SCHEMBL246714

SCHEMBL246714

CCCCNC(=O)C(c1ccccc1)N1CCc2cc(OC)c(OC)cc2C1Cc1ccc(OC)c(OC)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
HCRTR1 O43613 14/20 1.00
HCRTR2 O43614 13/20 1.00
MTNR1B P49286 6/20 0.55
MTNR1A P48039 1/20 0.52

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
SCHEMBL196582 1.00 HCRTR1 (1.00) HCRTR1HCRTR2MTNR1BMTNR1A
SCHEMBL196581 1.00 HCRTR1 (1.00) HCRTR1HCRTR2MTNR1BMTNR1A
SCHEMBL5207076 0.96 HCRTR1 (0.92) HCRTR1HCRTR2MTNR1BMTNR1A
SCHEMBL5210423 0.89 HCRTR1 (0.81) HCRTR1HCRTR2MTNR1BMTNR1A
SCHEMBL5207183 0.89 HCRTR1 (0.79) HCRTR1HCRTR2MTNR1BMTNR1A
SCHEMBL5207208 0.88 HCRTR1 (0.79) HCRTR1HCRTR2MTNR1BMTNR1A
SCHEMBL5207307 0.87 HCRTR1 (0.78) HCRTR1HCRTR2MTNR1BMTNR1A
SCHEMBL198063 0.87 HCRTR1 (1.00) HCRTR1HCRTR2MTNR1BMTNR1A
SCHEMBL30593432 0.87 HCRTR1 (1.00) HCRTR1HCRTR2MTNR1BMTNR1A
SCHEMBL198064 0.87 HCRTR1 (1.00) HCRTR1HCRTR2MTNR1BMTNR1A

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
EP-2402322-A1 1,2,3,4-tetrahydroisoquinoline derivative and its use as orexin receptor antagonist Actelion Pharmaceuticals Ltd. (CH) 2012-01-04 EP disclosed