SCHEMBL3317296

SCHEMBL3317296

CCCCCCC(C)OC

nearest known ligand 0.46

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
OPRM1 P35372 1/20 0.46
FAAH O00519 5/20 0.44
CNR1 P21554 1/20 0.43
CNR2 P34972 1/20 0.43
SPHK1 Q9NYA1 1/20 0.43
LMNA P02545 1/20 0.42
TSHR P16473 1/20 0.42
THRB P10828 1/20 0.42
ZDHHC7 Q9NXF8 1/20 0.42
DNM1 Q05193 2/20 0.42
ADH1B P00325 1/20 0.40
ADH1C P00326 1/20 0.40
ADH1A P07327 1/20 0.40
ADH4 P08319 1/20 0.40
ADH7 P40394 1/20 0.40
SMPD1 P17405 2/20 0.39
ACE2 Q9BYF1 1/20 0.39

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
SCHEMBL3316130 1.00 OPRM1 (0.46) OPRM1FAAHCNR1CNR2SPHK1
SCHEMBL28216704 1.00 OPRM1 (0.46) OPRM1FAAHCNR1CNR2SPHK1
SCHEMBL11579490 1.00 OPRM1 (0.46) OPRM1FAAHCNR1CNR2SPHK1
SCHEMBL29518544 1.00 OPRM1 (0.46) OPRM1FAAHCNR1CNR2SPHK1
SCHEMBL13555001 1.00 OPRM1 (0.46) OPRM1FAAHCNR1CNR2SPHK1
SCHEMBL3315441 1.00 OPRM1 (0.46) OPRM1FAAHCNR1CNR2SPHK1
SCHEMBL12424296 1.00 OPRM1 (0.46) OPRM1FAAHCNR1CNR2SPHK1
SCHEMBL1142792 1.00 OPRM1 (0.46) OPRM1FAAHCNR1CNR2SPHK1
SCHEMBL22817316 1.00 OPRM1 (0.46) OPRM1FAAHCNR1CNR2SPHK1
SCHEMBL10447343 0.97 OPRM1 (0.44) OPRM1FAAHCNR1CNR2SPHK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11771712-B2 Carborane compounds and methods of use thereof OHIO STATE INNOVATION FOUNDATION (US) 2023-10-03 US disclosed
CN-112300099-A Ketal derivatives of drugs, preparation method thereof, pharmaceutical compositions and uses 南开大学 2021-02-02 CN disclosed
CN-109851485-A The method and system of differential pressure heat coupling reaction rectifying production 2- methoxyl group -2- methyl heptane 重庆大学 2019-06-07 CN disclosed
WO-2017174953-A1 ALKYLATION METHOD PIVERT (FR) 2017-10-12 WO disclosed
US-9670410-B2 Liquid crystal composition INDUSTRY-UNIVERSITY COOPERATION FOUNDATION HANYANG UNIVERSITY (KR) 2017-06-06 US disclosed
US-20150137036-A1 LIQUID CRYSTAL COMPOSITION INDUSTRY-UNIVERSITY COOPERATION FOUNDATION HANYANG UNIVERSITY (KR) 2015-05-21 US disclosed
US-8633245-B2 PAI-1 inhibitor INSTITUTE OF MEDICINAL MOLECULAR DESIGN, INC. (JP) 2014-01-21 US disclosed
EP-2132167-B1 METHOD FOR THE PRODUCTION OF beta-KETONITRILES BASF SE (DE) 2013-12-25 EP disclosed
US-8501748-B2 Method for the production of β-ketonitriles BASF SE (DE) 2013-08-06 US disclosed
US-8404160-B2 Metallic ink APPLIED NANOTECH HOLDINGS, INC. (US) 2013-03-26 US disclosed
EP-1160250-A1 Silicon derivative, liquid crystal composition and liquid crystal display CHISSO CORPORATION (JP) 2001-12-05 EP disclosed
EP-1114825-A1 SILICON COMPOUNDS, LIQUID CRYSTAL COMPOSITIONS AND LIQUID CRYSTAL DISPLAYS CHISSO CORPORATION (JP) 2001-07-11 EP disclosed
EP-1010692-A1 LIQUID-CRYSTAL COMPOUNDS HAVING LARGE VALUE OF PERMITTIVITY ANISOTROPY, LIQUID-CRYSTAL COMPOSITION CONTAINING THE SAME, AND LIQUID-CRYSTAL DISPLAY ELEMENT MADE USING THE LIQUID-CRYSTAL COMPOSITION CHISSO CORPORATION (JP) 2000-06-21 EP disclosed
US-5993690-A Organosilicon compound, liquid crystal composition, and liquid-crystal display element CHISSO CORPORATION (JP) 1999-11-30 US disclosed
EP-0959060-A1 CHLOROBENZENE DERIVATIVES, LIQUID-CRYSTAL COMPOSITION, AND LIQUID-CRYSTAL DISPLAY ELEMENTS CHISSO CORPORATION (JP) 1999-11-24 EP disclosed
EP-0872484-A1 ORGANOSILICON COMPOUNDS, LIQUID-CRYSTAL COMPOSITION, AND LIQUID-CRYSTAL DISPLAY ELEMENT CHISSO CORPORATION (JP) 1998-10-21 EP disclosed
US-5324451-A Excellent response and memory DAINIPPON INK AND CHEMICALS, INC. (JP) 1994-06-28 US disclosed
EP-0329153-B1 NOVEL LACTIC ACID DERIVATIVES AND LIQUID CRYSTAL COMPOSITIONS CONTAINING THE SAME DAINIPPON INK AND CHEMICALS, INC. (JP) 1992-10-21 EP disclosed
EP-0329153-A2 Novel lactic acid derivatives and liquid crystal compositions containing the same DAINIPPON INK AND CHEMICALS, INC. (JP) 1989-08-23 EP disclosed
US-4376094-A Method of disinfecting and a method for destroying bacteria and fungi using 2-substituted glutaraldehydes STERLING DRUG INC. (US) 1983-03-08 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 (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-11771712-B2 Carborane compounds and methods of use thereof ESR2, GPER1, ESRRB OPRM1 309/4885FAAH 1683/4885CNR1 11/4885

“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.