Predicted protein targets (top 8)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CHRM2 | P08172 | 3/20 | 0.47 |
| ▸ | CHRM4 | P08173 | 3/20 | 0.47 |
| ▸ | CHRM5 | P08912 | 3/20 | 0.47 |
| ▸ | CHRM1 | P11229 | 3/20 | 0.47 |
| ▸ | CHRM3 | P20309 | 3/20 | 0.47 |
| ▸ | P2RX7 | Q99572 | 9/20 | 0.39 |
| ▸ | PER2 | O15055 | 6/20 | 0.39 |
| ▸ | CRY2 | Q49AN0 | 1/20 | 0.36 |
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 | |
|---|---|---|---|---|
| SCHEMBL17946144 | 0.94 | — | — | |
| SCHEMBL2379257 | 0.94 | — | — | |
| SCHEMBL10587336 | 0.82 | CHRM2 (0.45) | CHRM2CHRM4CHRM5CHRM1CHRM3 | |
| Hydrochloric Acid SCHEMBL3337122 | 0.78 | CHRM2 (0.47) | CHRM2CHRM4CHRM5CHRM1CHRM3 | |
| SCHEMBL4330615 | 0.78 | CHRM2 (0.49) | CHRM2CHRM4CHRM5CHRM1CHRM3 | |
| Hydrochloric Acid SCHEMBL1948450 | 0.76 | CHRM2 (0.44) | CHRM2CHRM4CHRM5CHRM1CHRM3 | |
| SCHEMBL11463019 | 0.75 | — | — | |
| SCHEMBL11479479 | 0.75 | — | — | |
| SCHEMBL11288962 | 0.75 | — | — | |
| SCHEMBL13232234 | 0.75 | — | — |
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 19 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20100204522-A1 | PROCESS FOR MAKING DIBUTYL ETHERS FROM ISOBUTANOL | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2010-08-12 | — | — | US | disclosed |
| US-20100197975-A1 | PROCESS FOR MAKING DIALKYL ETHERS FROM ALCOHOLS | E.I. DU PONT DE NEMOURS & COMPANY (DE) | 2010-08-05 | — | — | US | disclosed |
| US-20100179355-A1 | PROCESSES FOR MAKING DIALKYL ETHERS FROM ALCOHOLS | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2010-07-15 | — | — | US | disclosed |
| US-7625941-B2 | N-substituted pyrrolidinone having a separated pendant ammonium cation by a variable length alkyl spacer and fluoroalkyl sulfonate anions; environmentally friendly solvent; catalysts for reactions, including nitration, acylation, esterification, etherification | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-12-01 | — | — | US | disclosed |
| EP-1940761-B1 | PREPARATION OF POLYTRIMETHYLENE ETHER GLYCOL AND COPOLYMERS THEREOF | DU PONT (US) | 2009-05-06 | — | — | EP | disclosed |
| EP-1951647-A2 | OLEFIN ISOMERIZATION | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2008-08-06 | — | — | EP | disclosed |
| US-7405330-B2 | Preparation of polytrimethylene ether glycol and copolymers thereof | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2008-07-29 | — | — | US | disclosed |
| US-7402711-B2 | Preparation of poly(tetramethylene) glycol | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2008-07-22 | — | — | US | disclosed |
| EP-1940761-A1 | PREPARATION OF POLYTRIMETHYLENE ETHER GLYCOL AND COPOLYMERS THEREOF | E.I.Du pont de nemours and company (US) | 2008-07-09 | — | — | EP | disclosed |
| US-7314962-B2 | Alkylation of aromatic compounds | E. I. DU PONT DE NEMOURS & CO. (US) | 2008-01-01 | — | — | US | disclosed |
| US-20070123737-A1 | Preparation of polytrimethylene ether glycol and copolymers thereof | E. I. DU PONT DE NEMOURS AND COMPANY | 2007-05-31 | — | — | US | disclosed |
| WO-2007050490-A2 | OLEFIN ISOMERIZATION | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2007-05-03 | — | — | WO | disclosed |
| US-20070100192-A1 | Olefin isomerization | E. I. DU PONT DE NEMOURS AND COMPANY | 2007-05-03 | — | — | US | disclosed |
| WO-2007038362-A1 | PREPARATION OF POLYTRIMETHYLENE ETHER GLYCOL AND COPOLYMERS THEREOF | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2007-04-05 | — | — | WO | disclosed |
| US-20070066853-A1 | Preparation of poly(tetramethylene) glycol | E. I. DU PONT DE NEMOURS AND COMPANY | 2007-03-22 | — | — | US | disclosed |
| US-20070066834-A1 | Ionic liquids | E. I. DU PONT DE NEMOURS AND COMPANY | 2007-03-22 | — | — | US | disclosed |
| US-7157588-B2 | Ionic liquids | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2007-01-02 | — | — | US | disclosed |
| US-20060235230-A1 | Based on an N-substituted pyrrolidinone having a pendant ammonium cation that is separated from the pyrrolidone ring by a variable length alkyl spacer; use as solvents, catalysts; can be readily prepared from levulinic acid or derivatives obtained from the hydrolysis of inexpensive biomass feedstock | THE CHEMOURS COMPANY FC, LLC | 2006-10-19 | — | — | US | disclosed |
| US-20060235249-A1 | Alkylation of aromatic compounds | E. I. DU PONT DE NEMOURS AND COMPANY | 2006-10-19 | — | — | 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 (9 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-20070066853-A1 | Preparation of poly(tetramethylene) glycol | PARG, PUF60, TPR | CHRM2 4672/4885CHRM4 4575/4885CHRM5 3941/4885 |
| US-20100179355-A1 | PROCESSES FOR MAKING DIALKYL ETHERS FROM ALCOHOLS | ADH1C, DAGLA, DCLK1 | CHRM2 3356/4885CHRM4 3134/4885CHRM5 3600/4885 |
| US-20070066834-A1 | Ionic liquids | NUP205, PML, AQP4 | CHRM2 4192/4885CHRM4 4264/4885CHRM5 3308/4885 |
| US-20070123737-A1 | Preparation of polytrimethylene ether glycol and copolymers thereof | PARG, PTGES3, PGD | CHRM2 3146/4885CHRM4 3594/4885CHRM5 3264/4885 |
| US-20060235249-A1 | Alkylation of aromatic compounds | TYR, ALK, AHR | CHRM2 1525/4885CHRM4 752/4885CHRM5 941/4885 |
| US-20060235230-A1 | Based on an N-substituted pyrrolidinone having a pendant ammonium cation that is separated from the pyrrolidone ring by a variable length alkyl spacer; use as solvents, catalysts; can be readily prepared from levulinic acid or derivatives obtained from the hydrolysis of inexpensive biomass feedstock | ALAD, ASS1, ADSL | CHRM2 3911/4885CHRM4 4063/4885CHRM5 2812/4885 |
| US-20070100192-A1 | Olefin isomerization | OSBP, OXER1, OSBPL3 | CHRM2 3157/4885CHRM4 2323/4885CHRM5 3238/4885 |
| US-20100204522-A1 | PROCESS FOR MAKING DIBUTYL ETHERS FROM ISOBUTANOL | EBP, PPIP5K2, PCBP1 | CHRM2 4171/4885CHRM4 3516/4885CHRM5 3580/4885 |
| US-20100197975-A1 | PROCESS FOR MAKING DIALKYL ETHERS FROM ALCOHOLS | ADH1C, DCLK1, DCLK3 | CHRM2 1763/4885CHRM4 1254/4885CHRM5 2485/4885 |
“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.