Predicted protein targets (top 14)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | LMNA | P02545 | 3/20 | 0.63 |
| ▸ | MEN1 | O00255 | 1/20 | 0.63 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.63 |
| ▸ | KDM4E | B2RXH2 | 3/20 | 0.62 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.62 |
| ▸ | HPGD | P15428 | 1/20 | 0.62 |
| ▸ | HSD17B10 | Q99714 | 1/20 | 0.62 |
| ▸ | RORC | P51449 | 4/20 | 0.49 |
| ▸ | KCNH2 | Q12809 | 2/20 | 0.48 |
| ▸ | PIM1 | P11309 | 3/20 | 0.47 |
| ▸ | CAPN1 | P07384 | 1/20 | 0.46 |
| ▸ | POLB | P06746 | 1/20 | 0.43 |
| ▸ | HSP90AA1 | P07900 | 1/20 | 0.43 |
| ▸ | RXFP1 | Q9HBX9 | 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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL31683747 | 1.00 | LMNA (0.63) | LMNAMEN1KMT2AKDM4EALDH1A1 | |
| SCHEMBL6214246 | 0.95 | LMNA (0.60) | LMNAMEN1KMT2AKDM4EALDH1A1 | |
| SCHEMBL9443566 | 0.93 | LMNA (0.54) | LMNAMEN1KMT2AKDM4EALDH1A1 | |
| SCHEMBL9443520 | 0.91 | CAPN1 (0.56) | LMNAMEN1KMT2AKDM4EALDH1A1 | |
| SCHEMBL9126186 | 0.91 | LMNA (0.53) | LMNAMEN1KMT2AKDM4EALDH1A1 | |
| SCHEMBL9443626 | 0.90 | LMNA (0.55) | LMNAMEN1KMT2AKDM4EALDH1A1 | |
| SCHEMBL5868709 | 0.90 | LMNA (0.68) | LMNAMEN1KMT2AKDM4EALDH1A1 | |
| SCHEMBL10475589 | 0.89 | LMNA (0.51) | LMNAMEN1KMT2AKDM4EALDH1A1 | |
| SCHEMBL9443476 | 0.88 | CAPN1 (0.55) | LMNAMEN1KMT2AKDM4EALDH1A1 | |
| SCHEMBL9443486 | 0.87 | LMNA (0.53) | LMNAMEN1KMT2AKDM4EALDH1A1 |
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 51 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-1063747-C | Quinolone- and naphthyridonecarboxylic acid derivatives | BAYER AG (DE) | 2001-03-28 | — | — | CN | disclosed |
| EP-0704443-B1 | Quinolone and naphthyridone carboxylic acid derivatives | BAYER AG (DE) | 2000-12-27 | — | — | EP | disclosed |
| US-6018054-A | INTERMEDIATE COMPOUNDS FOR PREPARING NOVEL QUINOLONE AND NAPHTHYRIDONE DERIVATIVES WHICH ARE SUBSTITUTED IN THE 7-POSITION BY A PARTIALLY HYDROGENATED ISOINDOLINYL RING, USE AS ANTIBACTERIAL AGENTS AND AS FEED ADDITIVES | BAYER AKTIENGESELLSCHAFT (DE) | 2000-01-25 | — | — | US | disclosed |
| EP-0705828-B1 | Quinolone- and naphthyridone carboxylic acid derivatives as antibacterial agents | BAYER AG (DE) | 1999-12-01 | — | — | EP | disclosed |
| US-5990122-A | SUBSTITUTED IN THE 7-POSITION BY A TRICYCLIC AMINE RADICAL; REDUCED GENOTOXIC PROPERTIES AND INCREASED ANTIBACTERIAL ACTIVITY | BAYER AKTIENGESELLSCHAFT (DE) | 1999-11-23 | — | — | US | disclosed |
| US-5986105-A | ENANTIOMORPHS AS BACTERICIDES | BAYER AKTIENGESELLSCHAFT (DE) | 1999-11-16 | — | — | US | disclosed |
| CN-1044118-C | 7-isoindolinyl-quinolone derivatives and process for their preparation | BAYER AG (DE) | 1999-07-14 | — | — | CN | disclosed |
| CN-1189494-A | Substituted isoazalene compound | BAYER AG (DE) | 1998-08-05 | — | — | CN | disclosed |
| US-5783708-A | HEXAHYDROISOINDOLE DERIVATIVES | BAYER AKTIENGESELLSCHAFT (DE) | 1998-07-21 | — | — | US | disclosed |
| US-5753669-A | BACTERICIDES | BAYER AKTIENGESELLSCHAFT (DE) | 1998-05-19 | — | — | US | disclosed |
| US-4994599-A | Antibacterial agents | ABBOTT LABORATORIES (US) | 1991-02-19 | — | — | US | disclosed |
| US-4940794-A | INTERMEDIATES FOR PREPARING ANTIBACTERIAL QUINOLINE-3-CARBOXYLIC ACIDS | CHINOIN GYOGYSZER ES VEGYESZETI TERMEKEK GYARA/RT. (HU) | 1990-07-10 | — | — | US | disclosed |
| US-4940710-A | 7-(substituted)piperazinyl-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acids | AMERICAN CYANAMID COMPANY (US) | 1990-07-10 | — | — | US | disclosed |
| EP-0310647-A1 | QUINOLINE CARBOXYLIC ACID BORIC ACID ANHYDRIDES AND PROCESS FOR THE PREPARATION THEREOF. | CHINOIN GYOGYSZER ES VEGYESZET (HU) | 1989-04-12 | — | — | EP | disclosed |
| EP-0131839-B1 | QUINOLINE ANTIBACTERIAL COMPOUNDS | ABBOTT LABORATORIES (US) | 1989-02-01 | — | — | EP | disclosed |
| CN-88101941-A | Process for preparing quinoline carboxylic acid boric anhydride | — | 1988-10-26 | — | — | CN | disclosed |
| WO-1988007998-A1 | QUINOLINE CARBOXYLIC ACID BORIC ACID ANHYDRIDES AND PROCESS FOR THE PREPARATION THEREOF | Chinoin Gyógyszer és Vegyészeti Termékek Gyára Rt. (HU) | 1988-10-20 | — | — | WO | disclosed |
| US-4730000-A | 7-SUBSTITUTED AMINO-6-FLUORO-1,4-DIHYDRO-4-OXOQUINOLINE-3-CARBOXYLIC ACIDS AND ESTERS | ABBOTT LABORATORIES (US) | 1988-03-08 | — | — | US | disclosed |
| EP-0230053-A2 | 7-(Substituted)piperazinyl-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acids | AMERICAN CYANAMID COMPANY (US) | 1987-07-29 | — | — | EP | disclosed |
| EP-0131839-A1 | Quinoline antibacterial compounds | ABBOTT LABORATORIES (US) | 1985-01-23 | — | — | EP | disclosed |