SCHEMBL4946068

SCHEMBL4946068

CC(C)=CCC#N

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
SCHEMBL4307163 0.78 KMT2A (0.60)
SCHEMBL806716 0.78 KMT2A (0.60)
SCHEMBL9814899 0.77
SCHEMBL551890 0.77
SCHEMBL28356297 0.77
SCHEMBL1105232 0.77 KMT2A (0.64)
SCHEMBL8940810 0.77 KMT2A (0.64)
SCHEMBL60485 0.75
SCHEMBL30705403 0.75
SCHEMBL15980884 0.75

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 16 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114573751-B Dispersing agent for lithium ion battery, preparation method of dispersing agent, positive electrode slurry, positive electrode plate and lithium ion battery 比亚迪股份有限公司 2023-12-12 CN claimed
WO-2023123024-A1 ELECTROCHEMICAL APPARATUS AND ELECTRONIC APPARATUS 宁德新能源科技有限公司 2023-07-06 WO disclosed
EP-0941671-B1 Taste agent from Saccharum Officinarum, process for preparing it, products containing it INT FLAVORS & FRAGRANCES INC (US) 2015-09-09 EP disclosed
EP-2487149-A1 METHOD FOR PRODUCING KETONE JX Nippon Oil & Energy Corporation (JP) 2012-08-15 EP disclosed
US-20120197036-A1 METHOD FOR MANUFACTURING KETONE OSAKA UNIVERSITY (JP) 2012-08-02 US disclosed
CN-102548942-A Method for producing ketone JX NIPPON OIL & ENERGY CORP 2012-07-04 CN disclosed
US-7319129-B2 Silsesquioxane derivative and process for producing the same CHISSO CORPORATION (JP) 2008-01-15 US disclosed
US-7053167-B2 Silsesquioxane derivative having functional group CHISSO CORPORATION (JP) 2006-05-30 US disclosed
US-20060089504-A1 Silsesquioxane derivative having functional group ITO KENYA 2006-04-27 US disclosed
US-20060052623-A1 Having two cyclotetrasiloxne rings connected by O-Si groups obtained through hydrolysis and condensation of trifunctional hydrolyzable silicon compounds; functionalization; fireproofing, thermostability, weathproofing, photostability, dielectric, hardness, strength and chemical resistance CHISSO CORPORATION (JP) 2006-03-09 US disclosed
CN-1572754-A Method for producing organic compound by substituting halogen atoms MITSUI CHEMICALS INC (JP) 2005-02-02 CN disclosed
US-20040068074-A1 Production process for silsesquioxane derivative having functional group and silsesquioxane derivative JNC CORPORATION (JP) 2004-04-08 US disclosed
EP-0241690-A2 Aliphatic diisocyanates and their use for the preparation of polyurethane polymers BAYER AG (DE) 1987-10-21 EP disclosed
US-4331562-A IN THE PRESENCE OF A PALLADIUM OR RUTHENIUM CATALYST PHILLIPS PETROLEUM COMPANY (US) 1982-05-25 US disclosed
US-4261927-A PLLADIUM OR RUTHENIUM CATALYST, METAL NITRATE PROMOTER PHILLIPS PETROLEUM COMPANY (US) 1981-04-14 US disclosed
US-4067906-A BIRCH REDUCTION, ISOMERIZATION; PERFUMES GIVAUDAN CORPORATION (US) 1978-01-10 US disclosed