SCHEMBL28111302

SCHEMBL28111302

CS(=O)(=O)n1c(-c2ccccc2)cc2ccccc21

nearest known ligand 0.56

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 2/20 0.56
CA12 O43570 2/20 0.55
CA9 Q16790 2/20 0.55
CA2 P00918 1/20 0.55
HRH3 Q9Y5N1 1/20 0.54
L3MBTL1 Q9Y468 1/20 0.51
ACLY P53396 7/20 0.50
ALDH1A1 P00352 2/20 0.49
KDM4E B2RXH2 1/20 0.49
HPGD P15428 1/20 0.49
HSD17B10 Q99714 1/20 0.49
MTNR1A P48039 1/20 0.45
MTNR1B P49286 1/20 0.45
AGTR1 P30556 1/20 0.44
PTGS2 P35354 2/20 0.44
PDE4A P27815 1/20 0.41
PDE4B Q07343 1/20 0.41
PDE4C Q08493 1/20 0.41
PDE4D Q08499 1/20 0.41

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
SCHEMBL4065720 0.87 HRH3 (0.53) KMT2ACA12CA9CA2HRH3
SCHEMBL28111780 0.84 ACLY (0.56) CA12CA9CA2HRH3ACLY
SCHEMBL3558164 0.81 CA12 (0.78) KMT2ACA12CA9CA2L3MBTL1
SCHEMBL28111778 0.79 PPARG (0.46) HRH3ACLYPTGS2
SCHEMBL28017014 0.79 CA12 (0.69) KMT2ACA12CA9CA2L3MBTL1
SCHEMBL14583988 0.78 CYP19A1 (0.56) KMT2ACA12CA9CA2HRH3
SCHEMBL4073243 0.77 HRH3 (0.52) CA12CA9CA2HRH3L3MBTL1
SCHEMBL4073241 0.76 HRH3 (0.48) KMT2ACA12CA9CA2HRH3
SCHEMBL4073246 0.76 HRH3 (0.51) KMT2ACA12CA9CA2HRH3
SCHEMBL6295031 0.76 HRH3 (0.64) KMT2AHRH3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112358432-B Synthetic method of indole derivatives 天津大学 2022-06-10 CN disclosed
CN-112358432-A Synthetic method of indole derivatives 天津大学 2021-02-12 CN disclosed
CN-106179294-A A kind of method that hydrotalcite catalyst economic benefits and social benefits catalyze and synthesize benzazolyl compounds 山东师范大学 2016-12-07 CN disclosed