SCHEMBL778104

SCHEMBL778104

O=S(=O)(CC(F)(F)F)c1ccccc1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PSIP1 O75475 1/20 0.54
HSD11B1 P28845 6/20 0.46
HTR6 P50406 1/20 0.44
ALDH1A1 P00352 3/20 0.43
APOBEC3G Q9HC16 1/20 0.41
CYP3A4 P08684 1/20 0.41
CYP2C9 P11712 1/20 0.41
HPGD P15428 1/20 0.41
CYP2C19 P33261 1/20 0.41
POLB P06746 1/20 0.41
HSD17B10 Q99714 1/20 0.41
TDP1 Q9NUW8 1/20 0.41
CA12 O43570 1/20 0.41
CA1 P00915 1/20 0.41
CA2 P00918 1/20 0.41
CA3 P07451 1/20 0.41
CA4 P22748 1/20 0.41
CA6 P23280 1/20 0.41
CA5A P35218 1/20 0.41
CA7 P43166 1/20 0.41

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
SCHEMBL9303097 0.84 PNMT (0.44) PSIP1ALDH1A1CYP3A4CYP2C9HPGD
SCHEMBL775887 0.83 PSIP1 (0.50) PSIP1HSD11B1HTR6ALDH1A1APOBEC3G
SCHEMBL19248406 0.83 PSIP1 (0.56) PSIP1HSD11B1HTR6ALDH1A1CYP3A4
SCHEMBL776676 0.80 ALDH1A1 (0.43) HSD11B1ALDH1A1CA1CA2KMT2A
SCHEMBL19239760 0.79 PSIP1 (0.52) PSIP1HSD11B1HTR6ALDH1A1CYP3A4
SCHEMBL7967868 0.79 PSIP1 (0.56) PSIP1HSD11B1HTR6ALDH1A1POLB
SCHEMBL776537 0.78 PSIP1 (0.50) PSIP1HSD11B1HTR6ALDH1A1CA2
SCHEMBL23501536 0.78 GAA (0.55) HTR6ALDH1A1CYP3A4CYP2C9TDP1
SCHEMBL3109115 0.78 PLCG1 (0.59) HSD11B1ALDH1A1CYP3A4CYP2C9CYP2C19
SCHEMBL8795743 0.78 CA2 (0.52) ALDH1A1CA12CA1CA2CA7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120473558-A Solid electrolyte, solid battery, preparation method of solid electrolyte and power utilization device 深圳供电局有限公司 2025-08-12 CN disclosed
US-12100809-B2 Non-aqueous liquid electrolyte and non-aqueous liquid electrolyte secondary battery MITSUBISHI CHEMICAL CORPORATION (JP) 2024-09-24 US disclosed
US-11466375-B1 Low temperature lithium production Consolidated Nuclear Security, LLC (US) 2022-10-11 US 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
US-10718057-B1 Low temperature lithium production Consolidated Nuclear Security, LLC (US) 2020-07-21 US disclosed
EP-3621141-A1 NON-AQUEOUS LIQUID ELECTROLYTE AND NON-AQUEOUS LIQUID ELECTROLYTE SECONDARY BATTERY MITSUBISHI CHEMICAL CORPORATION (JP) 2020-03-11 EP disclosed
CN-110198941-A Pyrrolopyridine N- oxidized derivatives and its preparation method and application 江苏豪森药业集团有限公司 2019-09-03 CN 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-20150056503-A1 NON-AQUEOUS LIQUID ELECTROLYTE AND NON-AQUEOUS LIQUID ELECTROLYTE SECONDARY BATTERY MITSUBISHI CHEMICAL CORPORATION (JP) 2015-02-26 US disclosed
US-20120177988-A1 NON-AQUEOUS LIQUID ELECTROLYTE AND NON-AQUEOUS LIQUID ELECTROLYTE SECONDARY BATTERY MITSUBISHI CHEMICAL CORPORATION (JP) 2012-07-12 US disclosed
US-20120070731-A1 NON-AQUEOUS LIQUID ELECTROLYTE AND NON-AQUEOUS LIQUID ELECTROLYTE SECONDARY BATTERY MITSUBISHI CHEMICAL CORPORATION (JP) 2012-03-22 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
EP-2012386-A1 NONAQUEOUS ELECTROLYTE SOLUTION AND NONAQUEOUS ELECTROLYTE SECONDARY BATTERY Mitsubishi Chemical Corporation (JP) 2009-01-07 EP disclosed
EP-1451199-A4 MAGNESIUM MEDIATED PREPARATION OF FLUORINATED ALKYLSILANES UNIV SOUTHERN CALIFORNIA (US) 2006-04-26 EP disclosed
US-6803477-B2 EFFICIENT PREPARATION OF TRIFLUOROMETHYL- AND DIFLUORO-METHYLSILANES USING MAGNESIUM MEDIATED REDUCTION OF CHLOROSILANES REACTING WITH TRI- AND DIFLUOROMETHYL SULFIDES, SULFOXIDES AND SULFONES; AUTOCATALYSIS UNIVERSITY OF SOUTHERN CALIFORNIA 2004-10-12 US disclosed
EP-1451199-A2 MAGNESIUM MEDIATED PREPARATION OF FLUORINATED ALKYLSILANES University Of Southern California (US) 2004-09-01 EP disclosed
US-20030153778-A1 Magnesium mediated preparation of fluorinated alkyl silanes UNIVERSITY OF SOUTHERN CALIFORNIA 2003-08-14 US disclosed
WO-2003048033-A2 MAGNESIUM MEDIATED PREPARATION OF FLUORINATED ALKYLSILANES UNIVERSITY OF SOUTHERN CALIFORNIA (US) 2003-06-12 WO 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 (1 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-20030153778-A1 Magnesium mediated preparation of fluorinated alkyl silanes TST, STS, PFAS PSIP1 292/4885HSD11B1 1371/4885HTR6 2734/4885

“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.