SCHEMBL7032199

SCHEMBL7032199

COc1ccc(CB(O)Cc2ccc(OC)cc2)cc1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ IDO1 P14902 4/20 0.52
▸ CA1 P00915 2/20 0.52
▸ CA2 P00918 2/20 0.52
▸ ENPP2 Q13822 1/20 0.52
▸ CA12 O43570 1/20 0.50
▸ CA7 P43166 1/20 0.50
▸ CA9 Q16790 1/20 0.50
▸ CA14 Q9ULX7 1/20 0.50
▸ CALM1 P0DP23 1/20 0.48
▸ AGXT P21549 2/20 0.48
▸ LTA4H P09960 1/20 0.48
▸ TAAR1 Q96RJ0 1/20 0.48
▸ ALDH1A1 P00352 2/20 0.47
▸ HTT P42858 1/20 0.47
▸ PKM P14618 1/20 0.47
▸ LDHA P00338 1/20 0.47
▸ APP P05067 1/20 0.47
▸ TP53 P04637 1/20 0.47
▸ CYP3A4 P08684 1/20 0.47
▸ ALOX15 P16050 1/20 0.47

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
SCHEMBL1453650 0.86 IDO1 (0.52) IDO1CA1CA2ENPP2CA12
SCHEMBL28200387 0.83 IDO1 (0.48) IDO1CA1CA2ENPP2CA12
SCHEMBL3898145 0.81 IDO1 (0.56) IDO1CA1CA2CA12CA7
SCHEMBL28046123 0.79 IDO1 (0.45) IDO1CA1CA2ENPP2CA12
1,4-Dimethoxybenzene SCHEMBL27700725 0.77 CA1 (0.85) CA1CA2ENPP2CA12CA7
Methyl Alcohol SCHEMBL28311094 0.76 IDO1 (0.56) IDO1CA1CA2CA12CA7
Methyl Alcohol SCHEMBL28823289 0.74 IDO1 (0.61) IDO1CA1CA2CA12CA7
Methyl Alcohol SCHEMBL28283803 0.74 MAOB (0.68) IDO1CA1CA2CA12CA7
SCHEMBL28891213 0.74 TAAR1 (0.55) IDO1CA1CA2CALM1TAAR1
SCHEMBL6273725 0.74 IDO1 (0.55) IDO1CA1CA2ENPP2CA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6600066-B1 Process for preparing perhalogenated monoorganoboranes or diorganoboranes which makes it possible to obtain these compounds under conditions which can readily be implemented in the industry is described. BASELL POLYOLEFINE GMBH (DE) 2003-07-29 — — US claimed
EP-1140947-B1 METHOD FOR PRODUCING MONO-ORGANOBORANES OR DI-ORGANOBORANES BASELL POLYOLEFINE GMBH (DE) 2003-03-12 — — EP claimed
US-6600066-B1 Process for preparing perhalogenated monoorganoboranes or diorganoboranes which makes it possible to obtain these compounds under conditions which can readily be implemented in the industry is described. BASELL POLYOLEFINE GMBH (DE) 2003-07-29 — — US disclosed
EP-1140947-B1 METHOD FOR PRODUCING MONO-ORGANOBORANES OR DI-ORGANOBORANES BASELL POLYOLEFINE GMBH (DE) 2003-03-12 — — EP disclosed
US-6417302-B1 REACTION PRODUCT OF DI(PENTAFLUOROPHENYL) BORINIC ACID AND ORGANOALUMINUM COMPOUND; OLEFIN POLYMERIZATION COORDINATION CATALYSTS BASELL POLYOLEFINE GMBH (DE) 2002-07-09 — — US disclosed
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