SCHEMBL6311852

SCHEMBL6311852

CC(C)c1cccc(Oc2cccc(N(Cc3ccccc3SC(F)(F)F)CC(O)C(C)C)c2)c1

nearest known ligand 0.50

Predicted protein targets (top 1)

geneUniProtsupporting neighboursconfidence
CETP P11597 20/20 0.50

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
SCHEMBL6311777 0.89 CETP (0.55) CETP
SCHEMBL7652626 0.89 CETP (0.52) CETP
SCHEMBL7648089 0.88 CETP (0.52) CETP
SCHEMBL6307087 0.87 CETP (0.47) CETP
SCHEMBL6307690 0.86 CETP (0.46) CETP
SCHEMBL6308353 0.85 CETP (0.56) CETP
SCHEMBL6307336 0.84 CETP (0.50) CETP
SCHEMBL6311849 0.83 CETP (0.66) CETP
SCHEMBL6307988 0.80 CETP (0.59) CETP
SCHEMBL6304952 0.79 CETP (0.54) 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