SCHEMBL28068111

SCHEMBL28068111

Cc1ccc(C2=NS(=O)(=O)c3ccccc32)cc1

nearest known ligand 0.56

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
GAA P10253 4/20 0.56
HTT P42858 2/20 0.56
MEN1 O00255 2/20 0.48
KMT2A Q03164 2/20 0.48
HSD17B10 Q99714 2/20 0.48
POLB P06746 1/20 0.47
LMNA P02545 2/20 0.45
PKM P14618 1/20 0.45
ALDH1A1 P00352 3/20 0.45
SMN1; SMN2 Q16637 2/20 0.43
HPGD P15428 1/20 0.43
NPSR1 Q6W5P4 1/20 0.43
KCNA3 P22001 1/20 0.42
TSHR P16473 1/20 0.42

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
SCHEMBL7638951 0.85 ALDH1A1 (0.51) GAAHTTHSD17B10LMNAPKM
SCHEMBL28297388 0.83 ALDH1A1 (0.42) GAAHTTHSD17B10POLBLMNA
SCHEMBL7638472 0.82 GAA (0.48) GAAHTTMEN1KMT2AHSD17B10
SCHEMBL7633990 0.79 LMNA (0.55) GAAHTTMEN1KMT2AHSD17B10
SCHEMBL652970 0.74 PKM (0.53) GAAHTTMEN1KMT2AHSD17B10
SCHEMBL31154056 0.73 ALDH1A1 (0.46) HTTMEN1KMT2AHSD17B10LMNA
SCHEMBL7640758 0.72 MAOB (0.43) MEN1KMT2APKMALDH1A1SMN1; SMN2
SCHEMBL7642811 0.72 MAOB (0.43) GAAHSD17B10POLBPKMALDH1A1
SCHEMBL7634824 0.72 EPAS1 (0.56) GAAMEN1KMT2APOLBPKM
SCHEMBL2207008 0.71 GAA (0.44) GAAHTTMEN1KMT2AHSD17B10

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
CN-106866574-B A kind of method of reduction amination synthesis of chiral sulfanilamide (SN) in palladium chtalyst asymmetric molecult 中国科学院大连化学物理研究所 2019-06-04 CN disclosed
CN-105693653-A Method for synthesizing chiral amine through palladium catalyzed asymmetric hydrogenolysis of racemic oxazirine 中国科学院大连化学物理研究所 2016-06-22 CN disclosed