SCHEMBL30718969

SCHEMBL30718969

O=S(=O)(Oc1ccccc1-c1c(OCc2ccccc2)ccc2ccccc12)C(F)(F)F

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 5/20 0.50
NPC1 O15118 4/20 0.50
MAPT P10636 4/20 0.50
SMN1; SMN2 Q16637 3/20 0.50
L3MBTL1 Q9Y468 1/20 0.50
LMNA P02545 2/20 0.44
NPSR1 Q6W5P4 2/20 0.44
HPGD P15428 1/20 0.44
HTT P42858 1/20 0.44
MRGPRX4 Q96LA9 1/20 0.39
PRMT5 O14744 1/20 0.37
WDR77 Q9BQA1 1/20 0.37
BRD4 O60885 2/20 0.37
DHODH Q02127 1/20 0.37
ALDH1A1 P00352 3/20 0.37
MEN1 O00255 2/20 0.37
KMT2A Q03164 2/20 0.37
XBP1 P17861 1/20 0.37
C5AR1 P21730 1/20 0.36
GAA P10253 1/20 0.36

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
SCHEMBL30719046 0.83 KMT2A (0.54) RAB9AMAPTSMN1; SMN2LMNANPSR1
SCHEMBL6547054 0.82 NPC1 (0.45) RAB9ANPC1MAPTSMN1; SMN2L3MBTL1
SCHEMBL30718956 0.81 MAPT (0.46) MAPTL3MBTL1BRD4DHODH
SCHEMBL30719034 0.80 MAPT (0.47) RAB9AMAPTSMN1; SMN2ALDH1A1MEN1
SCHEMBL30719032 0.80 MAPT (0.47) RAB9AMAPTSMN1; SMN2ALDH1A1MEN1
SCHEMBL3811084 0.80 MAPT (0.43) RAB9AMAPTSMN1; SMN2ALDH1A1MEN1
SCHEMBL16072722 0.79 KCNA3 (0.46) MAPTSMN1; SMN2L3MBTL1LMNAHTT
SCHEMBL591400 0.79 MAPT (0.46) RAB9ANPC1MAPTSMN1; SMN2L3MBTL1
SCHEMBL635407 0.78 MAPT (0.49) RAB9ANPC1MAPTSMN1; SMN2L3MBTL1
SCHEMBL29560409 0.78 MAPT (0.49) RAB9ANPC1MAPTSMN1; SMN2L3MBTL1

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-117362141-A Method for synthesizing axial chiral biaryl compound by palladium-catalyzed asymmetric hydrogenolysis 中国科学院大连化学物理研究所 2024-01-09 CN disclosed