SCHEMBL5664504

SCHEMBL5664504

C=C(C)C=NO

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
SCHEMBL10425988 1.00
SCHEMBL5664500 1.00
SCHEMBL26646659 0.71
SCHEMBL8179076 0.71
SCHEMBL15382249 0.71
SCHEMBL15835931 0.71
SCHEMBL7296060 0.69
SCHEMBL7296055 0.69
SCHEMBL8011418 0.69
SCHEMBL10465705 0.69

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1527165-A4 A RHODOCOCCUS GENE ENCODING ALDOXIME DEHYDRATASE DU PONT (US) 2006-06-07 EP claimed
EP-1527165-A2 A RHODOCOCCUS GENE ENCODING ALDOXIME DEHYDRATASE E.I. du Pont de Nemours and Company (US) 2005-05-04 EP claimed
WO-2003078581-A2 A RHODOCOCCUS GENE ENCODING ALDOXIME DEHYDRATASE E.I. DU PONT DE NEMOURS AND COMPANY (US) 2003-09-25 WO claimed
US-20260114475-A1 ANIMAL FOOD COMPOSITIONS WITH IMPROVED PALATABILITY AND CUSTOMIZABILITY, AND METHODS FOR PREPARING THE SAME MARS, INCORPORATED (US) 2026-04-30 US disclosed
EP-4593631-A1 ANIMAL FOOD COMPOSITIONS WITH IMPROVED PALATABILITY AND CUSTOMIZABILITY, AND METHODS FOR PREPARING THE SAME Mars, Incorporated (US) 2025-08-06 EP disclosed
WO-2024073025-A1 ANIMAL FOOD COMPOSITIONS WITH IMPROVED PALATABILITY AND CUSTOMIZABILITY, AND METHODS FOR PREPARING THE SAME MARS, INCORPORATED (US) 2024-04-04 WO disclosed
EP-4344552-A1 ANIMAL FOOD COMPOSITIONS WITH IMPROVED PALATABILITY, AND METHODS FOR PREPARING THE SAME MARS, INCORPORATED (US) 2024-04-03 EP disclosed
CN-109384714-A The recovery method and production method of substituted or unsubstituted 2,3- pyridinedicarboxylic acid 北京颖泰嘉和生物科技股份有限公司 2019-02-26 CN disclosed
US-9783523-B2 N-acylimino heterocyclic compounds BASF SE (DE) 2017-10-10 US disclosed
US-20160297793-A1 N-ACYLIMINO HETEROCYCLIC COMPOUNDS BASF SE (DE) 2016-10-13 US disclosed
EP-1527165-A4 A RHODOCOCCUS GENE ENCODING ALDOXIME DEHYDRATASE DU PONT (US) 2006-06-07 EP disclosed
US-5227491-A Process for the preparation of dialkyl 2,3-pyridinedicarboxylate and derivatives thereof from an α,β-unsaturated oxime and an aminobutenedioate AMERICAN CYANAMID COMPANY (US) 1993-07-13 US disclosed
US-4921839-A Erythromycin a 11,12-carbonate 9-oxime derivatives BEECHAM GROUP P.L.C. (GB) 1990-05-01 US disclosed
EP-0284203-A2 Erythromycin derivatives, process for their preparation and their pharmaceutical use BEECHAM GROUP PLC (GB) 1988-09-28 EP disclosed
US-4686302-A Simultaneous preparation of nitriles and acrylamide or methacrylamide BASF AKTIENGESELLSCHAFT (DE) 1987-08-11 US disclosed
US-4634558-A Preparation of α-substituted acrylamides BASF AKTIENGESELLSCHAFT (DE) 1987-01-06 US disclosed
US-4597907-A Preparation of α-substituted acrylamides BASF AKTIENGESELLSCHAFT (DE) 1986-07-01 US disclosed
EP-0087666-A1 Process for preparing methacryl amide BASF Aktiengesellschaft (DE) 1983-09-07 EP disclosed
EP-0021072-A1 Production of alpha-hydroxy oximes ALLIED CORPORATION (US) 1981-01-07 EP disclosed
US-4237069-A REACTING AN ALPHA-HALO-ALDEHYDE WITH AN HYDROXYLAMINE-GENERATING REAGENT ALLIED CHEMICAL CORPORATION (US) 1980-12-02 US disclosed