Predicted protein targets (top 4)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CA1 | P00915 | 2/20 | 0.36 |
| ▸ | CA2 | P00918 | 2/20 | 0.36 |
| ▸ | KCNH2 | Q12809 | 6/20 | 0.32 |
| ▸ | ACHE | P22303 | 2/20 | 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 | |
|---|---|---|---|---|
| Hydrochloric Acid SCHEMBL4622494 | 0.99 | CA1 (0.35) | CA1CA2KCNH2ACHE | |
| Trifluoromethanesulfonic Acid SCHEMBL707413 | 0.88 | KCNH2 (0.41) | CA1CA2KCNH2ACHE | |
| Sulfuric Acid SCHEMBL4247474 | 0.84 | CA1 (0.44) | CA1CA2 | |
| Trifluoromethanesulfonic Acid SCHEMBL1330197 | 0.83 | CA1 (0.47) | CA1CA2KCNH2ACHE | |
| Trifluoromethanesulfonic Acid SCHEMBL1329120 | 0.83 | CA1 (0.47) | CA1CA2KCNH2ACHE | |
| Trifluoromethanesulfonic Acid SCHEMBL711975 | 0.83 | CA1 (0.47) | CA1CA2KCNH2ACHE | |
| Trifluoromethanesulfonic Acid SCHEMBL1329985 | 0.83 | CA1 (0.47) | CA1CA2KCNH2ACHE | |
| SCHEMBL4247119 | 0.82 | CA1 (0.43) | CA1CA2 | |
| Sulfuric Acid SCHEMBL21195055 | 0.82 | CA1 (0.43) | CA1CA2 | |
| SCHEMBL17162136 | 0.81 | CA1 (0.35) | CA1CA2KCNH2ACHE |
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 88 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-1954680-B1 | IONIC LIQUIDS | DU PONT (US) | 2012-05-23 | — | — | EP | claimed |
| US-20120011886-A1 | IONIC COMPOUNDS IN LITHIUM BROMIDE/WATER ABSORPTION CYCLE SYSTEMS | E. I. DU PONT DE NEMOURS AND COMPANY | 2012-01-19 | — | — | US | claimed |
| US-20110195212-A1 | Flame Retardant Polycarbonate Compositions | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2011-08-11 | — | — | US | claimed |
| US-20100204521-A1 | PROCESSES FOR MAKING DIBUTYL ETHERS FROM 2-BUTANOL | E. I. DU PONT DE NEMOURS AND COMPANY | 2010-08-12 | — | — | US | claimed |
| US-20100197974-A1 | PROCESSES FOR MAKING DIALKYL ETHERS FROM ALCOHOLS | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2010-08-05 | — | — | US | claimed |
| EP-2205545-A2 | PROCESSES FOR MAKING DIBUTYL ETHERS FROM 2-BUTANOL | E. I. du Pont de Nemours and Company (US) | 2010-07-14 | — | — | EP | claimed |
| US-20100174120-A1 | PROCESSES FOR MAKING DIBUTYL ETHERS FROM ISOBUTANOL | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2010-07-08 | — | — | US | claimed |
| EP-2185494-A2 | PROCESSES FOR MAKING DIBUTYL ETHERS FROM ISOBUTANOL | E. I. du Pont de Nemours and Company (US) | 2010-05-19 | — | — | EP | claimed |
| US-7544813-B2 | Ionic liquids | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-06-09 | — | — | US | claimed |
| EP-1940914-B1 | PREPARATION OF POLYTRIMETHYLENE ETHER GLYCOL AND COPOLYMERS THEREOF | DU PONT (US) | 2009-05-13 | — | — | EP | claimed |
| US-7528287-B2 | Preparation of poly(tetramethylene) glycol | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-05-05 | — | — | US | claimed |
| WO-2009032961-A2 | PROCESSES FOR MAKING DIBUTYL ETHERS FROM 2-BUTANOL | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-03-12 | — | — | WO | claimed |
| WO-2009032962-A2 | PROCESSES FOR MAKING DIBUTYL ETHERS FROM ISOBUTANOL | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-03-12 | — | — | WO | claimed |
| US-20080221241-A1 | Flame Retardant Polycarbonate Compositions | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2008-09-11 | — | — | US | claimed |
| US-7238772-B2 | Preparation of polytrimethylene ether glycol and copolymers thereof | E. I. DU PONT DE NEMOURS AND COMPANY (DE) | 2007-07-03 | — | — | US | claimed |
| US-20070100184-A1 | Alkylation of aromatic compounds | E. I. DU PONT DE NEMOURS AND COMPANY | 2007-05-03 | — | — | US | claimed |
| US-20070066822-A1 | Ionic liquids | THE CHEMOURS COMPANY FC, LLC | 2007-03-22 | — | — | US | claimed |
| US-20070066852-A1 | Preparation of poly(tetramethylene) glycol | THE CHEMOURS COMPANY FC, LLC | 2007-03-22 | — | — | US | claimed |
| US-20070066854-A1 | Preparation of polytrimethylene ether glycol and copolymers thereof | THE CHEMOURS COMPANY FC, LLC | 2007-03-22 | — | — | US | claimed |
| EP-2118194-B1 | FLAME RETARDANT POLYCARBONATE COMPOSITIONS | DU PONT (US) | 2014-12-03 | — | — | EP | disclosed |
| US-20140286849-A1 | Mixtures of Ammonia and Ionic Liquids | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2014-09-25 | — | — | US | disclosed |
| US-8715521-B2 | Absorption cycle utilizing ionic liquid as working fluid | E I DU PONT DE NEMOURS AND COMPANY (US) | 2014-05-06 | — | — | US | disclosed |
| US-8707720-B2 | Hybrid vapor compression-absorption cycle | E I DU PONT DE NEMOURS AND COMPANY (US) | 2014-04-29 | — | — | US | disclosed |
| US-8628644-B2 | Utilizing ionic liquids for hydrofluorocarbon separation | E I DU PONT NEMOURS AND COMPANY (US) | 2014-01-14 | — | — | US | disclosed |
| US-8568608-B2 | Vapor compression cycle utilizing ionic liquid as compressor lubricant | E I DU PONT DE NEMOURS AND COMPANY (US) | 2013-10-29 | — | — | US | disclosed |
| US-20130231448-A1 | PROCESS FOR SEPARATION OF TETRAFLUOROETHYLENE FROM CARBON DIOXIDE USING IONIC LIQUIDS | E I DU PONT DE NEMOURS AND COMPANY (US) | 2013-09-05 | — | — | US | disclosed |
| US-8313558-B2 | Process for separation of tetrafluoroethylene from carbon dioxide using ionic liquids | E I DU PONT DE NEMOURS AND COMPANY (US) | 2012-11-20 | — | — | US | disclosed |
| EP-2129737-B1 | HEAT TRANSFER SYSTEMS USING MIXTURES OF POLYOLS AND IONIC LIQUIDS | DU PONT (US) | 2012-10-17 | — | — | EP | disclosed |
| EP-1954680-B1 | IONIC LIQUIDS | DU PONT (US) | 2012-05-23 | — | — | EP | disclosed |
| US-20120011886-A1 | IONIC COMPOUNDS IN LITHIUM BROMIDE/WATER ABSORPTION CYCLE SYSTEMS | E. I. DU PONT DE NEMOURS AND COMPANY | 2012-01-19 | — | — | US | disclosed |
| US-8075777-B2 | Process for the separation of diastereomers | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2011-12-13 | — | — | US | disclosed |
| EP-1846535-B1 | ABSORPTION CYCLE UTILIZING IONIC LIQUID AS WORKING FLUID | DU PONT (US) | 2011-11-16 | — | — | EP | disclosed |
| EP-2368960-A1 | Vapor compression utilizing ionic liquid as compressor lubricant | E. I. du Pont de Nemours and Company (US) | 2011-09-28 | — | — | EP | disclosed |
| US-20110195212-A1 | Flame Retardant Polycarbonate Compositions | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2011-08-11 | — | — | US | disclosed |
| US-7947770-B2 | blend of polycarbonate resin prepared from diphenylcarbonate and 2,2-bis(4-hydroxyphenyl)propane; polytetrafluoroethylene antidrip agent; tetrafluoroalkylsulfonate or hexafluorodialkylsulfonimide salt of Na, K, Cs, Li or a pyridium, pydridazinium, phosphonium, ammonium etc.; protective devices | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2011-05-24 | — | — | US | disclosed |
| EP-2258787-A2 | Absorption cycle utilizing ionic liquid as working fluid | E. I. du Pont de Nemours and Company (US) | 2010-12-08 | — | — | EP | disclosed |
| US-7838679-B2 | Pyridinium cation and fluoroalkylsulfonate or fluoroalkylsulfonimide anions; solvents and catalysts | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2010-11-23 | — | — | US | disclosed |
| US-7838684-B2 | Fluorinated anions; cation selected from pyridinium, pyridazinium, pyrimidinium, pyrazinium, imidazolium, pyrazolium, thiazolium, oxazolium, triazolium, and phosphonium, ammonium cations with specified substituents, and anion is fluorinated sulfonium, sulfonylimide | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2010-11-23 | — | — | US | disclosed |
| US-7834189-B2 | Oxazolium cation and fluoroalkylsulfonate or fluoroalkylsulfonimide anions; solvents and catalysts | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2010-11-16 | — | — | US | disclosed |
| US-7834192-B2 | Ionic liquids | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2010-11-16 | — | — | US | disclosed |
| US-7829710-B2 | Ionic liquids | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2010-11-09 | — | — | US | disclosed |
| US-7829725-B2 | Ionic liquids | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2010-11-09 | — | — | US | disclosed |
| US-7829704-B2 | pyridazinium cation and fluoroalkylsulfonate or fluoroalkylsulfonimide anions; solvents and catalysts | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2010-11-09 | — | — | US | disclosed |
| US-7829722-B2 | Ionic liquids | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2010-11-09 | — | — | US | disclosed |
| US-7829706-B2 | Ionic liquids | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2010-11-09 | — | — | US | disclosed |
| US-7829739-B2 | Ionic liquids | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2010-11-09 | — | — | US | disclosed |
| US-20100257879-A1 | HYBRID VAPOR COMPRESSION-ABSORPTION CYCLE | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2010-10-14 | — | — | US | disclosed |
| US-20100204521-A1 | PROCESSES FOR MAKING DIBUTYL ETHERS FROM 2-BUTANOL | E. I. DU PONT DE NEMOURS AND COMPANY | 2010-08-12 | — | — | US | disclosed |
| US-20100197974-A1 | PROCESSES FOR MAKING DIALKYL ETHERS FROM ALCOHOLS | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2010-08-05 | — | — | US | disclosed |
| US-7765823-B2 | Cooling or heating systems using refrigerants and absorbentssuch as fluorocarbon gases in fluorinated ionic liquids;comprising an absorber, generator, condenser, pressure reductiondevice, evaporator, compressor, and conduit fromm the evaporator tothe absorber; efficiency | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2010-08-03 | — | — | US | disclosed |
| EP-2205545-A2 | PROCESSES FOR MAKING DIBUTYL ETHERS FROM 2-BUTANOL | E. I. du Pont de Nemours and Company (US) | 2010-07-14 | — | — | EP | disclosed |
| US-20100174120-A1 | PROCESSES FOR MAKING DIBUTYL ETHERS FROM ISOBUTANOL | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2010-07-08 | — | — | US | disclosed |
| US-20100155660-A1 | MIXTURES OF AMMONIA AND IONIC LIQUIDS | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2010-06-24 | — | — | US | disclosed |
| US-20100144994-A1 | Process for Separation of Tetrafluoroethylene from Carbon Dioxide using Ionic Liquids | PATENT RECORDS CENTER/DUPONT LEGAL (US) | 2010-06-10 | — | — | US | disclosed |
| US-20100132384-A1 | HEAT TRANSFER SYSTEMS USING MIXTURES OF POLYOLS AND ICONIC LIQUIDS | E. I. DU PONT DE NEMOURS AND COMPANY | 2010-06-03 | — | — | US | disclosed |
| EP-2185495-A2 | PROCESSES FOR MAKING DIALKYL ETHERS FROM ALCOHOLS | E. I. du Pont de Nemours and Company (US) | 2010-05-19 | — | — | EP | disclosed |
| EP-2185494-A2 | PROCESSES FOR MAKING DIBUTYL ETHERS FROM ISOBUTANOL | E. I. du Pont de Nemours and Company (US) | 2010-05-19 | — | — | EP | disclosed |
| US-20090292126-A1 | Ionic Liquids | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-11-26 | — | — | US | disclosed |
| US-20090234118-A1 | Ionic Liquids | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-09-17 | — | — | US | disclosed |
| US-20090234134-A1 | Ionic Liquids | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-09-17 | — | — | US | disclosed |
| US-20090233788-A1 | Ionic Liquids | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-09-17 | — | — | US | disclosed |
| US-20090234135-A1 | Ionic Liquids | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-09-17 | — | — | US | disclosed |
| US-20090234120-A1 | Ionic Liquids | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-09-17 | — | — | US | disclosed |
| US-20090234119-A1 | Ionic Liquids | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-09-17 | — | — | US | disclosed |
| US-20090234116-A1 | Ionic Liquids | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-09-17 | — | — | US | disclosed |
| US-20090234133-A1 | Ionic Liquids | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-09-17 | — | — | US | disclosed |
| US-20090227447-A1 | Ionic Liquids | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-09-10 | — | — | US | disclosed |
| US-7544813-B2 | Ionic liquids | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-06-09 | — | — | US | disclosed |
| US-20090131728-A1 | PROCESS FOR THE SEPARATION OF DIASTEREOMERS | E. I. DU PONT DE NEMOURS AND COMPANY | 2009-05-21 | — | — | US | disclosed |
| EP-1940914-B1 | PREPARATION OF POLYTRIMETHYLENE ETHER GLYCOL AND COPOLYMERS THEREOF | DU PONT (US) | 2009-05-13 | — | — | EP | disclosed |
| US-7528287-B2 | Preparation of poly(tetramethylene) glycol | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-05-05 | — | — | US | disclosed |
| WO-2009032961-A2 | PROCESSES FOR MAKING DIBUTYL ETHERS FROM 2-BUTANOL | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-03-12 | — | — | WO | disclosed |
| WO-2009032959-A2 | PROCESSES FOR MAKING DIALKYL ETHERS FROM ALCOHOLS | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-03-12 | — | — | WO | disclosed |
| WO-2009032962-A2 | PROCESSES FOR MAKING DIBUTYL ETHERS FROM ISOBUTANOL | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2009-03-12 | — | — | WO | disclosed |
| WO-2008143925-A1 | PROCESS FOR THE SEPARATION OF DIASTEREOMERS | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2008-11-27 | — | — | WO | disclosed |
| US-20080221241-A1 | Flame Retardant Polycarbonate Compositions | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2008-09-11 | — | — | US | disclosed |
| EP-1954658-A1 | ALKYLATION OF AROMATIC COMPOUNDS | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2008-08-13 | — | — | EP | disclosed |
| US-20080153697-A1 | For use as absorption cooling fluids in absorption cycles, and ammonia storage; refrigerants | E. I. DUPONT DE NEMOURS AND COMPANY (US) | 2008-06-26 | — | — | US | disclosed |
| US-20070295478-A1 | Vapor Compression Cycle Utilizing Ionic Liquid as Compressor Lubricant | E. I. DU PONT DE NEMOURS AND COMPANY | 2007-12-27 | — | — | US | disclosed |
| US-7238772-B2 | Preparation of polytrimethylene ether glycol and copolymers thereof | E. I. DU PONT DE NEMOURS AND COMPANY (DE) | 2007-07-03 | — | — | US | disclosed |
| US-20070131535-A1 | Utilizing ionic liquids for hydrofluorocarbon separation | THE CHEMOURS COMPANY FC, LLC | 2007-06-14 | — | — | US | disclosed |
| US-20070100184-A1 | Alkylation of aromatic compounds | E. I. DU PONT DE NEMOURS AND COMPANY | 2007-05-03 | — | — | US | disclosed |
| WO-2007050492-A1 | ALKYLATION OF AROMATIC COMPOUNDS | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2007-05-03 | — | — | WO | disclosed |
| US-20070066822-A1 | Ionic liquids | THE CHEMOURS COMPANY FC, LLC | 2007-03-22 | — | — | US | disclosed |
| US-20070066852-A1 | Preparation of poly(tetramethylene) glycol | THE CHEMOURS COMPANY FC, LLC | 2007-03-22 | — | — | US | disclosed |
| US-20070066854-A1 | Preparation of polytrimethylene ether glycol and copolymers thereof | THE CHEMOURS COMPANY FC, LLC | 2007-03-22 | — | — | US | disclosed |
| US-20070019708-A1 | Hybrid vapor compression-absorption cycle | E. I. DU PONT DE NEMOURS AND COMPANY | 2007-01-25 | — | — | US | disclosed |
| US-20060197053-A1 | Absorption cycle utilizing ionic liquid as working fluid | E. I. DU PONT DE NEMOURS AND COMPANY | 2006-09-07 | — | — | US | disclosed |
| US-20060197053-A1 | Absorption cycle utilizing ionic liquid as working fluid | E. I. DU PONT DE NEMOURS AND COMPANY | 2006-09-07 | — | — | 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 (19 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-20100174120-A1 | PROCESSES FOR MAKING DIBUTYL ETHERS FROM ISOBUTANOL | EBP, PPIP5K2, PCBP1 | CA1 4453/4885CA2 4552/4885KCNH2 1554/4885 |
| US-20100197974-A1 | PROCESSES FOR MAKING DIALKYL ETHERS FROM ALCOHOLS | ADH1C, DCLK1, GK | CA1 3525/4885CA2 4364/4885KCNH2 325/4885 |
| US-20090234134-A1 | Ionic Liquids | INF2, MOGAT2, FLI1 | CA1 592/4885CA2 545/4885KCNH2 1220/4885 |
| US-20090234120-A1 | Ionic Liquids | INF2, MOGAT2, FLI1 | CA1 592/4885CA2 545/4885KCNH2 1220/4885 |
| US-20130231448-A1 | PROCESS FOR SEPARATION OF TETRAFLUOROETHYLENE FROM CARBON DIOXIDE USING IONIC LIQUIDS | CNOT9, CA9, TAF9 | CA1 75/4885CA2 49/4885KCNH2 1474/4885 |
| US-20090234135-A1 | Ionic Liquids | INF2, MOGAT2, FLI1 | CA1 592/4885CA2 545/4885KCNH2 1220/4885 |
| US-20070100184-A1 | Alkylation of aromatic compounds | TYR, ALK, AHR | CA1 3741/4885CA2 2648/4885KCNH2 1186/4885 |
| US-20100144994-A1 | Process for Separation of Tetrafluoroethylene from Carbon Dioxide using Ionic Liquids | CNOT9, CA9, TAF9 | CA1 75/4885CA2 49/4885KCNH2 1474/4885 |
| US-20090131728-A1 | PROCESS FOR THE SEPARATION OF DIASTEREOMERS | DHPS, DHODH, GALE | CA1 1575/4885CA2 1013/4885KCNH2 811/4885 |
| US-20070066854-A1 | Preparation of polytrimethylene ether glycol and copolymers thereof | PARG, PTGES3, PGD | CA1 2257/4885CA2 3765/4885KCNH2 2378/4885 |
| US-20100204521-A1 | PROCESSES FOR MAKING DIBUTYL ETHERS FROM 2-BUTANOL | TRIB2, EBP, DAB2IP | CA1 4339/4885CA2 3539/4885KCNH2 1685/4885 |
| US-20090234133-A1 | Ionic Liquids | INF2, MOGAT2, FLI1 | CA1 592/4885CA2 545/4885KCNH2 1220/4885 |
| US-20090234118-A1 | Ionic Liquids | INF2, MOGAT2, FLI1 | CA1 592/4885CA2 545/4885KCNH2 1220/4885 |
| US-20070131535-A1 | Utilizing ionic liquids for hydrofluorocarbon separation | AQP3, AQP1, SLC26A3 | CA1 208/4885CA2 295/4885KCNH2 38/4885 |
| US-20090234119-A1 | Ionic Liquids | INF2, MOGAT2, FLI1 | CA1 592/4885CA2 545/4885KCNH2 1220/4885 |
| US-20070066822-A1 | Ionic liquids | AFF2, AFF1, ZYX | CA1 2794/4885CA2 432/4885KCNH2 273/4885 |
| US-20090234116-A1 | Ionic Liquids | INF2, MOGAT2, FLI1 | CA1 592/4885CA2 545/4885KCNH2 1220/4885 |
| US-20090292126-A1 | Ionic Liquids | INF2, MOGAT2, FLI1 | CA1 592/4885CA2 545/4885KCNH2 1220/4885 |
| US-20070066852-A1 | Preparation of poly(tetramethylene) glycol | PARG, PUF60, TPR | CA1 2718/4885CA2 4710/4885KCNH2 860/4885 |
“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.