Predicted protein targets (top 11)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | DGAT1 | O75907 | 1/20 | 0.41 |
| ▸ | TSHR | P16473 | 3/20 | 0.33 |
| ▸ | KCNN4 | O15554 | 1/20 | 0.32 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.32 |
| ▸ | POLB | P06746 | 1/20 | 0.31 |
| ▸ | HSD17B10 | Q99714 | 1/20 | 0.31 |
| ▸ | MGAM | O43451 | 1/20 | 0.31 |
| ▸ | GAA | P10253 | 1/20 | 0.31 |
| ▸ | SI | P14410 | 1/20 | 0.31 |
| ▸ | MGAM2 | Q2M2H8 | 1/20 | 0.31 |
| ▸ | TET2 | Q6N021 | 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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL17574065 | 0.89 | DGAT1 (0.44) | DGAT1TSHRKCNN4ALDH1A1HSD17B10 | |
| SCHEMBL17124363 | 0.82 | DGAT1 (0.39) | DGAT1TSHRKCNN4ALDH1A1 | |
| SCHEMBL10078130 | 0.82 | DGAT1 (0.39) | DGAT1TSHRKCNN4ALDH1A1 | |
| SCHEMBL12690945 | 0.82 | DGAT1 (0.39) | DGAT1TSHRKCNN4ALDH1A1 | |
| SCHEMBL12690948 | 0.82 | DGAT1 (0.39) | DGAT1TSHRKCNN4ALDH1A1 | |
| SCHEMBL10093742 | 0.82 | DGAT1 (0.39) | DGAT1TSHRKCNN4ALDH1A1 | |
| SCHEMBL10027501 | 0.82 | DGAT1 (0.39) | DGAT1TSHRKCNN4ALDH1A1 | |
| SCHEMBL16807263 | 0.82 | DGAT1 (0.39) | DGAT1TSHRKCNN4ALDH1A1 | |
| SCHEMBL28447095 | 0.81 | — | — | |
| SCHEMBL12449512 | 0.81 | PRSS1 (0.37) | TSHR |
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 41 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-109721448-B | Method for preparing alkyl derivative by liquid-phase oxidative carbonylation of methyl tert-butyl ether | 河北工业大学 | 2021-06-08 | — | — | CN | claimed |
| US-6818049-B1 | HALOGEN FREE INDUSTRIAL SOLVENT FORMULATION; LOW REACTIVITY TO OZONE FORMATION | EXXONMOBIL CHEMICAL PATENTS INC. | 2004-11-16 | — | — | US | claimed |
| US-6506243-B1 | Industrial solvents; dialkyl carbonates, alkyl acetates, dioxolanes, pivalates, isobutyrates, nitriles | EXXONMOBIL CHEMICAL PATENTS INC. | 2003-01-14 | — | — | US | claimed |
| WO-2002064687-A1 | ENVIRONMENTALLY PREFERRED FLUIDS AND FLUID BLENDS | EXXONMOBIL CHEMICAL PATENTS INC. (US) | 2002-08-22 | — | — | WO | claimed |
| EP-1090085-A1 | ENVIRONMENTALLY PREFERRED FLUIDS AND FLUID BLENDS | EXXON CHEMICAL PATENTS INC. (US) | 2001-04-11 | — | — | EP | claimed |
| WO-1999057217-A1 | ENVIRONMENTALLY PREFERRED FLUIDS AND FLUID BLENDS | EXXON CHEMICAL PATENTS INC. (US) | 1999-11-11 | — | — | WO | claimed |
| CN-110605145-B | Catalyst for methyl hydrogen esterification reaction and method for preparing isononanoic acid | 万华化学集团股份有限公司 | 2022-04-22 | — | — | CN | disclosed |
| CN-109721448-B | Method for preparing alkyl derivative by liquid-phase oxidative carbonylation of methyl tert-butyl ether | 河北工业大学 | 2021-06-08 | — | — | CN | disclosed |
| EP-2654794-B1 | MATERIALS AND METHODS FOR CONJUGATING A WATER SOLUBLE FATTY ACID DERIVATIVE TO A PROTEIN | Baxalta GmbH (CH) | 2020-03-04 | — | — | EP | disclosed |
| CN-110605145-A | Catalyst for methyl hydrogen esterification reaction and method for preparing isononanoic acid | 万华化学集团股份有限公司 | 2019-12-24 | — | — | CN | disclosed |
| EP-2902212-B1 | IMAGE FORMATION METHOD | FUJIFILM CORP (JP) | 2017-09-06 | — | — | EP | disclosed |
| US-20170210734-A1 | Substituted Azaspiro(4.5)Decane Derivatives | GRUENENTHAL GMBH (DE) | 2017-07-27 | — | — | US | disclosed |
| US-9291893-B2 | Resist composition and method for producing resist pattern | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2016-03-22 | — | — | US | disclosed |
| WO-2002064687-A1 | ENVIRONMENTALLY PREFERRED FLUIDS AND FLUID BLENDS | EXXONMOBIL CHEMICAL PATENTS INC. (US) | 2002-08-22 | — | — | WO | disclosed |
| US-20020002933-A1 | Environmentally preferred fluids and fluid blends | YEZRIELEV ALBERT ILYA (US) | 2002-01-10 | — | — | US | disclosed |
| US-20010041808-A1 | Production of esters | EXXONMOBIL CHEMICAL PATENTS INC. | 2001-11-15 | — | — | US | disclosed |
| US-6280519-B1 | Environmentally preferred fluids and fluid blends | EXXON CHEMICAL PATENTS INC. | 2001-08-28 | — | — | US | disclosed |
| WO-2001047861-A1 | PRODUCTION OF ESTERS | EXXONMOBIL CHEMICAL PATENTS INC. (US) | 2001-07-05 | — | — | WO | disclosed |
| EP-1090085-A1 | ENVIRONMENTALLY PREFERRED FLUIDS AND FLUID BLENDS | EXXON CHEMICAL PATENTS INC. (US) | 2001-04-11 | — | — | EP | disclosed |
| WO-1999057217-A1 | ENVIRONMENTALLY PREFERRED FLUIDS AND FLUID BLENDS | EXXON CHEMICAL PATENTS INC. (US) | 1999-11-11 | — | — | WO | 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.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20170210734-A1 | Substituted Azaspiro(4.5)Decane Derivatives | OPRL1, OPRM1, OPRD1 | DGAT1 2614/4885TSHR 1767/4885KCNN4 2070/4885 |
“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.