SCHEMBL8201062

SCHEMBL8201062

c1ccc(OCCOCCOCCOCCOCCOCCOCC2CO2)cc1

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 1/20 0.68
TSHR P16473 4/20 0.51
ALDH1A1 P00352 4/20 0.51
TP53 P04637 3/20 0.51
HIF1A Q16665 2/20 0.51
SMN1; SMN2 Q16637 2/20 0.51
CYP3A4 P08684 1/20 0.51
MEN1 O00255 3/20 0.49
KMT2A Q03164 3/20 0.49
HTR1A P08908 2/20 0.46
ADRA1D P25100 1/20 0.46
ADRA1A P35348 1/20 0.46
KCNA3 P22001 1/20 0.45
GLA P06280 1/20 0.45
TAAR1 Q96RJ0 1/20 0.43
MAPT P10636 2/20 0.42
HPGD P15428 2/20 0.42
PKM P14618 2/20 0.42
CYP1A2 P05177 1/20 0.42
PPARG P37231 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
SCHEMBL2882808 1.00 TDP1 (0.68) TDP1TSHRALDH1A1TP53HIF1A
SCHEMBL8198198 1.00 TDP1 (0.68) TDP1TSHRALDH1A1TP53HIF1A
SCHEMBL7933696 0.98 TDP1 (0.70) TDP1TSHRALDH1A1TP53HIF1A
SCHEMBL9952595 0.93 TDP1 (0.79) TDP1TSHRALDH1A1TP53HIF1A
SCHEMBL27991659 0.91 TDP1 (0.82) TDP1TSHRALDH1A1TP53HIF1A
SCHEMBL11682636 0.90 TDP1 (0.68) TDP1TSHRALDH1A1TP53HIF1A
SCHEMBL9325190 0.89 TDP1 (0.55) TDP1TSHRALDH1A1TP53HIF1A
SCHEMBL28371423 0.89 TDP1 (0.57) TDP1TSHRALDH1A1TP53HIF1A
SCHEMBL29148825 0.86 TDP1 (0.85) TDP1TSHRALDH1A1TP53HIF1A
SCHEMBL20492157 0.85 MEN1 (0.59) TDP1TSHRALDH1A1TP53HIF1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6019908-A ACTIVE HYDROGEN COMPOUND IS REACTED WITH GLYCIDYL ETHERS TOGETHER WITH ETHYLENE OXIDES TO OBTAIN A POLYETHER COMPOUND AND THE POLYETHER COMPOUND IS REACTED WITH A COMPOUND HAVING A POLYMERIZABLE FUNCTIONAL GROUP; CROSSLINKING DAI-ICHI KOGYO SEIYAKU, CO., LTD. (JP) 2000-02-01 US disclosed
EP-0460876-B1 Ion-conductive polymer electrolyte DAI ICHI KOGYO SEIYAKU CO LTD (JP) 1995-10-25 EP disclosed
US-5433877-A Ion-conductive polymer electrolyte DAI-ICHI KOGYO SEIYAKU CO., LTD. (JP) 1995-07-18 US disclosed
EP-0392839-B1 Ion-conductive polymer electrolyte DAI ICHI KOGYO SEIYAKU CO LTD (JP) 1995-07-12 EP disclosed
EP-0425255-B1 Ion-conductive polymer electrolyte DAI ICHI KOGYO SEIYAKU CO LTD (JP) 1995-04-26 EP disclosed
US-5169921-A Composing branched propylene/1,2-/ segment of polyol for flexibility and adhesion at low temperature DAI-ICHI KOGYO SEIYAKU CO., LTD. (JP) 1992-12-08 US disclosed
US-5159001-A Crosslinked polyether and soluble salt DAI-ICHI KOGYO SEIYAKU CO., LTD. (JP) 1992-10-27 US disclosed
EP-0498370-A2 Polyurethane type curable coating composition DAI-ICHI KOGYO SEIYAKU CO., LTD. (JP) 1992-08-12 EP disclosed
US-5116541-A Polyether DAI-ICHI KOGYO SEIYAKU CO., LTD. (JP) 1992-05-26 US disclosed
US-5098589-A Modified polyether polymers or polyepoxides DAI-ICHI KOGYO SEIYAKU CO., LTD. (JP) 1992-03-24 US disclosed
EP-0460876-A1 Ion-conductive polymer electrolyte DAI-ICHI KOGYO SEIYAKU CO., LTD. (JP) 1991-12-11 EP disclosed
EP-0425255-A2 Ion-conductive polymer electrolyte DAI-ICHI KOGYO SEIYAKU CO., LTD. (JP) 1991-05-02 EP disclosed
EP-0392839-A2 Ion-conductive polymer electrolyte DAI-ICHI KOGYO SEIYAKU CO., LTD. (JP) 1990-10-17 EP disclosed