SCHEMBL8370127

SCHEMBL8370127

O=c1c(OCc2ccccc2)c(OCc2ccccc2)c1=O

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 3/20 0.53
▸ GAA P10253 2/20 0.53
▸ POLB P06746 1/20 0.53
▸ MAOA P21397 2/20 0.50
▸ MAOB P27338 2/20 0.50
▸ TSHR P16473 1/20 0.50
▸ HPGD P15428 2/20 0.49
▸ HTT P42858 2/20 0.49
▸ SMN1; SMN2 Q16637 2/20 0.49
▸ MEN1 O00255 2/20 0.49
▸ KMT2A Q03164 2/20 0.49
▸ ALDH1A1 P00352 1/20 0.49
▸ GSTP1 P09211 1/20 0.48
▸ CYP1A2 P05177 1/20 0.48
▸ PTGS1 P23219 1/20 0.48
▸ SLC6A2 P23975 1/20 0.48
▸ CYP2C19 P33261 1/20 0.48
▸ PTGS2 P35354 1/20 0.48
▸ SLC6A3 Q01959 1/20 0.48
▸ HIF1A Q16665 1/20 0.48

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
SCHEMBL7534835 0.86 LMNA (0.50) LMNAGAAPOLBMAOAMAOB
SCHEMBL23258887 0.78 KDM1A (0.54) LMNAGAAPOLBMAOAMAOB
SCHEMBL756581 0.78 TSHR (0.52) LMNAGAAPOLBMAOAMAOB
SCHEMBL29366230 0.78 TSHR (0.52) LMNAGAAPOLBMAOAMAOB
SCHEMBL8639557 0.77 AGXT (0.50) MAOAMAOBHTTALDH1A1CYP1A2
SCHEMBL11629996 0.77 NPC1 (0.50) MAOAMAOBSMN1; SMN2TDP1RAB9A
SCHEMBL9467731 0.77 TSHR (0.46) LMNAGAAPOLBMAOAMAOB
SCHEMBL1127799 0.76 TSHR (0.50) LMNAGAAPOLBMAOAMAOB
SCHEMBL24968079 0.76 L3MBTL1 (0.63) LMNAGAAPOLBMAOAMAOB
SCHEMBL29366541 0.76 TSHR (0.50) LMNAGAAPOLBMAOAMAOB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5334489-A Hydroxylating 3,4-disubstituted-cyclobut-3-ene-1,2-dione by heating in presence of acid catalysts which is generated by exposing actinic radiation from superacid precursor POLAROID CORPORATION (US) 1994-08-02 — — US claimed
US-6004719-A ACID-GENERATING LAYER OR PHASE COMPRISING A MIXTURE OF A SUPERACID PRECURSOR, A SENSITIZING DYE AND A SECONDARY ACID GENERATOR, AND A COLOR-CHANGE LAYER OR PHASE COMPRISING AN IMAGE DYE. POLAROID CORPORATION (US) 1999-12-21 — — US disclosed
EP-0757629-B1 IMAGING MEDIUM AND PROCESS POLAROID CORP (US) 1999-01-20 — — EP disclosed
EP-0757628-B1 PROCESS FOR FIXING AN IMAGE POLAROID CORP (US) 1998-12-02 — — EP disclosed
EP-0665960-B1 IMAGING MEDIUM AND PROCESS POLAROID CORP (US) 1998-08-19 — — EP disclosed
US-5783593-A FUNGICIDE; ANTICHOLESTEROL AGENT ABBOTT LABORATORIES (US) 1998-07-21 — — US disclosed
US-5741630-A ACID-CATALYZED THERMAL DECOMPOSITION OF SECONDARY ACID GENERATOR AND FORMATION OF SECOND ACID; COPPER COMPOUND AND REACTIVE MATERIAL USED TO DECOMPOSE SUPERACID PRECURSOR POLAROID CORPORATION (US) 1998-04-21 — — US disclosed
US-5631118-A MULTILAYER ELEMENT WITH ACID GENERATING LAYER, ACID PRECURSOR, SENSITIZING DYE, ACID GENERATOR AND COLOR CHANGING LAYER POLAROID CORPORATION (US) 1997-05-20 — — US disclosed
EP-0757628-A1 PROCESS FOR FIXING AN IMAGE POLAROID CORPORATION (US) 1997-02-12 — — EP disclosed
EP-0757629-A1 IMAGING MEDIUM AND PROCESS POLAROID CORPORATION (US) 1997-02-12 — — EP disclosed
US-5441850-A Exposing medium to actinic radiation in specified wavelength so sensitizing dye decomposes superacid precursor, heating to decompose secondary acid generator, mixing acid generating and color change layers to form image, providing base to restore POLAROID CORPORATION (US) 1995-08-15 — — US disclosed
EP-0665961-A1 IMAGING MEDIUM AND PROCESS. POLAROID CORP (US) 1995-08-09 — — EP disclosed
EP-0665789-A1 HEAT-SENSITIVE IMAGE RECORDING MEDIUM AND PROCESS. POLAROID CORP (US) 1995-08-09 — — EP disclosed
EP-0665960-A1 IMAGING MEDIUM AND PROCESS POLAROID CORPORATION (US) 1995-08-09 — — EP disclosed
US-5395736-A Exposing superoxide precursor to actinic radiation, generating superacid, mixing with oxalic acid diester, heating POLAROID CORPORATION (US) 1995-03-07 — — US disclosed
US-5334489-A Hydroxylating 3,4-disubstituted-cyclobut-3-ene-1,2-dione by heating in presence of acid catalysts which is generated by exposing actinic radiation from superacid precursor POLAROID CORPORATION (US) 1994-08-02 — — US disclosed
WO-1994010607-A1 IMAGING MEDIUM AND PROCESS POLAROID CORPORATION (US) 1994-05-11 — — WO disclosed
WO-1994009992-A1 HEAT-SENSITIVE IMAGE RECORDING MEDIUM AND PROCESS POLAROID CORPORATION (US) 1994-05-11 — — WO disclosed
WO-1994010606-A1 IMAGING MEDIUM AND PROCESS POLAROID CORPORATION (US) 1994-05-11 — — WO disclosed
US-5286612-A Mixture of superacid precursor and dye POLAROID CORPORATION (US) 1994-02-15 — — US disclosed
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