SCHEMBL813882

SCHEMBL813882

CCCCCCCC/C=C\CCCCCCCC(=O)OC1CCCCC1

nearest known ligand 0.82

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NAAA Q02083 2/20 0.82
TERT O14746 3/20 0.50
CYP1A2 P05177 2/20 0.50
MAPT P10636 2/20 0.50
CYP2C19 P33261 2/20 0.50
BLM P54132 2/20 0.50
HSD17B10 Q99714 2/20 0.50
FABP4 P15090 2/20 0.50
FAAH O00519 2/20 0.50
PTPN1 P18031 2/20 0.50
PPARG P37231 2/20 0.50
KMT2A Q03164 2/20 0.50
PPARD Q03181 2/20 0.50
PPARA Q07869 2/20 0.50
GMNN O75496 1/20 0.50
USP2 O75604 1/20 0.50
LMNA P02545 1/20 0.50
POLB P06746 1/20 0.50
CYP2C9 P11712 1/20 0.50
ALOX15 P16050 1/20 0.50

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
SCHEMBL8982662 1.00 NAAA (0.82) NAAATERTCYP1A2MAPTCYP2C19
SCHEMBL8982712 1.00 NAAA (0.82) NAAATERTCYP1A2MAPTCYP2C19
SCHEMBL3658245 1.00 NAAA (0.82) NAAATERTCYP1A2MAPTCYP2C19
SCHEMBL8982688 1.00 NAAA (0.82) NAAATERTCYP1A2MAPTCYP2C19
SCHEMBL8982686 1.00 NAAA (0.82) NAAATERTCYP1A2MAPTCYP2C19
SCHEMBL8982701 1.00 NAAA (0.82) NAAATERTCYP1A2MAPTCYP2C19
SCHEMBL8982705 1.00 NAAA (0.82) NAAATERTCYP1A2MAPTCYP2C19
SCHEMBL8982880 1.00 NAAA (0.82) NAAATERTCYP1A2MAPTCYP2C19
SCHEMBL8982670 1.00 NAAA (0.82) NAAATERTCYP1A2MAPTCYP2C19
SCHEMBL8982760 1.00 NAAA (0.82) NAAATERTCYP1A2MAPTCYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119875591-A Liquid cooling composition, preparation method and application thereof 中国石油化工股份有限公司 2025-04-25 CN claimed
US-8425784-B2 Ozonolysis reactions in liquid CO2 and CO2-expanded solvents UNIVERSITY OF KANSAS (US) 2013-04-23 US claimed
US-12619006-B2 Wavelength selective absorption filter and display device FUJIFILM CORPORATION (JP) 2026-05-05 US disclosed
CN-116568763-B Wavelength selective absorption filter and display device 富士胶片株式会社 2025-05-13 CN disclosed
CN-119875591-A Liquid cooling composition, preparation method and application thereof 中国石油化工股份有限公司 2025-04-25 CN disclosed
US-20230288610-A1 WAVELENGTH SELECTIVE ABSORPTION FILTER AND DISPLAY DEVICE FUJIFILM CORPORATION (JP) 2023-09-14 US disclosed
CN-116568763-A Wavelength selective absorption filter and display device 富士胶片株式会社 2023-08-08 CN disclosed
WO-2022138925-A1 WAVELENGTH-SELECTIVE ABSORPTION FILTER AND DISPLAY DEVICE 富士フイルム株式会社 2022-06-30 WO disclosed
EP-2209547-B1 OZONOLYSIS REACTIONS IN LIQUID CO2 AND CO2-EXPANDED SOLVENTS UNIV KANSAS (US) 2018-06-20 EP disclosed
US-9354356-B2 Polymer film, and optically-compensatory film, polarizer and liquid-crystal display device comprising the same FUJIFILM CORPORATION (JP) 2016-05-31 US disclosed
US-9091804-B2 Polymer film, and optically-compensatory film, polarizer and liquid-crystal display device comprising the same FUJIFILM CORPORATION (JP) 2015-07-28 US disclosed
US-6153794-A Phosphine sulfide, a manufacturing process therefor and use thereof MITSUI CHEMICALS, INC. (JP) 2000-11-28 US disclosed
CN-1262276-A Phosphine sulfide preparing process and use thereof MITSUI CHEMICALS INC (JP) 2000-08-09 CN disclosed
EP-0972776-A1 A phosphine sulfide, a manufacturing process therefor and a use thereof Mitsui Chemicals, Inc. (JP) 2000-01-19 EP disclosed
EP-0713855-A1 Novel liquid fatty acid derivatives NEW JAPAN CHEMICAL CO.,LTD. (JP) 1996-05-29 EP disclosed
EP-0631607-A4 METHOD FOR LUBRICATING METAL-METAL CONTACT SYSTEMS IN METALWORKING OPERATIONS WITH CYCLOHEXYL ESTERS. QUAKER CHEM CORP (US) 1995-11-15 EP disclosed
EP-0631607-A1 METHOD FOR LUBRICATING METAL-METAL CONTACT SYSTEMS IN METALWORKING OPERATIONS WITH CYCLOHEXYL ESTERS QUAKER CHEMICAL CORPORATION (US) 1995-01-04 EP disclosed
WO-1994017162-A1 METHOD FOR LUBRICATING METAL-METAL CONTACT SYSTEMS IN METALWORKING OPERATIONS WITH CYCLOHEXYL ESTERS QUAKER CHEMICAL CORPORATION (US) 1994-08-04 WO disclosed
US-5318711-A For high pressure, high speed cold working of metals and/or alloys QUAKER CHEMICAL CORPORATION (US) 1994-06-07 US disclosed
US-4364743-A ESTER AND MIDDLE OIL ERNER WILLIAM E 1982-12-21 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-12619006-B2 Wavelength selective absorption filter and display device STRA6, SULT1A1, SLC7A1 NAAA 1052/4885TERT 3862/4885CYP1A2 827/4885

“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.