SCHEMBL7369040

SCHEMBL7369040

O=c1c(Br)c(-c2ccccc2Br)oc2ccccc12

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NTRK1 P04629 1/20 0.53
PLK3 Q9H4B4 1/20 0.53
CYP3A4 P08684 5/20 0.50
KDM4E B2RXH2 4/20 0.50
HSD17B10 Q99714 4/20 0.50
ALDH1A1 P00352 3/20 0.50
HPGD P15428 3/20 0.50
MAOA P21397 3/20 0.50
SMN1; SMN2 Q16637 2/20 0.50
GLA P06280 1/20 0.50
MAPT P10636 1/20 0.50
PGAM1 P18669 1/20 0.50
CASP1 P29466 1/20 0.50
CASP7 P55210 1/20 0.50
NMUR2 Q9GZQ4 4/20 0.49
TRPC5 Q9UL62 1/20 0.47
KMT2A Q03164 4/20 0.46
MEN1 O00255 3/20 0.46
TSHR P16473 2/20 0.46
CYP2C9 P11712 1/20 0.46

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
SCHEMBL1423153 0.84 NMUR2 (0.54) NTRK1PLK3CYP3A4KDM4EHSD17B10
SCHEMBL1534666 0.79 KMT2A (0.65) NTRK1PLK3CYP3A4KDM4EHSD17B10
SCHEMBL29501080 0.79 KMT2A (0.65) NTRK1PLK3CYP3A4KDM4EHSD17B10
SCHEMBL10514551 0.77 NMUR2 (0.53) NTRK1PLK3CYP3A4KDM4EHSD17B10
SCHEMBL28381107 0.73 MAOA (0.51) NTRK1PLK3CYP3A4KDM4EHSD17B10
SCHEMBL6978811 0.73 PTGS1 (0.59) CYP3A4KDM4EHSD17B10ALDH1A1HPGD
SCHEMBL13978680 0.72 MAOA (0.57) CYP3A4KDM4EHSD17B10ALDH1A1HPGD
SCHEMBL21585300 0.72 MAOA (0.63) CYP3A4KDM4EHSD17B10ALDH1A1HPGD
SCHEMBL6977307 0.71 KDM4E (0.55) CYP3A4KDM4EHSD17B10ALDH1A1HPGD
SCHEMBL3267918 0.70 MAOA (0.64) CYP3A4KDM4EHSD17B10ALDH1A1HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0714296-B1 FLAVONOID AND BIFLAVONOID DERIVATIVES, THEIR PHARMACEUTICAL COMPOSITIONS, THEIR ANXIOLYTIC ACTIVITY UNIV STRATHCLYDE (GB) 2001-11-07 EP disclosed
EP-0973516-A1 USE OF HALO AND/OR NITRO-SUBSTITUTED FLAVONOIDS AS ANXYOLITICS University of Strathclyde (GB) 2000-01-26 EP disclosed
US-6004998-A FLAVONOID 6,8-DIBROMOCHRYSIN UNIVERSITY OF STRATHCLYDE (GB) 1999-12-21 US disclosed
WO-1998044920-A1 USE OF HALO AND/OR NITRO-SUBSTITUTED FLAVONOIDS AS ANXYOLITICS UNIVERSITY OF STRATHCLYDE (GB) 1998-10-15 WO disclosed
US-5756538-A REDUCING THE SEDATIVE AND RELAXANT SIDE EFFECT UNIVERSITY OF STRATHCLYDE (GB) 1998-05-26 US disclosed
EP-0714296-A1 FLAVONOID AND BIFLAVONOID DERIVATIVES, THEIR PHARMACEUTICAL COMPOSITIONS, THEIR ANXIOLYTIC ACTIVITY UNIVERSITY OF STRATHCLYDE (GB) 1996-06-05 EP disclosed
WO-1995005169-A1 FLAVONOID AND BIFLAVONOID DERIVATIVES, THEIR PHARMACEUTICAL COMPOSITIONS, THEIR ANXIOLYTIC ACTIVITY THE UNIVERSITY OF STRATHCLYDE (GB) 1995-02-23 WO disclosed