Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | MTNR1A | P48039 | 1/20 | 0.60 |
| ▸ | MTNR1B | P49286 | 1/20 | 0.60 |
| ▸ | LOXL2 | Q9Y4K0 | 1/20 | 0.55 |
| ▸ | NLRP3 | Q96P20 | 1/20 | 0.54 |
| ▸ | FLT3 | P36888 | 1/20 | 0.50 |
| ▸ | IDO1 | P14902 | 1/20 | 0.49 |
| ▸ | KDM4E | B2RXH2 | 3/20 | 0.49 |
| ▸ | MAPT | P10636 | 2/20 | 0.49 |
| ▸ | DAO | P14920 | 2/20 | 0.49 |
| ▸ | HPGD | P15428 | 1/20 | 0.49 |
| ▸ | SRD5A2 | P31213 | 1/20 | 0.49 |
| ▸ | HSD17B10 | Q99714 | 1/20 | 0.49 |
| ▸ | GSK3B | P49841 | 1/20 | 0.48 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.47 |
| ▸ | GAA | P10253 | 1/20 | 0.47 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.47 |
| ▸ | HRH4 | Q9H3N8 | 1/20 | 0.46 |
| ▸ | HDAC3 | O15379 | 1/20 | 0.45 |
| ▸ | HDAC1 | Q13547 | 1/20 | 0.45 |
| ▸ | HDAC2 | Q92769 | 1/20 | 0.45 |
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 | |
|---|---|---|---|---|
| SCHEMBL9027547 | 0.85 | LOXL2 (0.58) | MTNR1AMTNR1BLOXL2NLRP3KDM4E | |
| SCHEMBL3451201 | 0.85 | LOXL2 (0.58) | MTNR1AMTNR1BLOXL2NLRP3FLT3 | |
| SCHEMBL31336079 | 0.84 | LOXL2 (0.56) | MTNR1AMTNR1BLOXL2NLRP3FLT3 | |
| SCHEMBL49270 | 0.84 | LOXL2 (0.56) | MTNR1AMTNR1BLOXL2NLRP3FLT3 | |
| SCHEMBL29365671 | 0.84 | LOXL2 (0.56) | MTNR1AMTNR1BLOXL2NLRP3FLT3 | |
| SCHEMBL12714834 | 0.83 | MTNR1A (0.66) | MTNR1AMTNR1BLOXL2NLRP3FLT3 | |
| SCHEMBL27736989 | 0.83 | MTNR1A (0.54) | MTNR1AMTNR1BLOXL2NLRP3FLT3 | |
| SCHEMBL31514826 | 0.82 | LOXL2 (0.55) | MTNR1AMTNR1BLOXL2NLRP3IDO1 | |
| SCHEMBL31511816 | 0.82 | LOXL2 (0.55) | MTNR1AMTNR1BLOXL2NLRP3FLT3 | |
| SCHEMBL630523 | 0.82 | SIRT1 (0.64) | MTNR1AMTNR1BLOXL2NLRP3FLT3 |
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 153 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119306681-A | Synthesis method of 3-oxazoline-5-ketone and derivative thereof | 湖南医药学院 | 2025-01-14 | — | — | CN | claimed |
| CN-113862234-B | Transaminase and application thereof in preparation of (R) -alpha-methyl tryptamine compound | 弈柯莱生物科技(集团)股份有限公司 | 2024-09-10 | — | — | CN | claimed |
| CN-113862234-A | Transaminase and application thereof in preparation of (R) -alpha-methyltryptamine compounds | 弈柯莱生物科技(上海)股份有限公司 | 2021-12-31 | — | — | CN | claimed |
| US-10143679-B2 | Phytoestrogen compositions and associated methods | NSE PRODUCTS, INC. (US) | 2018-12-04 | — | — | US | claimed |
| US-20180271834-A1 | PHYTOESTROGEN COMPOSITIONS AND ASSOCIATED METHODS | NSE PRODUCTS, INC. (US) | 2018-09-27 | — | — | US | claimed |
| CN-106795531-A | Methods, reagents and cells for biosynthesis of compounds | 英威达技术有限责任公司 | 2017-05-31 | — | — | CN | claimed |
| CN-105189764-A | Methods of producing 7-carbon chemicals via C1 carbon chain elongation associated with coenzyme B synthesis | INVISTA TECH SARL | 2015-12-23 | — | — | CN | claimed |
| CN-104903455-A | Method for biosynthesis of isobutene | INVISTA TECH SARL | 2015-09-09 | — | — | CN | claimed |
| CN-104768560-A | Diagnosis and treatment of autism spectrum disorders | CALIFORNIA INST OF TECHN | 2015-07-08 | — | — | CN | claimed |
| US-20150005360-A1 | PHYTOESTROGEN COMPOSITIONS AND ASSOCIATED METHODS | NSE PRODUCTS, INC. (US) | 2015-01-01 | — | — | US | claimed |
| CN-102317464-B | Biological Synthesis of Difunctional Alkanes from Carbohydrate Feedstocks | CELEXION, LLC (US) | 2014-10-29 | — | — | CN | claimed |
| CN-102317464-A | From alpha-ketoacid biosynthesizing difunctionality alkane | CELEXION LLC | 2012-01-11 | — | — | CN | claimed |
| CN-100390189-C | Production of 2 '-deoxynucleosides and 2' -deoxynucleoside precursors from 2-dehydro-3-deoxy-D-gluconic acid | EVOLOGIC S A (FR) | 2008-05-28 | — | — | CN | claimed |
| CN-1832954-A | Production of 2 '-deoxynucleosides and 2' -deoxynucleoside precursors from 2-dehydro-3-deoxy-D-gluconic acid | EVOLOGIC S A (FR) | 2006-09-13 | — | — | CN | claimed |
| CN-1207569-C | Method for assaying virus-containing sample, virus assaying method and diagnostic kit | ADVANCED LIFE SCIENCE INST INC (JP) | 2005-06-22 | — | — | CN | claimed |
| CN-1330716-A | Method for controlling gene expression in bacteria, i.e., Agrobacterium rhizogenes, to improve root nodule development, nitrogen fixation, and plant biomass production | G IN E ST R A SOCIETA CONSORTI (IT) | 2002-01-09 | — | — | CN | claimed |
| CN-1239548-A | Method for detecting or determining viruses | TONEN CORP (JP) | 1999-12-22 | — | — | CN | claimed |
| EP-0025727-B1 | INDOLE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND MEDICAMENTS CONTAINING THEM | SANOFI S.A. (FR) | 1984-03-28 | — | — | EP | claimed |
| EP-0025727-A1 | Indole derivatives, process for their preparation and medicaments containing them | SANOFI S.A. (FR) | 1981-03-25 | — | — | EP | claimed |
| CN-118956653-B | Probiotic with uric acid reducing activity, composite probiotic agent and application thereof | 齐鲁工业大学(山东省科学院) | 2025-03-18 | — | — | CN | disclosed |
| CN-119615198-A | Electrocatalytic oxidation modification method for indole skeleton-containing compound | 浙江工业大学 | 2025-03-14 | — | — | CN | disclosed |
| CN-119306681-A | Synthesis method of 3-oxazoline-5-ketone and derivative thereof | 湖南医药学院 | 2025-01-14 | — | — | CN | disclosed |
| CN-118956653-A | Probiotic with uric acid reducing activity, composite probiotic agent and application thereof | 齐鲁工业大学(山东省科学院) | 2024-11-15 | — | — | CN | disclosed |
| CN-113862234-B | Transaminase and application thereof in preparation of (R) -alpha-methyl tryptamine compound | 弈柯莱生物科技(集团)股份有限公司 | 2024-09-10 | — | — | CN | disclosed |
| CN-113862234-B | Transaminase and application thereof in preparation of (R) -alpha-methyl tryptamine compound | 弈柯莱生物科技(集团)股份有限公司 | 2024-09-10 | — | — | CN | disclosed |
| CN-117925502-B | Shinyleaf yellowhorn tissue culture solution | 山东沃奇农业开发有限公司 | 2024-07-05 | — | — | CN | disclosed |
| CN-117925502-A | Shinyleaf yellowhorn tissue culture solution | 山东沃奇农业开发有限公司 | 2024-04-26 | — | — | CN | disclosed |
| CN-107312028-B | Halogenated organoaminosilane precursors and methods of depositing thin films comprising the same | 弗萨姆材料美国有限责任公司 | 2023-04-14 | — | — | CN | disclosed |
| CN-115896823-A | D 2 Method for preparing alpha, beta-deuterated amine medicine and prodrug by electrocatalysis of nitrile with O as deuterium source | 天津大学 | 2023-04-04 | — | — | CN | disclosed |
| CN-112891343-B | Application of 3-indole acetonitrile in preparing medicine for inhibiting novel coronavirus SARS-CoV-2 | 华中农业大学 | 2022-04-01 | — | — | CN | disclosed |
| CN-113862234-A | Transaminase and application thereof in preparation of (R) -alpha-methyltryptamine compounds | 弈柯莱生物科技(上海)股份有限公司 | 2021-12-31 | — | — | CN | disclosed |
| CN-113862234-A | Transaminase and application thereof in preparation of (R) -alpha-methyltryptamine compounds | 弈柯莱生物科技(上海)股份有限公司 | 2021-12-31 | — | — | CN | disclosed |
| CN-112891343-A | Application of 3-indole acetonitrile in preparing medicine for inhibiting novel coronavirus SARS-CoV-2 | 华中农业大学 | 2021-06-04 | — | — | CN | disclosed |
| CN-105209626-B | 3- hydracrylic acid is produced by recombination yeast | 诺维信股份有限公司 | 2019-09-03 | — | — | CN | disclosed |
| US-10143679-B2 | Phytoestrogen compositions and associated methods | NSE PRODUCTS, INC. (US) | 2018-12-04 | — | — | US | disclosed |
| US-20180271834-A1 | PHYTOESTROGEN COMPOSITIONS AND ASSOCIATED METHODS | NSE PRODUCTS, INC. (US) | 2018-09-27 | — | — | US | disclosed |
| CN-107828671-A | For producing the composition and method of 3 hydracrylic acids | 卡吉尔公司 | 2018-03-23 | — | — | CN | disclosed |
| CN-107746834-A | For preparing the method and intermediate of Pregabalin | 辉瑞爱尔兰制药公司 | 2018-03-02 | — | — | CN | disclosed |
| CN-107709568-A | Method for producing and processing diamines | 基因组股份公司 | 2018-02-16 | — | — | CN | disclosed |
| CN-107586753-A | Collaboration produces isopropanol and primary alconol, the microorganism and method of dihydric alcohol and acid | 基因组股份公司 | 2018-01-16 | — | — | CN | disclosed |
| CN-107556273-A | For preparing the method and intermediate of Pregabalin | 辉瑞爱尔兰制药公司 | 2018-01-09 | — | — | CN | disclosed |
| CN-107406821-A | For producing the mutation host cell of 3 hydracrylic acids | 诺维信公司 | 2017-11-28 | — | — | CN | disclosed |
| CN-105051022-B | Process and intermediates for the preparation of pregabalin | 辉瑞爱尔兰制药公司 | 2017-10-27 | — | — | CN | disclosed |
| CN-107109444-A | Method and material for producing 6-carbon monomers | 英威达技术有限责任公司 | 2017-08-29 | — | — | CN | disclosed |
| CN-107109347-A | Recombinant host cell for producing 3 hydracrylic acids | 诺维信公司 | 2017-08-29 | — | — | CN | disclosed |
| CN-106795534-A | Method, reagent and cell for biosynthesis compound | 英威达技术有限责任公司 | 2017-05-31 | — | — | CN | disclosed |
| CN-106795531-A | Methods, reagents and cells for biosynthesis of compounds | 英威达技术有限责任公司 | 2017-05-31 | — | — | CN | disclosed |
| CN-106795530-A | Methods, reagents and cells for biosynthesis of compounds | 英威达技术有限责任公司 | 2017-05-31 | — | — | CN | disclosed |
| CN-104388443-B | Strawberry auxin synthetic rate-limiting enzyme gene FaYUC11 and application | 上海市农业科学院 | 2017-05-03 | — | — | CN | disclosed |
| CN-106119113-A | For producing the biology of 1,3 butanediols | 基因组股份公司 | 2016-11-16 | — | — | CN | disclosed |
| CN-102625846-B | Organisms for the production of 1, 3-butanediol | 基因组股份公司 | 2016-08-03 | — | — | CN | disclosed |
| CN-102762735-B | Microorganisms producing 1, 4-butanediol, 4-hydroxybutyraldehyde, 4-hydroxybutyryl-COA, putrescine and related compounds and related methods | 基因组股份公司 | 2016-08-03 | — | — | CN | disclosed |
| CN-105473726-A | Keto-isovalerate decarboxylase enzymes and methods of use thereof | BUTAMAX(TM) ADVANCED BIOFUELS LLC | 2016-04-06 | — | — | CN | disclosed |
| CN-105441374-A | Microorganism for producing 1, 4-butanediol, 4-hydroxybutyraldehyde, 4-maloyl-COA, putrescine and related compound and related method thereof | GENOMATICA INC | 2016-03-30 | — | — | CN | disclosed |
| CN-105431520-A | 3-hydroxypropionic acid production using recombinant yeast expressing insect aspartate 1-decarboxylase | NOVOZYMES AS | 2016-03-23 | — | — | CN | disclosed |
| CN-105209626-A | 3-hydroxypropionic acid production by recombinant yeasts | NOVOZYMES INC | 2015-12-30 | — | — | CN | disclosed |
| CN-105189764-A | Methods of producing 7-carbon chemicals via C1 carbon chain elongation associated with coenzyme B synthesis | INVISTA TECH SARL | 2015-12-23 | — | — | CN | disclosed |
| CN-105189770-A | Methods of producing 7-carbon chemicals via carbon chain elongation associated with cyclohexane carboxylate synthesis | INVISTA TECH SARL | 2015-12-23 | — | — | CN | disclosed |
| EP-2465929-B1 | R-HNL random variants and their use for preparing optically pure, sterically hindered cyanohydrins | DSM IP ASSETS BV (NL) | 2015-12-02 | — | — | EP | disclosed |
| CN-105051022-A | Process and intermediates for the preparation of pregabalin | PFIZER IRELAND PHARMACEUTICALS | 2015-11-11 | — | — | CN | disclosed |
| CN-104903455-A | Method for biosynthesis of isobutene | INVISTA TECH SARL | 2015-09-09 | — | — | CN | disclosed |
| CN-104884629-A | Microorganisms and methods for producing fatty alcohols of specific length and related compounds | GENOMATICA INC | 2015-09-02 | — | — | CN | disclosed |
| CN-104768560-A | Diagnosis and treatment of autism spectrum disorders | CALIFORNIA INST OF TECHN | 2015-07-08 | — | — | CN | disclosed |
| CN-104520426-A | Biosynthetic pathways, recombinant cells, and methods | UNIV MINNESOTA | 2015-04-15 | — | — | CN | disclosed |
| CN-102245780-B | Production of branched-chain alcohols by photosynthetic microoraganisms | SYNTHETIC GENOMICS INC | 2015-03-25 | — | — | CN | disclosed |
| US-20150005360-A1 | PHYTOESTROGEN COMPOSITIONS AND ASSOCIATED METHODS | NSE PRODUCTS, INC. (US) | 2015-01-01 | — | — | US | disclosed |
| CN-102317464-B | Biological Synthesis of Difunctional Alkanes from Carbohydrate Feedstocks | CELEXION, LLC (US) | 2014-10-29 | — | — | CN | disclosed |
| US-8846366-B2 | R-hydroxynitrile lyase (R-HNL) random variants and their use for preparing optically pure, sterically hindered cyanohydrins | DSM IP ASSETS BV (NL) | 2014-09-30 | — | — | US | disclosed |
| CN-103946383-A | Microorganisms and methods for producing olefins | GENOMATICA INC | 2014-07-23 | — | — | CN | disclosed |
| CN-103917651-A | Eukaryotic organisms and methods for producing 1,3-butanediol | GENOMATICA INC | 2014-07-09 | — | — | CN | disclosed |
| CN-103890185-A | Microorganisms and methods for producing 2,4-pentadienoate, butadiene, propylene, 1,3-butanediol and related alcohols | GENOMATICA INC | 2014-06-25 | — | — | CN | disclosed |
| CN-101611141-B | Random variants of R-HNL and their use for the preparation of optically pure sterically hindered cyanohydrins | DSM IP ASSETS BV | 2014-05-07 | — | — | CN | disclosed |
| EP-2092060-B1 | R-HNL RANDOM VARIANTS AND THEIR USE FOR PREPARING OPTICALLY PURE, STERICALLY HINDERED CYANOHYDRINS | DSM IP ASSETS BV (NL) | 2014-01-22 | — | — | EP | disclosed |
| CN-103502432-A | Compositions and methods for producing 3-hydroxypropionic acid | NOVOZYMES INC | 2014-01-08 | — | — | CN | disclosed |
| EP-2141148-B1 | INDOLE DERIVATIVE HAVING CPLA2 INHIBITORY ACTIVITY, USE OF THE SAME AND METHOD FOR PRODUCING THE SAME | DAIICHI SANKYO CO LTD (JP) | 2013-07-03 | — | — | EP | disclosed |
| CN-102762735-A | Microorganisms producing 1, 4-butanediol, 4-hydroxybutyraldehyde, 4-hydroxybutyryl-COA, putrescine and related compounds and related methods | GENOMATICA INC | 2012-10-31 | — | — | CN | disclosed |
| US-8293781-B2 | Indole derivatives having cPLA2 inhibiting activity and applications and production methods of the same | DAIICHI SANKYO COMPANY, LIMITED (JP) | 2012-10-23 | — | — | US | disclosed |
| CN-102625846-A | Organisms for the production of 1, 3-butanediol | GENOMATICA INC | 2012-08-01 | — | — | CN | disclosed |
| CN-102625845-A | Microorganisms and methods for the synergistic production of isopropanol and primary alcohols, glycols and acids | GENOMATICA INC | 2012-08-01 | — | — | CN | disclosed |
| EP-2465929-A1 | R-HNL random variants and their use for preparing optically pure, sterically hindered cyanohydrins | DSM IP Assets B.V. (NL) | 2012-06-20 | — | — | EP | disclosed |
| CN-101321775-B | ODCASE inhibitors for the treatment of malaria | UNIV HEALTH NETWORK | 2012-05-23 | — | — | CN | disclosed |
| CN-102317464-A | From alpha-ketoacid biosynthesizing difunctionality alkane | CELEXION LLC | 2012-01-11 | — | — | CN | disclosed |
| CN-102245780-A | Production of branched-chain alcohols by photosynthetic microoraganisms | SYNTHETIC GENOMICS INC | 2011-11-16 | — | — | CN | disclosed |
| US-20100143986-A1 | R-HNL RANDOM VARIANTS AND THEIR USE FOR PREPARING OPTICALLY PURE, STERICALLY HINDERED CYANOHYDRINS | DSM IP ASSETS BV (NL) | 2010-06-10 | — | — | US | disclosed |
| US-20100113777-A1 | INDOLE DERIVATIVES HAVING cPLA2 INHIBITING ACTIVITY AND APPLICATIONS AND PRODUCTION METHODS OF THE SAME | ASUBIO PHARMA CO., LTD. (JP) | 2010-05-06 | — | — | US | disclosed |
| US-20100041110-A1 | R-Hydroxynitrile Lyases Having Improved Substrate Acceptance and the Use Thereof | DSM FINE CHEMICALS AUSTRIA NFG GMBH & CO KG (AT) | 2010-02-18 | — | — | US | disclosed |
| EP-2141148-A1 | INDOLE DERIVATIVE HAVING CPLA2 INHIBITORY ACTIVITY, USE OF THE SAME AND METHOD FOR PRODUCING THE SAME | Asubio Pharma Co., Ltd. (JP) | 2010-01-06 | — | — | EP | disclosed |
| CN-101611141-A | Random variants of R-HNL and their use for the preparation of optically pure sterically hindered cyanohydrins | DSM IP ASSETS BV (NL) | 2009-12-23 | — | — | CN | disclosed |
| EP-2092060-A1 | R-HNL RANDOM VARIANTS AND THEIR USE FOR PREPARING OPTICALLY PURE, STERICALLY HINDERED CYANOHYDRINS | DSMIP Assets B.V. (NL) | 2009-08-26 | — | — | EP | disclosed |
| US-7572608-B2 | R-hydroxynitrillyases having improved substrate tolerance and the use thereof | DSM FINE CHEMICALS AUSTRIA NFG GMBH & CO. KG (AT) | 2009-08-11 | — | — | US | disclosed |
| CN-101495643-A | Process for preparing pentamethylene 1,5-diisocyanate | BASF SE (DE) | 2009-07-29 | — | — | CN | disclosed |
| EP-1613748-B1 | R-HYDROXYNITRILLYASES HAVING IMPROVED SUBSTRATE TOLERANCE AND THE USE THEREOF | DSM FINE CHEM AUSTRIA GMBH (AT) | 2009-04-15 | — | — | EP | disclosed |
| US-7514245-B2 | Method for producing chiral α-hydroxycarboxylic acids by enzymatic hydrolysis of chiral cyanohydrins | DSM FINE CHEMICALS AUSTRIA NFG GMBH & CO. KG (AT) | 2009-04-07 | — | — | US | disclosed |
| EP-1566441-B1 | Genes coding for hydroxynitrile lyase, recombinant proteins with hydroxynitrile lyase activity and their use | DSM FINE CHEM AUSTRIA GMBH (AT) | 2009-02-18 | — | — | EP | disclosed |
| CN-101321775-A | ODCASE inhibitors for the treatment of malaria | UNIV HEALTH NETWORK (CA) | 2008-12-10 | — | — | CN | disclosed |
| CN-101297042-A | Fermentive production of four carbon alcohols | DU PONT (US) | 2008-10-29 | — | — | CN | disclosed |
| US-20080206827-A1 | Method for producing chiral a-hydroxycarboxylic crystalline acids | DSM FINE CHEMICALS AUSTRIA NFG GMBH & CO. KG (AT) | 2008-08-28 | — | — | US | disclosed |
| US-7390647-B2 | Method for producing chiral α-hydroxycarboxylic crystalline acids | DSM FINE CHEMICALS AUSTRIA NFG GMBH & CO KG (AT) | 2008-06-24 | — | — | US | disclosed |
| WO-2008071695-A1 | R-HNL RANDOM VARIANTS AND THEIR USE FOR PREPARING OPTICALLY PURE, STERICALLY HINDERED CYANOHYDRINS | DSM IP ASSETS BV (NL) | 2008-06-19 | — | — | WO | disclosed |
| CN-100390189-C | Production of 2 '-deoxynucleosides and 2' -deoxynucleoside precursors from 2-dehydro-3-deoxy-D-gluconic acid | EVOLOGIC S A (FR) | 2008-05-28 | — | — | CN | disclosed |
| CN-101103113-A | R-hydroxynitrile lyases having improved substrate acceptance and the use thereof | DSM FINE CHEM AUSTRIA GMBH (AT) | 2008-01-09 | — | — | CN | disclosed |
| EP-1838855-A1 | R-HYDROXYNITRILE LYASES HAVING IMPROVED SUBSTRATE ACCEPTANCE AND THE USE THEREOF | DSM Fine Chemicals Austria Nfg GmbH & Co KG (AT) | 2007-10-03 | — | — | EP | disclosed |
| US-7202075-B2 | Isolated protein having hydroxynitrile lyase activity | DSM FINE CHEMICALS AUSTRIA NFG GMBH & CO KG (AT) | 2007-04-10 | — | — | US | disclosed |
| CN-1287154-C | Method for detecting or determining virus | ADVANCED LIFE SCIENCE INST INC (JP) | 2006-11-29 | — | — | CN | disclosed |
| CN-1832954-A | Production of 2 '-deoxynucleosides and 2' -deoxynucleoside precursors from 2-dehydro-3-deoxy-D-gluconic acid | EVOLOGIC S A (FR) | 2006-09-13 | — | — | CN | disclosed |
| US-20060199256-A1 | Method for producing chiral alpha-hydroxycarboxylic acids by enzymatic hydrolysis of chiral cyanohydrins | DSM FINE CHEMICALS AUSTRIA NFG GMBH & CO KG (AT) | 2006-09-07 | — | — | US | disclosed |
| WO-2006076965-A1 | R-HYDROXYNITRILE LYASES HAVING IMPROVED SUBSTRATE ACCEPTANCE AND THE USE THEREOF | DSM FINE CHEMICALS AUSTRIA NFG GMBH & CO KG (AT) | 2006-07-27 | — | — | WO | disclosed |
| EP-0927766-B1 | Enzymatic process for the preparation of (S)-cyanhydrines | DSM FINE CHEM AUSTRIA GMBH (AT) | 2006-06-14 | — | — | EP | disclosed |
| US-7052885-B2 | Process for preparing heterocyclic (R)- and (S)-cyanohydrins | DSM FINE CHEMICALS AUSTRIA NFG GMBH & CO KG (AT) | 2006-05-30 | — | — | US | disclosed |
| US-20060105434-A1 | R-hydroxynitrillyases havign improved substrate tolerance and the use thereof | DSM FINE CHEMICALS AUSTRIA NFG GMBH & COKG (AT) | 2006-05-18 | — | — | US | disclosed |
| US-20060099696-A1 | Method for Producing Chiral Alpha-Hydroxycarboxylic Crystalline Acids | DSM FINE CHEMICALS AUSTRIA NFG GMBH & CO KG (AT) | 2006-05-11 | — | — | US | disclosed |
| EP-1323830-B1 | Process for the preparation of heterocyclic (R)- et (S)-cyanohydrines | DSM FINE CHEM AUSTRIA GMBH (AT) | 2006-04-26 | — | — | EP | disclosed |
| EP-1223220-B1 | Genes coding for hydroxynitrile lyase, recombinant proteins with hydroxynitrile lyase activity and their use | DSM FINE CHEM AUSTRIA GMBH (AT) | 2006-03-01 | — | — | EP | disclosed |
| EP-1566441-A1 | Genes coding for hydroxynitrile lyase, recombinant proteins with hydroxynitrile lyase activity and their use | DSM Fine Chemicals Austria Nfg GmbH & Co KG (AT) | 2005-08-24 | — | — | EP | disclosed |
| EP-1148042-B1 | Method for producing optically and chemically pure (R)- and (S)-hydroxycarboxylic acids | DSM FINE CHEM AUSTRIA GMBH (AT) | 2005-07-06 | — | — | EP | disclosed |
| CN-1207569-C | Method for assaying virus-containing sample, virus assaying method and diagnostic kit | ADVANCED LIFE SCIENCE INST INC (JP) | 2005-06-22 | — | — | CN | disclosed |
| US-20050064552-A1 | Genes containing a DNA sequence coding for hydroxynitrile lyase, recombinant proteins derived therefrom and having hydroxynitrile lyase activity, and use thereof | DSM FINE CHEMICALS AUSTRIA NFG GMBH & COKG (AT) | 2005-03-24 | — | — | US | disclosed |
| US-6861243-B2 | Genes containing a DNA sequence coding for hydroxynitrile lyase, recombinant proteins derived therefrom and having hydroxynitrile lyase activity, and use thereof | DSM FINE CHEMICALS AUSTRIA NFG GMBH & CO. KG (AT) | 2005-03-01 | — | — | US | disclosed |
| WO-2004090124-A2 | SEQUENCES ENCODING S-HYDROXYNITRIL LYASES AND THEIR USE IN METHODS FOR THE PRODUCTION OF CYANOHYDRINS | BASF AKTIENGESELLSCHAFT (DE) | 2004-10-21 | — | — | WO | disclosed |
| US-6781012-B2 | ACID HYDROLYSIS OF THE CORRESPONDING CYANOHYDRIN; EXTRACTION; COOLING | DSM FINE CHEMICALS AUSTRIA NFG GMBH & CO KG (AT) | 2004-08-24 | — | — | US | disclosed |
| EP-1010702-B1 | Process for preparing ortho-substituted aryl metal compounds and their conversion with electrophiles | MERCK PATENT GMBH (DE) | 2004-07-28 | — | — | EP | disclosed |
| CN-1492231-A | Method for detecting or determining virus | 株式会社先端生命科学研究所 | 2004-04-28 | — | — | CN | disclosed |
| US-6717006-B1 | REACTING ALDEHYDE OR KETONE WITH HYDROCYANIC ACID STIRRED AQUEOUS-SOLVENT EMULSION; REDUCED ENZYME AND TIME REQUIREMENTS | DSM FINE CHEMICALS AUSTRIA NFG GMBH & CO KG (AT) | 2004-04-06 | — | — | US | disclosed |
| EP-1010703-B1 | Process for preparing aryl metal compounds and their conversion with electrophiles | MERCK PATENT GMBH (DE) | 2004-02-25 | — | — | EP | disclosed |
| EP-1238094-B1 | METHOD FOR THE PRODUCTION OF OPTICALLY ACTIVE CYANOHYDRINS USING R-OXYNITRILASE | DSM FINE CHEM AUSTRIA GMBH (AT) | 2004-02-04 | — | — | EP | disclosed |
| US-20030129712-A1 | Process for preparing heterocyclic (R)- and (S)-cyanohydrins | DSM FINE CHEMICALS AUSTRIA NFG GMBH & COKG (AT) | 2003-07-10 | — | — | US | disclosed |
| EP-1323830-A2 | Process for the preparation of heterocyclic (R)- and (S)-cyanohydrines | DSM Fine Chemicals Austria Nfg GmbH & Co KG (AT) | 2003-07-02 | — | — | EP | disclosed |
| US-20030119099-A1 | Genes containing a DNA sequence coding for hydroxynitrile lyase, recombinant proteins derived therefrom and having hydroxynitrile lyase activity, and use thereof | DSM FINE CHEMICALS AUSTRIA NFG GMBH & COKG (AT) | 2003-06-26 | — | — | US | disclosed |
| EP-1223220-A1 | Genes coding for hydroxynitrile lyase, recombinant proteins with hydroxynitrile lyase activity and their use | DSM Fine Chemicals Austria Nfg GmbH & Co KG (AT) | 2002-07-17 | — | — | EP | disclosed |
| EP-1223168-A1 | Method for the preparation of enantiomerically enriched amino and hydroxyfuranones | DSM Fine Chemicals Austria Nfg GmbH & Co KG (AT) | 2002-07-17 | — | — | EP | disclosed |
| US-6417377-B1 | Process for preparing enantiomer-enriched amino- and hydroxyfuranones | DSM FINE CHEMICALS AUSTRIA NFG GMBH & CO KG (AT) | 2002-07-09 | — | — | US | disclosed |
| EP-0957083-B1 | Process for stabilising cyanhydrines | DSM FINE CHEM AUSTRIA GMBH (AT) | 2002-04-10 | — | — | EP | disclosed |
| CN-1330716-A | Method for controlling gene expression in bacteria, i.e., Agrobacterium rhizogenes, to improve root nodule development, nitrogen fixation, and plant biomass production | G IN E ST R A SOCIETA CONSORTI (IT) | 2002-01-09 | — | — | CN | disclosed |
| US-20010041359-A1 | Process for the preparation of optically and chemically highly pure (R) - or (S) -alpha- hydroxycarboxylic acids | DSM FINE CHEMICALS AUSTRIA NFG GMBH & COKG (AT) | 2001-11-15 | — | — | US | disclosed |
| EP-1148042-A2 | Method for producing optically and chemically pure (R)- and (S)-hydroxycarboxylic acids | DSM Fine Chemicals Austria Nfg GmbH & Co KG (AT) | 2001-10-24 | — | — | EP | disclosed |
| US-6225095-B1 | REACTING ALDEHYDE OR KETONE DISSOLVED IN AN ORGANIC, WATER-IMMISCIBLE OR SLIGHTLY MISCIBLE DILUENT, AN AQUEOUS HYDROXYNITRILE LYASE SOLUTION, AND A CYANIDE GROUP DONOR TO FORM AN EMULSION WHICH IS MAINTAINED BY STIRRING | DSM FINE CHEMICALS AUSTRIA GMBH (AT) | 2001-05-01 | — | — | US | disclosed |
| US-6207835-B1 | DEPROTONATION IN CONTINUOUS FLOW REACTOR | MERCK KGAA (DE) | 2001-03-27 | — | — | US | disclosed |
| EP-1010702-A2 | Process for preparing ortho-substituted aryl metal compounds and their conversion with electrophiles | MERCK PATENT GmbH (DE) | 2000-06-21 | — | — | EP | disclosed |
| EP-1010703-A2 | Process for preparing aryl metal compounds and their conversion with electrophiles | MERCK PATENT GmbH (DE) | 2000-06-21 | — | — | EP | disclosed |
| US-6031123-A | Process for stabilizing cyanohydrins | DSM FINE CHEMICALS AUSTRIA GMBH (AT) | 2000-02-29 | — | — | US | disclosed |
| CN-1239548-A | Method for detecting or determining viruses | TONEN CORP (JP) | 1999-12-22 | — | — | CN | disclosed |
| EP-0957083-A2 | Process for stabilising cyanhydrines | DSM Fine Chemicals Austria GmbH (AT) | 1999-11-17 | — | — | EP | disclosed |
| EP-0927766-A1 | Enzymatic process for the preparation of (S)-cyanhydrines | DSM Fine Chemicals Austria GmbH (AT) | 1999-07-07 | — | — | EP | disclosed |
| US-4510315-A | CARDIOVASCULAR DISORDERS | SANOFI, S.A. (FR) | 1985-04-09 | — | — | US | disclosed |
| EP-0025727-B1 | INDOLE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND MEDICAMENTS CONTAINING THEM | SANOFI S.A. (FR) | 1984-03-28 | — | — | EP | disclosed |
| US-4404217-A | DRUGS ACTIVE ON CARDIOVASCULAR SYSTEM | C. M. INDUSTRIES (FR) | 1983-09-13 | — | — | US | disclosed |
| EP-0025727-A1 | Indole derivatives, process for their preparation and medicaments containing them | SANOFI S.A. (FR) | 1981-03-25 | — | — | EP | disclosed |
| US-4104402-A | BRONCHODILATORS | TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) | 1978-08-01 | — | — | US | disclosed |
| US-4035512-A | Aminotetralols | TAKEDA CHEMICAL INDUSTRIES, LTD. (JA) | 1977-07-12 | — | — | US | disclosed |
| US-4010202-A | TREATMENT OF ASTHMA AND ARRHYTHMIA | TAKEDA CHEMICAL INDUSTRIES, LTD. (JA) | 1977-03-01 | — | — | US | disclosed |
| US-3953442-A | ANALGESICS, CENTRAL NERVOUS SYSTEM | CLIN MIDY (FR) | 1976-04-27 | — | — | US | disclosed |
| US-3953442-A | ANALGESICS, CENTRAL NERVOUS SYSTEM | CLIN MIDY (FR) | 1976-04-27 | — | — | US | disclosed |
| US-3933853-A | ANALGESICS, TRANQUILIZERS | CLIN MIDY (FR) | 1976-01-20 | — | — | US | disclosed |
| US-3933853-A | ANALGESICS, TRANQUILIZERS | CLIN MIDY (FR) | 1976-01-20 | — | — | 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 (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-20100113777-A1 | INDOLE DERIVATIVES HAVING cPLA2 INHIBITING ACTIVITY AND APPLICATIONS AND PRODUCTION METHODS OF THE SAME | PLA2G4A, PLA2G2E, PLA2G6 | MTNR1A 342/4885MTNR1B 387/4885LOXL2 267/4885 |
“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.