SCHEMBL4649825

SCHEMBL4649825

C1CCCC2CCCC2=NCC1

nearest known ligand 0.39

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
NISCH Q9Y2I1 1/20 0.39
NOS3 P29474 7/20 0.36
NOS1 P29475 7/20 0.36
NOS2 P35228 7/20 0.36
MEN1 O00255 1/20 0.32
KMT2A Q03164 1/20 0.32
HSD17B10 Q99714 1/20 0.32
ADRA2A P08913 1/20 0.31
ADRA2B P18089 1/20 0.31
ADRA2C P18825 1/20 0.31
ADRA1A P35348 1/20 0.31
HRH2 P25021 1/20 0.31
HRH3 Q9Y5N1 1/20 0.31
CRBN Q96SW2 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
SCHEMBL4649152 0.95 NOS3 (0.41) NISCHNOS3NOS1NOS2MEN1
SCHEMBL22477358 0.95 NOS3 (0.41) NISCHNOS3NOS1NOS2MEN1
SCHEMBL5011983 0.95 NOS3 (0.41) NISCHNOS3NOS1NOS2MEN1
SCHEMBL15743712 0.95 NOS3 (0.41) NISCHNOS3NOS1NOS2MEN1
SCHEMBL4611302 0.95 NOS3 (0.41) NISCHNOS3NOS1NOS2MEN1
SCHEMBL14993410 0.95 NOS3 (0.41) NISCHNOS3NOS1NOS2MEN1
SCHEMBL15665415 0.93 NISCH (0.40) NISCHNOS3NOS1NOS2HSD17B10
SCHEMBL6498120 0.93 NOS1 (0.39) NISCHNOS3NOS1NOS2MEN1
SCHEMBL15526124 0.91 NISCH (0.39) NISCHNOS3NOS1NOS2MEN1
SCHEMBL14993640 0.91 NISCH (0.39) NISCHNOS3NOS1NOS2MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2785726-A2 ESTER-FUNCTIONAL SILANES AND THE PREPARATION AND USE THEREOF; AND USE OF IMINIUM COMPOUNDS AS PHASE TRANSFER CATALYSTS Dow Corning Corporation (US) 2014-10-08 EP disclosed
WO-2013081820-A2 ESTER-FUNCTIONAL SILANES AND THE PREPARATION AND USE THEREOF;AND USE OF IMINIUM COMPOUNDS AS PHASE TRANSFER CATALYSTS DOW CORNING CORPORATION (US) 2013-06-06 WO disclosed
EP-1963388-A1 POLYURETHANE ELASTOMERS COMPRISING ALLOPHANATE MODIFIED ISOCYANATES Bayer MaterialScience LLC (US) 2008-09-03 EP disclosed
EP-1963390-A1 RIM ELASTOMERS BASED ON ISOCYANURATES OF ISOPHORONE DIISOCYANATE AND PREPOLYMERS THEREOF Bayer MaterialScience LLC (US) 2008-09-03 EP disclosed
WO-2007075329-A1 RIM ELASTOMERS BASED ON ISOCYANURATES OF ISOPHORONE DIISOCYANATE AND PREPOLYMERS THEREOF BAYER MATERIALSCIENCE LLC (US) 2007-07-05 WO disclosed
WO-2007075330-A1 POLYURETHANE ELASTOMERS COMPRISING ALLOPHANATE MODIFIED ISOCYANATES BAYER MATERIALSCIENCE LLC (US) 2007-07-05 WO disclosed