SCHEMBL8418957

SCHEMBL8418957

CCCCCCCC[C@@H](CC)CO

nearest known ligand 0.81

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 0.81
ALDH1A1 P00352 4/20 0.81
CYP2D6 P10635 2/20 0.48
CYP3A4 P08684 2/20 0.48
SPHK1 Q9NYA1 1/20 0.48
GMNN O75496 1/20 0.48
POLB P06746 1/20 0.48
THPO P40225 1/20 0.48
MTOR P42345 1/20 0.48
BLM P54132 1/20 0.48
KDM4E B2RXH2 1/20 0.48
TP53 P04637 1/20 0.48
CYP1A2 P05177 1/20 0.48
MAPT P10636 1/20 0.48
CETP P11597 1/20 0.48
HTT P42858 1/20 0.48
UBE2N P61088 1/20 0.48
TDP1 Q9NUW8 1/20 0.46
TSHR P16473 2/20 0.44
HSD17B10 Q99714 1/20 0.43

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
SCHEMBL11782392 1.00 LMNA (0.81) LMNAALDH1A1CYP2D6CYP3A4SPHK1
SCHEMBL29904 1.00 LMNA (0.81) LMNAALDH1A1CYP2D6CYP3A4SPHK1
SCHEMBL4264099 1.00 LMNA (0.81) LMNAALDH1A1CYP2D6CYP3A4SPHK1
SCHEMBL4174962 1.00 LMNA (0.81) LMNAALDH1A1CYP2D6CYP3A4SPHK1
SCHEMBL13389943 1.00 LMNA (0.81) LMNAALDH1A1CYP2D6CYP3A4SPHK1
SCHEMBL812360 1.00 LMNA (0.81) LMNAALDH1A1CYP2D6CYP3A4SPHK1
SCHEMBL21551897 1.00 LMNA (0.81) LMNAALDH1A1CYP2D6CYP3A4SPHK1
SCHEMBL20679010 1.00 LMNA (0.81) LMNAALDH1A1CYP2D6CYP3A4SPHK1
SCHEMBL20678914 1.00 LMNA (0.81) LMNAALDH1A1CYP2D6CYP3A4SPHK1
SCHEMBL503146 1.00 LMNA (0.81) LMNAALDH1A1CYP2D6CYP3A4SPHK1

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-6002037-A INTERMEDIATES OF CHIRAL ORGANIC COMPOUNDS, E.G., ISOALKYL ALCOHOLS, IN HIGHLY ENANTIOMERIC EXCESS FOR PREPARING VITAMINS, DRUGS AND BIOMOLECULES; METALLOCENE CATALYSTS PURDUE RESEARCH FOUNDATION (US) 1999-12-14 US disclosed