SCHEMBL13896395

SCHEMBL13896395

CCCCCCOC(=O)N[C@H]1CCCCC/C=C\[C@@H]2C[C@@]2(C(=O)NS(=O)(=O)C(C)CC)NC(=O)[C@@H]2C[C@@H](OC(=O)N3CCc4ccccc4C3)CN2C1=O

nearest known ligand 0.44

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
▸ ADRB3 P13945 1/20 0.39
▸ ADRA2B P18089 1/20 0.39
▸ ADRA2C P18825 1/20 0.39
▸ CYP3A4 P08684 2/20 0.33
▸ CTSB P07858 1/20 0.32
▸ CTSS P25774 1/20 0.30

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
SCHEMBL11975739 0.88 ADRB3 (0.45) ADRB3ADRA2BADRA2CCYP3A4CTSB
SCHEMBL13623487 0.87 ADRB3 (0.37) ADRB3ADRA2BADRA2CCYP3A4CTSB
SCHEMBL3975668 0.86 CTSB (0.37) ADRB3ADRA2BADRA2CCYP3A4CTSB
SCHEMBL8279917 0.86 CTSB (0.37) ADRB3ADRA2BADRA2CCYP3A4CTSB
SCHEMBL4245010 0.85 ADRB3 (0.41) ADRB3ADRA2BADRA2CCYP3A4CTSB
SCHEMBL8279044 0.85 ADRB3 (0.41) ADRB3ADRA2BADRA2CCYP3A4CTSB
SCHEMBL13880420 0.85 ADRB3 (0.41) ADRB3ADRA2BADRA2CCYP3A4CTSB
SCHEMBL4245015 0.85 ADRB3 (0.41) ADRB3ADRA2BADRA2CCYP3A4CTSB
SCHEMBL11975740 0.85 ADRB3 (0.45) ADRB3ADRA2BADRA2CCYP3A4CTSB
SCHEMBL8277040 0.85 CYP3A4 (0.39) ADRB3ADRA2BADRA2CCYP3A4CTSB

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-1680137-B1 Macrocyclic carboxylic acid and acylsulfonamide compound as inhibitor of HCV replication HOFFMANN LA ROCHE (CH) 2012-11-21 — — EP disclosed
Send feedback