Predicted protein targets (top 16)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CA1 | P00915 | 3/20 | 0.42 |
| ▸ | CA2 | P00918 | 3/20 | 0.42 |
| ▸ | CA12 | O43570 | 2/20 | 0.42 |
| ▸ | CA9 | Q16790 | 2/20 | 0.42 |
| ▸ | EPHX1 | P07099 | 2/20 | 0.37 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.37 |
| ▸ | CES2 | O00748 | 1/20 | 0.33 |
| ▸ | CES1 | P23141 | 1/20 | 0.33 |
| ▸ | NPC1 | O15118 | 1/20 | 0.33 |
| ▸ | TSHR | P16473 | 1/20 | 0.33 |
| ▸ | ACHE | P22303 | 1/20 | 0.32 |
| ▸ | NAAA | Q02083 | 1/20 | 0.31 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.31 |
| ▸ | HTT | P42858 | 1/20 | 0.30 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.30 |
| ▸ | HSD17B10 | Q99714 | 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 | |
|---|---|---|---|---|
| SCHEMBL3415461 | 1.00 | CA1 (0.42) | CA1CA2CA12CA9EPHX1 | |
| Cyclohexane SCHEMBL10804991 | 1.00 | CA1 (0.42) | CA1CA2CA12CA9EPHX1 | |
| SCHEMBL221594 | 1.00 | — | — | |
| SCHEMBL3416195 | 1.00 | CA1 (0.42) | CA1CA2CA12CA9EPHX1 | |
| SCHEMBL3415460 | 1.00 | CA1 (0.42) | CA1CA2CA12CA9EPHX1 | |
| SCHEMBL3415468 | 1.00 | CA1 (0.42) | CA1CA2CA12CA9EPHX1 | |
| SCHEMBL3413582 | 1.00 | — | — | |
| SCHEMBL8530196 | 1.00 | CA1 (0.42) | CA1CA2CA12CA9EPHX1 | |
| SCHEMBL4473841 | 1.00 | CA1 (0.42) | CA1CA2CA12CA9EPHX1 | |
| SCHEMBL1683865 | 0.96 | — | — |
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 152 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-108473526-A | Process for producing oligonucleotide and nucleoside, nucleotide or oligonucleotide | 味之素株式会社 | 2018-08-31 | — | — | CN | claimed |
| US-20120310012-A1 | METHOD FOR PREPARING A DEPEROXIDATION CATALYST | RHODIA OPERATIONS (FR) | 2012-12-06 | — | — | US | claimed |
| EP-1440050-B1 | METHOD FOR CATALYTIC DECOMPOSITION OF ORGANIC HYDROPEROXIDES | RHODIA OPERATIONS (FR) | 2010-03-31 | — | — | EP | claimed |
| EP-1492754-B1 | METHOD FOR MAKING CARBOXYLIC ACIDS | RHODIA POLYAMIDE INTERMEDIATES (FR) | 2008-11-05 | — | — | EP | claimed |
| US-7396961-B2 | Process for catalytically decomposing organic hydroperoxides | RHODIA POLYAMIDE INTERMEDIATES (FR) | 2008-07-08 | — | — | US | claimed |
| CN-100341837-C | Method for making carboxylic acids | RHODIA POLYAMIDES INTERMEDIATE (FR) | 2007-10-10 | — | — | CN | claimed |
| US-20070129575-A1 | Process for catalytically decomposing organic hydroperoxides | PERFORMANCE POLYAMIDES, SAS (FR) | 2007-06-07 | — | — | US | claimed |
| CN-1309696-C | Method for catalytic decomposition of organic hydroperoxides | RHODIA POLYAMIDE INTERMEDIATES (FR) | 2007-04-11 | — | — | CN | claimed |
| CN-1649818-A | Method for making carboxylic acids | RHODIA POLYAMIDES INTERMEDIATE (FR) | 2005-08-03 | — | — | CN | claimed |
| CN-1596239-A | Method for catalytic decomposition of organic hydroperoxides | RHODIA POLYAMIDE INTERMEDIATES (FR) | 2005-03-16 | — | — | CN | claimed |
| US-20040267052-A1 | Method for catalytic decomposition of organic hydroperoxides | RHODIA POLYAMIDE INTERMEDIATES (FR) | 2004-12-30 | — | — | US | claimed |
| CN-1167657-C | Process for producing mixture contg. cyclododecanone and cyclododecanol | ��Ļ���Ű˾ | 2004-09-22 | — | — | CN | claimed |
| JP-3439193-B2 | — | — | 2003-08-25 | — | — | JP | claimed |
| EP-1051380-B1 | PROCESS FOR PRODUCING A MIXTURE CONTAINING CYCLODODECANONE AND CYCLODODECANOL | DU PONT (US) | 2003-05-21 | — | — | EP | claimed |
| JP-2002502835-A | — | — | 2002-01-29 | — | — | JP | claimed |
| CN-1284054-A | Process for producing a mixture containing cyclododecanone and cyclododecanol | DU PONT (US) | 2001-02-14 | — | — | CN | claimed |
| EP-1051380-A1 | PROCESS FOR PRODUCING A MIXTURE CONTAINING CYCLODODECANONE AND CYCLODODECANOL | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2000-11-15 | — | — | EP | claimed |
| WO-1999040054-A1 | PROCESS FOR PRODUCING A MIXTURE CONTAINING CYCLODODECANONE AND CYCLODODECANOL | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 1999-08-12 | — | — | WO | claimed |
| US-5892123-A | BY CATALYTIC OXIDATION OF CYCLODODECANE | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 1999-04-06 | — | — | US | claimed |
| JP-11269158-A | — | — | None | — | — | JP | disclosed |
| JP-11228554-A | — | — | None | — | — | JP | disclosed |
| CN-119798056-A | Energy-saving method for producing cyclododecanone | 万华化学集团股份有限公司 | 2025-04-11 | — | — | CN | disclosed |
| US-12023649-B2 | Plant leaves-derived carbon material doped with two metals and preparation and use thereof | ZHEJIANG UNIVERSITY OF TECHNOLOGY (CN) | 2024-07-02 | — | — | US | disclosed |
| CN-112090449-B | Bimetal central metalloporphyrin as well as preparation method and application thereof | 浙江工业大学 | 2023-03-31 | — | — | CN | disclosed |
| CN-113603564-B | Method for catalytically oxidizing cycloalkane by using trimetal center (Co & Cu & Zn) 2D MOFs/ultraviolet light | 浙江工业大学 | 2023-03-14 | — | — | CN | disclosed |
| US-20230069145-A1 | PLANT LEAVES-DERIVED CARBON MATERIAL DOPED WITH TWO METALS AND PREPARATION AND USE THEREOF | ZHEJIANG UNIVERSITY OF TECHNOLOGY (CN) | 2023-03-02 | — | — | US | disclosed |
| CN-110882724-B | Platinum-supported catalyst, preparation method thereof and application thereof in cyclododecanol synthesis | 万华化学集团股份有限公司 | 2022-11-08 | — | — | CN | disclosed |
| US-11420991-B2 | Confined porphyrin Co(II) and preparation method and application thereof | ZHEJIANG UNIVERSITY OF TECHNOLOGY (CN) | 2022-08-23 | — | — | US | disclosed |
| CN-113769746-A | Co (II) and Ni (II) doped montmorillonite and preparation method and application thereof | 浙江工业大学 | 2021-12-10 | — | — | CN | disclosed |
| CN-113769744-A | Transition metal doped camphor tree leaf derived carbon material and preparation method and application thereof | 浙江工业大学 | 2021-12-10 | — | — | CN | disclosed |
| CN-113694947-A | Co (II) and Zn (II) and Cu (II) doped hydrotalcite and preparation method and application thereof | 浙江工业大学 | 2021-11-26 | — | — | CN | disclosed |
| CN-113694926-A | Bimetal-doped plant leaf derived carbon material and preparation method and application thereof | 浙江工业大学 | 2021-11-26 | — | — | CN | disclosed |
| CN-113683619-A | Metalloporphyrin trimetal center 2D MOFs, and preparation method and application thereof | 浙江工业大学 | 2021-11-23 | — | — | CN | disclosed |
| CN-113649013-A | Co (II), Zn (II) bimetal doped carbon material and preparation method and application thereof | 浙江工业大学 | 2021-11-16 | — | — | CN | disclosed |
| CN-113649073-A | Method for catalytic oxidation of cycloparaffin by metalloporphyrin bimetallic center 2D MOFs | 浙江工业大学 | 2021-11-16 | — | — | CN | disclosed |
| CN-113603564-A | Method for catalytically oxidizing cycloalkane by using trimetal center (Co & Cu & Zn)2D MOFs/ultraviolet light | 浙江工业大学 | 2021-11-05 | — | — | CN | disclosed |
| US-20210155650-A1 | CONFINED PORPHYRIN CO(II) AND PREPARATION METHOD AND APPLICATION THEREOF | ZHEJIANG UNIVERSITY OF TECHNOLOGY (CN) | 2021-05-27 | — | — | US | disclosed |
| CN-110938078-B | Limited porphyrin Co (II) and preparation method and application thereof | 浙江工业大学 | 2021-01-01 | — | — | CN | disclosed |
| CN-112121858-A | Heterogeneous bimetal central metalloporphyrin and preparation method and application thereof | 浙江工业大学 | 2020-12-25 | — | — | CN | disclosed |
| CN-112108186-A | Method for oxidizing cycloalkane under synergetic catalysis of metalloporphyrin MOFs PCN-224(Co)/Cu (II) salt | 浙江工业大学 | 2020-12-22 | — | — | CN | disclosed |
| CN-112094178-A | Method for catalytic oxidation of cycloalkane by bimetallic porphyrin MOFs PCN-222(Co & Cu) | 浙江工业大学 | 2020-12-18 | — | — | CN | disclosed |
| CN-112090449-A | Bimetal central metalloporphyrin and preparation method and application thereof | 浙江工业大学 | 2020-12-18 | — | — | CN | disclosed |
| CN-112094179-A | Method for catalytic oxidation of cycloalkane by bimetallic porphyrin MOFs PCN-224(Co & Cu) | 浙江工业大学 | 2020-12-18 | — | — | CN | disclosed |
| CN-112094180-A | Method for catalytic oxidation of cycloalkane by bimetallic porphyrin MOFs PCN-224(Co & Zn) | 浙江工业大学 | 2020-12-18 | — | — | CN | disclosed |
| CN-112076789-A | Method for oxidizing cycloalkane under synergetic catalysis of metalloporphyrin MOFs PCN-224(Co)/Zn (II) salt | 浙江工业大学 | 2020-12-15 | — | — | CN | disclosed |
| CN-112076787-A | Method for oxidizing cycloalkane under synergetic catalysis of metalloporphyrin MOFs PCN-222(Co)/Zn (II) salt | 浙江工业大学 | 2020-12-15 | — | — | CN | disclosed |
| CN-112076788-A | Method for oxidizing cycloalkane under concerted catalysis of metalloporphyrin MOFs PCN-222(Co)/Cu (II) salt | 浙江工业大学 | 2020-12-15 | — | — | CN | disclosed |
| CN-112062653-A | Method for oxidizing cycloalkane under concerted catalysis of metalloporphyrin MOFs PCN-224(Mn)/Cu (II) salt | 浙江工业大学 | 2020-12-11 | — | — | CN | disclosed |
| CN-112047810-A | Method for catalytic oxidation of cycloalkane by bimetallic porphyrin MOFs PCN-222(Co & Zn) | 浙江工业大学 | 2020-12-08 | — | — | CN | disclosed |
| CN-111995506-A | Method for oxidizing cycloparaffin through synergistic catalysis of limited-domain metalloporphyrin manganese (II)/Zn (II) salt | 浙江工业大学 | 2020-11-27 | — | — | CN | disclosed |
| CN-111995505-A | Method for oxidizing cycloparaffin through synergistic catalysis of limited-domain metalloporphyrin cobalt (II)/Cu (II) salt | 浙江工业大学 | 2020-11-27 | — | — | CN | disclosed |
| CN-111943808-A | Method for oxidizing cycloalkane under concerted catalysis of metalloporphyrin MOFs PCN-224(Mn)/Zn (II) salt | 浙江工业大学 | 2020-11-17 | — | — | CN | disclosed |
| CN-111943809-A | Method for oxidizing cycloparaffin through synergistic catalysis of limited-domain metalloporphyrin cobalt (II)/Zn (II) salt | 浙江工业大学 | 2020-11-17 | — | — | CN | disclosed |
| CN-111943810-A | Method for oxidizing cycloparaffin through synergistic catalysis of limited-domain metalloporphyrin manganese (II)/Cu (II) salt | 浙江工业大学 | 2020-11-17 | — | — | CN | disclosed |
| EP-2803408-B1 | Method and apparatus for producing oxide of hydrocarbon compound using same | UBE INDUSTRIES (JP) | 2020-11-04 | — | — | EP | disclosed |
| CN-111018673-A | Method for catalytic oxidation of cycloparaffin by limited porphyrin Co (II) | 浙江工业大学 | 2020-04-17 | — | — | CN | disclosed |
| CN-110938078-A | Limited porphyrin Co (II) and preparation method and application thereof | 浙江工业大学 | 2020-03-31 | — | — | CN | disclosed |
| CN-110918122-A | Heterogeneous copper porphyrin and preparation method and application thereof | 浙江工业大学 | 2020-03-27 | — | — | CN | disclosed |
| CN-110882724-A | Platinum-supported catalyst, preparation method thereof and application thereof in cyclododecanol synthesis | 万华化学集团股份有限公司 | 2020-03-17 | — | — | CN | disclosed |
| US-10392334-B2 | Method for producing ketone and/or alcohol, and system thereof | UBE INDUSTRIES, LTD. (JP) | 2019-08-27 | — | — | US | disclosed |
| US-20180346399-A1 | METHOD FOR PRODUCING KETONE AND/OR ALCOHOL, AND SYSTEM THEREOF | UBE INDUSTRIES, LTD. (JP) | 2018-12-06 | — | — | US | disclosed |
| EP-2623199-B1 | OXIDATION CATALYST FOR HYDROCARBON COMPOUND, AND METHOD AND APPARATUS FOR PRODUCING OXIDE OF HYDROCARBON COMPOUND USING SAME | UBE INDUSTRIES (JP) | 2018-11-07 | — | — | EP | disclosed |
| EP-3388409-A1 | KETONE AND/OR ALCOHOL PRODUCTION METHOD, AND SYSTEM FOR SAME | UBE Industries, Ltd. (JP) | 2018-10-17 | — | — | EP | disclosed |
| US-10099985-B2 | Method for producing ketone and/or alcohol, and system thereof | UBE INDUSTRIES, LTD. (JP) | 2018-10-16 | — | — | US | disclosed |
| CN-108602736-A | Method and system for producing ketone and/or alcohol | 宇部兴产株式会社 | 2018-09-28 | — | — | CN | disclosed |
| US-20170313641-A1 | Method For Producing Ketone And/Or Alcohol, And System Thereof | UBE INDUSTRIES, LTD. (JP) | 2017-11-02 | — | — | US | disclosed |
| EP-3214061-A1 | METHOD FOR PRODUCING KETONE AND/OR ALCOHOL, AND SYSTEM THEREOF | UBE Industries, Ltd. (JP) | 2017-09-06 | — | — | EP | disclosed |
| CN-104114569-B | Oligonucleotide with protected base moiety | 味之素株式会社 | 2017-04-26 | — | — | CN | disclosed |
| EP-2803408-A1 | Method and apparatus for producing oxide of hydrocarbon compound using same | Ube Industries, Ltd. (JP) | 2014-11-19 | — | — | EP | disclosed |
| EP-2623199-A1 | OXIDATION CATALYST FOR HYDROCARBON COMPOUND, AND METHOD AND APPARATUS FOR PRODUCING OXIDE OF HYDROCARBON COMPOUND USING SAME | Ube Industries, Ltd. (JP) | 2013-08-07 | — | — | EP | disclosed |
| US-20130184494-A1 | Oxidation Catalyst for Hydrocarbon Compound, and Method and Apparatus for Producing Oxide of Hydrocarbon Compound Using Same | USE Industries, Ltd. (JP) | 2013-07-18 | — | — | US | disclosed |
| CN-103140286-A | Oxidation catalyst for hydrocarbon compound, and method and apparatus for producing oxide of hydrocarbon compound using same | UBE INDUSTRIES | 2013-06-05 | — | — | CN | disclosed |
| EP-2096097-B1 | METHOD FOR PRODUCING OXIDATION PRODUCT OF CYCLOALKANE | DAICEL CHEM (JP) | 2012-08-22 | — | — | EP | disclosed |
| US-7834217-B2 | Method for producing oxidation product of cycloalkane | DAICEL CHEMICAL INDUSTRIES, LTD. (JP) | 2010-11-16 | — | — | US | disclosed |
| CN-101848912-A | Organic metal compound, composition for trapping moisture and oxygen, cured body, and organic EL device | JSR CORP | 2010-09-29 | — | — | CN | disclosed |
| US-20100081848-A1 | METHOD FOR PRODUCING OXIDATION PRODUCT OF CYCLOALKANE | DAICEL CHEMICAL INDUSTRIES, LTD. (JP) | 2010-04-01 | — | — | US | disclosed |
| EP-2096097-A1 | METHOD FOR PRODUCING OXIDATION PRODUCT OF CYCLOALKANE | DAICEL CHEMICAL INDUSTRIES, LTD. (JP) | 2009-09-02 | — | — | EP | disclosed |
| US-7396961-B2 | Process for catalytically decomposing organic hydroperoxides | RHODIA POLYAMIDE INTERMEDIATES (FR) | 2008-07-08 | — | — | US | disclosed |
| CN-100341837-C | Method for making carboxylic acids | RHODIA POLYAMIDES INTERMEDIATE (FR) | 2007-10-10 | — | — | CN | disclosed |
| US-20070129575-A1 | Process for catalytically decomposing organic hydroperoxides | PERFORMANCE POLYAMIDES, SAS (FR) | 2007-06-07 | — | — | US | disclosed |
| CN-1309696-C | Method for catalytic decomposition of organic hydroperoxides | RHODIA POLYAMIDE INTERMEDIATES (FR) | 2007-04-11 | — | — | CN | disclosed |
| US-20070053572-A1 | Method for operating an x-ray diagnostics device | SIEMENS AKTIENGESELLSCHAFT (DE) | 2007-03-08 | — | — | US | disclosed |
| EP-1309534-B1 | IMPROVED HYDROPEROXIDE DECOMPOSITION CATALYST | INVISTA TECH SARL (US) | 2005-10-19 | — | — | EP | disclosed |
| CN-1649818-A | Method for making carboxylic acids | RHODIA POLYAMIDES INTERMEDIATE (FR) | 2005-08-03 | — | — | CN | disclosed |
| CN-1203041-C | Improved hydroperoxide decomposition catalyst | DU PONT (US) | 2005-05-25 | — | — | CN | disclosed |
| CN-1596239-A | Method for catalytic decomposition of organic hydroperoxides | RHODIA POLYAMIDE INTERMEDIATES (FR) | 2005-03-16 | — | — | CN | disclosed |
| US-20040267052-A1 | Method for catalytic decomposition of organic hydroperoxides | RHODIA POLYAMIDE INTERMEDIATES (FR) | 2004-12-30 | — | — | US | disclosed |
| US-6806390-B1 | LONGER CATALYST LIFE, IMPROVED YIELDS OF USEFUL PRODUCTS, AND THE ABSENCE OF SOLUBLE METAL COMPOUNDS; CONTACTING THE HYDROPEROXIDE WITH A CATALYTIC AMOUNT OF A HETEROGENEOUS GOLD CATALYST WHEREIN THE GOLD CATALYST HAS BEEN SILANIZED | Inuista North America S.àr.l. | 2004-10-19 | — | — | US | disclosed |
| CN-1167657-C | Process for producing mixture contg. cyclododecanone and cyclododecanol | ��Ļ���Ű˾ | 2004-09-22 | — | — | CN | disclosed |
| CN-1167657-C | Process for producing mixture contg. cyclododecanone and cyclododecanol | ��Ļ���Ű˾ | 2004-09-22 | — | — | CN | disclosed |
| CN-1454199-A | Improved hydroperoxide decomposition catalyst | DU PONT (US) | 2003-11-05 | — | — | CN | disclosed |
| EP-1051380-B1 | PROCESS FOR PRODUCING A MIXTURE CONTAINING CYCLODODECANONE AND CYCLODODECANOL | DU PONT (US) | 2003-05-21 | — | — | EP | disclosed |
| EP-1051380-B1 | PROCESS FOR PRODUCING A MIXTURE CONTAINING CYCLODODECANONE AND CYCLODODECANOL | DU PONT (US) | 2003-05-21 | — | — | EP | disclosed |
| EP-1309534-A1 | IMPROVED HYDROPEROXIDE DECOMPOSITION CATALYST | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2003-05-14 | — | — | EP | disclosed |
| EP-1012130-B9 | HYDROPEROXIDE DECOMPOSITION PROCESS | DU PONT (US) | 2003-05-02 | — | — | EP | disclosed |
| EP-1107952-B1 | HYDROPEROXIDE DECOMPOSITION PROCESS | DU PONT (US) | 2003-01-29 | — | — | EP | disclosed |
| EP-1012130-B1 | HYDROPEROXIDE DECOMPOSITION PROCESS | DU PONT (US) | 2003-01-22 | — | — | EP | disclosed |
| EP-0931044-B1 | HYDROPEROXIDE DECOMPOSITION PROCESSES | DU PONT (US) | 2002-11-20 | — | — | EP | disclosed |
| CN-1093109-C | Hydroperoxide decomposition process | DU PONT (US) | 2002-10-23 | — | — | CN | disclosed |
| WO-2002016296-A1 | IMPROVED HYDROPEROXIDE DECOMPOSITION CATALYST | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2002-02-28 | — | — | WO | disclosed |
| EP-1159240-A1 | HYDROPEROXIDE DECOMPOSITION PROCESS | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2001-12-05 | — | — | EP | disclosed |
| EP-1151984-A2 | Hydroperoxide decomposition processes | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2001-11-07 | — | — | EP | disclosed |
| US-6284927-B1 | FORMING ALCOHOL OR KETONE FROM DECOMPOSITION OF HYDROPEROXIDE | E. I. DU PONT NEMOURS AND COMPANY | 2001-09-04 | — | — | US | disclosed |
| EP-1107952-A1 | HYDROPEROXIDE DECOMPOSITION PROCESS | E.I. DUPONT DE NEMOURS AND COMPANY (US) | 2001-06-20 | — | — | EP | disclosed |
| US-6191311-B1 | DECOMPOSING HYDROPEROXIDE TO FORM REACTION MIXTURE CONTAINING CORRESPONDING ALCOHOL AND KETONE, THE IMPROVEMENT COMPRISING DECOMPOSING THE HYDROPEROXIDE BY CONTACTING WITH A CATALYTIC AMOUNT OF A HETEROGENEOUS NIOBIUM OXIDE OR HYDROXIDE | E. I. DU PONT DE NEMOURS AND COMPANY | 2001-02-20 | — | — | US | disclosed |
| CN-1284054-A | Process for producing a mixture containing cyclododecanone and cyclododecanol | DU PONT (US) | 2001-02-14 | — | — | CN | disclosed |
| CN-1284054-A | Process for producing a mixture containing cyclododecanone and cyclododecanol | DU PONT (US) | 2001-02-14 | — | — | CN | disclosed |
| EP-1051380-A1 | PROCESS FOR PRODUCING A MIXTURE CONTAINING CYCLODODECANONE AND CYCLODODECANOL | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2000-11-15 | — | — | EP | disclosed |
| EP-1051380-A1 | PROCESS FOR PRODUCING A MIXTURE CONTAINING CYCLODODECANONE AND CYCLODODECANOL | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2000-11-15 | — | — | EP | disclosed |
| WO-2000053550-A1 | HYDROPEROXIDE DECOMPOSITION PROCESS | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2000-09-14 | — | — | WO | disclosed |
| EP-1012130-A2 | HYDROPEROXIDE DECOMPOSITION PROCESS | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2000-06-28 | — | — | EP | disclosed |
| WO-2000012470-A1 | HYDROPEROXIDE DECOMPOSITION PROCESS | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2000-03-09 | — | — | WO | disclosed |
| JP-2000007668-A | PRODUCTION OF EPOXYCYCLODODECADIENE | UBE IND LTD | 2000-01-11 | — | — | JP | disclosed |
| JP-2000001473-A | PRODUCTION OF CYCLODODECYL HYDROPEROXIDE | UBE IND LTD | 2000-01-07 | — | — | JP | disclosed |
| CN-1047587-C | Process for preparing alkanone and/or alkanol | DSM NV (NL) | 1999-12-22 | — | — | CN | disclosed |
| EP-0659726-B1 | Process for preparing a cycloalkanone and/or a cycloalkanol | DSM NV (NL) | 1999-11-03 | — | — | EP | disclosed |
| JP-H11269158-A | PREPARATION OF 1,2-EPOXY-5,9-CYCLODODECADIENE | UBE IND LTD | 1999-10-05 | — | — | JP | disclosed |
| CN-1228755-A | Hydroperoxide decomposition process | DU PONT (US) | 1999-09-15 | — | — | CN | disclosed |
| JP-H11228554-A | PRODUCTION OF 1,2-EPOXY-5,9-CYCLODODECADIENE | UBE IND LTD | 1999-08-24 | — | — | JP | disclosed |
| WO-1999040054-A1 | PROCESS FOR PRODUCING A MIXTURE CONTAINING CYCLODODECANONE AND CYCLODODECANOL | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 1999-08-12 | — | — | WO | disclosed |
| WO-1999040054-A1 | PROCESS FOR PRODUCING A MIXTURE CONTAINING CYCLODODECANONE AND CYCLODODECANOL | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 1999-08-12 | — | — | WO | disclosed |
| EP-0931044-A1 | HYDROPEROXIDE DECOMPOSITION PROCESSES | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 1999-07-28 | — | — | EP | disclosed |
| US-5892123-A | BY CATALYTIC OXIDATION OF CYCLODODECANE | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 1999-04-06 | — | — | US | disclosed |
| US-5892123-A | BY CATALYTIC OXIDATION OF CYCLODODECANE | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 1999-04-06 | — | — | US | disclosed |
| US-5859301-A | OXIDIZING AN ALKANE OR ALKENE TO FORM AN ALKYLHYDROPEROXIDE WHICH IS THEN DECOMPOSED IN THE PRESENCE OF A CATALYST | DSM N.V. (NL) | 1999-01-12 | — | — | US | disclosed |
| EP-0713846-B1 | PROCESS FOR PRODUCING CYCLOALKANOL AND CYCLOALKANONE | UBE INDUSTRIES (JP) | 1998-10-28 | — | — | EP | disclosed |
| WO-1998034894-A2 | HYDROPEROXIDE DECOMPOSITION PROCESS | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 1998-08-13 | — | — | WO | disclosed |
| US-5728890-A | DECOMPOSING CYCLOALKYLHYDROPEROXIDE BY CONTACT WITH A RUTHENIUM COMPLEX | UBE INDUSTRIES, LTD. (JP) | 1998-03-17 | — | — | US | disclosed |
| WO-1998009931-A1 | HYDROPEROXIDE DECOMPOSITION PROCESSES | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 1998-03-12 | — | — | WO | disclosed |
| EP-0674613-B1 | METHOD FOR THE CONTINUOUS PREPARATION OF A MIXTURE OF A CYCLOALKANONE, CYCLOALKANOL AND A CYCLOALKYLHYDROPEROXIDE | DSM NV (NL) | 1997-09-17 | — | — | EP | disclosed |
| EP-0577709-B1 | PROCESS FOR PREPARING AN ALKANONE AND/OR ALKANOL | DSM NV (NL) | 1997-01-08 | — | — | EP | disclosed |
| EP-0713846-A1 | PROCESS FOR PRODUCING CYCLOALKANOL AND CYCLOALKANONE | UBE INDUSTRIES, LTD. (JP) | 1996-05-29 | — | — | EP | disclosed |
| EP-0549068-B1 | Alkyl peroxides and uses | DSM NV (NL) | 1996-02-21 | — | — | EP | disclosed |
| EP-0674613-A1 | METHOD FOR THE CONTINUOUS PREPARATION OF A MIXTURE OF A CYCLOALKANONE, CYCLOALKANOL AND A CYCLOALKYLHYDROPEROXIDE. | DSM NV (NL) | 1995-10-04 | — | — | EP | disclosed |
| EP-0665827-A1 | METHOD FOR THE CATALYZED DECOMPOSITION OF ORGANIC HYDROPEROXIDES | TECHNISCHE UNIVERSITEIT DELFT (NL) | 1995-08-09 | — | — | EP | disclosed |
| EP-0659726-A1 | Process for preparing an alkanone and/or an alkanol | DSM N.V. (NL) | 1995-06-28 | — | — | EP | disclosed |
| US-5406001-A | Oxidizing cycloalkane with oxygen-containing gas in presence of phenolic compound | DSM N.V. (NL) | 1995-04-11 | — | — | US | disclosed |
| WO-1994013613-A1 | METHOD FOR THE CONTINUOUS PREPARATION OF A MIXTURE OF A CYCLOALKANONE, CYCLOALKANOL AND A CYCLOALKYLHYDROPEROXIDE | DSM N.V. (NL) | 1994-06-23 | — | — | WO | disclosed |
| US-5319146-A | Alkyl peroxides and uses | DSM N.V. (NL) | 1994-06-07 | — | — | US | disclosed |
| WO-1994008932-A1 | METHOD FOR THE CATALYZED DECOMPOSITION OF ORGANIC HYDROPEROXIDES | TECHNISCHE UNIVERSITEIT DELFT (NL) | 1994-04-28 | — | — | WO | disclosed |
| US-5298665-A | Decomposing alkyl hydroperoxide in solvent in presence of catalytic metal compound immobilized on a carrier | DSM N.V. (NL) | 1994-03-29 | — | — | US | disclosed |
| EP-0577709-A1 | PROCESS FOR PREPARING AN ALKANONE AND/OR ALKANOL. | DSM NV (NL) | 1994-01-12 | — | — | EP | disclosed |
| EP-0549068-A1 | Alkyl peroxides and uses | DSM N.V. (NL) | 1993-06-30 | — | — | EP | disclosed |
| WO-1993008159-A1 | PROCESS FOR THE PREPARATION OF A KETOXIME | DSM N.V. (NL) | 1993-04-29 | — | — | WO | disclosed |
| WO-1993008160-A1 | PROCESS FOR THE PREPARATION OF A KETOXIME | DSM N.V. (NL) | 1993-04-29 | — | — | WO | disclosed |
| CN-1066839-A | The method for preparing alkane ketone and/or alkanol | DSM NV (NL) | 1992-12-09 | — | — | CN | disclosed |
| WO-1992016487-A1 | PROCESS FOR PREPARING AN ALKANONE AND/OR ALKANOL | DSM N.V. (NL) | 1992-10-01 | — | — | WO | disclosed |
| EP-0164463-B1 | METHOD FOR PRODUCING A MIXTURE CONTAINING CYCLOALKANONES AND CYCLOALKANOLS | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1988-05-11 | — | — | EP | disclosed |
| US-4568769-A | Method for producing a mixture containing cycloalkanones and cycloalkanols | SUMITOMO CHEMICAL COMPANY (JP) | 1986-02-04 | — | — | US | disclosed |
| EP-0164463-A1 | Method for producing a mixture containing cycloalkanones and cycloalkanols | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1985-12-18 | — | — | EP | disclosed |
| US-4147883-A | Conversion of cycloalkylhydroperoxides to alkane dicarboxylic acids | IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) | 1979-04-03 | — | — | US | disclosed |
| US-3956397-A | Process for extracting cycloaliphatic hydroperoxides | RHONE-POULENC INDUSTRIES (FR) | 1976-05-11 | — | — | US | disclosed |
| US-3956397-A | Process for extracting cycloaliphatic hydroperoxides | RHONE-POULENC INDUSTRIES (FR) | 1976-05-11 | — | — | 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 (4 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-11420991-B2 | Confined porphyrin Co(II) and preparation method and application thereof | PPOX, PPIF, PPIC | CA1 385/4885CA2 80/4885CA12 212/4885 |
| US-20100081848-A1 | METHOD FOR PRODUCING OXIDATION PRODUCT OF CYCLOALKANE | CBR3, CBR1, CYCS | CA1 3560/4885CA2 2302/4885CA12 3864/4885 |
| US-20210155650-A1 | CONFINED PORPHYRIN CO(II) AND PREPARATION METHOD AND APPLICATION THEREOF | PPOX, PPIF, PPIC | CA1 385/4885CA2 80/4885CA12 212/4885 |
| US-20130184494-A1 | Oxidation Catalyst for Hydrocarbon Compound, and Method and Apparatus for Producing Oxide of Hydrocarbon Compound Using Same | ALKBH3, HAO2, ALKBH2 | CA1 303/4885CA2 212/4885CA12 581/4885 |
“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.