SCHEMBL7238207

SCHEMBL7238207

O=C(Cl)c1ccccc1/N=N/c1ccc([N+](=O)[O-])cc1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 8/20 0.50
MEN1 O00255 7/20 0.50
ALDH1A1 P00352 6/20 0.50
MAPT P10636 6/20 0.50
POLB P06746 3/20 0.50
NPSR1 Q6W5P4 2/20 0.50
HTT P42858 2/20 0.50
LMNA P02545 1/20 0.50
SMN1; SMN2 Q16637 3/20 0.49
TDP1 Q9NUW8 2/20 0.49
IDE P14735 1/20 0.48
RAB9A P51151 4/20 0.47
MAPK1 P28482 4/20 0.47
NPC1 O15118 3/20 0.47
HSP90AA1 P07900 2/20 0.47
RECQL P46063 1/20 0.47
CASP3 P42574 1/20 0.46
SENP8 Q96LD8 1/20 0.46
SENP7 Q9BQF6 1/20 0.46
SENP6 Q9GZR1 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
SCHEMBL7238211 1.00 KMT2A (0.50) KMT2AMEN1ALDH1A1MAPTPOLB
SCHEMBL38666081 0.87 IDE (0.65) KMT2AMEN1ALDH1A1MAPTPOLB
SCHEMBL3626928 0.87 IDE (0.65) KMT2AMEN1ALDH1A1MAPTPOLB
SCHEMBL10385044 0.81 IDE (0.59) KMT2AMEN1ALDH1A1MAPTPOLB
SCHEMBL10385043 0.81 IDE (0.59) KMT2AMEN1ALDH1A1MAPTPOLB
SCHEMBL2266910 0.79 ALDH1A1 (0.52) KMT2AMEN1ALDH1A1MAPTPOLB
SCHEMBL2266902 0.79 ALDH1A1 (0.52) KMT2AMEN1ALDH1A1MAPTPOLB
SCHEMBL4278058 0.78 MEN1 (0.68) KMT2AMEN1ALDH1A1MAPTPOLB
SCHEMBL29238056 0.78 KMT2A (0.55) KMT2AMEN1ALDH1A1MAPTPOLB
SCHEMBL29238060 0.78 KMT2A (0.55) KMT2AMEN1ALDH1A1MAPTPOLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6559303-B1 Bridgehead atoms are bonded to one or more bridges that interconnect one or more ring systems thereby forming a large cyclic structure. Located in each bridge are two or more nitrogenous moieties that are derivatized with chemical ISIS PHARMACEUTICALS, INC. 2003-05-06 US disclosed
EP-0865439-A4 COMBINATORIAL LIBRARIES HAVING AMINODIOL MONOMER SUBUNITS ISIS PHARMACEUTICALS INC (US) 1998-11-11 EP disclosed
EP-0865439-A1 COMBINATORIAL LIBRARIES HAVING AMINODIOL MONOMER SUBUNITS ISIS PHARMACEUTICALS, INC. (US) 1998-09-23 EP disclosed
WO-1996040672-A1 COMBINATORIAL LIBRARIES HAVING AMINODIOL MONOMER SUBUNITS ISIS PHARMACEUTICALS, INC. (US) 1996-12-19 WO disclosed