SCHEMBL5860190

SCHEMBL5860190

C[C@@](O)(c1ccccc1)[C@@H](Br)C(=O)O

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 1/20 0.44
KMT2A Q03164 1/20 0.44
CYP2C19 P33261 1/20 0.42
HIF1A Q16665 1/20 0.42
HDAC3 O15379 1/20 0.41
HDAC4 P56524 1/20 0.41
HDAC1 Q13547 1/20 0.41
HDAC7 Q8WUI4 1/20 0.41
HDAC2 Q92769 1/20 0.41
HDAC10 Q969S8 1/20 0.41
HDAC11 Q96DB2 1/20 0.41
HDAC8 Q9BY41 1/20 0.41
HDAC6 Q9UBN7 1/20 0.41
HDAC9 Q9UKV0 1/20 0.41
HDAC5 Q9UQL6 1/20 0.41
KIF11 P52732 6/20 0.41
CYP1A2 P05177 2/20 0.40
CYP2D6 P10635 1/20 0.40
KCNN4 O15554 1/20 0.38
ALDH1A1 P00352 2/20 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
SCHEMBL11779390 0.82 MAPT (0.45) MAPTKMT2ACYP2C19HIF1AHDAC3
SCHEMBL17093302 0.78 MAPT (0.45) MAPTKMT2ACYP2C19HIF1AHDAC3
SCHEMBL6874329 0.78 MAPT (0.45) MAPTKMT2ACYP2C19HIF1AHDAC3
SCHEMBL20184853 0.78 CYP2D6 (0.46) MAPTKMT2ACYP2C19HIF1AHDAC3
SCHEMBL7019907 0.78 MAPT (0.45) MAPTKMT2ACYP2C19HIF1AHDAC3
SCHEMBL17582896 0.78 CYP2D6 (0.46) MAPTKMT2ACYP2C19HIF1AHDAC3
SCHEMBL20184852 0.78 CYP2D6 (0.46) MAPTKMT2ACYP2C19HIF1AHDAC3
SCHEMBL9683891 0.78 CYP2D6 (0.46) MAPTKMT2ACYP2C19HIF1AHDAC3
SCHEMBL6529290 0.77 ALDH1A1 (0.41) MAPTKMT2ACYP2C19HIF1AHDAC3
SCHEMBL5860569 0.76 MAPT (0.44) MAPTKMT2ACYP2C19HIF1AHDAC3

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
US-7060471-B2 Stereoselective chemoenzymatic process for the preparation of optically enriched phenylglycidates as precursors of taxol side chain COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2006-06-13 US disclosed