SCHEMBL8070410

SCHEMBL8070410

c1ccc2c(c1)CCCC2c1ccc(C2CCCCC2)cc1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ HAO1 Q9UJM8 1/20 0.52
▸ GID4 Q8IVV7 1/20 0.51
▸ MAPK1 P28482 1/20 0.51
▸ MAPK14 Q16539 1/20 0.51
▸ TAOK1 Q7L7X3 1/20 0.49
▸ TAOK3 Q9H2K8 1/20 0.49
▸ ADRA2A P08913 2/20 0.47
▸ ADRA1A P35348 2/20 0.47
▸ CYP2D6 P10635 2/20 0.47
▸ ADRA1D P25100 1/20 0.47
▸ ADRA1B P35368 1/20 0.47
▸ HTR1A P08908 1/20 0.47
▸ OPRM1 P35372 1/20 0.47
▸ IGF1R P08069 1/20 0.46
▸ ALOX15 P16050 1/20 0.46
▸ TAAR1 Q96RJ0 2/20 0.46
▸ MEN1 O00255 1/20 0.46
▸ ALDH1A1 P00352 1/20 0.46
▸ BLM P54132 1/20 0.46
▸ KMT2A Q03164 1/20 0.46

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
SCHEMBL29842306 0.84 GID4 (0.62) HAO1GID4MAPK1MAPK14ADRA2A
SCHEMBL395087 0.84 GID4 (0.62) HAO1GID4MAPK1MAPK14ADRA2A
SCHEMBL20863599 0.81 HAO1 (0.53) HAO1GID4MAPK1MAPK14ADRA2A
SCHEMBL20863578 0.81 HAO1 (0.53) HAO1GID4MAPK1MAPK14ADRA2A
SCHEMBL7059074 0.81 HAO1 (0.57) HAO1GID4MAPK1MAPK14TAOK1
SCHEMBL20874477 0.78 GID4 (0.56) HAO1GID4MAPK1MAPK14ADRA2A
SCHEMBL29155816 0.78 GID4 (0.52) HAO1GID4MAPK1MAPK14ADRA2A
SCHEMBL20856005 0.78 HAO1 (0.53) HAO1GID4MAPK1MAPK14ADRA2A
SCHEMBL13444088 0.78 GID4 (0.72) HAO1GID4MAPK1MAPK14ALDH1A1
SCHEMBL7324670 0.78 GID4 (0.72) HAO1GID4MAPK1MAPK14ALDH1A1

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-6025177-A ENANTIOSELECTIVE SYNTHESIS OF CHIRAL ALPHA-HYDROXYCARBOXYLATE BY REACTING A PROCHIRAL ALPHA-KETOCARBOXYLIC ACID WITH A SINGLE ENANTIOMER OF AN N-SUBSTITUTED VICINAL AMINOALCOHOL OF SPECIFIC CYCLOHYDROCARBONS TO FORM ALPHA-HYDROXYCARBOXYLATE SEPRACOR INC. (US) 2000-02-15 — — US disclosed
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