Gemifloxacin

Gemifloxacin

SCHEMBL1444728

CON=C1CN(c2nc3c(cc2F)c(=O)c(C(=O)O)cn3C2CC2)CC1CN

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

gyrAgyrBparCparE

The experimentally established mechanism targets of Gemifloxacin. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
DPP4 P27487 6/20 1.00
CHRM2 P08172 1/20 1.00
DRD1 P21728 1/20 1.00
LMNA P02545 2/20 0.93
KDM4E B2RXH2 1/20 0.93
ABCC4 O15439 1/20 0.93
HSD17B10 Q99714 1/20 0.93
KCNH2 Q12809 2/20 0.47
DHFR P00374 1/20 0.46
CYP2C9 P11712 1/20 0.43
ATP6V1B2 P21281 1/20 0.43
TBXA2R P21731 1/20 0.43
EDNRA P25101 1/20 0.43
TARBP2 Q15633 1/20 0.43
TOP2A P11388 1/20 0.43
TOP2B Q02880 1/20 0.43
KMT2A Q03164 1/20 0.43
EPHA2 P29317 1/20 0.42
FLT4 P35916 1/20 0.42
GSK3B P49841 1/20 0.42

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
Gemifloxacin SCHEMBL136635 1.00 DPP4 (1.00) DPP4CHRM2DRD1LMNAKDM4E
Gemifloxacin SCHEMBL29662144 1.00 DPP4 (1.00) DPP4CHRM2DRD1LMNAKDM4E
Gemifloxacin SCHEMBL13414391 1.00 DPP4 (1.00) DPP4CHRM2DRD1LMNAKDM4E
Gemifloxacin SCHEMBL2419850 1.00 DPP4 (1.00) DPP4CHRM2DRD1LMNAKDM4E
Gemifloxacin SCHEMBL136634 1.00 DPP4 (1.00) DPP4CHRM2DRD1LMNAKDM4E
Gemifloxacin SCHEMBL3252334 1.00 DPP4 (1.00) DPP4CHRM2DRD1LMNAKDM4E
Gemifloxacin SCHEMBL1950144 1.00 DPP4 (1.00) DPP4CHRM2DRD1LMNAKDM4E
Gemifloxacin SCHEMBL6930951 1.00 DPP4 (1.00) DPP4CHRM2DRD1LMNAKDM4E
Gemifloxacin SCHEMBL136633 1.00 DPP4 (1.00) DPP4CHRM2DRD1LMNAKDM4E
Gemifloxacin SCHEMBL1948042 0.99 DPP4 (0.98) DPP4CHRM2DRD1LMNAKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20170253588-A1 SALT OF NAPHTHYRIDINE CARBOXYLIC ACID DERIVATIVE LG LIFE SCIENCES, LTD. (KR) 2017-09-07 US claimed
US-20160264569-A1 SALT OF NAPHTHYRIDINE CARBOXYLIC ACID DERIVATIVE LG LIFE SCIENCES, LTD. (KR) 2016-09-15 US claimed
US-20160045490-A1 USE OF CHEMOTHERAPEUTIC AGENTS BAYER INNOVATION GMBH (DE) 2016-02-18 US claimed
US-20150291585-A1 SALT OF NAPHTHYRIDINE CARBOXYLIC ACID DERIVATIVE LG Life Sciences, Ltd (KR) 2015-10-15 US claimed
US-20140287028-A1 Use of Chemotherapeutic Agents BAYER INNOVATION GMBH (DE) 2014-09-25 US claimed
US-20130065917-A1 SALT OF NAPHTHYRIDINE CARBOXYLIC ACID DERIVATIVE LG CHEMICAL LTD. 2013-03-14 US claimed
US-20110312987-A1 SALT OF NAPHTHYRIDINE CARBOXYLIC ACID DERIVATIVE LG CHEMICAL LTD. 2011-12-22 US claimed
US-20100240694-A1 SALT OF NAPHTHYRIDINE CARBOXYLIC ACID DERIVATIVE LG LIFE SCIENCES, LTD. 2010-09-23 US claimed
US-20090182006-A1 Treating a respiratory disorder by administering a hydrate of Gemifloxacinwith a carrier or excipient; chemical resistance; humidity; storage stability; thermodynamics; materials handling; sksin disorders; soft tissue-targeted therapy; sexual disorders; bovine mastitis; veterinary medicine LG LIFE SCIENCES, LTD. 2009-07-16 US claimed
US-20070197501-A1 Use Of Chemotherapeutic Agents BAYER INNOVATION GMBH (DE) 2007-08-23 US claimed
US-20030050321-A1 Salt of naphthyridine carboxylic acid derivative LG CHEMICAL LTD. 2003-03-13 US claimed
US-20030045544-A1 Bactericides for the oral region of animals using 3-carboxy-4-oxo quinoline or 1,8-naphthyridine derivatives or 1-cyclopropyl-3-carboyx-4-oxo quinolizine derivatives BAYER INNOVATION GMBH (DE) 2003-03-06 US claimed
US-20020032216-A1 Salt of naphthyridine carboxylic acid derivative LG CHEMICAL LTD. 2002-03-14 US claimed
EP-1179533-A2 Salt of naphthyridine carboxylic acid derivative LG CHEMICAL LIMITED (KR) 2002-02-13 EP claimed
EP-1114050-A1 PROCESS FOR THE PRODUCTION OF A NAPHTHYRIDINE CARBOXYLIC ACID DERIVATIVE ( METHANESULFONATE SESQUIHYDRATE ) SMITHKLINE BEECHAM PLC (GB) 2001-07-11 EP claimed
WO-2000017199-A1 PROCESS FOR THE PRODUCTION OF A NAPHTHYRIDINE CARBOXYLIC ACID DERIVATIVE (METHANESULFONATE SESQUIHYDRATE) SMITHKLINE BEECHAM P.L.C. (GB) 2000-03-30 WO claimed
US-5962468-A ANTIBACTERIAL ACTIVITY LG CHEMICAL LTD. (KR) 1999-10-05 US claimed
EP-0688772-B1 Quinoline carboxylic acid derivatives having 7-(4-amino-methyl-3-oxime) pyrrolidine substituents and processes for their preparation LG CHEMICAL LTD (KR) 1999-05-06 EP claimed
US-5869670-A BACTERICIDES LG CHEMICAL LTD. (KR) 1999-02-09 US claimed
US-5776944-A 7-(4-aminomethyl-3-methyloxyiminopyrroplidin-1-yl)-1-cyclopropyl-6-flu oro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid and the process for the preparation thereof LG CHEMICAL LTD. (KR) 1998-07-07 US claimed

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

For each of this compound's patents that has machine-readable text (13 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-20030045544-A1 Bactericides for the oral region of animals using 3-carboxy-4-oxo quinoline or 1,8-naphthyridine derivatives or 1-cyclopropyl-3-carboyx-4-oxo quinolizine derivatives NQO2, BROX, CYP4X1 DPP4 307/4885CHRM2 3393/4885DRD1 265/4885
US-20150291585-A1 SALT OF NAPHTHYRIDINE CARBOXYLIC ACID DERIVATIVE NANP, NRDC, ABCB11 DPP4 253/4885CHRM2 3340/4885DRD1 1350/4885
US-20090182006-A1 Treating a respiratory disorder by administering a hydrate of Gemifloxacinwith a carrier or excipient; chemical resistance; humidity; storage stability; thermodynamics; materials handling; sksin disorders; soft tissue-targeted therapy; sexual disorders; bovine mastitis; veterinary medicine FIS1, GSDMD, SUCNR1 DPP4 3045/4885CHRM2 3329/4885DRD1 1594/4885
US-20130065917-A1 SALT OF NAPHTHYRIDINE CARBOXYLIC ACID DERIVATIVE NANP, NRDC, ABCB11 DPP4 253/4885CHRM2 3340/4885DRD1 1350/4885
US-20020032216-A1 Salt of naphthyridine carboxylic acid derivative NANP, NRDC, ABCB11 DPP4 253/4885CHRM2 3340/4885DRD1 1350/4885
US-20070197501-A1 Use Of Chemotherapeutic Agents TYMP, TP53, MSH2 DPP4 2790/4885CHRM2 4725/4885DRD1 3984/4885
US-20160264569-A1 SALT OF NAPHTHYRIDINE CARBOXYLIC ACID DERIVATIVE NANP, NRDC, ABCB11 DPP4 253/4885CHRM2 3340/4885DRD1 1350/4885
US-20110312987-A1 SALT OF NAPHTHYRIDINE CARBOXYLIC ACID DERIVATIVE NANP, NRDC, ABCB11 DPP4 253/4885CHRM2 3340/4885DRD1 1350/4885
US-20100240694-A1 SALT OF NAPHTHYRIDINE CARBOXYLIC ACID DERIVATIVE NANP, NRDC, ABCB11 DPP4 253/4885CHRM2 3340/4885DRD1 1350/4885
US-20170253588-A1 SALT OF NAPHTHYRIDINE CARBOXYLIC ACID DERIVATIVE NANP, NRDC, ABCB11 DPP4 253/4885CHRM2 3340/4885DRD1 1350/4885
US-20140287028-A1 Use of Chemotherapeutic Agents TYMP, TP53, MSH2 DPP4 2790/4885CHRM2 4725/4885DRD1 3984/4885
US-20160045490-A1 USE OF CHEMOTHERAPEUTIC AGENTS TYMP, TP53, MSH2 DPP4 2790/4885CHRM2 4725/4885DRD1 3984/4885
US-20030050321-A1 Salt of naphthyridine carboxylic acid derivative NANP, NRDC, ABCB11 DPP4 253/4885CHRM2 3340/4885DRD1 1350/4885

“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.