SCHEMBL9635290

SCHEMBL9635290

CCOC(=O)c1c[nH]c2c(F)c(F)c(F)cc2c1=O

nearest known ligand 0.66

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.66
CYP3A4 P08684 1/20 0.66
CYP2C19 P33261 1/20 0.66
CLEC4M Q9H2X3 1/20 0.60
KDM4E B2RXH2 3/20 0.56
GABRA1 P14867 3/20 0.54
GABRB2 P47870 3/20 0.54
GABRB1 P18505 2/20 0.53
GABRA3 P34903 2/20 0.53
MAPT P10636 2/20 0.52
KMT2A Q03164 4/20 0.51
MEN1 O00255 2/20 0.51
ALDH1A1 P00352 2/20 0.47
STAT3 P40763 1/20 0.47
TP53 P04637 1/20 0.46
HPGD P15428 1/20 0.46
HSD17B10 Q99714 1/20 0.46
L3MBTL1 Q9Y468 1/20 0.46

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
SCHEMBL29376920 1.00 CYP1A2 (0.66) CYP1A2CYP3A4CYP2C19CLEC4MKDM4E
SCHEMBL11235716 0.92 CYP1A2 (0.63) CYP1A2CYP3A4CYP2C19CLEC4MKDM4E
SCHEMBL19971590 0.91 CYP1A2 (0.62) CYP1A2CYP3A4CYP2C19CLEC4MKDM4E
SCHEMBL30540821 0.91 CYP1A2 (0.62) CYP1A2CYP3A4CYP2C19CLEC4MKDM4E
SCHEMBL10519082 0.90 CYP1A2 (0.60) CYP1A2CYP3A4CYP2C19CLEC4MKDM4E
SCHEMBL1345017 0.89 CYP1A2 (0.59) CYP1A2CYP3A4CYP2C19CLEC4MKDM4E
SCHEMBL10618700 0.89 CYP1A2 (0.59) CYP1A2CYP3A4CYP2C19CLEC4MKDM4E
SCHEMBL15999499 0.87 CYP1A2 (0.67) CYP1A2CYP3A4CYP2C19CLEC4MKDM4E
SCHEMBL10766497 0.87 CYP1A2 (0.57) CYP1A2CYP3A4CYP2C19CLEC4MKDM4E
SCHEMBL13368169 0.87 CYP1A2 (0.57) CYP1A2CYP3A4CYP2C19CLEC4MKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115403521-A Synthesis method of lomefloxacin hydrochloride intermediate 常州兰陵制药有限公司 2022-11-29 CN claimed
CN-111208221-B Method for detecting lomefloxacin hydrochloride related substances 宜宾市南溪区红光制药有限公司 2022-07-05 CN claimed
JP-2231477-A None JP disclosed
CN-115403521-A Synthesis method of lomefloxacin hydrochloride intermediate 常州兰陵制药有限公司 2022-11-29 CN disclosed
CN-115403521-A Synthesis method of lomefloxacin hydrochloride intermediate 常州兰陵制药有限公司 2022-11-29 CN disclosed
CN-111208221-B Method for detecting lomefloxacin hydrochloride related substances 宜宾市南溪区红光制药有限公司 2022-07-05 CN disclosed
CN-111208221-B Method for detecting lomefloxacin hydrochloride related substances 宜宾市南溪区红光制药有限公司 2022-07-05 CN disclosed
CN-114609260-A Method for detecting lomefloxacin hydrochloride intermediate related substances 江苏吉贝尔药业股份有限公司 2022-06-10 CN disclosed
CN-111208221-A Method for detecting lomefloxacin hydrochloride related substances 宜宾市南溪区红光制药有限公司 2020-05-29 CN disclosed
CN-111208221-A Method for detecting lomefloxacin hydrochloride related substances 宜宾市南溪区红光制药有限公司 2020-05-29 CN disclosed
US-20160030443-A1 METHODS AND COMPOSITIONS FOR MODULATING REGULATORY T CELL FUNCTION WANG RONGFU (US) 2016-02-04 US disclosed
EP-0265230-A1 Substituted-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acids, derivatives thereof, pharmaceutical compositions comprising the compounds, and processes for producing the compounds WARNER-LAMBERT COMPANY (US) 1988-04-27 EP disclosed
US-4665079-A QUINOLINE DERIVATIVES WARNER-LAMBERT COMPANY (US) 1987-05-12 US disclosed
US-4638067-A NAPHTHYRIDINE AND QUINOLINE CARBOXYLIC ACIDS WARNER-LAMBERT CO. (US) 1987-01-20 US disclosed
EP-0172651-A1 Substituted-9-fluoro-3-methyl-7-oxo-2,3-dihydro-7H-pyrido[1,2,3-de][1,4]benzoxazine-6-carboxylic acids; substituted-5-amino-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acids; substituted-5-amino-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acids; derivatives thereof; pharmaceutical compositions comprising the compounds; and processes for producing the compounds WARNER-LAMBERT COMPANY (US) 1986-02-26 EP disclosed
US-4571396-A Antibacterial agents WARNER-LAMBERT COMPANY (US) 1986-02-18 US disclosed
EP-0159174-A2 Substituted naphthyridine-, quinoline- and benzoxazine- carboxylic acids as antibacterial agents and processes for their production WARNER-LAMBERT COMPANY (US) 1985-10-23 EP disclosed
EP-0153163-A2 7-Substituted-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acids; 7-substituted-1-cyclopropyl-1,4-dihydro-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acids; their derivatives; and a process for preparing the compounds WARNER-LAMBERT COMPANY (US) 1985-08-28 EP disclosed
EP-0106489-A2 Antibacterial agents WARNER-LAMBERT COMPANY (US) 1984-04-25 EP disclosed
US-4398029-A BACTERICIDES KYORIN SEIYAKU KABUSHIKI KAISHA (JP) 1983-08-09 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-20160030443-A1 METHODS AND COMPOSITIONS FOR MODULATING REGULATORY T CELL FUNCTION IRAK4, TLR8, TLR4 CYP1A2 3095/4885CYP3A4 826/4885CYP2C19 2675/4885

“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.