Predicted protein targets (top 15)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | MAOA | P21397 | 1/20 | 0.48 |
| ▸ | MAOB | P27338 | 1/20 | 0.48 |
| ▸ | OPRM1 | P35372 | 1/20 | 0.41 |
| ▸ | OPRK1 | P41145 | 1/20 | 0.41 |
| ▸ | OPRL1 | P41146 | 1/20 | 0.41 |
| ▸ | SLC6A4 | P31645 | 3/20 | 0.40 |
| ▸ | SLC6A2 | P23975 | 1/20 | 0.40 |
| ▸ | SLC6A3 | Q01959 | 1/20 | 0.40 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.40 |
| ▸ | ADRB2 | P07550 | 1/20 | 0.40 |
| ▸ | HTT | P42858 | 1/20 | 0.40 |
| ▸ | ELANE | P08246 | 1/20 | 0.39 |
| ▸ | HTR2A | P28223 | 1/20 | 0.39 |
| ▸ | HTR2C | P28335 | 1/20 | 0.39 |
| ▸ | KMT2A | Q03164 | 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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL27488335 | 1.00 | MAOA (0.48) | MAOAMAOBOPRM1OPRK1OPRL1 | |
| SCHEMBL5639001 | 0.98 | MAOA (0.50) | MAOAMAOBOPRM1OPRK1OPRL1 | |
| SCHEMBL6672640 | 0.93 | MAOA (0.50) | MAOAMAOBOPRM1OPRK1OPRL1 | |
| SCHEMBL28259694 | 0.89 | OPRL1 (0.41) | MAOAMAOBOPRM1OPRK1OPRL1 | |
| SCHEMBL2374703 | 0.89 | MAOA (0.54) | MAOAMAOBOPRM1OPRK1OPRL1 | |
| SCHEMBL11365074 | 0.83 | MAOA (0.48) | MAOAMAOBOPRM1OPRK1OPRL1 | |
| SCHEMBL11817033 | 0.81 | ACAT2 (0.39) | KMT2A | |
| SCHEMBL28161193 | 0.79 | MAOA (0.48) | MAOAMAOBOPRM1OPRK1OPRL1 | |
| SCHEMBL18114513 | 0.79 | OPRM1 (0.42) | MAOAMAOBOPRM1OPRL1SLC6A3 | |
| SCHEMBL13757097 | 0.79 | TSHR (0.46) | MAOAMAOBOPRM1OPRK1OPRL1 |
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 264 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-4302350-A2 | LIQUID CARBON-NEUTRAL ENERGY FACILITY SYSTEM | The Claire Technologies Corporation (US) | 2024-01-10 | — | — | EP | claimed |
| US-11848468-B2 | Liquid carbon-neutral energy facility system | CLAIRE Technologies (US) | 2023-12-19 | — | — | US | claimed |
| EP-4225694-A1 | CARBON-NEUTRAL PROCESS FOR GENERATING ELECTRICITY | The Claire Technologies Corporation (US) | 2023-08-16 | — | — | EP | claimed |
| WO-2022203824-A2 | LIQUID CARBON-NEUTRAL ENERGY FACILITY SYSTEM | The Claire Technologies Corporation (US) | 2022-09-29 | — | — | WO | claimed |
| US-20220285714-A1 | LIQUID CARBON-NEUTRAL ENERGY FACILITY SYSTEM | The Claire Technologies Corporation (US) | 2022-09-08 | — | — | US | claimed |
| WO-2022076219-A1 | CARBON-NEUTRAL PROCESS FOR GENERATING ELECTRICITY | The Claire Technologies Corporation (US) | 2022-04-14 | — | — | WO | claimed |
| US-11236028-B2 | Production and use of 3,4′ and 4,4′-dimethylbiphenyl isomers | EXXONMOBIL CHEMICAL PATENTS INC. (US) | 2022-02-01 | — | — | US | claimed |
| US-20210053890-A1 | Production and Use of 3,4' and 4,4'-Dimethylbiphenyl Isomers | EXXONMOBIL CHEMICAL PATENTS INC. | 2021-02-25 | — | — | US | claimed |
| US-20200325096-A1 | Oxidation of Methyl-substituted Biphenyl Compounds | EXXONMOBIL CHEMICAL PATENTS INC. | 2020-10-15 | — | — | US | claimed |
| US-10710945-B2 | Aromatic compositions and methods for obtaining them | EXXONMOBIL CHEMICAL PATENTS INC. (US) | 2020-07-14 | — | — | US | claimed |
| WO-2014159101-A1 | METHYL-SUBSTITUTED BIPHENYL COMPOUNDS, THEIR PRODUCTION AND THEIR USE IN THE MANUFACTURE OF PLASTICIZERS | EXXONMOBIL CHEMICAL PATENTS INC. (US) | 2014-10-02 | — | — | WO | claimed |
| WO-2014159100-A1 | (METHYLCYCLOHEXYL)TOLUENE ISOMER MIXTURES, THEIR PRODUCTION AND THEIR USE IN THE MANUFACTURE OF PLASTICIZERS | EXXONMOBIL CHEMICAL PATENTS INC. (US) | 2014-10-02 | — | — | WO | claimed |
| US-20140275605-A1 | (Methylcyclohexyl)Toluene Isomer Mixtures,Their Production and Their Use in the Manufacture of Plasticizers | EXXONMOBIL CHEMICAL PATENTS INC. | 2014-09-18 | — | — | US | claimed |
| US-20140275606-A1 | Methyl-Substituted Biphenyl Compounds, Their Production and Their Use in the Manufacture of Plasticizers | EXXONMOBIL CHEMICAL PATENTS INC. | 2014-09-18 | — | — | US | claimed |
| US-20140275607-A1 | Methyl-Substituted Biphenyl Compounds, Their Production and Their Use in the Manufacture of Plasticizers | EXXONMOBIL CHEMICAL PATENTS INC. | 2014-09-18 | — | — | US | claimed |
| US-20140275609-A1 | Methyl-Substituted Biphenyl Compounds, Their Production and Their Use in the Manufacture of Plasticizers | EXXONMOBIL CHEMICAL PATENTS INC. | 2014-09-18 | — | — | US | claimed |
| US-20050215433-A1 | Aromatic fluid as agricultural solvent | EXXONMOBIL CHEMICAL PATENTS INC. | 2005-09-29 | — | — | US | claimed |
| US-20050054819-A1 | Cycloalkyl ketoamides derivatives useful as cathepsin k inhibitors | SMITHKLINE BEECHAM CORPORATION | 2005-03-10 | — | — | US | claimed |
| EP-1465862-A1 | CYCLOALKYL KETOAMIDES DERIVATIVES USEFUL AS CATHEPSIN K INHIBITORS | SmithKline Beecham Corporation (US) | 2004-10-13 | — | — | EP | claimed |
| WO-2003062192-A1 | CYCLOALKYL KETOAMIDES DERIVATIVES USEFUL AS CATHEPSIN K INHIBITORS | SMITHKLINE BEECHAM CORPORATION (US) | 2003-07-31 | — | — | WO | claimed |
Patent text — is the patent's own abstract consistent with the prediction?
For each of this compound's patents that has machine-readable text (10 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-20140275605-A1 | (Methylcyclohexyl)Toluene Isomer Mixtures,Their Production and Their Use in the Manufacture of Plasticizers | DDT, CYP3A4, TERT | MAOA 2360/4885MAOB 2678/4885OPRM1 413/4885 |
| US-20050054819-A1 | Cycloalkyl ketoamides derivatives useful as cathepsin k inhibitors | CTSK, CTSS, CTSE | MAOA 2083/4885MAOB 2350/4885OPRM1 4338/4885 |
| US-20140275606-A1 | Methyl-Substituted Biphenyl Compounds, Their Production and Their Use in the Manufacture of Plasticizers | BMI1, DNMT3B, DNMT1 | MAOA 465/4885MAOB 194/4885OPRM1 2645/4885 |
| US-20200325096-A1 | Oxidation of Methyl-substituted Biphenyl Compounds | CYP1B1, CYP1A1, CYP4B1 | MAOA 238/4885MAOB 79/4885OPRM1 357/4885 |
| US-20140275607-A1 | Methyl-Substituted Biphenyl Compounds, Their Production and Their Use in the Manufacture of Plasticizers | DNMT3B, DNMT1, BMI1 | MAOA 488/4885MAOB 219/4885OPRM1 1880/4885 |
| US-20210053890-A1 | Production and Use of 3,4' and 4,4'-Dimethylbiphenyl Isomers | BMP4, DBF4, EIF4B | MAOA 2449/4885MAOB 952/4885OPRM1 3097/4885 |
| US-10710945-B2 | Aromatic compositions and methods for obtaining them | AHR, ARNT, TDO2 | MAOA 842/4885MAOB 570/4885OPRM1 4139/4885 |
| US-20050215433-A1 | Aromatic fluid as agricultural solvent | DDT, AHR, ALB | MAOA 762/4885MAOB 952/4885OPRM1 4523/4885 |
| US-11236028-B2 | Production and use of 3,4′ and 4,4′-dimethylbiphenyl isomers | BMP4, DBF4, EIF4B | MAOA 2459/4885MAOB 945/4885OPRM1 3137/4885 |
| US-20140275609-A1 | Methyl-Substituted Biphenyl Compounds, Their Production and Their Use in the Manufacture of Plasticizers | DDT, HPD, AHR | MAOA 388/4885MAOB 295/4885OPRM1 948/4885 |
“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.