SCHEMBL6217185

SCHEMBL6217185

O=C(O)Oc1cn(C2CC2)c2cc(F)c(F)cc2c1=O

nearest known ligand 0.50

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
▸ KDM4E B2RXH2 4/20 0.50
▸ ALDH1A1 P00352 4/20 0.50
▸ TOP2A P11388 4/20 0.50
▸ TOP2B Q02880 4/20 0.50
▸ LMNA P02545 3/20 0.50
▸ HPGD P15428 2/20 0.50
▸ HSD17B10 Q99714 2/20 0.50
▸ CYP1A2 P05177 1/20 0.50
▸ CYP2C9 P11712 1/20 0.50
▸ MAPT P10636 1/20 0.47
▸ PIK3CG P48736 6/20 0.41
▸ PIK3CD O00329 4/20 0.41
▸ PIK3R1 P27986 4/20 0.41
▸ PIK3CA P42336 4/20 0.41
▸ HTT P42858 1/20 0.39
▸ SMN1; SMN2 Q16637 1/20 0.39

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

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
SCHEMBL6240583 0.90 ALDH1A1 (0.47) KDM4EALDH1A1TOP2ATOP2BLMNA
SCHEMBL10875722 0.90 ALDH1A1 (0.47) KDM4EALDH1A1TOP2ATOP2BLMNA
SCHEMBL10923486 0.90 KDM4E (0.47) KDM4EALDH1A1TOP2ATOP2BLMNA
SCHEMBL8131496 0.89 KDM4E (0.40) KDM4EALDH1A1TOP2ATOP2BLMNA
SCHEMBL10591014 0.86 KDM4E (0.44) KDM4EALDH1A1TOP2ATOP2BLMNA
SCHEMBL9370629 0.86 KDM4E (0.61) KDM4EALDH1A1TOP2ATOP2BLMNA
SCHEMBL9370160 0.85 KDM4E (0.55) KDM4EALDH1A1TOP2ATOP2BLMNA
SCHEMBL6660578 0.85 KDM4E (0.36) KDM4EALDH1A1TOP2ATOP2BLMNA
SCHEMBL7501881 0.85 KDM4E (0.36) KDM4EALDH1A1TOP2ATOP2BLMNA
SCHEMBL9234576 0.85 KDM4E (0.36) KDM4EALDH1A1TOP2ATOP2BLMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3784656-B1 PROCESS FOR THE HYDROLYSIS OF QUINOLONE CARBOXYLIC ESTERS ELANCO ANIMAL HEALTH GMBH (DE) 2023-06-28 — — EP claimed
EP-1236718-B1 Improved process for the preparation of fluoro-quinolonecarboxylic acids BAYER CHEMICALS AG (DE) 2004-08-11 — — EP claimed
EP-1236718-A1 Improved process for the preparation of fluoro-quinolonecarboxylic acids BAYER AG (DE) 2002-09-04 — — EP claimed
EP-0775114-B1 PROCESS FOR MAKING ANTIMICROBIAL COMPOUNDS PROCTER & GAMBLE (US) 2000-03-22 — — EP claimed
EP-0274033-B1 PROCESS FOR THE PREPARATION OF QUINOLINECARBOXYLIC ACIDS BAYER AG (DE) 1992-03-11 — — EP claimed
EP-0274033-A1 Process for the preparation of quinolinecarboxylic acids BAYER AG (DE) 1988-07-13 — — EP claimed
EP-3784656-B1 PROCESS FOR THE HYDROLYSIS OF QUINOLONE CARBOXYLIC ESTERS ELANCO ANIMAL HEALTH GMBH (DE) 2023-06-28 — — EP disclosed
EP-0757990-B1 7-(1-Pyrrolidoinyl)-3-quinolone and naphthyridone carboxylic acid derivatives, method for their preparation and for substituted mono- and bicyclic pyrrolidine intermediates, and their antibacterial and feed additive compositions BAYER HEALTHCARE AG (DE) 2005-03-30 — — EP disclosed
EP-1236718-B1 Improved process for the preparation of fluoro-quinolonecarboxylic acids BAYER CHEMICALS AG (DE) 2004-08-11 — — EP disclosed
EP-1236718-A1 Improved process for the preparation of fluoro-quinolonecarboxylic acids BAYER AG (DE) 2002-09-04 — — EP disclosed
EP-0704443-B1 Quinolone and naphthyridone carboxylic acid derivatives BAYER AG (DE) 2000-12-27 — — EP disclosed
EP-0401623-B1 Process for the preparation of 7-(3-amino- and 3-aminomethyl-1-pyrrolidinyl)-3-quinolinonecarboxylic and -naphthyridinonecarboxylic acids BAYER AG (DE) 2000-01-26 — — EP disclosed
EP-0705828-B1 Quinolone- and naphthyridone carboxylic acid derivatives as antibacterial agents BAYER AG (DE) 1999-12-01 — — EP disclosed
EP-0224178-A1 1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7(1-piperazinyl)-3-quinoline-carboxylic acids, process for their preparation and antibacterial compositions containing them BAYER AG (DE) 1987-06-03 — — EP disclosed
EP-0203488-A2 7-Azolyl-1-cyclopropyl-1,4-dihydro-4-oxo-3-quinoline carboxylic acids and 1,8-naphthyridine carboxylic acids, process for their preparation and bactericidal agents containing them BAYER AG (DE) 1986-12-03 — — EP disclosed
EP-0113091-B1 MICROBIOCIDAL AGENTS BASED ON QUINOLONE-CARBOXYLIC ACIDS BAYER AG (DE) 1986-07-30 — — EP disclosed
EP-0169993-A2 7-(3-Aryl-1-piperazinyl) and 7-(3-cyclohexyl-1-piperazinyl) 3-quinoline carboxylic acids BAYER AG (DE) 1986-02-05 — — EP disclosed
EP-0168733-A2 Process for the preparation of quinolinone and naphthyridoncarboxylic acids BAYER AG (DE) 1986-01-22 — — EP disclosed
EP-0166939-A1 1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7(3-oxo-1-piperazinyl)-3-quinoline-carboxylic acids, process for their preparation and bactericidal agents containing them BAYER AG (DE) 1986-01-08 — — EP disclosed
EP-0113091-A1 Microbiocidal agents based on quinolone-carboxylic acids BAYER AG (DE) 1984-07-11 — — EP disclosed
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