SCHEMBL29131267

SCHEMBL29131267

CCOP(=O)(C[S@@+]([O-])Cc1ccccc1)OCC

nearest known ligand 0.41

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
NPSR1 Q6W5P4 2/20 0.41
KCNH2 Q12809 1/20 0.40
POLB P06746 1/20 0.38
ACHE P22303 1/20 0.38
MAPT P10636 1/20 0.38
MAPK1 P28482 1/20 0.38
NR1I2 O75469 1/20 0.37
L3MBTL1 Q9Y468 1/20 0.37
TSHR P16473 2/20 0.36
AOX1 Q06278 1/20 0.36
MEN1 O00255 1/20 0.35
KMT2A Q03164 1/20 0.35

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
SCHEMBL11553770 1.00 NPSR1 (0.41) NPSR1KCNH2POLBACHEMAPT
SCHEMBL1330697 0.77 NPSR1 (0.43) NPSR1KCNH2POLBACHEMAPT
SCHEMBL17050984 0.77 NPSR1 (0.43) NPSR1KCNH2POLBACHEMAPT
SCHEMBL11662478 0.74 ANPEP (0.43) TSHR
SCHEMBL366215 0.73 NPY5R (0.50) NPSR1KCNH2POLBACHEMAPT
Hydrogen Peroxide SCHEMBL8609887 0.72 NPY5R (0.49) NPSR1KCNH2POLBACHEMAPT
SCHEMBL914767 0.72 NPY5R (0.49) NPSR1KCNH2POLBACHEMAPT
SCHEMBL916329 0.72 NPY5R (0.49) NPSR1KCNH2POLBACHEMAPT
SCHEMBL9000152 0.71 TSHR (0.32) TSHR
SCHEMBL777260 0.70 TP53 (0.46) MAPTTSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117303992-A Preparation method of polyfunctional group substituted chiral sulfoxide compound 厦门大学 2023-12-29 CN claimed