Predicted protein targets (top 19)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ALDH1A1 | P00352 | 4/20 | 0.39 |
| ▸ | TP53 | P04637 | 3/20 | 0.39 |
| ▸ | TSHR | P16473 | 3/20 | 0.39 |
| ▸ | MAPT | P10636 | 2/20 | 0.39 |
| ▸ | HPGD | P15428 | 2/20 | 0.39 |
| ▸ | MEN1 | O00255 | 2/20 | 0.39 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.39 |
| ▸ | HIF1A | Q16665 | 2/20 | 0.39 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.39 |
| ▸ | PPARG | P37231 | 1/20 | 0.39 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.37 |
| ▸ | PKM | P14618 | 2/20 | 0.36 |
| ▸ | LMNA | P02545 | 1/20 | 0.36 |
| ▸ | GAA | P10253 | 1/20 | 0.36 |
| ▸ | GRM2 | Q14416 | 1/20 | 0.35 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.34 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.34 |
| ▸ | HRH3 | Q9Y5N1 | 2/20 | 0.32 |
| ▸ | GLA | P06280 | 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 | |
|---|---|---|---|---|
| SCHEMBL12922174 | 0.94 | ALDH1A1 (0.39) | ALDH1A1TP53TSHRMAPTHPGD | |
| SCHEMBL974403 | 0.92 | TP53 (0.35) | ALDH1A1TP53TSHRMAPTHPGD | |
| SCHEMBL7110426 | 0.92 | TP53 (0.38) | ALDH1A1TP53TSHRMAPTHPGD | |
| SCHEMBL977193 | 0.91 | ALDH1A1 (0.40) | ALDH1A1TP53TSHRMAPTHPGD | |
| SCHEMBL974715 | 0.91 | ALDH1A1 (0.40) | ALDH1A1TP53TSHRMAPTHPGD | |
| SCHEMBL974683 | 0.91 | TP53 (0.37) | ALDH1A1TP53TSHRMAPTHPGD | |
| SCHEMBL977824 | 0.91 | TP53 (0.37) | ALDH1A1TP53TSHRMAPTHPGD | |
| SCHEMBL976626 | 0.90 | ALDH1A1 (0.40) | ALDH1A1TP53TSHRMAPTHPGD | |
| SCHEMBL978636 | 0.90 | TP53 (0.36) | ALDH1A1TP53TSHRMAPTHPGD | |
| SCHEMBL975153 | 0.90 | TP53 (0.38) | ALDH1A1TP53TSHRMAPTHPGD |
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 82 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-7868171-B2 | N-alkoxy-4, 4-dioxy-polyalkyl-piperidines as radical polymerization initiators | CIBA SPECIALTY CHEMICALS CORP. (US) | 2011-01-11 | — | — | US | claimed |
| EP-1592722-B1 | PARTICLE SIZE AND MORPHOLOGY CONTROL IN RUBBER MODIFIED MONOVINYLIDENE AROMATIC POLYMERS | DOW GLOBAL TECHNOLOGIES INC (US) | 2010-09-15 | — | — | EP | claimed |
| EP-1618148-B1 | HIGH GLOSS RUBBER MODIFIED MONOVINYLIDENE AROMATIC POLYMERS PRODUCED BY A MASS POLYMERIZATION PROCESS | DOW GLOBAL TECHNOLOGIES INC (US) | 2009-03-25 | — | — | EP | claimed |
| EP-1740632-B1 | IMPROVED MASS POLYMERIZED RUBBER-MODIFIED MONOVINYLIDENE AROMATIC COPOLYMER COMPOSITION | DOW GLOBAL TECHNOLOGIES INC (US) | 2008-08-13 | — | — | EP | claimed |
| US-7312277-B2 | Mass polymerized rubber-modified monovinylidene aromatic copolymer composition | DOW GLOBAL TECHNOLOGIES INC. (US) | 2007-12-25 | — | — | US | claimed |
| US-20070173570-A1 | N-alkoxy-4, 4-dioxy-polyalkyl-piperidine compounds, with glycidyl or alkylcarbonyl groups as functional initiators for controlled radical polymerization | FUSO FRANCESCO | 2007-07-26 | — | — | US | claimed |
| US-7235663-B2 | N-alkoxy-4,4-dioxy-polyalkyl-piperidines as radical polymerization inhibitors | CIBA SPECIALTY CHEMICALS CORP. (US) | 2007-06-26 | — | — | US | claimed |
| US-20070106028-A1 | low temperature impact; polymerized acrylonitrile-styrene copolymer crosslinked with polybutadiene rubber and butadiene-styrene block copolymer rubber; GLOSS; MOLDING MATERIALS, light absorbance; molded objects | ALTER DOMUS (US) LLC | 2007-05-10 | — | — | US | claimed |
| EP-1740632-A1 | IMPROVED MASS POLYMERIZED RUBBER-MODIFIED MONOVINYLIDENE AROMATIC COPOLYMER COMPOSITION | Dow Global Technologies Inc. (US) | 2007-01-10 | — | — | EP | claimed |
| US-7115684-B2 | High gloss rubber modified monovinylidene aromatic polymers produced by a mass polymerization process | DOW GLOBAL TECHNOLOGIES INC. (US) | 2006-10-03 | — | — | US | claimed |
| US-20060122331-A1 | High gloss rubber modified monovinylidene aromatic polymers produced by a mass polymerization process | TRINSEO EUROPE GMBH (CH) | 2006-06-08 | — | — | US | claimed |
| US-20060058465-A1 | Particle size and morphology control in rubber modified monovinylidene aromatic polymers | TRINSEO EUROPE GMBH (CH) | 2006-03-16 | — | — | US | claimed |
| EP-1618148-A2 | HIGH GLOSS RUBBER MODIFIED MONOVINYLIDENE AROMATIC POLYMERS PRODUCED BY A MASS POLYMERIZATION PROCESS | DOW GLOBAL TECHNOLOGIES INC. (US) | 2006-01-25 | — | — | EP | claimed |
| WO-2005108447-A1 | IMPROVED MASS POLYMERIZED RUBBER-MODIFIED MONOVINYLIDENE AROMATIC COPOLYMER COMPOSITION | DOW GLOBAL TECHNOLOGIES INC. (US) | 2005-11-17 | — | — | WO | claimed |
| WO-2004072172-A2 | HIGH GLOSS RUBBER MODIFIED MONOVINYLIDENE AROMATIC POLYMERS PRODUCED BY A MASS POLYMERIZATION PROCESS | DOW GLOBAL TECHNOLOGIES INC. (US) | 2004-08-26 | — | — | WO | claimed |
| EP-1341763-B1 | N-ALKOXY-4,4-DIOXY-POLYALKYL-PIPERIDINE COMPOUNDS, WITH GLYCIDYL OR ALKYLCARBONYL GROUPS AS FUNCTIONAL INITIATORS FOR CONTROLLED RADICAL POLYMERIZATION | CIBA SC HOLDING AG (CH) | 2004-06-16 | — | — | EP | claimed |
| US-20040049043-A1 | N-alkoxy-4,4-dioxy-polyalkyl-piperidine compounds, with glycidyl or alkylcarbonyl groups as functional initiators for controlled radical polymerization | CIBA SPECIALTY CHEMICALS CORP. | 2004-03-11 | — | — | US | claimed |
| EP-1341763-A2 | N-ALKOXY-4,4-DIOXY-POLYALKYL-PIPERIDINE COMPOUNDS, WITH GLYCIDYL OR ALKYLCARBONYL GROUPS AS FUNCTIONAL INITIATORS FOR CONTROLLED RADICAL POLYMERIZATION | Ciba SC Holding AG (CH) | 2003-09-10 | — | — | EP | claimed |
| WO-2002048109-A2 | N-ALKOXY-4,4-DIOXY-POLYALKYL-PIPERIDINES AS RADICAL POLYMERIZATION INITIATORS | CIBA SPECIALTY CHEMICLAS HOLDING INC. (CH) | 2002-06-20 | — | — | WO | claimed |
| US-8544658-B2 | Functionalized thin film polyamide membranes | POLYMERS CRC LIMITED (AU) | 2013-10-01 | — | — | US | disclosed |
| US-8544658-B2 | Functionalized thin film polyamide membranes | POLYMERS CRC LIMITED (AU) | 2013-10-01 | — | — | US | disclosed |
| US-8544658-B2 | Functionalized thin film polyamide membranes | POLYMERS CRC LIMITED (AU) | 2013-10-01 | — | — | US | disclosed |
| EP-2313184-B1 | FUNCTIONALIZED THIN FILM POLYAMIDE MEMBRANES | POLYMERS CRC LTD (AU) | 2012-10-10 | — | — | EP | disclosed |
| EP-2313184-B1 | FUNCTIONALIZED THIN FILM POLYAMIDE MEMBRANES | POLYMERS CRC LTD (AU) | 2012-10-10 | — | — | EP | disclosed |
| US-20110189469-A1 | FUNCTIONALIZED THIN FILM POLYAMIDE MEMBRANES | POLYMERS CRC LIMITED (AU) | 2011-08-04 | — | — | US | disclosed |
| US-20110189469-A1 | FUNCTIONALIZED THIN FILM POLYAMIDE MEMBRANES | POLYMERS CRC LIMITED (AU) | 2011-08-04 | — | — | US | disclosed |
| US-20110189469-A1 | FUNCTIONALIZED THIN FILM POLYAMIDE MEMBRANES | POLYMERS CRC LIMITED (AU) | 2011-08-04 | — | — | US | disclosed |
| EP-2313184-A1 | FUNCTIONALIZED THIN FILM POLYAMIDE MEMBRANES | Polymers CRC Limited (AU) | 2011-04-27 | — | — | EP | disclosed |
| US-7868171-B2 | N-alkoxy-4, 4-dioxy-polyalkyl-piperidines as radical polymerization initiators | CIBA SPECIALTY CHEMICALS CORP. (US) | 2011-01-11 | — | — | US | disclosed |
| US-7868171-B2 | N-alkoxy-4, 4-dioxy-polyalkyl-piperidines as radical polymerization initiators | CIBA SPECIALTY CHEMICALS CORP. (US) | 2011-01-11 | — | — | US | disclosed |
| US-7868171-B2 | N-alkoxy-4, 4-dioxy-polyalkyl-piperidines as radical polymerization initiators | CIBA SPECIALTY CHEMICALS CORP. (US) | 2011-01-11 | — | — | US | disclosed |
| EP-1866343-B1 | PROCESS FOR THE PREPARATION OF STAR AND BLOCK-COPOLYMERS VIA EPOXY-FUNCTIONALIZED ALKOXYAMINES | BASF SE (DE) | 2010-09-29 | — | — | EP | disclosed |
| EP-1592722-B1 | PARTICLE SIZE AND MORPHOLOGY CONTROL IN RUBBER MODIFIED MONOVINYLIDENE AROMATIC POLYMERS | DOW GLOBAL TECHNOLOGIES INC (US) | 2010-09-15 | — | — | EP | disclosed |
| WO-2010015599-A1 | FUNCTIONALIZED THIN FILM POLYAMIDE MEMBRANES | POLYMERS CRC LIMITED (AU) | 2010-02-11 | — | — | WO | disclosed |
| WO-2010015599-A1 | FUNCTIONALIZED THIN FILM POLYAMIDE MEMBRANES | POLYMERS CRC LIMITED (AU) | 2010-02-11 | — | — | WO | disclosed |
| US-7632891-B2 | Grafting of nitroxyl terminated oligomers or polymers onto thermoplastic polymers | CIBA SPECIALTY CHEMICALS CORPORATION (US) | 2009-12-15 | — | — | US | disclosed |
| US-7632891-B2 | Grafting of nitroxyl terminated oligomers or polymers onto thermoplastic polymers | CIBA SPECIALTY CHEMICALS CORPORATION (US) | 2009-12-15 | — | — | US | disclosed |
| US-20090306294-A1 | Method of producing comb block-copolymers from epoxy-functionalized nitroxylethers and anionically polymerizable monomers | CIBA SPECIALTY CHEMICALS CORP. | 2009-12-10 | — | — | US | disclosed |
| US-20090306294-A1 | Method of producing comb block-copolymers from epoxy-functionalized nitroxylethers and anionically polymerizable monomers | CIBA SPECIALTY CHEMICALS CORP. | 2009-12-10 | — | — | US | disclosed |
| US-20090299013-A1 | Process for the Preparation of Star and Block-Copolymers Via Epoxy-Functionalized Alkoxyamines | CIBA SPECIALTY CHEMICALS CORP. | 2009-12-03 | — | — | US | disclosed |
| US-20090299013-A1 | Process for the Preparation of Star and Block-Copolymers Via Epoxy-Functionalized Alkoxyamines | CIBA SPECIALTY CHEMICALS CORP. | 2009-12-03 | — | — | US | disclosed |
| EP-1877457-B1 | METHOD OF PRODUCING COMB BLOCK-COPOLYMERS FROM EPOXY-FUNCTIONALIZED NITROXYLETHERS AND ANIONICALLY POLYMERIZABLE MONOMERS | BASF SE (DE) | 2009-08-12 | — | — | EP | disclosed |
| US-7528194-B2 | Comb copolymers with defined side chains and process for their manufacture | CIBA SPECIALTY CHEMICALS CORP. (US) | 2009-05-05 | — | — | US | disclosed |
| US-7528194-B2 | Comb copolymers with defined side chains and process for their manufacture | CIBA SPECIALTY CHEMICALS CORP. (US) | 2009-05-05 | — | — | US | disclosed |
| US-7528194-B2 | Comb copolymers with defined side chains and process for their manufacture | CIBA SPECIALTY CHEMICALS CORP. (US) | 2009-05-05 | — | — | US | disclosed |
| EP-1618148-B1 | HIGH GLOSS RUBBER MODIFIED MONOVINYLIDENE AROMATIC POLYMERS PRODUCED BY A MASS POLYMERIZATION PROCESS | DOW GLOBAL TECHNOLOGIES INC (US) | 2009-03-25 | — | — | EP | disclosed |
| EP-1534765-B1 | METHOD OF PRODUCING COMB OR STAR COPOLYMERS USING EPOXY-FUNCTIONALIZED NITROXYLETHERS | CIBA HOLDING INC (CH) | 2008-12-17 | — | — | EP | disclosed |
| EP-1740632-B1 | IMPROVED MASS POLYMERIZED RUBBER-MODIFIED MONOVINYLIDENE AROMATIC COPOLYMER COMPOSITION | DOW GLOBAL TECHNOLOGIES INC (US) | 2008-08-13 | — | — | EP | disclosed |
| US-7312277-B2 | Mass polymerized rubber-modified monovinylidene aromatic copolymer composition | DOW GLOBAL TECHNOLOGIES INC. (US) | 2007-12-25 | — | — | US | disclosed |
| US-7291682-B2 | Method of producing comb or star copolymers using epoxy-functionalized nitroxylethers | CIBA SPECIALTY CHEMICALS CORP. (US) | 2007-11-06 | — | — | US | disclosed |
| US-7291682-B2 | Method of producing comb or star copolymers using epoxy-functionalized nitroxylethers | CIBA SPECIALTY CHEMICALS CORP. (US) | 2007-11-06 | — | — | US | disclosed |
| US-20070173570-A1 | N-alkoxy-4, 4-dioxy-polyalkyl-piperidine compounds, with glycidyl or alkylcarbonyl groups as functional initiators for controlled radical polymerization | FUSO FRANCESCO | 2007-07-26 | — | — | US | disclosed |
| US-20070173570-A1 | N-alkoxy-4, 4-dioxy-polyalkyl-piperidine compounds, with glycidyl or alkylcarbonyl groups as functional initiators for controlled radical polymerization | FUSO FRANCESCO | 2007-07-26 | — | — | US | disclosed |
| US-20070173570-A1 | N-alkoxy-4, 4-dioxy-polyalkyl-piperidine compounds, with glycidyl or alkylcarbonyl groups as functional initiators for controlled radical polymerization | FUSO FRANCESCO | 2007-07-26 | — | — | US | disclosed |
| US-7235663-B2 | N-alkoxy-4,4-dioxy-polyalkyl-piperidines as radical polymerization inhibitors | CIBA SPECIALTY CHEMICALS CORP. (US) | 2007-06-26 | — | — | US | disclosed |
| US-7235663-B2 | N-alkoxy-4,4-dioxy-polyalkyl-piperidines as radical polymerization inhibitors | CIBA SPECIALTY CHEMICALS CORP. (US) | 2007-06-26 | — | — | US | disclosed |
| US-7235663-B2 | N-alkoxy-4,4-dioxy-polyalkyl-piperidines as radical polymerization inhibitors | CIBA SPECIALTY CHEMICALS CORP. (US) | 2007-06-26 | — | — | US | disclosed |
| US-20070106028-A1 | low temperature impact; polymerized acrylonitrile-styrene copolymer crosslinked with polybutadiene rubber and butadiene-styrene block copolymer rubber; GLOSS; MOLDING MATERIALS, light absorbance; molded objects | ALTER DOMUS (US) LLC | 2007-05-10 | — | — | US | disclosed |
| EP-1740632-A1 | IMPROVED MASS POLYMERIZED RUBBER-MODIFIED MONOVINYLIDENE AROMATIC COPOLYMER COMPOSITION | Dow Global Technologies Inc. (US) | 2007-01-10 | — | — | EP | disclosed |
| US-7144691-B2 | Color photographic recording material | CIBA SPECIALTY CHEMICALS CORPORATION (US) | 2006-12-05 | — | — | US | disclosed |
| US-7115684-B2 | High gloss rubber modified monovinylidene aromatic polymers produced by a mass polymerization process | DOW GLOBAL TECHNOLOGIES INC. (US) | 2006-10-03 | — | — | US | disclosed |
| US-20060194053-A1 | Comb copolymers with defined side chains and process for their manufacture | CIBA SPECIALTY CHEMICALS CORP. | 2006-08-31 | — | — | US | disclosed |
| US-20060122331-A1 | High gloss rubber modified monovinylidene aromatic polymers produced by a mass polymerization process | TRINSEO EUROPE GMBH (CH) | 2006-06-08 | — | — | US | disclosed |
| US-20060058465-A1 | Particle size and morphology control in rubber modified monovinylidene aromatic polymers | TRINSEO EUROPE GMBH (CH) | 2006-03-16 | — | — | US | disclosed |
| EP-1618148-A2 | HIGH GLOSS RUBBER MODIFIED MONOVINYLIDENE AROMATIC POLYMERS PRODUCED BY A MASS POLYMERIZATION PROCESS | DOW GLOBAL TECHNOLOGIES INC. (US) | 2006-01-25 | — | — | EP | disclosed |
| EP-1615962-A2 | COMB COPOLYMERS WITH DEFINED SIDE CHAINS AND PROCESS FOR THEIR MANUFACTURE | Ciba SC Holding AG (CH) | 2006-01-18 | — | — | EP | disclosed |
| US-6967228-B2 | Stable free radical polymers | FIRESTONE POLYMERS, LLC (US) | 2005-11-22 | — | — | US | disclosed |
| WO-2005108447-A1 | IMPROVED MASS POLYMERIZED RUBBER-MODIFIED MONOVINYLIDENE AROMATIC COPOLYMER COMPOSITION | DOW GLOBAL TECHNOLOGIES INC. (US) | 2005-11-17 | — | — | WO | disclosed |
| EP-1592722-A1 | PARTICLE SIZE AND MORPHOLOGY CONTROL IN RUBBER MODIFIED MONOVINYLIDENE AROMATIC POLYMERS | Dow Global Technologies Inc. (US) | 2005-11-09 | — | — | EP | disclosed |
| US-20050079455-A1 | Colour photographic recording material | CIBA SPECIALTY CHEMICALS CORP. | 2005-04-14 | — | — | US | disclosed |
| EP-1493057-A1 | COLOUR PHOTOGRAPHIC RECORDING MATERIAL | Ciba SC Holding AG (CH) | 2005-01-05 | — | — | EP | disclosed |
| US-20040220345-A1 | Stable free radical polymers | FIRESTONE POLYMERS, LLC | 2004-11-04 | — | — | US | disclosed |
| US-20040220344-A1 | Stable free radical polymers | FIRESTONE POLYMERS, LLC. | 2004-11-04 | — | — | US | disclosed |
| EP-1473312-A2 | Stable free radical polymers | Firestone Polymers, LLC (US) | 2004-11-03 | — | — | EP | disclosed |
| WO-2004072172-A2 | HIGH GLOSS RUBBER MODIFIED MONOVINYLIDENE AROMATIC POLYMERS PRODUCED BY A MASS POLYMERIZATION PROCESS | DOW GLOBAL TECHNOLOGIES INC. (US) | 2004-08-26 | — | — | WO | disclosed |
| WO-2004072136-A1 | PARTICLE SIZE AND MORPHOLOGY CONTROL IN RUBBER MODIFIED MONOVINYLIDENE AROMATIC POLYMERS | DOW GLOBAL TECHNOLOGIES INC. (US) | 2004-08-26 | — | — | WO | disclosed |
| WO-2004069887-A2 | COMB COPOLYMERS WITH DEFINED SIDE CHAINS AND PROCESS FOR THEIR MANUFACTURE | CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) | 2004-08-19 | — | — | WO | disclosed |
| EP-1341763-B1 | N-ALKOXY-4,4-DIOXY-POLYALKYL-PIPERIDINE COMPOUNDS, WITH GLYCIDYL OR ALKYLCARBONYL GROUPS AS FUNCTIONAL INITIATORS FOR CONTROLLED RADICAL POLYMERIZATION | CIBA SC HOLDING AG (CH) | 2004-06-16 | — | — | EP | disclosed |
| US-20040049043-A1 | N-alkoxy-4,4-dioxy-polyalkyl-piperidine compounds, with glycidyl or alkylcarbonyl groups as functional initiators for controlled radical polymerization | CIBA SPECIALTY CHEMICALS CORP. | 2004-03-11 | — | — | US | disclosed |
| WO-2003075091-A1 | COLOUR PHOTOGRAPHIC RECORDING MATERIAL | CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) | 2003-09-12 | — | — | WO | disclosed |
| EP-1341763-A2 | N-ALKOXY-4,4-DIOXY-POLYALKYL-PIPERIDINE COMPOUNDS, WITH GLYCIDYL OR ALKYLCARBONYL GROUPS AS FUNCTIONAL INITIATORS FOR CONTROLLED RADICAL POLYMERIZATION | Ciba SC Holding AG (CH) | 2003-09-10 | — | — | EP | disclosed |
| WO-2002048109-A2 | N-ALKOXY-4,4-DIOXY-POLYALKYL-PIPERIDINES AS RADICAL POLYMERIZATION INITIATORS | CIBA SPECIALTY CHEMICLAS HOLDING INC. (CH) | 2002-06-20 | — | — | WO | disclosed |
| WO-2002048109-A2 | N-ALKOXY-4,4-DIOXY-POLYALKYL-PIPERIDINES AS RADICAL POLYMERIZATION INITIATORS | CIBA SPECIALTY CHEMICLAS HOLDING INC. (CH) | 2002-06-20 | — | — | 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 (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-20070173570-A1 | N-alkoxy-4, 4-dioxy-polyalkyl-piperidine compounds, with glycidyl or alkylcarbonyl groups as functional initiators for controlled radical polymerization | PTGER4, ALKBH3, PIGO | ALDH1A1 737/4885TP53 4722/4885TSHR 4817/4885 |
| US-20040049043-A1 | N-alkoxy-4,4-dioxy-polyalkyl-piperidine compounds, with glycidyl or alkylcarbonyl groups as functional initiators for controlled radical polymerization | PAOX, ALKBH3, PTGER4 | ALDH1A1 1472/4885TP53 4311/4885TSHR 4856/4885 |
“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.