SCHEMBL6306808

SCHEMBL6306808

OCC(c1ccc(C(F)(F)F)cc1)N(Cc1cccc(OC(F)(F)C(F)F)c1)c1cccc(OCc2cccc(OC(F)(F)F)c2)c1

nearest known ligand 0.60

Predicted protein targets (top 1)

geneUniProtsupporting neighboursconfidence
CETP P11597 19/20 0.60

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
SCHEMBL6307720 0.95 CETP (0.64) CETP
SCHEMBL6388020 0.92 CETP (0.61) CETP
SCHEMBL6312909 0.91 CETP (0.58) CETP
SCHEMBL6311997 0.90 CETP (0.49) CETP
SCHEMBL6306279 0.89 CETP (0.65) CETP
SCHEMBL7084162 0.88 CETP (0.47) CETP
SCHEMBL6304631 0.87 CETP (0.47) CETP
SCHEMBL6311951 0.87 CETP (0.59) CETP
SCHEMBL6304540 0.86 CETP (0.47) CETP
SCHEMBL6306809 0.85 CETP (0.59) CETP

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
US-6861561-B2 Substituted aromatic policyclic tertiary-heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity G. D. SEARLE & CO. (US) 2005-03-01 US claimed
US-6482862-B1 Method of using substituted N-benzyl-N-phenyl aminoalcohols for inhibiting cholesteryl ester transfer protein activity G.D. SEARLE & CO. 2002-11-19 US claimed