337-B1 4-CYANOPIPERIDINE DERIVATIVES, PREPARATION AND USE THEREOF Eisai Co., Ltd. (JP) 1991-05-15 EP disclosed
EP-0326526-A1 Aminoketones of substituted dibenzo- and pyridobenzo-azepinones and pharmaceutical compositions ISTITUTO DE ANGELI S.p.A. (IT) 1989-08-02 EP disclosed
EP-0269991-A1 Process for the synthesis of 4-cyanoquinuclidine or a salt thereof Eisai Chemical Co., Ltd. (JP) 1988-06-08 EP disclosed
US-4721788-A 4-cyanopiperidine derivatives EISAI CO., LTD. (JP) 1988-01-26 US disclosed
EP-0213337-A1 4-cyanopiperidine derivatives, preparation and use thereof Eisai Co., Ltd. (JP) 1987-03-11 EP disclosed