SCHEMBL2998258

SCHEMBL2998258

CCOC(=O)c1cc(OCCCCCCOc2ccc(N=Nc3ccc(C)cc3)cc2)cc(C(=O)OCC)c1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 2/20 0.50
TDP1 Q9NUW8 1/20 0.50
KMT2A Q03164 2/20 0.48
MEN1 O00255 1/20 0.48
MAPT P10636 3/20 0.45
NPC1 O15118 2/20 0.45
RAB9A P51151 2/20 0.45
SMN1; SMN2 Q16637 1/20 0.45
PPARD Q03181 1/20 0.45
PPARA Q07869 1/20 0.45
PLK1 P53350 1/20 0.42
ALDH1A1 P00352 1/20 0.42
GAA P10253 1/20 0.42
KCNH2 Q12809 1/20 0.42
HRH3 Q9Y5N1 1/20 0.42
TBXAS1 P24557 1/20 0.42
HTT P42858 1/20 0.42
ESR1 P03372 1/20 0.42
THRB P10828 1/20 0.42
PLA2G2A P14555 1/20 0.42

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
SCHEMBL3971125 1.00 L3MBTL1 (0.50) L3MBTL1TDP1KMT2AMEN1MAPT
SCHEMBL13900185 0.93 L3MBTL1 (0.45) L3MBTL1TDP1KMT2AMEN1MAPT
SCHEMBL6316002 0.89 PPARD (0.47) L3MBTL1TDP1KMT2AMEN1MAPT
SCHEMBL6320506 0.89 PPARD (0.47) L3MBTL1TDP1KMT2AMEN1MAPT
SCHEMBL13900198 0.89 MAPT (0.50) L3MBTL1TDP1MAPTNPC1RAB9A
SCHEMBL6413184 0.88 TDP1 (0.58) L3MBTL1TDP1KMT2AMEN1MAPT
SCHEMBL13004362 0.86 MAPT (0.44) L3MBTL1TDP1KMT2AMEN1MAPT
SCHEMBL3973334 0.86 PLA2G2A (0.55) L3MBTL1KMT2AMEN1PPARDPPARA
SCHEMBL3973336 0.86 PLA2G2A (0.55) L3MBTL1KMT2AMEN1PPARDPPARA
SCHEMBL13004357 0.85 MAPT (0.39) L3MBTL1TDP1KMT2AMEN1MAPT

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
US-7787346-B2 Hologram recording method and device, hologram reproduction method and device, and optical recording medium FUJI XEROX CO., LTD. (JP) 2010-08-31 US disclosed
US-7501210-B2 Photo-responsive high-molecular compound, photo-responsive high-molecular composition, dicarboxylic acid monomer, polyester, optical recording medium and optical record reproducing device FUJI XEROX CO., LTD. (JP) 2009-03-10 US disclosed
US-20080151734-A1 Hologram recording method and device, hologram reproduction method and device, and optical recording medium FUJI XEROX CO., LTD. (JP) 2008-06-26 US disclosed
US-20070184234-A1 PHOTO-RESPONSIVE HIGH-MOLECULAR COMPOUND, PHOTO-RESPONSIVE HIGH-MOLECULAR COMPOSITION, DICARBOXYLIC ACID MONOMER, POLYESTER, OPTICAL RECORDING MEDIUM AND OPTICAL RECORD REPRODUCING DEVICE FUJI XEROX CO., LTD., TOKYO, JAPAN 2007-08-09 US disclosed
US-20050228153-A1 Optical recording material, optical recording medium and optical recording/reproducing device FUJI XEROX CO. LTD. 2005-10-13 US disclosed
US-20040191684-A1 Optical recording medium and method for producing the same FUJI XEROX CO., LTD. (JP) 2004-09-30 US disclosed
US-20040029038-A1 Photo-responsive high-molecular compound, photo-responsive high-molecular composition, dicarboxylic acid monomer, polyester, optical recording medium and optical record reproducing device FUJI XEROX CO., LTD. (JP) 2004-02-12 US disclosed