SCHEMBL7640784

SCHEMBL7640784

Cc1ccc(S(=O)(=O)C[C@H]2OC(OCc3ccccc3)[C@@H](O)[C@@H](O)[C@@H]2O)cc1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.46
LGALS9 O00182 1/20 0.43
MAPT P10636 2/20 0.43
SLC5A2 P31639 2/20 0.42
MCHR1 Q99705 1/20 0.40
KMT2A Q03164 1/20 0.39
CA1 P00915 5/20 0.39
CA2 P00918 5/20 0.39
CA9 Q16790 5/20 0.39
FGF1 P05230 2/20 0.39
FGF2 P09038 2/20 0.39
VEGFA P15692 2/20 0.39
HPSE Q9Y251 2/20 0.39
SYNJ2 O15056 2/20 0.38
KDM4E B2RXH2 1/20 0.38
ABL1 P00519 1/20 0.38
ALPL P05186 1/20 0.38
POLB P06746 1/20 0.38
ALPI P09923 1/20 0.38
GAA P10253 1/20 0.38

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
SCHEMBL7640793 1.00 LMNA (0.46) LMNALGALS9MAPTSLC5A2MCHR1
SCHEMBL14890384 0.84 FGF1 (0.44) LMNALGALS9SLC5A2CA1CA2
SCHEMBL15504371 0.81 SLC5A2 (0.47) MAPTSLC5A2SYNJ2KDM4EABL1
SCHEMBL14903579 0.81 SLC5A2 (0.47) MAPTSLC5A2SYNJ2KDM4EABL1
SCHEMBL14903581 0.81 SLC5A2 (0.47) MAPTSLC5A2SYNJ2KDM4EABL1
SCHEMBL8347457 0.81 CA1 (0.39) LGALS9SLC5A2CA1CA2CA9
SCHEMBL8347450 0.81 CA1 (0.39) LGALS9SLC5A2CA1CA2CA9
SCHEMBL29193080 0.75 SLC5A2 (0.61) SLC5A2POLB
SCHEMBL2621543 0.75 SLC5A2 (0.61) SLC5A2POLB
SCHEMBL26071211 0.75 SYNJ2 (0.51) MAPTSLC5A2SYNJ2KDM4EABL1

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 2 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6462193-B1 ADDING 3-AZIDO-2-HYDROXYPROPANALDEHYDE WITH DIHYDROXYACETONE PHOSPHATE USING AN ALDOLASE, HYDROLYZING THE INTERMEDIATE WITH ACID PHOSPHATASE, ISOMERIZING USING AN ISOMERASE, CYCLIZING USING REDUCTIVE AMINATION TO PRODUCE TETRAHYDROXYAZEPINE THE SCRIPPS RESEARCH INSTITUTE 2002-10-08 US disclosed
WO-1998037218-A1 HYDROXYAZEPANES AS INHIBITORS OF GLYCOSIDASE AND HIV PROTEASE THE SCRIPPS RESEARCH INSTITUTE (US) 1998-08-27 WO disclosed