SCHEMBL803816

SCHEMBL803816

C/C=C(/C)CO

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
SCHEMBL10666 1.00
SCHEMBL196185 1.00
Phosphoric Acid SCHEMBL443105 0.84 BTN3A1 (0.50)
SCHEMBL9578998 0.78 TSHR (0.33)
SCHEMBL25227766 0.74
SCHEMBL28186956 0.73
SCHEMBL4623680 0.73 KMT2A (0.50)
SCHEMBL15655770 0.73 KMT2A (0.50)
SCHEMBL4671195 0.73 KMT2A (0.50)
SCHEMBL1301055 0.72

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3601205-B1 PROCESS FOR THE PREPARATION OF ALPHA, BETA UNSATURATED ALDEHYDES BY OXIDATION OF ALCOHOLS IN THE PRESENCE OF A LIQUID PHASE BASF SE (DE) 2025-12-24 EP disclosed
CN-117603025-A Process for preparing alpha, beta unsaturated aldehydes by oxidizing alcohols in the presence of a liquid phase 巴斯夫欧洲公司 2024-02-27 CN disclosed
CN-110418779-B Process for preparing alpha, beta unsaturated aldehydes by oxidizing alcohols in the presence of a liquid phase 巴斯夫欧洲公司 2023-12-15 CN disclosed
US-20230165839-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE ELIXIR MEDICAL CORPORATION (US) 2023-06-01 US disclosed
US-20230165839-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE ELIXIR MEDICAL CORPORATION (US) 2023-06-01 US disclosed
US-11332426-B2 Method of preparing trisubstituted ethylene compounds TRUSTEES OF BOSTON COLLEGE (US) 2022-05-17 US disclosed
US-11111197-B2 Process for the preparation of alpha, beta unsaturated aldehydes by oxidation of alcohols in the presence of a liquid phase BASF SE (DE) 2021-09-07 US disclosed
US-20210008040-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE ELIXIR MEDICAL CORPORATION (US) 2021-01-14 US disclosed
US-10875821-B2 Process for the preparation of alpha, beta unsaturated aldehydes by oxidation of alcohols in the presence of a liquid phase BASF SE 2020-12-29 US disclosed
US-20200392060-A1 PROCESS FOR THE PREPARATION OF ALPHA, BETA UNSATURATED ALDEHYDES BY OXIDATION OF ALCOHOLS IN THE PRESENCE OF A LIQUID PHASE BASF SE (DE) 2020-12-17 US disclosed
US-9149470-B2 Macrocyclic lactone compounds and methods for their use ELIXIR MEDICAL CORPORATION (US) 2015-10-06 US disclosed
US-8263644-B2 Cytotoxic xanthone compounds BRISTOL-MYERS SQUIBB COMPANY (US) 2012-09-11 US disclosed
US-20120071500-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE ELIXIR MEDICAL CORPORATION (US) 2012-03-22 US disclosed
US-20120071500-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE ELIXIR MEDICAL CORPORATION (US) 2012-03-22 US disclosed
US-8088789-B2 Administering hemiketal ring and seco-macrocyclic lactones; immunosuppressive, anti-proliferative, anti-fungal and anti-tumor ELIXIR MEDICAL CORPORATION (US) 2012-01-03 US disclosed
US-8088789-B2 Administering hemiketal ring and seco-macrocyclic lactones; immunosuppressive, anti-proliferative, anti-fungal and anti-tumor ELIXIR MEDICAL CORPORATION (US) 2012-01-03 US disclosed
US-20100311826-A1 CYTOTOXIC XANTHONE COMPOUNDS BRISTOL-MYERS SQUIBB COMPANY 2010-12-09 US disclosed
US-20080234309-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE ELIXIR MEDICAL CORPORATION (US) 2008-09-25 US disclosed
US-20080234309-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE ELIXIR MEDICAL CORPORATION (US) 2008-09-25 US disclosed
EP-1546134-B1 PIPERAZINE SUBSTITUTED ARYL BENZODIAZEPINES LILLY CO ELI (US) 2007-05-02 EP disclosed