SCHEMBL39918

SCHEMBL39918

CC(=O)N[C@@H]1CCNC1

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
SCHEMBL39851 1.00 — —
SCHEMBL39850 1.00 — —
Hydrochloric Acid SCHEMBL22655490 0.98 EPHX1 (0.48) —
Hydrochloric Acid SCHEMBL28300547 0.98 EPHX1 (0.48) —
Hydrochloric Acid SCHEMBL1898155 0.98 EPHX1 (0.48) —
Hydrochloric Acid SCHEMBL30998361 0.98 EPHX1 (0.48) —
Hydrochloric Acid SCHEMBL3948434 0.98 EPHX1 (0.48) —
SCHEMBL1321300 0.88 MAPK1 (0.50) —
SCHEMBL1006531 0.88 MAPK1 (0.50) —
SCHEMBL11949315 0.88 MAPK1 (0.50) —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-2007509075-A — — 2007-04-12 — — JP claimed
EP-1678167-A1 SUBSTITUTED CYCLIC HYDROXAMATES AS INHIBITORS OF MATRIX METALLOPROTEINASES Incyte Corporation (US) 2006-07-12 — — EP claimed
WO-2005037826-A1 SUBSTITUTED CYCLIC HYDROXAMATES AS INHIBITORS OF MATRIX METALLOPROTEINASES INCYTE CORPORATION (US) 2005-04-28 — — WO claimed
US-20260115194-A1 NEW TREATMENTS FOR PAIN SEVENLESS THERAPEUTICS LTD (GB) 2026-04-30 — — US disclosed
WO-2025091127-A1 HETEROCYCLIC COMPOUNDS, COMPOSITIONS COMPRISING THEM AND USES THEREOF UNIVERSITE DE MONTREAL (CA) 2025-05-08 — — WO disclosed
US-20250136598-A1 SUBSTITUTED PYRAZOLO-PYRIDINE AMIDES AND THEIR USE AS GLUN2B RECEPTOR MODULATORS JANSSEN PHARMACEUTICA NV (BE) 2025-05-01 — — US disclosed
CN-113166077-B Antibacterial compounds 布莱克史密斯医药公司 2025-01-28 — — CN disclosed
WO-2025003694-A1 NEW TREATMENTS FOR PAIN SEVENLESS THERAPEUTICS LIMITED (GB) 2025-01-02 — — WO disclosed
US-12172997-B2 Substituted pyrazolo-pyridine amides and their use as GluN2B receptor modulators JANSSEN PHARMACEUTICA NV (BE) 2024-12-24 — — US disclosed
WO-2024253416-A1 PYRIMIDINE/PYRIDINE DERIVATIVES OR SALTS THEREOF AND PHARMACEUTICAL COMPOSITIONS COMPRISING THE SAME YUHAN CORPORATION (KR) 2024-12-12 — — WO disclosed
WO-2024175043-A1 PYRIDOPYRIMIDINE DERIVATIVE AND USE THEREOF 广东东阳光药业股份有限公司 2024-08-29 — — WO disclosed
EP-1339684-A1 MCH ANTAGONISTS AND THEIR USE IN THE TREATMENT OF OBESITY SCHERING CORPORATION (US) 2003-09-03 — — EP disclosed
EP-1155013-B1 HETEROCYCLIC BENZENESULPHONAMIDE COMPOUNDS AS BRADYKININE ANTAGONISTS FOURNIER IND & SANTE (FR) 2003-07-23 — — EP disclosed
WO-2003051868-A1 LACTAMS AS TACHYKININ ANTAGONISTS PFIZER LIMITED (GB) 2003-06-26 — — WO disclosed
US-20030022891-A1 MCH antagonists and their use in the treatment of obesity SCHERING CORPORATION 2003-01-30 — — US disclosed
US-6479515-B1 FOR THE TREATMENT OF PAIN AND INFLAMMATION, AND ESPECIALLY IN THE TREATMENT OF ASTHMA, CEREBRAL TRAUMATIC SHOCK AND ALLERGIC RHINITIS FOURNIER INDUSTRIE ET SANTE (FR) 2002-11-12 — — US disclosed
US-20020132807-A1 Aryl phenylheterocyclyl sulfide derivatives and their use as cell adhesion-inhibiting anti-inflammatory and immune-suppressive agents ICOS CORPORATION 2002-09-19 — — US disclosed
EP-1233013-A1 NOVEL PHENYLALANINE DERIVATIVES Ajinomoto Co., Inc. (JP) 2002-08-21 — — EP disclosed
WO-2002057233-A1 MCH ANTAGONISTS AND THEIR USE IN THE TREATMENT OF OBESITY SCHERING CORPORATION (US) 2002-07-25 — — WO disclosed
CN-1340050-A Heterocyclic benzenesulphonamide compounds as bradykinine antagonists FOURNIER IND & SANTE (FR) 2002-03-13 — — CN disclosed
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