SCHEMBL970542

SCHEMBL970542

[Ga]CC(C1CCCCC1)C1CCCCC1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
EPHX1 P07099 2/20 0.55
SHBG P04278 1/20 0.42
TP53 P04637 3/20 0.41
LMNA P02545 3/20 0.41
CYP2D6 P10635 2/20 0.41
MEN1 O00255 2/20 0.41
KMT2A Q03164 2/20 0.41
ALDH1A1 P00352 2/20 0.41
CYP1A2 P05177 1/20 0.41
TSHR P16473 1/20 0.41
MLNR O43193 1/20 0.41
ABCB11 O95342 1/20 0.41
EGFR P00533 1/20 0.41
FYN P06241 1/20 0.41
CHRM2 P08172 1/20 0.41
CHRM4 P08173 1/20 0.41
HTR1A P08908 1/20 0.41
CHRM5 P08912 1/20 0.41
ADRA2A P08913 1/20 0.41
ADORA3 P0DMS8 1/20 0.41

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
SCHEMBL9821330 0.75 EPHX1 (0.60) EPHX1SHBGTP53LMNACYP2D6
SCHEMBL6518166 0.71 EPHX1 (0.55) EPHX1SHBGTP53LMNACYP2D6
SCHEMBL7318039 0.71 EPHX1 (0.55) EPHX1SHBGTP53LMNACYP2D6
SCHEMBL1323089 0.71 EPHX1 (0.55) EPHX1SHBGTP53LMNACYP2D6
SCHEMBL4358257 0.71 SHBG (0.62) EPHX1SHBGTP53LMNACYP2D6
SCHEMBL9358590 0.71 EPHX1 (0.55) EPHX1SHBGTP53LMNACYP2D6
SCHEMBL3887311 0.71 EPHX1 (0.55) EPHX1SHBGTP53LMNACYP2D6
SCHEMBL3209662 0.71 EPHX1 (0.55) EPHX1SHBGTP53LMNACYP2D6
SCHEMBL11003896 0.71 SHBG (0.62) EPHX1SHBGTP53LMNACYP2D6
SCHEMBL454466 0.71 SHBG (0.62) EPHX1SHBGTP53LMNACYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7871547-B2 reducing initial amount of soluble halide in solution of liquid organic medium, viscosity reducing agent, dihydrocarbylmagnesium compound, and the initial amount of soluble halide by mixing alkali metal with solution at mole ratio of metal to magnesium of less than 1:2.5, forming precipitated halide ALBEMARLE CORPORATION (US) 2011-01-18 US disclosed
EP-1809640-B1 HALIDE REDUCTION IN DIHYDROCARBYLMAGNESIUM MIXTURES ALBEMARLE CORP (US) 2008-07-16 EP disclosed
US-20080023856-A1 Halide Reduction in Dihydrocarbylmagnesium Mixtures ALBEMARLE CORPORATION (US) 2008-01-31 US disclosed
EP-1809640-A1 HALIDE REDUCTION DIHYDROCARBYLMAGNESIUM MIXTURES ALBEMARLE CORPORATION (US) 2007-07-25 EP disclosed
WO-2006054967-A1 HALIDE REDUCTION DIHYDROCARBYLMAGNESIUM MIXTURES ALBEMARLE CORPORATION (US) 2006-05-26 WO disclosed