SCHEMBL501152

SCHEMBL501152

O=C(O)c1cn(-c2ccc(F)cc2F)c2nc(Cl)c(F)cc2c1=O

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
EPHA2 P29317 1/20 0.63
FLT4 P35916 1/20 0.63
GSK3B P49841 1/20 0.63
RARB P10826 1/20 0.63
TBXAS1 P24557 1/20 0.63
SLC6A3 Q01959 1/20 0.63
KMT2A Q03164 2/20 0.61
LMNA P02545 4/20 0.57
KDM4E B2RXH2 3/20 0.57
ALDH1A1 P00352 3/20 0.57
HPGD P15428 2/20 0.57
HSD17B10 Q99714 2/20 0.57
POLB P06746 2/20 0.57
XBP1 P17861 1/20 0.57
NFKB1 P19838 1/20 0.57
HTT P42858 1/20 0.57
NFKB2 Q00653 1/20 0.57
RELA Q04206 1/20 0.57
MEN1 O00255 1/20 0.44
HSP90AA1 P07900 1/20 0.43

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
Fluoride SCHEMBL5143071 0.98 EPHA2 (0.61) EPHA2FLT4GSK3BRARBTBXAS1
SCHEMBL5143074 0.97 EPHA2 (0.60) EPHA2FLT4GSK3BRARBTBXAS1
SCHEMBL5316747 0.88 KMT2A (0.66) EPHA2FLT4GSK3BRARBTBXAS1
SCHEMBL6211205 0.87 LMNA (0.50) EPHA2FLT4GSK3BRARBTBXAS1
SCHEMBL8195587 0.86 EPHA2 (0.48) EPHA2FLT4GSK3BRARBTBXAS1
SCHEMBL13315750 0.86 EPHA2 (0.63) EPHA2FLT4GSK3BRARBTBXAS1
SCHEMBL9149681 0.86 EPHA2 (0.57) EPHA2FLT4GSK3BRARBTBXAS1
SCHEMBL7008249 0.86 EPHA2 (0.48) EPHA2FLT4GSK3BRARBTBXAS1
SCHEMBL19971429 0.86 KEAP1 (0.48) EPHA2FLT4GSK3BRARBTBXAS1
Trovafloxacin SCHEMBL8209872 0.85 EPHA2 (0.90) EPHA2FLT4GSK3BRARBTBXAS1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6114531-A Process for preparing quinolone and naphthyridone carboxylic acids PFIZER INC. (US) 2000-09-05 US claimed
EP-0775114-B1 PROCESS FOR MAKING ANTIMICROBIAL COMPOUNDS PROCTER & GAMBLE (US) 2000-03-22 EP claimed
EP-0976749-A1 Process for preparing quinolone and naphthyridone carboxylic acids Pfizer Products Inc. (US) 2000-02-02 EP claimed
US-5703231-A Process for making antimicrobial compounds THE PROCTER & GAMBLE COMPANY (US) 1997-12-30 US claimed
WO-1996004247-A1 PROCESS FOR MAKING ANTIMICROBIAL COMPOUNDS THE PROCTER & GAMBLE COMPANY (US) 1996-02-15 WO claimed
EP-0331960-B1 Process for the preparation of enantiomerically homogeneous aminopyrrolidinyl naphthyridine and quinolone carboxylic acids ABBOTT LAB (US) 1994-05-18 EP claimed
EP-0331960-A2 Process for the preparation of enantiomerically homogeneous aminopyrrolidinyl naphthyridine and quinolone carboxylic acids ABBOTT LABORATORIES (US) 1989-09-13 EP claimed
US-4859776-A (S)-7-(3-aminopyrrolidin-1-yl)-1-(ortho, para-difluorophenyl)-1,4-dihydro-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acid and method for its preparation ABBOTT LABORATORIES (US) 1989-08-22 US claimed
CN-110551124-B Quinolone compound or agriculturally and pharmaceutically acceptable salt thereof, and preparation method and application thereof 山东省联合农药工业有限公司 2021-01-08 CN disclosed
CN-110551124-A quinolone compound or agriculturally and pharmaceutically acceptable salt thereof, and preparation method and application thereof SHANDONG UNITED PESTICIDE IND CO LTD 2019-12-10 CN disclosed
EP-1861401-B1 7-AMINO ALKYLIDENYL-HETEROCYCLIC QUINOLONES AND NAPHTHYRIDONES JANSSEN PHARMACEUTICA NV (BE) 2015-11-18 EP disclosed
US-20140073631-A1 ANTIVIRAL AND ANTIMICROBIAL COMPOUNDS VYMED CORPORATION (US) 2014-03-13 US disclosed
US-20140073631-A1 ANTIVIRAL AND ANTIMICROBIAL COMPOUNDS VYMED CORPORATION (US) 2014-03-13 US disclosed
EP-1666477-B1 7-(4-SUBSTITUTED 3- CYCLOPROPYLAMINOMETHYL-1- PYRROLIDINYL) Q UINOLONECARBOXYLIC ACID DERIVATIVE KYORIN SEIYAKU KK (JP) 2013-07-03 EP disclosed
EP-0360258-A2 Amino acid quinoline and naphthyridine derivatives ABBOTT LABORATORIES (US) 1990-03-28 EP disclosed
EP-0331960-A2 Process for the preparation of enantiomerically homogeneous aminopyrrolidinyl naphthyridine and quinolone carboxylic acids ABBOTT LABORATORIES (US) 1989-09-13 EP disclosed
US-4859776-A (S)-7-(3-aminopyrrolidin-1-yl)-1-(ortho, para-difluorophenyl)-1,4-dihydro-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acid and method for its preparation ABBOTT LABORATORIES (US) 1989-08-22 US disclosed
US-4851535-A 2-(5-FLUORONICOTINOYL)ACETIC ACID DERIVATIVES, ANTIBACTERIAL 1-ARYL-1,4-DIHYDRO-4-OXONAPHTHYRIDINES TOYAMA CHEMICAL CO., LTD. (JP) 1989-07-25 US disclosed
EP-0302372-A1 Naphthyridine antianaerobic compounds ABBOTT LABORATORIES (US) 1989-02-08 EP disclosed
US-4704459-A VILSMEIER REAGENT TOYAMA CHEMICAL CO., LTD. (JP) 1987-11-03 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20140073631-A1 ANTIVIRAL AND ANTIMICROBIAL COMPOUNDS GDA, GMPS, GANC EPHA2 4871/4885FLT4 4218/4885GSK3B 2831/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.