SCHEMBL9340348

SCHEMBL9340348

C[Si](C)(C)[Si](C)(C)c1ccccc1

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ESR1 P03372 1/20 0.44
ESR2 Q92731 1/20 0.44
NR1H2 P55055 3/20 0.43
NR1H3 Q13133 3/20 0.43
TSHR P16473 3/20 0.35
ACHE P22303 2/20 0.35
LMNA P02545 1/20 0.35
ALOX12 P18054 1/20 0.35
MAPT P10636 1/20 0.34
NPC1 O15118 3/20 0.32
RAB9A P51151 3/20 0.32
SMN1; SMN2 Q16637 2/20 0.32
ALDH1A1 P00352 1/20 0.32
CES2 O00748 1/20 0.31
CES1 P23141 1/20 0.31
TP53 P04637 1/20 0.30
MAPK1 P28482 1/20 0.30
CA4 P22748 1/20 0.30
CHEK1 O14757 1/20 0.30
AKT2 P31751 1/20 0.30

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
SCHEMBL239179 0.87 ESR1 (0.48) ESR1ESR2NR1H2NR1H3TSHR
SCHEMBL11023990 0.81 ESR1 (0.44) ESR1ESR2NR1H2NR1H3TSHR
SCHEMBL23532344 0.81 ESR1 (0.44) ESR1ESR2NR1H2NR1H3TSHR
SCHEMBL10150936 0.79 ESR1 (0.42) ESR1ESR2NR1H2NR1H3TSHR
SCHEMBL244122 0.79 ESR1 (0.42) ESR1ESR2NR1H2NR1H3TSHR
SCHEMBL10616290 0.77 ESR1 (0.41) ESR1ESR2NR1H2NR1H3TSHR
SCHEMBL8939087 0.77 ESR1 (0.41) ESR1ESR2NR1H2NR1H3TSHR
SCHEMBL8214590 0.77 ESR1 (0.41) ESR1ESR2NR1H2NR1H3TSHR
SCHEMBL10355215 0.77 ESR1 (0.41) ESR1ESR2NR1H2NR1H3TSHR
SCHEMBL9757676 0.77 ESR1 (0.46) ESR1ESR2NR1H2NR1H3TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230253626-A1 NONAQUEOUS ELECTROLYTIC SOLUTION AND NONAQUEOUS ELECTROLYTIC SOLUTION SECONDARY BATTERY USING SAME MITSUBISHI CHEMICAL CORPORATION (JP) 2023-08-10 US disclosed
US-11688881-B2 Nonaqueous electrolytic solution and nonaqueous electrolytic solution secondary battery using same MITSUBISHI CHEMICAL CORPORATION (JP) 2023-06-27 US disclosed
US-11688881-B2 Nonaqueous electrolytic solution and nonaqueous electrolytic solution secondary battery using same MITSUBISHI CHEMICAL CORPORATION (JP) 2023-06-27 US disclosed
US-20200144670-A1 NONAQUEOUS ELECTROLYTIC SOLUTION AND NONAQUEOUS ELECTROLYTIC SOLUTION SECONDARY BATTERY USING SAME MITSUBISHI CHEMICAL CORPORATION (JP) 2020-05-07 US disclosed
US-20180019499-A1 NONAQUEOUS ELECTROLYTIC SOLUTION AND NONAQUEOUS ELECTROLYTIC SOLUTION SECONDARY BATTERY USING SAME MITSUBISHI CHEMICAL CORPORATION (JP) 2018-01-18 US disclosed
US-9806375-B2 Nonaqueous electrolytic solution and nonaqueous electrolytic solution secondary battery using same MITSUBISHI CHEMICAL CORPORATION (JP) 2017-10-31 US disclosed
US-20170018805-A1 NON-AQUEOUS ELECTROLYTIC SOLUTION AND NON-AQUEOUS ELECTROLYTE SECONDARY BATTERY USING THE SAME MITSUBISHI CHEMICAL CORPORATION (JP) 2017-01-19 US disclosed
US-20170018805-A1 NON-AQUEOUS ELECTROLYTIC SOLUTION AND NON-AQUEOUS ELECTROLYTE SECONDARY BATTERY USING THE SAME MITSUBISHI CHEMICAL CORPORATION (JP) 2017-01-19 US disclosed
US-20150080596-A1 Method Of Reducing A Halosilane Compound In A Micoreactor DOW CORNING CORPORATION 2015-03-19 US disclosed
US-20140363735-A1 NONAQUEOUS ELECTROLYTIC SOLUTION AND NONAQUEOUS ELECTROLYTIC SOLUTION SECONDARY BATTERY USING SAME MITSUBISHI CHEMICAL CORPORATION (JP) 2014-12-11 US disclosed
US-20140363735-A1 NONAQUEOUS ELECTROLYTIC SOLUTION AND NONAQUEOUS ELECTROLYTIC SOLUTION SECONDARY BATTERY USING SAME MITSUBISHI CHEMICAL CORPORATION (JP) 2014-12-11 US disclosed
US-20130309564-A1 NONAQUEOUS ELECTROLYTIC SOLUTION AND NONAQUEOUS ELECTROLYTIC SOLUTION SECONDARY BATTERY USING SAME MITSUBISHI CHEMICAL CORPORATION (JP) 2013-11-21 US disclosed
US-7169697-B2 Semiconductor device and manufacturing method of the same KABUSHIKI KAISHA TOSHIBA (JP) 2007-01-30 US disclosed
EP-0325248-B1 A process for the chlorodephenylation of phenylsilanes DOW CORNING (US) 1994-06-15 EP disclosed
US-5068381-A Reaction of silane with acetylene compound for use as a crosslinking agent and as a photosensitive agent SHIN-ETSU CHEMICAL CO., LTD. (JP) 1991-11-26 US disclosed
US-4855471-A Process for the chlorodephenylation of phenyldisilanes DOW CORNING CORPORATION (US) 1989-08-08 US disclosed
EP-0325248-A2 A process for the chlorodephenylation of phenylsilanes DOW CORNING CORPORATION (US) 1989-07-26 EP 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-20150080596-A1 Method Of Reducing A Halosilane Compound In A Micoreactor MSN, MGMT, BHMT2 ESR1 4824/4885ESR2 4758/4885NR1H2 2835/4885

“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.