SCHEMBL6906340

SCHEMBL6906340

O=S(=O)(c1ccc(O)c(-c2ccccc2O)c1)c1ccc(O)c(-c2ccccc2O)c1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 2/20 0.52
GAA P10253 2/20 0.52
PKLR P30613 3/20 0.45
POLB P06746 2/20 0.43
HSP90AA1 P07900 1/20 0.42
HSP90AB1 P08238 1/20 0.42
BCL2 P10415 1/20 0.42
MCL1 Q07820 1/20 0.42
MEN1 O00255 1/20 0.42
MAOA P21397 1/20 0.42
KMT2A Q03164 1/20 0.42
GFER P55789 1/20 0.42
ALDH1A1 P00352 1/20 0.40
HPGD P15428 1/20 0.40
BCL2L1 Q07817 1/20 0.40
HSD17B10 Q99714 1/20 0.40
HTR6 P50406 1/20 0.39
PTPN1 P18031 1/20 0.39
CA12 O43570 2/20 0.38
CA1 P00915 2/20 0.38

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
SCHEMBL8516332 0.86 HSD17B10 (0.53) MAPTGAAPKLRPOLBHSP90AA1
SCHEMBL9713722 0.82 BACE1 (0.56) MAPTGAAPOLBMEN1MAOA
SCHEMBL29429256 0.82 BACE1 (0.56) MAPTGAAPOLBMEN1MAOA
SCHEMBL1070330 0.82 BACE1 (0.56) MAPTGAAPOLBMEN1MAOA
SCHEMBL29706496 0.75 ALDH1A1 (0.63) MAPTPOLBBCL2MCL1MEN1
SCHEMBL30501700 0.75 ALDH1A1 (0.63) MAPTPOLBBCL2MCL1MEN1
SCHEMBL14760441 0.74 ESR1 (0.53) MAPTGAAPOLBMAOAALDH1A1
SCHEMBL8516709 0.74 ALDH1A1 (0.63) MAPTGAAPKLRALDH1A1HPGD
SCHEMBL1346857 0.73 HTR6 (0.58) MAPTGAAPKLRPOLBMEN1
SCHEMBL30110766 0.73 SERPINE1 (0.64) MAPTGAAPKLRPOLBALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0785235-B1 Compatibilized blends of polyetherimides and liquid crystalline polyesters GEN ELECTRIC (US) 2004-03-31 EP disclosed
US-6570038-B1 Phase transfer agent; reacting phosgene with sceondary amine SABIC INNOVATIVE PLASTICS IP B.V. (NL) 2003-05-27 US disclosed
EP-0784051-B1 Aqueous hexasubstituted guanidinium chlorides and methods for their preparation and use GEN ELECTRIC (US) 2002-08-07 EP disclosed
US-6235934-B1 MIXTURE WITH IMIDE AND SOLVENT GENERAL ELECTRIC COMPANY 2001-05-22 US disclosed
US-5872294-A Aqueous hexasubstituted guanidinium chlorides and methods for their preparation and use GENERAL ELECTRIC COMPANY (US) 1999-02-16 US disclosed
EP-0785235-A2 Compatibilized blends of polyetherimides and liquid crystalline polyesters GENERAL ELECTRIC COMPANY (US) 1997-07-23 EP disclosed
EP-0784051-A1 Aqueous hexasubstituted guanidinium chlorides and methods for their preparation and use GENERAL ELECTRIC COMPANY (US) 1997-07-16 EP disclosed
US-5633319-A NON-DELAMINATING; LOW VISCOSITY, HIGH WORKABILITY GENERAL ELECTRIC COMPANY (US) 1997-05-27 US disclosed
US-5132423-A Nucleophilic substitution reaction of alkali hydroxy- or mercaptoaromatic compound and heterocyclic substituted imide GENERAL ELECTRIC COMPANY (US) 1992-07-21 US disclosed
US-5116975-A Bis(guanidinium)alkane salts as phase transfer catalysts GENERAL ELECTRIC COMPANY (US) 1992-05-26 US disclosed
EP-0254994-B1 POLYETHERIMIDE BISHALOFORMATE COMPOSITIONS GENERAL ELECTRIC COMPANY (US) 1992-02-05 EP disclosed
US-5081298-A Bis(pentaalkylguanidinium) alkane salts as phase transfer catalysts GENERAL ELECTRIC COMPANY (US) 1992-01-14 US disclosed
US-4757150-A Polyetherimide bisphenol compositions GENERAL ELECTRIC COMPANY (US) 1988-07-12 US disclosed
EP-0254994-A1 Polyetherimide bishaloformate compositions GENERAL ELECTRIC COMPANY (US) 1988-02-03 EP disclosed