Predicted protein targets (top 5)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ACLY | P53396 | 2/20 | 0.37 |
| ▸ | THRB | P10828 | 1/20 | 0.36 |
| ▸ | HDAC4 | P56524 | 1/20 | 0.31 |
| ▸ | HDAC6 | Q9UBN7 | 1/20 | 0.31 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.31 |
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL10340794 | 0.81 | HDAC4 (0.31) | HDAC4HDAC6ALDH1A1 | |
| SCHEMBL16658459 | 0.79 | TSHR (0.32) | HDAC4HDAC6ALDH1A1 | |
| SCHEMBL7263038 | 0.79 | CES2 (0.39) | ALDH1A1 | |
| SCHEMBL8769260 | 0.77 | ACLY (0.34) | ACLYTHRBALDH1A1 | |
| SCHEMBL12762097 | 0.76 | ACLY (0.37) | ACLYTHRB | |
| SCHEMBL7262111 | 0.76 | CES2 (0.49) | — | |
| SCHEMBL9017248 | 0.75 | — | — | |
| SCHEMBL16653310 | 0.73 | THRB (0.38) | ACLYTHRB | |
| SCHEMBL11268258 | 0.73 | PTPN1 (0.34) | ALDH1A1 | |
| SCHEMBL11185102 | 0.73 | — | — |
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 20 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-12319594-B2 | Composition and method for capture and degradation of PFAS | BATTELLE MEMORIAL INSTITUTE (US) | 2025-06-03 | — | — | US | disclosed |
| US-11891313-B2 | Fluidic impedance platform for in-situ detection and quantification of PFAS in groundwater | BATTELLE MEMORIAL INSTITUTE (US) | 2024-02-06 | — | — | US | disclosed |
| WO-2023122143-A1 | METHODS AND COMPOSITIONS FOR PFAS DEFLUORINATION DETECTION | GINKGO BIOWORKS, INC. (US) | 2023-06-29 | — | — | WO | disclosed |
| US-20230089418-A1 | COMPOSITION AND METHOD FOR CAPTURE AND DEGRADATION OF PFAS | BATTELLE MEMORIAL INSTITUTE (US) | 2023-03-23 | — | — | US | disclosed |
| US-11518689-B2 | Composition and method for capture and degradation of PFAS | BATTELLE MEMORIAL INSTITUTE (US) | 2022-12-06 | — | — | US | disclosed |
| US-20220252536-A1 | FLUIDIC IMPEDANCE PLATFORM FOR IN-SITU DETECTION AND QUANTIFICATION OF PFAS IN GROUNDWATER | BATTELLE MEMORIAL INSTITUTE (US) | 2022-08-11 | — | — | US | disclosed |
| US-20210318613-A9 | RADIATION-SENSITIVE RESIN COMPOSITION AND RESIST PATTERN-FORMING METHOD | JSR CORPORATION (JP) | 2021-10-14 | — | — | US | disclosed |
| US-20200393761-A1 | RADIATION-SENSITIVE RESIN COMPOSITION AND RESIST PATTERN-FORMING METHOD | JSR CORPORATION (JP) | 2020-12-17 | — | — | US | disclosed |
| EP-2094633-B1 | HYDROFLUOROETHER COMPOUNDS AND PROCESSES FOR THEIR PREPARATION AND USE | 3M INNOVATIVE PROPERTIES CO (US) | 2017-08-02 | — | — | EP | disclosed |
| US-8193397-B2 | Comprising terminal (perfluoroalkyl) groups and intervening oxytetrafluoroethylidene moiety bonded through its central carbon atom to an alkoxy- or fluoroalkoxy-substituted fluoromethylene moiety, each of said terminal having at least one catenated heteroatom; ozone depletion potential, global warming | 3M INNOVATIVE PROPERTIES COMPANY (US) | 2012-06-05 | — | — | US | disclosed |
| EP-2094633-A1 | HYDROFLUOROETH R COMPOUNDS AND PROCESSES FOR THEIR PREPARATION AND USE | 3M Innovative Properties Company (US) | 2009-09-02 | — | — | EP | disclosed |
| WO-2008070606-A1 | HYDROFLUOROETHΞR COMPOUNDS AND PROCESSES FOR THEIR PREPARATION AND USE | 3M INNOVATIVE PROPERTIES COMPANY (US) | 2008-06-12 | — | — | WO | disclosed |
| US-20080139683-A1 | HYDROFLUOROETHER COMPOUNDS AND PROCESSES FOR THEIR PREPARATION AND USE | 3M INNOVATIVE PROPERTIES COMPANY | 2008-06-12 | — | — | US | disclosed |
| EP-1253133-B1 | Process of preparing halogenated esters | 3M INNOVATIVE PROPERTIES CO (US) | 2004-10-06 | — | — | EP | disclosed |
| US-6703520-B2 | REACTING AN ESTER WITH HALOGENATED UNSATURATED COMPOUND | 3M INNOVATIVE PROPERTIES COMPANY | 2004-03-09 | — | — | US | disclosed |
| US-20020177729-A1 | Process of preparing halogenated esters | 3M INNOVATIVE PROPERTIES COMPANY | 2002-11-28 | — | — | US | disclosed |
| WO-2002085837-A1 | PROCESS OF PREPARING HALOGENATED ESTERS | 3M INNOVATIVE PROPERTIES COMPANY (US) | 2002-10-31 | — | — | WO | disclosed |
| EP-1253133-A1 | Process of preparing halogenated esters | 3M Innovative Properties Company (US) | 2002-10-30 | — | — | EP | disclosed |
| US-5206422-A | Process for preparation of fluorinated carbonyl compounds | THE DOW CHEMICAL COMPANY (US) | 1993-04-27 | — | — | US | disclosed |
| US-4357282-A | CONTACTING A FLUORINATED METHYL OR ETHYL EHTER HAVING A METHOXYLATED CARBON ATOM WITH A LEWIS ACID CATALYST ACYLATION | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 1982-11-02 | — | — | 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.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20080139683-A1 | HYDROFLUOROETHER COMPOUNDS AND PROCESSES FOR THEIR PREPARATION AND USE | OGFOD1, AQP3, FOS | ACLY 4386/4885THRB 909/4885HDAC4 3666/4885 |
| US-20020177729-A1 | Process of preparing halogenated esters | ELOVL3, ELOVL1, EBP | ACLY 3686/4885THRB 1989/4885HDAC4 1245/4885 |
“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.