SCHEMBL3206927

SCHEMBL3206927

O=C(Oc1cccc([N+](=O)[O-])c1[N+](=O)[O-])C(=O)Oc1cccc([N+](=O)[O-])c1[N+](=O)[O-]

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GPR35 Q9HC97 2/20 0.55
TSHR P16473 2/20 0.50
ALDH1A1 P00352 4/20 0.46
TDP1 Q9NUW8 4/20 0.46
RAB9A P51151 3/20 0.44
NPC1 O15118 1/20 0.44
RECQL P46063 1/20 0.44
HTT P42858 1/20 0.43
MEN1 O00255 1/20 0.43
KMT2A Q03164 1/20 0.43
MAPT P10636 2/20 0.42
CYP1A2 P05177 1/20 0.42
CYP2C9 P11712 1/20 0.42
KDM4E B2RXH2 1/20 0.42
POLB P06746 1/20 0.41
L3MBTL1 Q9Y468 2/20 0.41
HPGD P15428 1/20 0.41
NPSR1 Q6W5P4 1/20 0.41
ESR2 Q92731 1/20 0.40
APEX1 P27695 1/20 0.40

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
SCHEMBL11250442 0.92 GPR35 (0.50) GPR35TSHRALDH1A1TDP1RAB9A
SCHEMBL11250446 0.92 GPR35 (0.50) GPR35TSHRALDH1A1TDP1RAB9A
SCHEMBL48359 0.89 GPR35 (0.55) GPR35TSHRALDH1A1TDP1RAB9A
SCHEMBL48361 0.88 GPR35 (0.53) GPR35TSHRALDH1A1TDP1RAB9A
SCHEMBL48360 0.88 GPR35 (0.53) GPR35TSHRALDH1A1TDP1RAB9A
SCHEMBL2373772 0.86 GPR35 (0.51) GPR35TSHRALDH1A1TDP1RAB9A
SCHEMBL1652615 0.86 GPR35 (0.51) GPR35TSHRALDH1A1TDP1RAB9A
SCHEMBL17005575 0.86 TSHR (0.51) GPR35TSHRALDH1A1TDP1RAB9A
SCHEMBL25331485 0.85 TSHR (0.50) GPR35TSHRALDH1A1TDP1RAB9A
SCHEMBL19713194 0.85 GPR35 (0.50) GPR35TSHRALDH1A1TDP1RAB9A

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 29 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7539006-B2 Electrolytic solution for driving electrolytic capacitor and electrolytic capacitor RUBYCON CORPORATION (JP) 2009-05-26 US claimed
US-20070029529-A1 Electrolytic solution for driving electrolytic capacitor and electrolytic capacitor KOMATSU AKIHIKO 2007-02-08 US claimed
US-20040245105-A1 Electrolyte solution for driving electrolytic capacitor and electrolytic capacitor RUBYCON CORPORATION (JP) 2004-12-09 US claimed
EP-1437749-A1 ELECTROLYTE SOLUTION FOR DRIVING ELECTROLYTIC CAPACITOR AND ELECTROLYTIC CAPACITOR Rubycon Corporation (JP) 2004-07-14 EP claimed
EP-0837141-B1 Process for detecting target nucleic acid, process for quantifying the same, and pyrylium compound for chemiluminescence analysis CANON KK (JP) 2003-01-08 EP claimed
US-20020115079-A1 Process for detecting target nucleic acid, process for quantifying the same, and pyrylium compound for chemiluminescence analysis OKAMOTO TADASHI (JP) 2002-08-22 US claimed
EP-0837141-A2 Process for detecting target nucleic acid, process for quantifying the same, and pyrylium compound for chemiluminescence analysis CANON KABUSHIKI KAISHA (JP) 1998-04-22 EP claimed
EP-0432017-B1 Derivatives of tetrahydro-2,3,6,7,1H,5H,11H-(1)benzopyrano(6,7,8,ij)quinolizinone-11 usable as markers for organic compounds for the purpose of detecting said compounds by chemiluminescence or fluorescence EUROBIO LAB (FR) 1995-08-16 EP claimed
EP-0419542-B1 NEW DERIVATIVES OF TETRAHYDRO-2,3,6,7,1H,5H,11H-(1)BENZOPYRANO(6,7,8,IJ)QUINOLIZONONE-11 USABLE AS MARKERS FOR ORGANIC COMPOUNDS FOR THE PURPOSE OF DETECTING SAID COMPOUNDS BY CHEMILUMINESCENCE OR FLUORESCENCE LABORATOIRES EUROBIO (FR) 1993-09-29 EP claimed
EP-3894862-A1 SUBSTRATE FOR AMPLIFYING THE CHEMILUMINESCENCE Fianostics GmbH (AT) 2021-10-20 EP disclosed
CN-113302496-A Enhanced chemiluminescent substrate 菲亚诺斯蒂克斯有限责任公司 2021-08-24 CN disclosed
WO-2020198771-A1 SUBSTRATE FOR AMPLIFYING THE CHEMILUMINESCENCE FIANOSTICS GMBH (AT) 2020-10-08 WO disclosed
EP-1460660-B1 ELECTROLYTIC CAPACITOR AND ELECTROLYTIC SOLUTION FOR DRIVING ELECTROLYTIC CAPACITOR RUBYCON CORP (JP) 2013-04-10 EP disclosed
US-7660101-B2 Electrolytic capacitor and electrolyte solution for use in an electrolytic capacitor RUBYCON CORPORATION (JP) 2010-02-09 US disclosed
US-20020115079-A1 Process for detecting target nucleic acid, process for quantifying the same, and pyrylium compound for chemiluminescence analysis OKAMOTO TADASHI (JP) 2002-08-22 US disclosed
US-6297008-B1 SIMPLE, SENSITIVE AND ACCURATE PROCESS BY HYBRIDIZING PROBE TO TARGET NUCLEIC ACID, ASSOCIATING CHEMILUMINESCENT COMPOUND OF DEFINED STRUCTURE WITH FORMED DOUBLE-STRAND, EXPOSING COMPOUND TO ACTIVATING COMPOUNDS, THEN DETECTING LUMINESCENCE CANON KABUSHIKI KAISHA (JP) 2001-10-02 US disclosed
EP-0837141-A2 Process for detecting target nucleic acid, process for quantifying the same, and pyrylium compound for chemiluminescence analysis CANON KABUSHIKI KAISHA (JP) 1998-04-22 EP disclosed
US-5151517-A Fluorescent marking compounds LABORATORIES EUROBIO (FR) 1992-09-29 US disclosed
US-4365018-A SELF-EXPOSING, CHEMILUMINESCENCE THE MEAD CORPORATION (US) 1982-12-21 US disclosed
US-4233402-A CHEMICAL ANALYSIS OF A BINDING PAIR OF LIGANDS AND ENZYMES BY LIGHT SIGNALS SYVA COMPANY (US) 1980-11-11 US disclosed