SCHEMBL6461550

SCHEMBL6461550

CCC(C)(OC(=O)CC(=O)OC(C)(CC)C(C)=O)C(C)=O

nearest known ligand 0.46

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
GAA P10253 3/20 0.46
MGAM O43451 2/20 0.37
SI P14410 2/20 0.37
MGAM2 Q2M2H8 2/20 0.37

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
SCHEMBL19036257 0.81 GAA (0.70) GAA
SCHEMBL31515323 0.77 GAA (0.43) GAAMGAMSIMGAM2
SCHEMBL13688674 0.73
SCHEMBL620517 0.73 GAA (0.42) GAAMGAMSIMGAM2
SCHEMBL9820088 0.73 GAA (0.42) GAAMGAMSIMGAM2
SCHEMBL3929481 0.73 GAA (0.42) GAAMGAMSIMGAM2
SCHEMBL15948299 0.71 MGAM (0.38) GAAMGAMSIMGAM2
SCHEMBL2967813 0.70 GAA (0.43) GAAMGAMSIMGAM2
SCHEMBL2046810 0.70 GAA (0.43) GAA
SCHEMBL6276282 0.70 GAA (0.44) GAAMGAMSIMGAM2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1578714-A1 NOVEL CHIRAL COMPOUNDS DERIVED FROM HEXANOIC ACID ESTERS, METHOD AND INTERMEDIATE CHEMICALS FOR THE PREPARATION AND USE THEREOF FOR SYNTHESIS OF 2-(BROMOMETHYL)2-ETHYL HEXANOIC CHIRAL ACID Aventis Pharma S.A. (FR) 2005-09-28 EP disclosed
WO-2004058678-A1 NOVEL CHIRAL COMPOUNDS DERIVED FROM HEXANOIC ACID ESTERS, METHOD AND INTERMEDIATE CHEMICALS FOR THE PREPARATION AND USE THEREOF FOR SYNTHESIS OF 2-(BROMOMETHYL)2-ETHYL HEXANOIC CHIRAL ACID AVENTIS PHARMA S.A (FR) 2004-07-15 WO disclosed