SCHEMBL863461

SCHEMBL863461

CC(C)N1CCN(C)C1

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
SCHEMBL20387008 0.95 MC4R (0.34)
SCHEMBL1116249 0.83
SCHEMBL9322170 0.83 ALDH1A1 (0.30)
SCHEMBL81580 0.81 MC4R (0.44)
SCHEMBL16316010 0.81 MC4R (0.44)
SCHEMBL22753497 0.81 MC4R (0.44)
SCHEMBL26844927 0.81 FDPS (0.30)
SCHEMBL840162 0.81 CHRNA7 (0.36)
SCHEMBL27966219 0.78
Hydrochloric Acid SCHEMBL21568420 0.78 CHRNA7 (0.35)

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
WO-2024145483-A1 COMPOUNDS FOR USE IN THE TREATMENT OF CANCER AND METHODS OF MAKING AND USING THE SAME HTG MOLECULAR DIAGNOSTICS, INC. (US) 2024-07-04 WO disclosed
WO-2024077023-A2 CEREBLON-RECRUITING BCL-XL/BCL-2 DUAL DEGRADERS UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INCORPORATED (US) 2024-04-11 WO disclosed
US-20240066029-A1 SUBSTITUTED PYRAZOLO[1,5-A]PYRIDINE COMPOUNDS AS RET KINASE INHIBITORS ARRAY BIOPHARMA INC. 2024-02-29 US disclosed
US-20230348658-A1 COPOLYMERS AND TERPOLYMERS OF POST MODIFIED POLYACRYLATES AS EFFICIENT GAS HYDRATE INHIBITORS SAUDI ARABIAN OIL COMPANY (SA) 2023-11-02 US disclosed
EP-3033066-B1 POLYUREA OR POLYURETHANE CAPSULES INT FLAVORS & FRAGRANCES INC (US) 2023-07-12 EP disclosed
WO-2023116835-A1 MULTI-PROTEIN DEGRADATION AGENT HAVING IMIDE SKELETON 苏州开拓药业股份有限公司 2023-06-29 WO disclosed
US-20230141913-A2 PHENOXY(HETERO)ARYL ETHERS OF ANTIPROLIFERACTIVE ACTIVITY Xeniopro GmbH (DE) 2023-05-11 US disclosed
US-20230141913-A2 PHENOXY(HETERO)ARYL ETHERS OF ANTIPROLIFERACTIVE ACTIVITY Xeniopro GmbH (DE) 2023-05-11 US disclosed
EP-4122499-A1 FIBROBLAST ACTIVATION PROTEIN INHIBITORS AND USE THEREOF 3B Pharmaceuticals GmbH (DE) 2023-01-25 EP disclosed
US-20220145461-A1 RARE EARTH PRECURSOR, METHOD OF PREPARING THE SAME, AND METHOD OF FORMING THIN FILM USING THE SAME HANSOL CHEMICAL CO., LTD. (KR) 2022-05-12 US disclosed
US-20110172217-A1 RING-FUSED MORPHOLINE DERIVATIVE HAVING PI3K-INHIBITING ACTIVITY SHIONOGI & CO., LTD. (JP) 2011-07-14 US disclosed
US-7893068-B2 Macrolide compounds comprising 18,19-epoxytricosa-8,12,14-trien-11-olide derivatives; angiogenesis inhibitors; anticarcinogenic, antimetastasis, antiinflammatory, and antitumor agents; antihypoxic agents; endothelial growth factor suppressors; retinal neovascularization, diabetic retinopathy MERCIAN CORPORATION (JP) 2011-02-22 US disclosed
US-7619100-B2 Physiologically active substances MERCIAN CORPORATION (JP) 2009-11-17 US disclosed
US-7576204-B2 Heterocyclic macrolide pharmaceutical agent, a method of producing the same and use of the same MERCIAN CORPORATION (JP) 2009-08-18 US disclosed
US-7550503-B2 Physiologically active substances EISAI R& D MANAGEMENT CO., LTD. (JP) 2009-06-23 US disclosed
US-20090105274-A1 Indolecarboxylic Acid Derivative Having PGD2 Receptor Antagonistic Activity SHIONOGI & CO., LTD. (JP) 2009-04-23 US disclosed
US-20080280288-A1 Assay Method to Predict Sensitivity of Cancer Cell to Anticancer Drug EISAI R&D MANAGEMENT CO., LTD. (JP) 2008-11-13 US disclosed
US-20080275059-A1 NOVEL PHYSIOLOGICALLY ACTIVE SUBSTANCES KOTAKE YOSHIHIKO 2008-11-06 US disclosed
US-20080255146-A1 NOVEL PHYSIOLOGICALLY ACTIVE SUBSTANCES MICROBIOPHARM JAPAN CO., LTD. (JP) 2008-10-16 US disclosed
US-7256178-B2 Physiologically active substances EISAI CO., LTD. (JP) 2007-08-14 US disclosed