SCHEMBL5148149

SCHEMBL5148149

CC(O)C(NS(=O)(=O)c1ccc(N)c2ccccc12)C(=O)O

nearest known ligand 0.51

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
SLC1A3 P43003 5/20 0.51
SLC1A2 P43004 5/20 0.51
SLC1A1 P43005 5/20 0.51
KDM4E B2RXH2 1/20 0.46
ALDH1A1 P00352 1/20 0.46
HPGD P15428 1/20 0.46
CASP1 P29466 1/20 0.46
CASP7 P55210 1/20 0.46
NPSR1 Q6W5P4 1/20 0.46
HSD17B10 Q99714 1/20 0.46
ADAMTS4 O75173 2/20 0.44
MMP13 P45452 5/20 0.44
MMP12 P39900 2/20 0.44
MMP2 P08253 3/20 0.43
MMP3 P08254 3/20 0.43
MMP1 P03956 2/20 0.43
MMP7 P09237 2/20 0.43
MMP9 P14780 2/20 0.43
NSD2 O96028 4/20 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
SCHEMBL5587395 0.86 SLC1A3 (0.48) SLC1A3SLC1A2SLC1A1KDM4EALDH1A1
SCHEMBL867348 0.85 ADAMTS4 (0.51) SLC1A3SLC1A2SLC1A1KDM4EALDH1A1
SCHEMBL4128594 0.80 F2 (0.52) SLC1A3SLC1A2SLC1A1KDM4EHSD17B10
SCHEMBL28739997 0.80 F2 (0.52) SLC1A3SLC1A2SLC1A1KDM4EHSD17B10
SCHEMBL10964796 0.80 F2 (0.52) SLC1A3SLC1A2SLC1A1KDM4EHSD17B10
SCHEMBL3813105 0.80 ALDH1A1 (0.54) SLC1A3SLC1A2SLC1A1KDM4EALDH1A1
SCHEMBL4128595 0.80 F2 (0.52) SLC1A3SLC1A2SLC1A1KDM4EHSD17B10
SCHEMBL9670221 0.79 NSD2 (0.45) SLC1A3SLC1A2SLC1A1ALDH1A1NSD2
SCHEMBL6266412 0.77 PKLR (0.50) SLC1A3SLC1A2SLC1A1MMP2MMP9
SCHEMBL5149287 0.77 MMP9 (0.44) ADAMTS4MMP13MMP12MMP2MMP9

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 7 patents. 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-113388128-B Imidazole dimethylamide bridged bis-beta-cyclodextrin stationary phase and preparation method and application thereof 南昌大学 2022-05-20 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
CN-113388128-A Imidazole dimethylamide bridged bis-beta-cyclodextrin stationary phase and preparation method and application thereof 南昌大学 2021-09-14 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
WO-2005056609-A1 CATIONIC OLIGOMER OF A SACCHARIDE FOR RESOLVING ENANTIOMERS AND ASYMMETRIC SYNTHESIS NATIONAL UNIVERSITY OF SINGAPORE (SG) 2005-06-23 WO disclosed