SCHEMBL5148151

SCHEMBL5148151

Nc1ccc(S(=O)(=O)NC(Cc2ccccc2)C(=O)O)c2ccccc12

nearest known ligand 0.56

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
MMP2 P08253 8/20 0.56
MMP9 P14780 6/20 0.56
ADAMTS4 O75173 1/20 0.56
ALDH1A1 P00352 1/20 0.54
MAPT P10636 1/20 0.54
HTT P42858 1/20 0.54
ADAMTS5 Q9UNA0 1/20 0.51
POLB P06746 1/20 0.51
MMP1 P03956 1/20 0.51
MMP3 P08254 1/20 0.51
MMP7 P09237 1/20 0.51
MMP13 P45452 1/20 0.51
NSD2 O96028 3/20 0.50
TYMS P04818 2/20 0.48

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
SCHEMBL4147220 1.00 MMP2 (0.56) MMP2MMP9ADAMTS4ALDH1A1MAPT
SCHEMBL27238700 1.00 MMP2 (0.56) MMP2MMP9ADAMTS4ALDH1A1MAPT
SCHEMBL6266412 0.87 PKLR (0.50) MMP2MMP9NSD2
SCHEMBL180020 0.86 NSD2 (0.45) MMP2MMP9ADAMTS4NSD2
SCHEMBL8842858 0.86 NSD2 (0.45) MMP9ADAMTS4MMP13NSD2
SCHEMBL9670221 0.86 NSD2 (0.45) ALDH1A1MAPTNSD2TYMS
SCHEMBL3813105 0.84 ALDH1A1 (0.54) MMP2MMP9ALDH1A1MMP1MMP3
SCHEMBL5706285 0.84 MMP9 (0.57) MMP2MMP9ADAMTS4MMP13NSD2
SCHEMBL5149287 0.84 MMP9 (0.44) MMP2MMP9ADAMTS4MMP13NSD2
SCHEMBL3863364 0.84 MMP9 (0.57) MMP2MMP9ADAMTS4MMP13NSD2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119174932-A Preparation method of capillary chromatographic column based on metal organic framework material and used for chiral separation 上海大学 2024-12-24 CN disclosed
CN-114504843-B Preparation method of capillary open-tube chromatographic column based on metal organic framework material 上海大学 2023-05-02 CN disclosed
CN-114504843-A Preparation method of capillary open-tube chromatographic column based on metal organic framework material 上海大学 2022-05-17 CN disclosed
EP-3313566-B1 PREPARATION OF MOLECULARLY IMPRINTED POLYMERS BY TWO-PHOTON STEREOLITHOGRAPHY CENTRE NAT RECH SCIENT (FR) 2019-06-05 EP disclosed
EP-3313566-A1 PREPARATION OF MOLECULARLY IMPRINTED POLYMERS BY TWO-PHOTON STEREOLITHOGRAPHY Centre National De La Recherche Scientifique (FR) 2018-05-02 EP disclosed
WO-2017001451-A1 PREPARATION OF MOLECULARLY IMPRINTED POLYMERS BY TWO-PHOTON STEREOLITHOGRAPHY CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2017-01-05 WO disclosed
EP-3112021-A1 PREPARATION OF MOLECULARLY IMPRINTED POLYMERS BY TWO-PHOTON STEREOLITHOGRAPHY Centre National de la Recherche Scientifique (C.N.R.S.) (FR) 2017-01-04 EP disclosed
CN-103464125-B Preparation method and application of novel triazole bridging compound cyclodextrin chiral stationary phase UNIV TIANJIN 2014-12-24 CN disclosed
CN-103464125-A Preparation method and application of novel triazole bridging compound cyclodextrin chiral stationary phase UNIV TIANJIN 2013-12-25 CN disclosed
US-20070225490-A1 Cationic Oligomer of a Saccharide for Resolving Enantiomers and Asymmetric Synthesis SELEX SENSORS AND AIRBORNE SYSTEMS LIMITED (GB) 2007-09-27 US disclosed
EP-1558368-A1 METHOD FOR PH-BIASED ISOELECTRIC TRAPPING SEPARATIONS The Texas A & M University System (US) 2005-08-03 EP disclosed
US-6923896-B2 Electrophoresis apparatus and method THE TEXAS A&M UNIVERSITY SYSTEM (US) 2005-08-02 US disclosed
WO-2005056609-A1 CATIONIC OLIGOMER OF A SACCHARIDE FOR RESOLVING ENANTIOMERS AND ASYMMETRIC SYNTHESIS NATIONAL UNIVERSITY OF SINGAPORE (SG) 2005-06-23 WO disclosed
WO-2003103811-A1 METHOD FOR PH-BIASED ISOELECTRIC TRAPPING SEPARATIONS THE TEXAS A & M UNIVERSITY SYSTEM (US) 2003-12-18 WO disclosed
US-20030226752-A1 Adjust concentration of sample; electrophoresis gradients GRADIPORE LIMITED (AU) 2003-12-11 US disclosed
CN-1460034-A Electrophoresis apparatus and method TEXAS A & M UNIV SYS (US) 2003-12-03 CN disclosed
EP-1333910-A1 ELECTROPHORESIS APPARATUS AND METHOD The Texas A & M University System (US) 2003-08-13 EP disclosed
US-20020043465-A1 Electrophoresis apparatus and method TEXAS A&M UNIVERSITY SYSTEM, THE 2002-04-18 US disclosed
WO-2002024314-A1 ELECTROPHORESIS APPARATUS AND METHOD THE TEXAS A & M UNIVERSITY SYSTEM (US) 2002-03-28 WO disclosed
US-5629424-A Stereoselective adsorptive bubble process THE CURATORS OF THE UNIVERSITY OF MISSOURI (US) 1997-05-13 US disclosed