SCHEMBL112469

SCHEMBL112469

O=C(C(Cl)Cl)C(F)(F)F

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
Water SCHEMBL6763348 0.97 LMNA (0.37)
Water SCHEMBL7929821 0.97 LMNA (0.37)
Water SCHEMBL5127632 0.97 LMNA (0.37)
Trifluoroacetic Acid SCHEMBL630048 0.91 LMNA (0.40)
SCHEMBL7211526 0.81 EPHX1 (0.31)
SCHEMBL7934605 0.78
SCHEMBL5860710 0.78
SCHEMBL6908016 0.78
SCHEMBL11635042 0.75
SCHEMBL6510412 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 697 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210332040-A1 SUBSTITUTED 4-AMINO-1H-IMIDAZO[4,5-c]QUINOLINE COMPOUNDS AND IMPROVED METHODS FOR THEIR PREPARATION INNATE TUMOR IMMUNITY INC (US) 2021-10-28 US claimed
EP-3837245-A1 SUBSTITUED 4-AMINO-1H-IMIDAZO[4,5-C]QUINOLINE COMPOUNDS AND IMPROVED METHODS FOR THEIR PREPARATION Innate Tumor Immunity, Inc. (US) 2021-06-23 EP claimed
WO-2020037094-A1 SUBSTITUED 4-AMINO-1H-IMIDAZO[4,5-C]QUINOLINE COMPOUNDS AND IMPROVED METHODS FOR THEIR PREPARATION INNATE TUMOR IMMUNITY, INC. (US) 2020-02-20 WO claimed
US-7002043-B2 Process for producing 1,1,1-trifluoroacetone CENTRAL GLASS COMPANY, LIMITED (JP) 2006-02-21 US claimed
EP-1127865-B1 Process for producing 1,1,1-Trifluoroacetone CENTRAL GLASS CO LTD (JP) 2005-11-02 EP claimed
US-20040034254-A1 Process for producing 1,1,1-trifluoroacetone CENTRAL GLASS COMPANY, LIMITED (JP) 2004-02-19 US claimed
US-6340776-B2 HYROGENOLYSIS OF HALOGENATED TRIFLUOROACETONE BY HYDROGEN GAS IN PRESENCE OF TRANSITION METAL CATALYST CENTRAL GLASS COMPANY, LIMITED (JP) 2002-01-22 US claimed
US-20010037041-A1 Process for producing 1,1,1,-trifluoroacetone CENTRAL GLASS COMPANY, LIMITED (JP) 2001-11-01 US claimed
EP-1127865-A1 Process for producing 1,1,1-Trifluoroacetone Central Glass Company, Limited (JP) 2001-08-29 EP claimed
EP-0872468-B1 Method for producing 3,3-dichloro-1,1,1-trifluoroacetone CENTRAL GLASS CO LTD (JP) 2001-07-25 EP claimed
US-6177595-B1 FLUORINATING IN A LIQUID PHASE A 1,1-DICHLORO-3-FLUORO-3,3-DICHLORO-, CHLORO/FLUORO-, OR DIFLUOROACETONE, PREFERABLY PENTACHLOROACETONE, BY HYDROGEN FLUORIDE USING A CATALYST OF TIN TETRAHALIDE; CORROSION RESISTANCE; EFFICIENCY CENTRAL GLASS COMPANY, LIMITED (JP) 2001-01-23 US claimed
US-5905174-A FLUORINATING PENTACHLOROACETONE WITH HYDROGEN FLUORIDE IN THE PRESENCE OF A CATALYST CENTRAL GLASS COMPANY, LIMITED (JP) 1999-05-18 US claimed
EP-0872468-A1 Method for producing 3,3-dichloro-1,1,1-trifluoroacetone Central Glass Company, Limited (JP) 1998-10-21 EP claimed
JP-11001451-A None JP disclosed
JP-11001451-A None JP disclosed
JP-9227440-A None JP disclosed
US-4704450-A OLIGO- AND POLYPEPTIDES SANOFI (FR) 1987-11-03 US disclosed
US-4581168-A COUPLING OF PEPTIDES, THEN HYDROLYSIS SANOFI (FR) 1986-04-08 US disclosed
US-4426324-A Immunopotentiating peptides HOFFMANN-LA ROCHE INC. (US) 1984-01-17 US disclosed
US-4247543-A OLIGOPEPTIDES; ANALGESICS; NERVOUS SYSTEM DISORDERS SANDOZ LTD. (CH) 1981-01-27 US disclosed