SCHEMBL2225149

SCHEMBL2225149

O=C(O)[N+]1([O-])CCC1

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
SCHEMBL431934 0.94
SCHEMBL4059820 0.91
SCHEMBL4062497 0.91
SCHEMBL1238338 0.91
SCHEMBL10371841 0.77
SCHEMBL9800820 0.75
SCHEMBL6538151 0.73
SCHEMBL4728246 0.73
SCHEMBL7338845 0.68 CA2 (0.43)
SCHEMBL18170327 0.67

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0190786-B1 AZETIDINE DERIVATIVES; PROCESS FOR THEIR PREPARATION; AND THEIR USE AS INTERMEDIATES SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 1990-04-04 EP claimed
EP-3814331-A1 NOVEL LXR MODULATORS WITH BICYCLIC CORE MOIETY Phenex-FXR GmbH (DE) 2021-05-05 EP disclosed
EP-2523664-A1 COMPOUNDS AND METHODS Tempero Pharmaceuticals, Inc. (US) 2012-11-21 EP disclosed
US-8232389-B2 Method for crystallization of azetidinonecarboxylic acid KANEKA CORPORATION (JP) 2012-07-31 US disclosed
US-8232389-B2 Method for crystallization of azetidinonecarboxylic acid KANEKA CORPORATION (JP) 2012-07-31 US disclosed
CN-101479281-B Improved method for crystallization of azetidinonecarboxylic acid KANEKA CORP 2012-07-11 CN disclosed
WO-2011088192-A1 COMPOUNDS AND METHODS TEMPERO PHARMACEUTICALS, INC. (US) 2011-07-21 WO disclosed
US-20100298556-A1 Method for crystallization of azetidinonecarboxylic acid KANEKA CORPORATION (JP) 2010-11-25 US disclosed
US-20100298556-A1 Method for crystallization of azetidinonecarboxylic acid KANEKA CORPORATION (JP) 2010-11-25 US disclosed
CN-101479281-A Improved method for crystallization of azetidinonecarboxylic acid KANEGAFUCHI CHEMICAL IND (JP) 2009-07-08 CN disclosed
EP-1187809-A1 PROCESS FOR REDUCTION OF (2R)-4-OXOAZETIDINONE-2-CARBOXYLIC ACID ABBOTT LABORATORIES (US) 2002-03-20 EP disclosed
WO-2000076964-A1 PROCESS FOR REDUCTION OF (2R)-4-OXOAZETIDINONE-2-CARBOXYLIC ACID ABBOTT LABORATORIES (US) 2000-12-21 WO disclosed
US-6103911-A Process for reduction of (2R)-4-oxoazetidinone-2-carboxylic acid ABBOTT LABORATORIES (US) 2000-08-15 US disclosed
EP-0944594-A4 INHIBITORS OF THE ENZYMATIC ACTIVITY OF PSA LILLY CO ELI (US) 2000-05-03 EP disclosed
EP-0944594-A1 INHIBITORS OF THE ENZYMATIC ACTIVITY OF PSA ELI LILLY AND COMPANY (US) 1999-09-29 EP disclosed
EP-0559533-B1 Process for preparing beta-lactam derivative and synthetic intermediate thereof TANABE SEIYAKU CO (JP) 1998-07-22 EP disclosed
WO-1998025895-A1 INHIBITORS OF THE ENZYMATIC ACTIVITY OF PSA ELI LILLY AND COMPANY (US) 1998-06-18 WO disclosed
US-5589592-A Process for preparing β-lactam derivative and synthetic intermediate TANABE SEIYAKU CO., LTD. (JP) 1996-12-31 US disclosed
US-5414081-A Treating a 1-aza-3-thiabicycloalkane with base and phosphine or phosphite desulfurizing agent, and reacting the product with an active esterifying agent TANABE SEIYAKU CO., LTD. (JP) 1995-05-09 US disclosed
EP-0559533-A1 Process for preparing beta-lactam derivative and synthetic intermediate thereof TANABE SEIYAKU CO., LTD. (JP) 1993-09-08 EP disclosed