SCHEMBL2222871

SCHEMBL2222871

CCN(C(=O)CC(CC(=O)O)c1ccccc1)c1ccccc1

nearest known ligand 0.58

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.53
GLA P06280 1/20 0.53
TSHR P16473 1/20 0.53
GABBR2 O75899 1/20 0.50
GABBR1 Q9UBS5 1/20 0.50
MAPT P10636 1/20 0.49
MEN1 O00255 4/20 0.45
KMT2A Q03164 4/20 0.45
POLB P06746 1/20 0.44
TP53 P04637 2/20 0.44
KDM4E B2RXH2 1/20 0.43
RECQL P46063 1/20 0.43
HTT P42858 1/20 0.40

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
SCHEMBL7815055 0.81 GABBR2 (0.53) ALDH1A1GABBR2GABBR1MAPTMEN1
SCHEMBL1114871 0.81 ALDH1A1 (0.56) ALDH1A1GLATSHRMAPTMEN1
Alcohol SCHEMBL28575312 0.78 GABBR2 (0.66) GABBR2GABBR1MAPTMEN1KMT2A
SCHEMBL503819 0.78 GABBR2 (0.76) TSHRGABBR2GABBR1MAPTMEN1
SCHEMBL20369046 0.76 ALDH1A1 (0.58) ALDH1A1GLATSHRMAPTMEN1
Hydrochloric Acid SCHEMBL7092228 0.76 GABBR2 (0.73) TSHRGABBR2GABBR1MAPTMEN1
SCHEMBL6734410 0.76 GABBR2 (0.73) TSHRGABBR2GABBR1MAPTMEN1
SCHEMBL308738 0.75 ALDH1A1 (0.66) ALDH1A1GLATSHRMAPTMEN1
SCHEMBL2484805 0.75 GABBR2 (0.66) TSHRGABBR2GABBR1MAPTMEN1
SCHEMBL2030599 0.75 ALDH1A1 (0.70) ALDH1A1GLATSHRMAPTMEN1

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
WO-2011086565-A1 METHOD FOR PREPARATION OF ENANTIOMERICALLY ENRICHED AND/OR RACEMIC GAMMA-AMINO ACIDS LUPIN LIMITED (IN) 2011-07-21 WO disclosed