Anthraquinone

Anthraquinone

SCHEMBL7142334

O=C1c2ccccc2C(=O)c2ccccc21.O=C=O

nearest known ligand 0.80

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Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 3/20 0.80
KMT2A Q03164 3/20 0.80
CDC25B P30305 3/20 0.80
MAOA P21397 4/20 0.65
RAB9A P51151 3/20 0.65
SMN1; SMN2 Q16637 3/20 0.65
MAPT P10636 3/20 0.65
APAF1 O14727 2/20 0.65
TDP2 O95551 2/20 0.65
KDM4E B2RXH2 2/20 0.65
NPC1 O15118 2/20 0.65
LMNA P02545 2/20 0.65
POLB P06746 2/20 0.65
S100A4 P26447 2/20 0.65
MAPK1 P28482 2/20 0.65
BLM P54132 2/20 0.65
CES2 O00748 1/20 0.65
TERT O14746 1/20 0.65
PLIN1 O60240 1/20 0.65
S1PR4 O95977 1/20 0.65

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
Anthraquinone SCHEMBL1901249 0.89 MEN1 (1.00) MEN1KMT2ACDC25BMAOARAB9A
Anthraquinone SCHEMBL14943 0.89 MEN1 (1.00) MEN1KMT2ACDC25BMAOARAB9A
Anthraquinone SCHEMBL29358690 0.89 MEN1 (1.00) MEN1KMT2ACDC25BMAOARAB9A
Anthraquinone SCHEMBL9650846 0.88 CDC25B (0.71) MEN1KMT2ACDC25BMAOARAB9A
Anthraquinone SCHEMBL9208192 0.86 MEN1 (0.92) MEN1KMT2ACDC25BMAOARAB9A
Anthraquinone SCHEMBL7205968 0.86 MEN1 (0.92) MEN1KMT2ACDC25BMAOARAB9A
Anthraquinone SCHEMBL11300863 0.86 MEN1 (0.92) MEN1KMT2ACDC25BMAOARAB9A
Anthraquinone SCHEMBL8081485 0.86 MEN1 (0.92) MEN1KMT2ACDC25BMAOARAB9A
Anthraquinone SCHEMBL10991985 0.86 MEN1 (0.92) MEN1KMT2ACDC25BMAOARAB9A
Anthraquinone SCHEMBL394493 0.86 MEN1 (0.92) MEN1KMT2ACDC25BMAOARAB9A

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-6656446-B1 Using carbon dioxide soluble secondary alcohol, free radical initiator and oxygen in carbon dioxide UNIVERSITY OF PITTSBURGH 2003-12-02 US disclosed
US-6596884-B2 Synthesizing an analog of anthraquinone that is soluble in or miscible with carbon dioxide; reacting with hydrogen in carbon dioxide to produce tetrahydroquinone; reacting with oxygen to produce hydrogen peroxide; regenerating analog UNIVERSITY OF PITTSBURGH 2003-07-22 US disclosed
US-20020110516-A1 Synthesis of hydrogen peroxide NATIONAL SCIENCE FOUNDATION 2002-08-15 US disclosed
US-6342196-B2 COMPRISES SYNTHESIZING ANALOG OF ANTHRAQUINONE SOLUBLE IN OR MISCIBLE WITH CARBON DIOXIDE, REACTING ANALOG WITH HYDROGEN PRODUCES TETRAHYDROQUINONE, REACTING WITH OXYGEN REGENERATES ANTHRAQUINONE AND PRODUCES HYDROGEN PEROXIDE; SOLVENT-FREE UNIVERSITY OF PITTSBURGH 2002-01-29 US disclosed
US-20010007045-A1 SYNTHESIS OF HYDROGEN PEROXIDE NATIONAL SCIENCE FOUNDATION 2001-07-05 US disclosed
WO-2000066489-A1 SYNTHESIS OF HYDROGEN PEROXIDE UNIVERSITY OF PITTSBURGH (US) 2000-11-09 WO disclosed
WO-2000000428-A1 SYNTHESIS OF HYDROGEN PEROXIDE UNIVERSITY OF PITTSBURGH (US) 2000-01-06 WO disclosed