SCHEMBL10712935

SCHEMBL10712935

CC(=O)OC(CC(=O)O)CC(=O)OO

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 0.55
SMN1; SMN2 Q16637 1/20 0.55
ALOX15 P16050 1/20 0.44
MMP12 P39900 1/20 0.43
CYP1A2 P05177 4/20 0.38
MEN1 O00255 3/20 0.38
KMT2A Q03164 3/20 0.38
HRH1 P35367 1/20 0.38
MAPK1 P28482 4/20 0.35
GMNN O75496 3/20 0.35
MAPT P10636 3/20 0.35
NPSR1 Q6W5P4 3/20 0.35
TSHR P16473 2/20 0.35
HSP90AA1 P07900 2/20 0.35
BLM P54132 2/20 0.35
NR1H4 Q96RI1 2/20 0.35
TP53 P04637 1/20 0.35
CYP2C9 P11712 1/20 0.35
HIF1A Q16665 1/20 0.35
PGD P52209 1/20 0.34

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
SCHEMBL6153718 0.87 LMNA (0.67) LMNASMN1; SMN2ALOX15MMP12CYP1A2
SCHEMBL5175797 0.81 LMNA (0.51) LMNASMN1; SMN2ALOX15MMP12CYP1A2
SCHEMBL6036839 0.81 LMNA (0.51) LMNASMN1; SMN2ALOX15MMP12CYP1A2
SCHEMBL10414980 0.77 LMNA (0.60) LMNASMN1; SMN2ALOX15MMP12CYP1A2
SCHEMBL4928056 0.75 LMNA (0.58) LMNASMN1; SMN2ALOX15MMP12CYP1A2
SCHEMBL13229795 0.75 LMNA (0.58) LMNASMN1; SMN2ALOX15MMP12CYP1A2
SCHEMBL4923275 0.75 LMNA (0.58) LMNASMN1; SMN2ALOX15MMP12CYP1A2
SCHEMBL4923280 0.75 LMNA (0.58) LMNASMN1; SMN2ALOX15MMP12CYP1A2
SCHEMBL27535340 0.73 LMNA (0.56) LMNASMN1; SMN2ALOX15MMP12CYP1A2
SCHEMBL31571128 0.73 LMNA (0.56) LMNASMN1; SMN2ALOX15MMP12CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0168480-A4 PROCESS FOR PREPARING OPTICALLY-ACTIVE 4-AMINO-3-HYDROXYBUTYRIC ACID. WISCONSIN ALUMNI RES FOUND (US) 1987-10-08 EP disclosed
US-4584270-A ENZYME CLEAVAGE OF ESTER GROUPING OF 3-HYDROXYGLUTARIC ACID DIESTER, FOLLOWED BY CHEMICAL CONVERSION WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 1986-04-22 US disclosed
EP-0168480-A1 PROCESS FOR PREPARING OPTICALLY-ACTIVE 4-AMINO-3-HYDROXYBUTYRIC ACID WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 1986-01-22 EP disclosed
WO-1985003307-A1 PROCESS FOR PREPARING OPTICALLY-ACTIVE 4-AMINO-3-HYDROXYBUTYRIC ACID WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 1985-08-01 WO disclosed