SCHEMBL777674

SCHEMBL777674

CCCCCOP(=O)(O)CC

nearest known ligand 0.65

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
LPAR3 Q9UBY5 14/20 0.65
LPAR2 Q9HBW0 8/20 0.65
LPAR1 Q92633 6/20 0.65
CYP3A4 P08684 1/20 0.50
LPAR5 Q9H1C0 1/20 0.44
LMNA P02545 1/20 0.43
ESR1 P03372 1/20 0.43
ADORA3 P0DMS8 1/20 0.43
CDC25A P30304 1/20 0.43
AGTR1 P30556 1/20 0.43
AKT1 P31749 1/20 0.43
ADRA1A P35348 1/20 0.43
KCNH2 Q12809 1/20 0.43

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
SCHEMBL18272681 0.98 LPAR3 (0.69) LPAR3LPAR2LPAR1CYP3A4LPAR5
SCHEMBL27935494 0.98 LPAR3 (0.69) LPAR3LPAR2LPAR1CYP3A4LPAR5
SCHEMBL17626411 0.98 LPAR3 (0.63) LPAR3LPAR2LPAR1CYP3A4LPAR5
SCHEMBL17626568 0.98 LPAR3 (0.63) LPAR3LPAR2LPAR1CYP3A4LPAR5
SCHEMBL15281699 0.98 LPAR3 (0.69) LPAR3LPAR2LPAR1CYP3A4LPAR5
SCHEMBL18715371 0.98 LPAR3 (0.69) LPAR3LPAR2LPAR1CYP3A4LPAR5
SCHEMBL17626485 0.98 LPAR3 (0.63) LPAR3LPAR2LPAR1CYP3A4LPAR5
SCHEMBL2486762 0.93 CYP3A4 (0.58) LPAR3LPAR2LPAR1CYP3A4
SCHEMBL18686723 0.93 LPAR3 (0.54) LPAR3LPAR2LPAR1CYP3A4LPAR5
SCHEMBL17626420 0.91 CYP3A4 (0.56) LPAR3LPAR2LPAR1CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12100809-B2 Non-aqueous liquid electrolyte and non-aqueous liquid electrolyte secondary battery MITSUBISHI CHEMICAL CORPORATION (JP) 2024-09-24 US disclosed
CN-112778511-B Catalyst composition for polyester production process 科莱恩塑料和涂料有限公司 2023-03-28 CN disclosed
US-20220149436-A1 NON-AQUEOUS LIQUID ELECTROLYTE AND NON-AQUEOUS LIQUID ELECTROLYTE SECONDARY BATTERY MITSUBISHI CHEMICAL CORPORATION (JP) 2022-05-12 US disclosed
US-11283107-B2 Non-aqueous liquid electrolyte and non-aqueous liquid electrolyte secondary battery MITSUBISHI CHEMICAL CORPORATION (JP) 2022-03-22 US disclosed
CN-113632282-A Electrolyte for secondary battery and secondary battery 株式会社村田制作所 2021-11-09 CN disclosed
EP-3621141-A1 NON-AQUEOUS LIQUID ELECTROLYTE AND NON-AQUEOUS LIQUID ELECTROLYTE SECONDARY BATTERY MITSUBISHI CHEMICAL CORPORATION (JP) 2020-03-11 EP disclosed
US-20190229372-A1 NON-AQUEOUS LIQUID ELECTROLYTE AND NON-AQUEOUS LIQUID ELECTROLYTE SECONDARY BATTERY MITSUBISHI CHEMICAL CORPORATION (JP) 2019-07-25 US disclosed
US-10333172-B2 Non-aqueous liquid electrolyte and non-aqueous liquid electrolyte secondary battery MITSUBISHI CHEMICAL CORPORATION (JP) 2019-06-25 US disclosed
US-10290901-B2 2019-05-14 US disclosed
US-9608291-B2 Non-aqueous liquid electrolyte and non-aqueous liquid electrolyte secondary battery MITSUBISHI CHEMICAL CORPORATION (JP) 2017-03-28 US disclosed
US-7749975-B2 Modulation of immunostimulatory properties of oligonucleotide-based compounds by optimal presentation of 5′ ends IDERA PHARMACEUTICALS, INC. (US) 2010-07-06 US disclosed
US-20100166805-A1 Modulation of immunostimulatory properties by small oligonucleotide-based compounds IDERA PHARMACEUTICALS, INC. 2010-07-01 US disclosed
US-7713535-B2 Modulation of immunostimulatory properties by small oligonucleotide-based compounds IDERA PHARMACEUTICALS, INC. (US) 2010-05-11 US disclosed
US-20090325065-A1 NON-AQUEOUS LIQUID ELECTROLYTE AND NON-AQUEOUS LIQUID ELECTROLYTE SECONDARY BATTERY MITSUBISHI CHEMICAL CORPORATION (JP) 2009-12-31 US disclosed
US-7632822-B2 Modulation of immunostimulatory properties of oligonucleotide-based compounds by utilizing modified immunostimulatory dinucleotides IDERA PHARMACEUTICALS, INC. (US) 2009-12-15 US disclosed
US-7595305-B2 Modulation of immunostimulatory properties of oligonucleotide-based compounds by utilizing modified immunostimulatory dinucleotides IDERA PHARMACEUTICALS (US) 2009-09-29 US disclosed
US-7517862-B2 Modulation of immunostimulatory properties of oligonucleotide-based compounds by optimal presentation of 5′ ends IDERA PHARMACEUTICALS, INC. (US) 2009-04-14 US disclosed
EP-2012386-A1 NONAQUEOUS ELECTROLYTE SOLUTION AND NONAQUEOUS ELECTROLYTE SECONDARY BATTERY Mitsubishi Chemical Corporation (JP) 2009-01-07 EP disclosed
US-7407944-B2 Modulation of immunostimulatory properties of oligonucleotide-based compounds by optimal presentation of 5′ ends IDERA PHARMACEUTICALS, INC. (US) 2008-08-05 US disclosed
US-20070173469-A1 Modulation of immunostimulatory properties of oligonucleotide-based compounds by optimal presentation of 5' ends HYBRIDON, INC. 2007-07-26 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20100166805-A1 Modulation of immunostimulatory properties by small oligonucleotide-based compounds TLR3, ENTPD5, TLR5 LPAR3 1251/4885LPAR2 1570/4885LPAR1 1973/4885
US-20070173469-A1 Modulation of immunostimulatory properties of oligonucleotide-based compounds by optimal presentation of 5' ends TLR5, TLR3, TLR9 LPAR3 1179/4885LPAR2 1594/4885LPAR1 1788/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.