SCHEMBL1145475

SCHEMBL1145475

CCCCOCC=O

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
SCHEMBL4246104 0.97
SCHEMBL8409214 0.97
SCHEMBL662064 0.97
SCHEMBL7889522 0.97
SCHEMBL7889517 0.97
SCHEMBL7890505 0.97
SCHEMBL9747732 0.97
SCHEMBL7882638 0.97
SCHEMBL10336190 0.97
SCHEMBL7889511 0.97

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6093832-A NEAR INFRARED RAY ABSORBING MATERIAL OR A LIGHT-HEAT CONVERSION MATERIAL YAMAMOTO CHEMICALS, INC. (JP) 2000-07-25 US claimed
US-4986885-A DISTILLATION OF AZEOTROPE WITH WATER, SEPARATION OF ORGANIC LAYER AND DISTILLATION THEREOF AT PROGRESSIVELY LOWER PRESSURES HOECHST AKTIENGESELLSCHAFT (DE) 1991-01-22 US claimed
EP-0335290-A2 Process for the separation of butanol and butoxyacetaldehyde HOECHST AKTIENGESELLSCHAFT (DE) 1989-10-04 EP claimed
US-4822854-A OXALIC ACID OR SALTS FOR COLORFASTNESS AND DEODORIZING THE DRACKETT COMPANY (US) 1989-04-18 US claimed
US-4803008-A Cleaning composition containing a colorant stabilized against fading THE DRACKETT COMPANY (US) 1989-02-07 US claimed
JP-1287045-A None JP disclosed
US-20240228507-A1 GREEN SOLVENTS FOR CHEMICAL REACTIONS Ecole polytechnique fédérale de Lausanne (EPFL) (CH) 2024-07-11 US disclosed
EP-4326725-A1 GREEN SOLVENTS FOR CHEMICAL REACTIONS ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE (EPFL) (CH) 2024-02-28 EP disclosed
CN-117321060-A Green solvent for chemical reaction 洛桑联邦理工学院 2023-12-29 CN disclosed
US-11697657-B2 Small molecule inhibitors of KRAS G12C mutant MERCK SHARP & DOHME LLC (US) 2023-07-11 US disclosed
US-20230212148-A1 THERAPEUTIC COMPOUNDS FOR HIV VIRUS INFECTION GILEAD SCIENCES, INC. 2023-07-06 US disclosed
EP-4118679-A1 METAL DEPOSITION PROCESSES Fujifilm Electronic Materials U.S.A., Inc. (US) 2023-01-18 EP disclosed
US-4260622-A Animal feedstuffs employing 3,4,5-trihydroxypiperidines BAYER AKTIENGESELLSCHAFT (DE) 1981-04-07 US disclosed
EP-0000947-B1 3,4,5-TRIHYDROXYPIPERIDINE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND MEDICAMENTS AND FODDER CONTAINING THEM BAYER AG (DE) 1981-01-14 EP disclosed
EP-0002781-B1 PROCESS FOR THE PREPARATION OF ALIPHATIC CARBONYLIC COMPOUNDS SUBSTITUTED BY HYDROXYLIC GROUPS WHICH ARE ETHERIFIED BY ALIPHATIC GROUPS BASF Aktiengesellschaft (DE) 1980-11-26 EP disclosed
US-4233246-A BY OXIDATION OF HYDROXY ALIPHATIC ETHERS BASF AKTIENGESELLSCHAFT (DE) 1980-11-11 US disclosed
US-4199572-A DERIVATIVES OF SISOMICINS BAYER AKTIENGESELLSCHAFT (DE) 1980-04-22 US disclosed
EP-0008058-A1 N-Amino-3,4,5-trihydroxypiperidines, methods for their preparation, medicaments containing them, method for the production of the medicaments and animal feedstuff containing said compounds BAYER AG (DE) 1980-02-20 EP disclosed
EP-0002781-A2 Process for the preparation of aliphatic carbonylic compounds substituted by hydroxylic groups which are etherified by aliphatic groups BASF Aktiengesellschaft (DE) 1979-07-11 EP disclosed
EP-0000947-A1 3,4,5-Trihydroxypiperidine derivatives, process for their preparation and medicaments and fodder containing them BAYER AG (DE) 1979-03-07 EP disclosed