SCHEMBL28836347

SCHEMBL28836347

N/C(=N\O)c1ccc(/C=C/c2ccc(O)c(O)c2)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM1A O60341 13/20 1.00
LCK P06239 3/20 0.59
NQO2 P16083 1/20 0.56
PTPN1 P18031 1/20 0.51
ALOX12 P18054 2/20 0.50
RGS12 O14924 1/20 0.50
TP53 P04637 1/20 0.50
CYP1A2 P05177 1/20 0.50
CYP3A4 P08684 1/20 0.50
CYP2C9 P11712 1/20 0.50
PKM P14618 1/20 0.50
ALOX15 P16050 1/20 0.50
CASP1 P29466 1/20 0.50
THPO P40225 1/20 0.50
GNAI1 P63096 1/20 0.50
HIF1A Q16665 1/20 0.50
HSD17B10 Q99714 1/20 0.50
KDM4E B2RXH2 1/20 0.50
MEN1 O00255 1/20 0.50
NPC1 O15118 1/20 0.50

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
SCHEMBL28111533 0.85 KDM1A (1.00) KDM1ALCKNQO2
SCHEMBL28111447 0.80 KDM1A (1.00) KDM1ANPC1MAPTMTOR
SCHEMBL28111935 0.80 KDM1A (1.00) KDM1A
SCHEMBL31236624 0.80 KDM1A (1.00) KDM1ANPC1MAPTMTOR
SCHEMBL4257370 0.79 KDM1A (0.66) KDM1ALCKNQO2PTPN1ALOX12
SCHEMBL4257368 0.79 KDM1A (0.66) KDM1ALCKNQO2PTPN1ALOX12
SCHEMBL18717464 0.79 KDM1A (0.65) KDM1AKDM4EPOLBMAPTHDAC6
SCHEMBL4167957 0.79 KDM1A (0.65) KDM1AKDM4EPOLBMAPTHDAC6
SCHEMBL12433083 0.79 KDM1A (0.65) KDM1AKDM4EPOLBMAPTHDAC6
SCHEMBL10335571 0.79 LCK (0.94) KDM1ALCKNQO2PTPN1ALOX12

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
CN-106045881-A Resveratrol derivative, preparation method thereof and application of resveratrol derivative serving as LSD1 inhibitor 新乡医学院 2016-10-26 CN disclosed