Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | NPSR1 | Q6W5P4 | 2/20 | 0.61 |
| ▸ | VCP | P55072 | 1/20 | 0.55 |
| ▸ | APP | P05067 | 1/20 | 0.50 |
| ▸ | NPC1 | O15118 | 5/20 | 0.48 |
| ▸ | RAB9A | P51151 | 5/20 | 0.48 |
| ▸ | HSP90AA1 | P07900 | 2/20 | 0.48 |
| ▸ | AGTR1 | P30556 | 1/20 | 0.48 |
| ▸ | PAX8 | Q06710 | 1/20 | 0.48 |
| ▸ | TLR9 | Q9NR96 | 1/20 | 0.48 |
| ▸ | MEN1 | O00255 | 2/20 | 0.46 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.46 |
| ▸ | POLB | P06746 | 1/20 | 0.46 |
| ▸ | NLRP3 | Q96P20 | 1/20 | 0.46 |
| ▸ | FFAR1 | O14842 | 5/20 | 0.45 |
| ▸ | MTOR | P42345 | 1/20 | 0.45 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.44 |
| ▸ | MAPT | P10636 | 1/20 | 0.44 |
| ▸ | OPRK1 | P41145 | 1/20 | 0.44 |
| ▸ | PAM | P19021 | 1/20 | 0.44 |
| ▸ | AR | P10275 | 1/20 | 0.42 |
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 | |
|---|---|---|---|---|
| SCHEMBL16803398 | 0.84 | NPSR1 (0.44) | NPSR1VCPNPC1RAB9AHSP90AA1 | |
| 4-Phenyl-3-Butyn-2-One SCHEMBL3986965 | 0.82 | GLA (0.68) | NPSR1VCPNPC1KMT2AFFAR1 | |
| Butenone SCHEMBL3986956 | 0.82 | GLA (0.68) | NPSR1VCPNPC1KMT2AFFAR1 | |
| SCHEMBL8605811 | 0.80 | APP (0.55) | NPSR1VCPAPPNPC1RAB9A | |
| SCHEMBL68968 | 0.80 | NPSR1 (0.59) | NPSR1VCPAPPNPC1RAB9A | |
| SCHEMBL3346483 | 0.80 | NPSR1 (0.59) | NPSR1VCPAPPNPC1RAB9A | |
| Benzene SCHEMBL28174766 | 0.80 | NPSR1 (0.59) | NPSR1VCPAPPNPC1RAB9A | |
| SCHEMBL8103677 | 0.80 | NPSR1 (0.59) | NPSR1VCPAPPNPC1RAB9A | |
| SCHEMBL12430908 | 0.79 | VCP (0.53) | NPSR1VCPRAB9AMEN1KMT2A | |
| SCHEMBL17957122 | 0.78 | NPSR1 (0.57) | NPSR1VCPAPPNPC1RAB9A |
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 221 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-117384199-A | Preparation of novel organic aluminum hydrogen compound and preparation method of unsaturated alcohol compound catalyzed by novel organic aluminum hydrogen compound | 北京理工大学 | 2024-01-12 | — | — | CN | claimed |
| CN-114874121-A | Method for preparing material containing monothiocarbonate group and product | 浙江大学 | 2022-08-09 | — | — | CN | claimed |
| CN-111822052-B | Preparation method of catalyst obtained by modifying palladium, catalyst and application | 厦门大学 | 2021-12-03 | — | — | CN | claimed |
| CN-111774096-B | Catalyst modified by thiol ligand and preparation method and application thereof | 厦门大学 | 2021-12-03 | — | — | CN | claimed |
| CN-111822052-A | Preparation method of catalyst obtained by modifying palladium, catalyst and application | 厦门大学 | 2020-10-27 | — | — | CN | claimed |
| CN-111774096-A | Catalyst modified by thiol ligand and preparation method and application thereof | 厦门大学 | 2020-10-16 | — | — | CN | claimed |
| WO-2019161649-A1 | 1-(8-ARYLNAPHTHYL)PHOSPHINE LIGAND AND PREPARATION METHOD THEREFOR, AND PHOSPHINE GOLD COMPLEX AND USE | 华中师范大学 | 2019-08-29 | — | — | WO | claimed |
| EP-2442783-B1 | NOVEL DEODORISING COMPOSITIONS AND DEODORISING PRODUCTS CONTAINING SAME | ROBERTET SA (FR) | 2017-08-09 | — | — | EP | claimed |
| US-9265852-B2 | Deordorising compositions and deodorising products containing same | ROBERTET S.A. (FR) | 2016-02-23 | — | — | US | claimed |
| US-20120201778-A1 | NOVEL DEORDORISING COMPOSITIONS AND DEODORISING PRODUCTS CONTAINING SAME | ROBERTET S.A. (FR) | 2012-08-09 | — | — | US | claimed |
| EP-2442783-A2 | NOVEL DEODORISING COMPOSITIONS AND DEODORISING PRODUCTS CONTAINING SAME | Robertet S.A. (FR) | 2012-04-25 | — | — | EP | claimed |
| EP-2272491-A1 | New deodorising compositions and deodorant products containing them | Robertet S.A. (FR) | 2011-01-12 | — | — | EP | claimed |
| WO-2010146258-A2 | NOVEL DEODORISING COMPOSITIONS AND DEODORISING PRODUCTS CONTAINING SAME | ROBERTET S.A. (FR) | 2010-12-23 | — | — | WO | claimed |
| US-20080275264-A1 | PROCESS FOR THE PREPARATION OF HALOGENOALKYLDIALKYL CHLOROSILANE | RHODIA CHIMIE (FR) | 2008-11-06 | — | — | US | claimed |
| EP-1633761-B1 | METHOD OF PREPARING HALOGENOALKYLDIALKYLCHLOROSILANE | RHODIA CHIMIE SA (FR) | 2008-05-07 | — | — | EP | claimed |
| US-20070185344-A1 | Method of preparing halogenoalkyldialkyl chlorosilane | RHODIA CHIMIE (FR) | 2007-08-09 | — | — | US | claimed |
| EP-1633761-A2 | METHOD OF PREPARING HALOGENOALKYLDIALKYLCHLOROSILANE | Rhodia Chimie (FR) | 2006-03-15 | — | — | EP | claimed |
| WO-2004113354-A2 | METHOD OF PREPARING HALOGENOALKYLDIALKYLCHLOROSILANE | RHODIA CHIMIE (FR) | 2004-12-29 | — | — | WO | claimed |
| US-4514267-A | Zinc electroplating additive concentrate | OMI INTERNATIONAL CORPORATION (US) | 1985-04-30 | — | — | US | claimed |
| JP-10236986-A | — | — | None | — | — | JP | disclosed |
| JP-6009631-A | — | — | None | — | — | JP | disclosed |
| US-12617765-B2 | Cannabinoid derivatives | CANOPY GROWTH CORPORATION (CA) | 2026-05-05 | — | — | US | disclosed |
| US-12618050-B2 | Engineered polypeptides that exhibit increased catalytic efficiency for unnatural cofactors and uses thereof | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 2026-05-05 | — | — | US | disclosed |
| US-20250059156-A1 | THERAPEUTIC ALKALOID COMPOUNDS | SENSORIUM THERAPEUTICS, INC. | 2025-02-20 | — | — | US | disclosed |
| EP-3997095-B1 | CANNABINOID DERIVATIVES | CANOPY GROWTH CORP (CA) | 2025-02-12 | — | — | EP | disclosed |
| EP-4165017-B1 | USE OF STROBILURIN TYPE COMPOUNDS FOR COMBATING PHYTOPATHOGENIC FUNGI CONTAINING AN AMINO ACID SUBSTITUTION F129L IN THE MITOCHONDRIAL CYTOCHROME B PROTEIN CONFERRING RESISTANCE TO QO INHIBITORS V | BASF SE (DE) | 2024-09-04 | — | — | EP | disclosed |
| WO-2024102991-A1 | THERAPEUTIC ALKALOID COMPOUNDS | SENSORIUM THERAPEUTICS, INC. (US) | 2024-05-16 | — | — | WO | disclosed |
| CN-114409501-B | Method for preparing propargyl alcohol compound by taking pinacol borane as hydrogen source | 云南民族大学 | 2024-05-10 | — | — | CN | disclosed |
| US-20240150345-A1 | GCN2 MODULATING COMPOUNDS AND USES THEREOF | PHARMARON UK LTD. (GB) | 2024-05-09 | — | — | US | disclosed |
| CN-117384199-A | Preparation of novel organic aluminum hydrogen compound and preparation method of unsaturated alcohol compound catalyzed by novel organic aluminum hydrogen compound | 北京理工大学 | 2024-01-12 | — | — | CN | disclosed |
| CN-115197108-B | Preparation method of gamma-ketosulfone compound | 南华大学 | 2023-11-28 | — | — | CN | disclosed |
| CN-114874121-B | Method for preparing substance containing monothiocarbonate group and product | 浙江大学 | 2023-10-03 | — | — | CN | disclosed |
| US-20230303483-A1 | USE OF STROBILURIN TYPE COMPOUNDS FOR COMBATING PHYTOPATHOGENIC FUNGI CONTAINING AN AMINO ACID SUBSTITUTION F129L IN THE MITOCHONDRIAL CYTOCHROME B PROTEIN CONFERRING RESISTANCE TO QO INHIBITORS V | BASF SE (DE) | 2023-09-28 | — | — | US | disclosed |
| EP-4242198-A1 | USE OF STROBILURIN TYPE COMPOUNDS FOR COMBATING PHYTOPATHOGENIC FUNGI CONTAINING AN AMINO ACID SUBSTITUTION F129L IN THE MITOCHONDRIAL CYTOCHROME B PROTEIN CONFERRING RESISTANCE TO QO INHIBITORS XIV | BASF SE (DE) | 2023-09-13 | — | — | EP | disclosed |
| CN-112939917-B | Preparation method of flavonoid compound | 中山大学 | 2023-08-22 | — | — | CN | disclosed |
| CN-113831272-B | Method for synthesizing 2-substituted indole compound by palladium-catalyzed iodobenzene and oxime ester | 华南理工大学 | 2023-07-18 | — | — | CN | disclosed |
| EP-4165017-A1 | USE OF STROBILURIN TYPE COMPOUNDS FOR COMBATING PHYTOPATHOGENIC FUNGI CONTAINING AN AMINO ACID SUBSTITUTION F129L IN THE MITOCHONDRIAL CYTOCHROME B PROTEIN CONFERRING RESISTANCE TO QO INHIBITORS V | BASF SE (DE) | 2023-04-19 | — | — | EP | disclosed |
| CN-113648291-B | Application of benzyl ketene compound in preparing lung cancer chemotherapy sensitization medicine and medicine | 丽水市中心医院 | 2023-03-14 | — | — | CN | disclosed |
| CN-115702139-A | Use of strobilurin-type compounds to control phytopathogenic fungi containing the amino acid substitution F129L in the mitochondrial cytochrome b protein conferring tolerance to Qo inhibitor V | 巴斯夫欧洲公司 | 2023-02-14 | — | — | CN | disclosed |
| US-20230024212-A1 | CANNABINOID DERIVATIVES | JGB COLLATERAL LLC | 2023-01-26 | — | — | US | disclosed |
| US-20230024212-A1 | CANNABINOID DERIVATIVES | JGB COLLATERAL LLC | 2023-01-26 | — | — | US | disclosed |
| US-20230002558-A1 | REACTIVE POLYAMIDEIMIDE OLIGOMERS, METHODS, AND ARTICLES | THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL | 2023-01-05 | — | — | US | disclosed |
| EP-4073053-A1 | CANNABINOID DERIVATIVES | Canopy Growth Corporation (CA) | 2022-10-19 | — | — | EP | disclosed |
| CN-115197108-A | Preparation method of gamma-ketosulfone compound | 南华大学 | 2022-10-18 | — | — | CN | disclosed |
| US-20220259221-A1 | CANNABINOID DERIVATIVES | CANOPY GROWTH CORPORATION (CA) | 2022-08-18 | — | — | US | disclosed |
| CN-114874121-A | Method for preparing material containing monothiocarbonate group and product | 浙江大学 | 2022-08-09 | — | — | CN | disclosed |
| US-20220242844-A1 | CANNABINOID DERIVATIVES | CANOPY GROWTH CORPORATION (CA) | 2022-08-04 | — | — | US | disclosed |
| WO-2022159745-A1 | GCN2 MODULATING COMPOUNDS AND USES THEREOF | HIBERCELL, INC. (US) | 2022-07-28 | — | — | WO | disclosed |
| EP-3997095-A1 | CANNABINOID DERIVATIVES | Canopy Growth Corporation (CA) | 2022-05-18 | — | — | EP | disclosed |
| EP-3994129-A1 | CANNABINOID DERIVATIVES | Canopy Growth Corporation (CA) | 2022-05-11 | — | — | EP | disclosed |
| CN-114409501-A | Method for preparing propargyl alcohol compound by taking pinacol borane as hydrogen source | 云南民族大学 | 2022-04-29 | — | — | CN | disclosed |
| US-20220090027-A1 | ENGINEERED POLYPEPTIDES THAT EXHIBIT INCREASED CATALYTIC EFFICIENCY FOR UNNATURAL COFACTORS AND USES THEREOF | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA | 2022-03-24 | — | — | US | disclosed |
| EP-3945089-A1 | USE OF STROBILURIN TYPE COMPOUNDS FOR COMBATING PHYTOPATHOGENIC FUNGI CONTAINING AN AMINO ACID SUBSTITUTION F129L IN THE MITOCHONDRIAL CYTOCHROME B PROTEIN CONFERRING RESISTANCE TO QO INHIBITORS V | BASF SE (DE) | 2022-02-02 | — | — | EP | disclosed |
| CN-113831272-A | Method for synthesizing 2-substituted indole compound by using palladium to catalyze iodobenzene and oxime ester | 华南理工大学 | 2021-12-24 | — | — | CN | disclosed |
| WO-2021249928-A1 | USE OF STROBILURIN TYPE COMPOUNDS FOR COMBATING PHYTOPATHOGENIC FUNGI CONTAINING AN AMINO ACID SUBSTITUTION F129L IN THE MITOCHONDRIAL CYTOCHROME B PROTEIN CONFERRING RESISTANCE TO QO INHIBITORS V | BASF SE (DE) | 2021-12-16 | — | — | WO | disclosed |
| CN-112158866-B | Preparation method of hydroxy alumina and catalyst thereof | 厦门大学 | 2021-12-03 | — | — | CN | disclosed |
| CN-111822052-B | Preparation method of catalyst obtained by modifying palladium, catalyst and application | 厦门大学 | 2021-12-03 | — | — | CN | disclosed |
| CN-111774096-B | Catalyst modified by thiol ligand and preparation method and application thereof | 厦门大学 | 2021-12-03 | — | — | CN | disclosed |
| CN-110218229-B | Beta-mercapto azaphospho heterocyclic derivative and preparation method thereof | 江苏强盛功能化学股份有限公司 | 2021-08-17 | — | — | CN | disclosed |
| CN-110272450-B | Beta-thiocarbonyl diphosphonic acid derivative and preparation method thereof | 江苏强盛功能化学股份有限公司 | 2021-08-17 | — | — | CN | disclosed |
| CN-110256496-B | Beta-thioindolone derivative and preparation method thereof | 江苏强盛功能化学股份有限公司 | 2021-08-17 | — | — | CN | disclosed |
| WO-2021113959-A1 | CANNABINOID DERIVATIVES | CANOPY GROWTH CORPORATION (CA) | 2021-06-17 | — | — | WO | disclosed |
| WO-2021113959-A1 | CANNABINOID DERIVATIVES | CANOPY GROWTH CORPORATION (CA) | 2021-06-17 | — | — | WO | disclosed |
| CN-112939917-A | Preparation method of flavonoid compound | 中山大学 | 2021-06-11 | — | — | CN | disclosed |
| WO-2021007660-A1 | CANNABINOID DERIVATIVES | CANOPY GROWTH CORPORATION (CA) | 2021-01-21 | — | — | WO | disclosed |
| WO-2021007660-A1 | CANNABINOID DERIVATIVES | CANOPY GROWTH CORPORATION (CA) | 2021-01-21 | — | — | WO | disclosed |
| US-20210009508-A1 | Automated Synthesis of Small Molecules Using Chiral, Non-Racemic Boronates | NATIONAL SCIENCE FOUNDATION | 2021-01-14 | — | — | US | disclosed |
| WO-2021000054-A1 | CANNABINOID DERIVATIVES | CANOPY GROWTH CORPORATION (CA) | 2021-01-07 | — | — | WO | disclosed |
| WO-2021000054-A1 | CANNABINOID DERIVATIVES | CANOPY GROWTH CORPORATION (CA) | 2021-01-07 | — | — | WO | disclosed |
| CN-112158866-A | Preparation method of hydroxy alumina and catalyst thereof | 厦门大学 | 2021-01-01 | — | — | CN | disclosed |
| CN-111822052-A | Preparation method of catalyst obtained by modifying palladium, catalyst and application | 厦门大学 | 2020-10-27 | — | — | CN | disclosed |
| CN-111774096-A | Catalyst modified by thiol ligand and preparation method and application thereof | 厦门大学 | 2020-10-16 | — | — | CN | disclosed |
| US-10752577-B2 | Automated synthesis of small molecules using chiral, non-racemic boronates | THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS (US) | 2020-08-25 | — | — | US | disclosed |
| WO-2020123563-A1 | ENGINEERED POLYPEPTIDES THAT EXHIBIT INCREASED CATALYTIC EFFICIENCY FOR UNNATURAL COFACTORS AND USES THEREOF | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 2020-06-18 | — | — | WO | disclosed |
| US-20190315676-A1 | AUTOMATED SYNTHESIS OF SMALL MOLECULES USING CHIRAL, NON-RACEMIC BORONATES | THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS | 2019-10-17 | — | — | US | disclosed |
| WO-2019161649-A1 | 1-(8-ARYLNAPHTHYL)PHOSPHINE LIGAND AND PREPARATION METHOD THEREFOR, AND PHOSPHINE GOLD COMPLEX AND USE | 华中师范大学 | 2019-08-29 | — | — | WO | disclosed |
| US-10287225-B2 | Chain multiyne compound, preparation method and application thereof | XIAMEN UNIVERSITY (CN) | 2019-05-14 | — | — | US | disclosed |
| US-10287225-B2 | Chain multiyne compound, preparation method and application thereof | XIAMEN UNIVERSITY (CN) | 2019-05-14 | — | — | US | disclosed |
| US-10239824-B2 | Automated synthesis of small molecules using chiral, non-racemic boronates | THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS (US) | 2019-03-26 | — | — | US | disclosed |
| US-20180065908-A1 | CHAIN MULTIYNE COMPOUND, PREPARATION METHOD AND APPLICATION THEREOF | XIAMEN UNIVERSITY (CN) | 2018-03-08 | — | — | US | disclosed |
| US-20180065908-A1 | CHAIN MULTIYNE COMPOUND, PREPARATION METHOD AND APPLICATION THEREOF | XIAMEN UNIVERSITY (CN) | 2018-03-08 | — | — | US | disclosed |
| US-20180065908-A1 | CHAIN MULTIYNE COMPOUND, PREPARATION METHOD AND APPLICATION THEREOF | XIAMEN UNIVERSITY (CN) | 2018-03-08 | — | — | US | disclosed |
| EP-2442783-B1 | NOVEL DEODORISING COMPOSITIONS AND DEODORISING PRODUCTS CONTAINING SAME | ROBERTET SA (FR) | 2017-08-09 | — | — | EP | disclosed |
| US-20170158614-A1 | AUTOMATED SYNTHESIS OF SMALL MOLECULES USING CHIRAL, NON-RACEMIC BORONATES | NATIONAL SCIENCE FOUNDATION | 2017-06-08 | — | — | US | disclosed |
| EP-2788359-B1 | COMPOSITION AND METHOD FOR NEUROPEPTIDE S RECEPTOR (NPSR) ANTAGONISTS | RES TRIANGLE INST (US) | 2017-03-01 | — | — | EP | disclosed |
| US-9388131-B2 | Automated synthesis of small molecules using chiral, non-racemic boronates | THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS (US) | 2016-07-12 | — | — | US | disclosed |
| US-9302970-B2 | Process for preparation of alkynyl carboxylic acids | COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) | 2016-04-05 | — | — | US | disclosed |
| US-9265852-B2 | Deordorising compositions and deodorising products containing same | ROBERTET S.A. (FR) | 2016-02-23 | — | — | US | disclosed |
| WO-2016012333-A1 | PESTICIDAL COMPOUNDS | SYNGENTA PARTICIPATIONS AG (CH) | 2016-01-28 | — | — | WO | disclosed |
| US-20150329567-A1 | Automated Synthesis of Small Molecules Using Chiral, Non-Racemic Boronates | THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS | 2015-11-19 | — | — | US | disclosed |
| US-9181265-B2 | Substituted 2,3-dihydro-1H-benzo[a]pyrano[2,3-c]phenazines as anti-angiogenic and anti-cancer agents | UNIVERSITE CATHOLIQUE DE LOUVAIN (BE) | 2015-11-10 | — | — | US | disclosed |
| US-9150582-B2 | Composition and method for neuropeptide S receptor (NPSR) antagonists | RESEARCH TRIANGLE INSTITUTE (US) | 2015-10-06 | — | — | US | disclosed |
| US-9150582-B2 | Composition and method for neuropeptide S receptor (NPSR) antagonists | RESEARCH TRIANGLE INSTITUTE (US) | 2015-10-06 | — | — | US | disclosed |
| WO-2015110502-A1 | COMBINATION OF CROSS-LINKERS | NEXAM CHEMICAL AB (SE) | 2015-07-30 | — | — | WO | disclosed |
| EP-2085220-B1 | Resin composition for laser engraving, relief printing plate precursor for laser engraving, relief printing plate and method of producing the same | FUJIFILM CORP (JP) | 2015-05-20 | — | — | EP | disclosed |
| US-9012658-B2 | Automated synthesis of small molecules using chiral, non-racemic boronates | THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS (US) | 2015-04-21 | — | — | US | disclosed |
| US-20150057268-A1 | COMPOSITION AND METHOD FOR NEUROPEPTIDE S RECEPTOR (NPSR) ANTAGONISTS | RESEARCH TRIANGLE INSTITUTE (US) | 2015-02-26 | — | — | US | disclosed |
| US-20150057268-A1 | COMPOSITION AND METHOD FOR NEUROPEPTIDE S RECEPTOR (NPSR) ANTAGONISTS | RESEARCH TRIANGLE INSTITUTE (US) | 2015-02-26 | — | — | US | disclosed |
| US-20150025269-A1 | PROCESS FOR PREPARATION OF ALKYNYL CARBOXYLIC ACIDS | COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) | 2015-01-22 | — | — | US | disclosed |
| US-20130289030-A1 | NOVEL PHENAZINE DERIVATIVES AND THEIR USES | UNIVERSITE LIBRE DE BRUXELLES (BE) | 2013-10-31 | — | — | US | disclosed |
| US-20130252972-A1 | ISOXAZOLE, ISOTHIAZOLE, FURANE AND THIOPHENE COMPOUNDS AS MICROBICIDES | SYNGENTA CROP PROTECTION LLC (US) | 2013-09-26 | — | — | US | disclosed |
| US-20130252972-A1 | ISOXAZOLE, ISOTHIAZOLE, FURANE AND THIOPHENE COMPOUNDS AS MICROBICIDES | SYNGENTA CROP PROTECTION LLC (US) | 2013-09-26 | — | — | US | disclosed |
| US-20130252972-A1 | ISOXAZOLE, ISOTHIAZOLE, FURANE AND THIOPHENE COMPOUNDS AS MICROBICIDES | SYNGENTA CROP PROTECTION LLC (US) | 2013-09-26 | — | — | US | disclosed |
| US-8519132-B2 | Mild and selective vanadium-catalyzed oxidation of benzylic, allylic, and propargylic alcohols using air | LOS ALAMOS NATIONAL SECURITY, LLC (US) | 2013-08-27 | — | — | US | disclosed |
| US-8519132-B2 | Mild and selective vanadium-catalyzed oxidation of benzylic, allylic, and propargylic alcohols using air | LOS ALAMOS NATIONAL SECURITY, LLC (US) | 2013-08-27 | — | — | US | disclosed |
| US-8519132-B2 | Mild and selective vanadium-catalyzed oxidation of benzylic, allylic, and propargylic alcohols using air | LOS ALAMOS NATIONAL SECURITY, LLC (US) | 2013-08-27 | — | — | US | disclosed |
| WO-2013086200-A1 | COMPOSITION AND METHOD FOR NEUROPEPTIDE S RECEPTOR (NPSR) ANTAGONISTS | RESEARCH TRIANGLE INSTITUTE (US) | 2013-06-13 | — | — | WO | disclosed |
| EP-2595985-A1 | ISOXAZOLE, ISOTHIAZOLE, FURANE AND THIOPHENE COMPOUNDS AS MICROBICIDES | Syngenta Participations AG (CH) | 2013-05-29 | — | — | EP | disclosed |
| US-8426592-B2 | Histone deacetylases, and uses related thereto | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2013-04-23 | — | — | US | disclosed |
| US-8399233-B2 | Histone deacetylases, and uses related thereto | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2013-03-19 | — | — | US | disclosed |
| US-8362084-B2 | Histone deacetylases, and uses related thereto | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2013-01-29 | — | — | US | disclosed |
| US-8329946-B2 | Histone deacetylases, and uses related thereto | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2012-12-11 | — | — | US | disclosed |
| US-8329945-B2 | Histone deacetylases, and uses related thereto | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2012-12-11 | — | — | US | disclosed |
| US-20120302510-A1 | HISTONE DEACETYLASES, AND USES RELATED THERETO | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2012-11-29 | — | — | US | disclosed |
| WO-2012149182-A2 | AUTOMATED SYNTHESIS OF SMALL MOLECULES USING CHIRAL, NON-RACEMIC BORONATES | THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS (US) | 2012-11-01 | — | — | WO | disclosed |
| US-20120265385-A1 | NONAQUEOUS ELECTROLYTE BATTERY AND NONAQUEOUS ELECTROLYTE, AND BATTERY PACK, ELECTRONIC APPLIANCE, ELECTRIC VEHICLE, ELECTRICITY STORAGE APPARATUS, AND ELECTRIC POWER SYSTEM | SONY CORPORATION (JP) | 2012-10-18 | — | — | US | disclosed |
| US-20120265385-A1 | NONAQUEOUS ELECTROLYTE BATTERY AND NONAQUEOUS ELECTROLYTE, AND BATTERY PACK, ELECTRONIC APPLIANCE, ELECTRIC VEHICLE, ELECTRICITY STORAGE APPARATUS, AND ELECTRIC POWER SYSTEM | SONY CORPORATION (JP) | 2012-10-18 | — | — | US | disclosed |
| US-8273520-B2 | Resin composition for laser engraving, relief printing plate precursor for laser engraving, relief printing plate and method of producing the same | FUJIFILM CORPORATION (JP) | 2012-09-25 | — | — | US | disclosed |
| US-20120232279-A1 | Mild and Selective Vanadium-Catalyzed Oxidation of Benzylic, Allylic, and Propargylic Alcohols Using Air | LOS ALAMOS NATIONAL SECURITY, LLC (US) | 2012-09-13 | — | — | US | disclosed |
| US-20120232279-A1 | Mild and Selective Vanadium-Catalyzed Oxidation of Benzylic, Allylic, and Propargylic Alcohols Using Air | LOS ALAMOS NATIONAL SECURITY, LLC (US) | 2012-09-13 | — | — | US | disclosed |
| US-20120201778-A1 | NOVEL DEORDORISING COMPOSITIONS AND DEODORISING PRODUCTS CONTAINING SAME | ROBERTET S.A. (FR) | 2012-08-09 | — | — | US | disclosed |
| US-8232420-B2 | Asymmetric catalyst and process for preparing optically active alcohols using the same | KANTO KAGAKU KABUSHIKI KAISHA (JP) | 2012-07-31 | — | — | US | disclosed |
| US-8227218-B2 | Method for the enzymatic reduction of alkyne derivates | BASF SE (DE) | 2012-07-24 | — | — | US | disclosed |
| US-8227218-B2 | Method for the enzymatic reduction of alkyne derivates | BASF SE (DE) | 2012-07-24 | — | — | US | disclosed |
| EP-2442783-A2 | NOVEL DEODORISING COMPOSITIONS AND DEODORISING PRODUCTS CONTAINING SAME | Robertet S.A. (FR) | 2012-04-25 | — | — | EP | disclosed |
| WO-2012010567-A1 | ISOXAZOLE, ISOTHIAZOLE, FURANE AND THIOPHENE COMPOUNDS AS MICROBICIDES | SYNGENTA PARTICIPATIONS AG (CH) | 2012-01-26 | — | — | WO | disclosed |
| WO-2012010567-A1 | ISOXAZOLE, ISOTHIAZOLE, FURANE AND THIOPHENE COMPOUNDS AS MICROBICIDES | SYNGENTA PARTICIPATIONS AG (CH) | 2012-01-26 | — | — | WO | disclosed |
| US-20110319493-A1 | HISTONE DEACETYLASES, AND USES RELATED THERETO | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2011-12-29 | — | — | US | disclosed |
| US-20110313045-A1 | HISTONE DEACETYLASES, AND USES RELATED THERETO | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2011-12-22 | — | — | US | disclosed |
| US-20110218154-A1 | HISTONE DEACETYLASES, AND USES RELATED THERETO | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2011-09-08 | — | — | US | disclosed |
| US-7994362-B2 | Histone deacetylases, and uses related thereto | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2011-08-09 | — | — | US | disclosed |
| EP-1741693-B1 | PROCESS FOR PRODUCTION OF OPTICALLY ACTIVE ALCOHOLS | NAGOYA IND SCIENCE RES INST (JP) | 2011-08-03 | — | — | EP | disclosed |
| US-7884225-B2 | Hydrosilation of chlorodimethylsilane with allyl chloride to give (3-chloropropyl)chlorodimethylsilane in the presence of catalytic dichlorobis(1,5-cyclooctadiene)diiridium and an auxilary mixture of cyclooctadiene and cyclohexanone; improved cost efficiency, lower amounts of catalyst required | RHODIA CHIMIE (FR) | 2011-02-08 | — | — | US | disclosed |
| EP-2272491-A1 | New deodorising compositions and deodorant products containing them | Robertet S.A. (FR) | 2011-01-12 | — | — | EP | disclosed |
| WO-2010146258-A2 | NOVEL DEODORISING COMPOSITIONS AND DEODORISING PRODUCTS CONTAINING SAME | ROBERTET S.A. (FR) | 2010-12-23 | — | — | WO | disclosed |
| US-20100261924-A1 | ASYMMETRIC CATALYST AND PROCESS FOR PREPARING OPTICALLY ACTIVE ALCOHOLS USING THE SAME | KANTO KAGAKU KABUSHIKI KAISHA (JP) | 2010-10-14 | — | — | US | disclosed |
| US-20100168441-A1 | PROCESS FOR PRODUCTION OF SUBSTITUTED BENZENE | NISSAN CHEMICAL INDUSTRIES, LTD. (JP) | 2010-07-01 | — | — | US | disclosed |
| US-20100137196-A1 | HISTONE DEACETYLASES, AND USES RELATED THERETO | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2010-06-03 | — | — | US | disclosed |
| US-20100069683-A1 | Organic metal compound and process for preparing optically-active alcohols using the same | KANTO KAGAKU KABUSHIKI KAISHA (JP) | 2010-03-18 | — | — | US | disclosed |
| US-20100056745-A1 | METHOD FOR PRODUCING ORGANOALKOXYDIALKYLSILANE | RHODIA CHIMIE (FR) | 2010-03-04 | — | — | US | disclosed |
| EP-1692148-B1 | METHOD FOR PRODUCING ORGANO ALCOXYDIALKYLSILANE | RHODIA CHIMIE SA (FR) | 2010-03-03 | — | — | EP | disclosed |
| US-20100009421-A1 | Method For The Enzymatic Reduction Of Alkyne Derivates | BASF SE (DE) | 2010-01-14 | — | — | US | disclosed |
| US-20100009421-A1 | Method For The Enzymatic Reduction Of Alkyne Derivates | BASF SE (DE) | 2010-01-14 | — | — | US | disclosed |
| EP-2061880-B1 | METHOD FOR THE ENZYMATIC REDUCTION OF ALKYNE DERIVATES | BASF SE (DE) | 2009-12-09 | — | — | EP | disclosed |
| US-20090247680-A1 | ADHESION PROMOTING ADDITIVE | AVERY DENNISON CORPORATION (US) | 2009-10-01 | — | — | US | disclosed |
| US-20090221474-A1 | HISTONE DEACETYLASES, AND USES RELATED THERETO | PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) | 2009-09-03 | — | — | US | disclosed |
| US-7582630-B2 | Pyradazine compounds as GSK-3 inhibitors | SMITHKLINE BEECHAM CORPORATION (US) | 2009-09-01 | — | — | US | disclosed |
| EP-2085220-A2 | Resin composition for laser engraving, relief printing plate precursor for laser engraving, relief printing plate and method of producing the same | FUJIFILM Corporation (JP) | 2009-08-05 | — | — | EP | disclosed |
| US-20090191479-A1 | RESIN COMPOSITION FOR LASER ENGRAVING, RELIEF PRINTING PLATE PRECURSOR FOR LASER ENGRAVING, RELIEF PRINTING PLATE AND METHOD OF PRODUCING THE SAME | FUJIFILM CORPORATION (JP) | 2009-07-30 | — | — | US | disclosed |
| US-20090062573-A1 | Organic metal compound and process for preparing optically-active alcohols using the same | KANTO KAGAKU KABUSHIKI KAISHA (JP) | 2009-03-05 | — | — | US | disclosed |
| US-20090053455-A1 | OPTICAL RECORDING MEDIUM, METAL COMPLEX COMPOUND AND ORGANIC DYE COMPOUND | MITSUBISHI KAGAKU MEDIA CO., LTD (JP) | 2009-02-26 | — | — | US | disclosed |
| EP-2024440-A2 | ADHESION PROMOTING ADDITIVE | AVERY DENNISON CORPORATION (US) | 2009-02-18 | — | — | EP | disclosed |
| US-20080275264-A1 | PROCESS FOR THE PREPARATION OF HALOGENOALKYLDIALKYL CHLOROSILANE | RHODIA CHIMIE (FR) | 2008-11-06 | — | — | US | disclosed |
| US-20080269425-A1 | Novel Catalyst | WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) | 2008-10-30 | — | — | US | disclosed |
| US-20080269425-A1 | Novel Catalyst | WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) | 2008-10-30 | — | — | US | disclosed |
| CN-100407454-C | Light-emitting device and method for manufacturing light-emitting device | SEMICONDUCTOR ENERGY LABORATORY CO., LTD. (JP) | 2008-07-30 | — | — | CN | disclosed |
| EP-1633761-B1 | METHOD OF PREPARING HALOGENOALKYLDIALKYLCHLOROSILANE | RHODIA CHIMIE SA (FR) | 2008-05-07 | — | — | EP | disclosed |
| US-20080103324-A1 | Method for Producing Organoalkoxydialkylsilane | RHODIA CHIMIE (FR) | 2008-05-01 | — | — | US | disclosed |
| US-7364841-B2 | Comprising support having thereon light-insensitive organic silver salt grains, photosensitive silver halide grains, a reducing agent for silver ions and a binder; improved storage stability, image lasting quality; use in medical diagnosis and graphic arts | KONICA MINOLTA & MEDICAL GRAPHIC, INC. (JP) | 2008-04-29 | — | — | US | disclosed |
| EP-1894999-A1 | Process for enzymatic reduction of alkyne derivatives | BASF SE (DE) | 2008-03-05 | — | — | EP | disclosed |
| WO-2007146603-A2 | ADHESION PROMOTING ADDITIVE | AVERY DENNISON CORPORATION (US) | 2007-12-21 | — | — | WO | disclosed |
| US-20070225528-A1 | Process for Producing Optically Active Alcohol | NAGOYA INDUSTRIAL SCIENCE RESEARCH CENTER (JP) | 2007-09-27 | — | — | US | disclosed |
| US-20070225528-A1 | Process for Producing Optically Active Alcohol | NAGOYA INDUSTRIAL SCIENCE RESEARCH CENTER (JP) | 2007-09-27 | — | — | US | disclosed |
| US-20070225528-A1 | Process for Producing Optically Active Alcohol | NAGOYA INDUSTRIAL SCIENCE RESEARCH CENTER (JP) | 2007-09-27 | — | — | US | disclosed |
| US-20070185344-A1 | Method of preparing halogenoalkyldialkyl chlorosilane | RHODIA CHIMIE (FR) | 2007-08-09 | — | — | US | disclosed |
| CN-1993348-A | Potassium channel inhibitors | MERCK & CO INC (US) | 2007-07-04 | — | — | CN | disclosed |
| US-20070093413-A1 | Histone deacetylases, and uses related thereto | HARVARD UNIVERSITY OTI (US) | 2007-04-26 | — | — | US | disclosed |
| CN-1309874-C | Tin plating method | SHIPLEY CO (US) | 2007-04-11 | — | — | CN | disclosed |
| US-7202019-B2 | Photothermographic imaging material | KONICA MINOLTA HOLDINGS, INC. (JP) | 2007-04-10 | — | — | US | disclosed |
| US-7202019-B2 | Photothermographic imaging material | KONICA MINOLTA HOLDINGS, INC. (JP) | 2007-04-10 | — | — | US | disclosed |
| US-7175978-B2 | Silver salt photothermographic dry imaging material | KONICA MINOLTA MEDICAL & GRAPHIC, INC. (JP) | 2007-02-13 | — | — | US | disclosed |
| US-7175978-B2 | Silver salt photothermographic dry imaging material | KONICA MINOLTA MEDICAL & GRAPHIC, INC. (JP) | 2007-02-13 | — | — | US | disclosed |
| EP-1741693-A1 | PROCESS FOR PRODUCTION OF OPTICALLY ACTIVE ALCOHOLS | Nagoya Industrial Science Research Institute (JP) | 2007-01-10 | — | — | EP | disclosed |
| EP-1741693-A1 | PROCESS FOR PRODUCTION OF OPTICALLY ACTIVE ALCOHOLS | Nagoya Industrial Science Research Institute (JP) | 2007-01-10 | — | — | EP | disclosed |
| US-20070003886-A1 | SILVER SALT PHOTOTHERMOGRAPHIC DRY IMAGING MATERIAL | KONICA MINOLTA MEDICAL & GRAPHIC, INC. (JP) | 2007-01-04 | — | — | US | disclosed |
| US-20070003886-A1 | SILVER SALT PHOTOTHERMOGRAPHIC DRY IMAGING MATERIAL | KONICA MINOLTA MEDICAL & GRAPHIC, INC. (JP) | 2007-01-04 | — | — | US | disclosed |
| EP-1692148-A2 | METHOD FOR PRODUCING ORGANO ALCOXYDIALKYLSILANE | Rhodia Chimie SA (FR) | 2006-08-23 | — | — | EP | disclosed |
| US-20060069097-A1 | Pyradazine compounds as gsk-3 inhibitors | SMITHKLINE BEECHAM CORPORATION | 2006-03-30 | — | — | US | disclosed |
| EP-1633761-A2 | METHOD OF PREPARING HALOGENOALKYLDIALKYLCHLOROSILANE | Rhodia Chimie (FR) | 2006-03-15 | — | — | EP | disclosed |
| CN-1716650-A | Light-emitting device and method for manufacturing light-emitting device | SEMICONDUCTOR ENERGY LAB (JP) | 2006-01-04 | — | — | CN | disclosed |
| US-20050209459-A1 | Processes for the preparation of 1,5-diryl-3-substituted-pyrazoles | REDDY M V R | 2005-09-22 | — | — | US | disclosed |
| EP-1551842-A1 | PYRADAZINE COMPOUNDS AS GSK-3 INHIBITORS | SMITHKLINE BEECHAM CORPORATION (US) | 2005-07-13 | — | — | EP | disclosed |
| WO-2005058922-A2 | METHOD FOR PRODUCING ORGANO ALCOXYDIALKYLSILANE | RHODIA CHIMIE (FR) | 2005-06-30 | — | — | WO | disclosed |
| US-6906196-B2 | Processes for the preparation of 1,5-diaryl-3-substituted-pyrazoles | ONCONOVA THERAPEUTICS, INC. (US) | 2005-06-14 | — | — | US | disclosed |
| EP-1121365-B1 | ORGANOBORON DERIVATIVES AND PROCESS FOR COUPLING ORGANIC COMPOUNDS | COMMW SCIENT IND RES ORG (AU) | 2005-06-08 | — | — | EP | disclosed |
| US-6864261-B2 | Therapeutic agents useful for treating pain | EURO-CELTIQUE S.A. (LU) | 2005-03-08 | — | — | US | disclosed |
| WO-2004113354-A2 | METHOD OF PREPARING HALOGENOALKYLDIALKYLCHLOROSILANE | RHODIA CHIMIE (FR) | 2004-12-29 | — | — | WO | disclosed |
| EP-1436285-A4 | PROCESSES FOR THE PREPARATION OF 1,5-DIARYL-3-SUBSTITUTED-PYRAZOLES | ONCONOVA THERAPEUTICS INC (US) | 2004-12-15 | — | — | EP | disclosed |
| CN-1530470-A | Tin-plating method | ϣ | 2004-09-22 | — | — | CN | disclosed |
| EP-1436285-A2 | PROCESSES FOR THE PREPARATION OF 1,5-DIARYL-3-SUBSTITUTED-PYRAZOLES | Onconova Therapeutics, Inc. (US) | 2004-07-14 | — | — | EP | disclosed |
| US-20040110763-A1 | Pyrazolopyridine compound and pharmaceutical use thereof | FUJISAWA PHARMACEUTICAL CO., LTD. (JP) | 2004-06-10 | — | — | US | disclosed |
| WO-2004035588-A1 | PYRADAZINE COMPOUNDS AS GSK-3 INHIBITORS | SMITHKLINE BEECHAM CORPORATION (US) | 2004-04-29 | — | — | WO | disclosed |
| US-6713566-B1 | CATALYTIC HYDROBORATION OF OLEFINIC OR ACETYLENIC FUNCTIONA-LIZED MATERIAL UNDER MILD CONDITIONS | COMMONWEALTH SCIENTIFIC AND INDUSTRIAL RESEARCH ORGANISATION (AU) | 2004-03-30 | — | — | US | disclosed |
| US-20040053914-A1 | Therapeutic agents useful for treating pain | PURDUE PHARMA L.P. | 2004-03-18 | — | — | US | disclosed |
| WO-2004018462-A1 | QUINAZOLINONE DERIVATIVES | CELLTECH R & D LIMITED (GB) | 2004-03-04 | — | — | WO | disclosed |
| CN-1458304-A | Tin plating method | SHIPLEY CO (US) | 2003-11-26 | — | — | CN | disclosed |
| WO-2003093236-A1 | 1-(PYRID-2-YL)-PIPERAZINE COMPOUNDS AS METABOTROPIC GLUTAMATE RECEPTOR INHIBITOR | EURO-CELTIQUE, S.A. (LU) | 2003-11-13 | — | — | WO | disclosed |
| US-20030109709-A1 | Processes for the preparation of 1,5-diaryl-3-substituted-pyrazoles | ONCONOVA THERAPEUTICS, INC. | 2003-06-12 | — | — | US | disclosed |
| EP-1313733-A1 | PYRAZOLOPYRIDINE COMPOUND AND PHARMACEUTICAL USE THEREOF | FUJISAWA PHARMACEUTICAL CO., LTD. (JP) | 2003-05-28 | — | — | EP | disclosed |
| WO-2003024958-A2 | PROCESSES FOR THE PREPARATION OF 1,5-DIARYL-3-SUBSTITUTED-PYRAZOLES | ONCONOVA THERAPEUTICS, INC. (US) | 2003-03-27 | — | — | WO | disclosed |
| WO-2002018382-A1 | PYRAZOLOPYRIDINE COMPOUND AND PHARMACEUTICAL USE THEREOF | FUJISAWA PHARMACEUTICAL CO., LTD. (JP) | 2002-03-07 | — | — | WO | disclosed |
| EP-1121365-A4 | ORGANOBORON DERIVATIVES AND PROCESS FOR COUPLING ORGANIC COMPOUNDS | COMMW SCIENT IND RES ORG (AU) | 2002-03-06 | — | — | EP | disclosed |
| EP-1121365-A1 | ORGANOBORON DERIVATIVES AND PROCESS FOR COUPLING ORGANIC COMPOUNDS | COMMONWEALTH SCIENTIFIC AND INDUSTRIAL RESEARCH ORGANISATION (AU) | 2001-08-08 | — | — | EP | disclosed |
| WO-2000021966-A1 | ORGANOBORON DERIVATIVES AND PROCESS FOR COUPLING ORGANIC COMPOUNDS | COMMONWEALTH SCIENTIFIC AND INDUSTRIAL RESEARCH ORGANISATION (AU) | 2000-04-20 | — | — | WO | disclosed |
| US-5945540-A | Synthesis of certain pyrazolo- 1,5-a! benzimidazole compounds | EASTMAN KODAK COMPANY (US) | 1999-08-31 | — | — | US | disclosed |
| JP-H10236986-A | PRODUCTION OF OPTICALLY ACTIVE ALCOHOLS | KAGAKU GIJUTSU SHINKO JIGYODAN | 1998-09-08 | — | — | JP | disclosed |
| JP-H069631-A | NEW PRODUCTION OF PYRAZOLOPYRIDINE | FUJISAWA PHARMACEUT CO LTD | 1994-01-18 | — | — | JP | disclosed |
| US-5220072-A | Reacting 2-ethylapopinene enantiomorph with haloborane-methyl sulfide complex | ALDRICH CHEMICAL CO., INC. (US) | 1993-06-15 | — | — | US | disclosed |
| US-5202502-A | Using b-halodiiso-2-ethylapopinocampheylborane as reducing agent | ALDRICH CHEMICAL COMPANY, INC. (US) | 1993-04-13 | — | — | US | disclosed |
| US-5159116-A | Reducing agents in the asymmetric reduction of ketones to optically active alcohols | ALDRICH CHEMICAL COMPANY, INC. (US) | 1992-10-27 | — | — | US | disclosed |
| US-4582578-A | Method for the electrochemical conversion of a quadricyclane to a norbornadiene | REGENTS OF THE UNIVERSITY OF MINNESOTA (US) | 1986-04-15 | — | — | US | disclosed |
| US-4514267-A | Zinc electroplating additive concentrate | OMI INTERNATIONAL CORPORATION (US) | 1985-04-30 | — | — | US | disclosed |
| US-4252619-A | Brightener for zinc electroplating solutions and process | OXY METAL INDUSTRIES CORPORATION (US) | 1981-02-24 | — | — | US | disclosed |
| US-4179561-A | REACTING A 3-DIAZOOXINDOLE WITH A SUBSTITUTED ACETYLENE | E. R. SQUIBB & SONS, INC. (US) | 1979-12-18 | — | — | US | disclosed |
| EP-0001516-A1 | Beta-Lactam compounds, processes for their preparation, pharmaceutical compositions containing them and intermediates of use in their preparation | GLAXO GROUP LIMITED (GB) | 1979-04-18 | — | — | EP | disclosed |
| US-4112096-A | ANTIALLERGENS | E. R. SQUIBB & SONS, INC. (US) | 1978-09-05 | — | — | US | disclosed |
| US-4076818-A | ANTIALLERGENS | E. R. SQUIBB & SONS, INC. (US) | 1978-02-28 | — | — | US | disclosed |
| US-3985765-A | ANTIINFLAMMATORY OR ANTIPYRETIC ACTIVITY | MILES LABORATORIES, INC. (US) | 1976-10-12 | — | — | US | disclosed |
| US-3948930-A | ANTIINFLAMMATORY, ANTIPYRETIC | MILES LABORATORIES, INC. (US) | 1976-04-06 | — | — | US | disclosed |
| US-3948930-A | ANTIINFLAMMATORY, ANTIPYRETIC | MILES LABORATORIES, INC. (US) | 1976-04-06 | — | — | US | disclosed |
| US-3948929-A | ANTIINFLAMMATORY, ANTIPYRETIC | MILES LABORATORIES, INC. (US) | 1976-04-06 | — | — | US | disclosed |
| US-3948932-A | ANTIINFLAMMATORY, ANTIPYRETIC | MILES LABORATORIES, INC. (US) | 1976-04-06 | — | — | 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 (44 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-20120302510-A1 | HISTONE DEACETYLASES, AND USES RELATED THERETO | HDAC1, HDAC8, HDAC11 | NPSR1 4476/4885VCP 2581/4885APP 4636/4885 |
| US-20090062573-A1 | Organic metal compound and process for preparing optically-active alcohols using the same | ADH1C, ADH1A, ADH5 | NPSR1 2956/4885VCP 4064/4885APP 3554/4885 |
| US-20150329567-A1 | Automated Synthesis of Small Molecules Using Chiral, Non-Racemic Boronates | BTD, POLL, POLR1A | NPSR1 2594/4885VCP 4193/4885APP 3568/4885 |
| US-20110319493-A1 | HISTONE DEACETYLASES, AND USES RELATED THERETO | HDAC1, HDAC8, HDAC11 | NPSR1 4476/4885VCP 2581/4885APP 4636/4885 |
| US-20040053914-A1 | Therapeutic agents useful for treating pain | SMN1; SMN2, OPRM1, PSEN1 | NPSR1 186/4885VCP 1026/4885APP 184/4885 |
| US-20100261924-A1 | ASYMMETRIC CATALYST AND PROCESS FOR PREPARING OPTICALLY ACTIVE ALCOHOLS USING THE SAME | ADH1A, ADH1C, ADH5 | NPSR1 1157/4885VCP 4120/4885APP 3585/4885 |
| US-20070225528-A1 | Process for Producing Optically Active Alcohol | ADH1C, ADH1A, ADH5 | NPSR1 2553/4885VCP 3141/4885APP 3805/4885 |
| US-20050209459-A1 | Processes for the preparation of 1,5-diryl-3-substituted-pyrazoles | CYP2E1, CYP1A1, CYP1B1 | NPSR1 2524/4885VCP 3953/4885APP 2937/4885 |
| US-20070185344-A1 | Method of preparing halogenoalkyldialkyl chlorosilane | HACL2, UBE3C, MCCC2 | NPSR1 2918/4885VCP 796/4885APP 4695/4885 |
| US-20150057268-A1 | COMPOSITION AND METHOD FOR NEUROPEPTIDE S RECEPTOR (NPSR) ANTAGONISTS | NPSR1, TACR1, NPFFR1 | NPSR1 1/4885VCP 2142/4885APP 314/4885 |
| US-20080103324-A1 | Method for Producing Organoalkoxydialkylsilane | STS, ARSA, SULT2A1 | NPSR1 303/4885VCP 2646/4885APP 2912/4885 |
| US-20080275264-A1 | PROCESS FOR THE PREPARATION OF HALOGENOALKYLDIALKYL CHLOROSILANE | HDHD5, DDC, HACL2 | NPSR1 3762/4885VCP 1186/4885APP 4785/4885 |
| US-20080269425-A1 | Novel Catalyst | PPOX, PNMT, POLRMT | NPSR1 3015/4885VCP 4615/4885APP 2555/4885 |
| US-20110218154-A1 | HISTONE DEACETYLASES, AND USES RELATED THERETO | HDAC1, HDAC8, HDAC11 | NPSR1 4476/4885VCP 2581/4885APP 4636/4885 |
| US-20090053455-A1 | OPTICAL RECORDING MEDIUM, METAL COMPLEX COMPOUND AND ORGANIC DYE COMPOUND | KCNJ2, KCNN2, KCNN3 | NPSR1 4617/4885VCP 4739/4885APP 1890/4885 |
| US-12617765-B2 | Cannabinoid derivatives | CNR2, CNR1, GPR18 | NPSR1 110/4885VCP 3282/4885APP 2267/4885 |
| US-20120232279-A1 | Mild and Selective Vanadium-Catalyzed Oxidation of Benzylic, Allylic, and Propargylic Alcohols Using Air | OR10J3, CBR3, CBR1 | NPSR1 1883/4885VCP 2987/4885APP 4709/4885 |
| US-10752577-B2 | Automated synthesis of small molecules using chiral, non-racemic boronates | BTD, POLL, POLR1A | NPSR1 2594/4885VCP 4193/4885APP 3568/4885 |
| US-20240150345-A1 | GCN2 MODULATING COMPOUNDS AND USES THEREOF | EIF2AK4, GCN1, CLN6 | NPSR1 3425/4885VCP 1535/4885APP 1124/4885 |
| US-20110313045-A1 | HISTONE DEACETYLASES, AND USES RELATED THERETO | HDAC1, HDAC8, HDAC11 | NPSR1 4476/4885VCP 2581/4885APP 4636/4885 |
| US-20170158614-A1 | AUTOMATED SYNTHESIS OF SMALL MOLECULES USING CHIRAL, NON-RACEMIC BORONATES | BTD, POLL, POLR1A | NPSR1 2594/4885VCP 4193/4885APP 3568/4885 |
| US-20230024212-A1 | CANNABINOID DERIVATIVES | CNR2, GPR18, CNR1 | NPSR1 44/4885VCP 3638/4885APP 1502/4885 |
| US-20190315676-A1 | AUTOMATED SYNTHESIS OF SMALL MOLECULES USING CHIRAL, NON-RACEMIC BORONATES | BTD, POLL, POLR1A | NPSR1 2594/4885VCP 4193/4885APP 3568/4885 |
| US-12618050-B2 | Engineered polypeptides that exhibit increased catalytic efficiency for unnatural cofactors and uses thereof | NNMT, NAPRT, NQO1 | NPSR1 1665/4885VCP 2912/4885APP 1585/4885 |
| US-20230303483-A1 | USE OF STROBILURIN TYPE COMPOUNDS FOR COMBATING PHYTOPATHOGENIC FUNGI CONTAINING AN AMINO ACID SUBSTITUTION F129L IN THE MITOCHONDRIAL CYTOCHROME B PROTEIN CONFERRING RESISTANCE TO QO INHIBITORS V | COX5B, SQOR, COX5A | NPSR1 2993/4885VCP 1253/4885APP 1167/4885 |
| US-20130252972-A1 | ISOXAZOLE, ISOTHIAZOLE, FURANE AND THIOPHENE COMPOUNDS AS MICROBICIDES | NOX1, NOX5, NOS1 | NPSR1 1513/4885VCP 4429/4885APP 4355/4885 |
| US-20150025269-A1 | PROCESS FOR PREPARATION OF ALKYNYL CARBOXYLIC ACIDS | CPS1, ALDH7A1, ACACA | NPSR1 2833/4885VCP 2094/4885APP 4736/4885 |
| US-20250059156-A1 | THERAPEUTIC ALKALOID COMPOUNDS | PDE4A, PDE4B, PDE4C | NPSR1 413/4885VCP 4774/4885APP 3856/4885 |
| US-10239824-B2 | Automated synthesis of small molecules using chiral, non-racemic boronates | BTD, POLL, POLR1A | NPSR1 2594/4885VCP 4193/4885APP 3568/4885 |
| US-20040110763-A1 | Pyrazolopyridine compound and pharmaceutical use thereof | ADRB1, ADRA1D, ADRB3 | NPSR1 39/4885VCP 3652/4885APP 49/4885 |
| US-20210009508-A1 | Automated Synthesis of Small Molecules Using Chiral, Non-Racemic Boronates | BTD, POLL, POLR1A | NPSR1 2594/4885VCP 4193/4885APP 3568/4885 |
| US-20180065908-A1 | CHAIN MULTIYNE COMPOUND, PREPARATION METHOD AND APPLICATION THEREOF | SQLE, COASY, MCCC2 | NPSR1 3871/4885VCP 2755/4885APP 3963/4885 |
| US-20070093413-A1 | Histone deacetylases, and uses related thereto | HDAC1, HDAC8, HDAC11 | NPSR1 4476/4885VCP 2581/4885APP 4636/4885 |
| US-10287225-B2 | Chain multiyne compound, preparation method and application thereof | SQLE, COASY, MCCC2 | NPSR1 3871/4885VCP 2755/4885APP 3963/4885 |
| US-20090221474-A1 | HISTONE DEACETYLASES, AND USES RELATED THERETO | HDAC1, HDAC8, HDAC11 | NPSR1 4476/4885VCP 2581/4885APP 4636/4885 |
| US-20100056745-A1 | METHOD FOR PRODUCING ORGANOALKOXYDIALKYLSILANE | STS, ARSA, SULT2A1 | NPSR1 303/4885VCP 2646/4885APP 2912/4885 |
| US-20130289030-A1 | NOVEL PHENAZINE DERIVATIVES AND THEIR USES | VEGFA, KDR, FLT4 | NPSR1 959/4885VCP 4566/4885APP 4778/4885 |
| US-20100069683-A1 | Organic metal compound and process for preparing optically-active alcohols using the same | ADH1C, ADH1A, ADH5 | NPSR1 2956/4885VCP 4064/4885APP 3554/4885 |
| US-20060069097-A1 | Pyradazine compounds as gsk-3 inhibitors | GSK3B, GSK3A, GSKIP | NPSR1 4512/4885VCP 4622/4885APP 1070/4885 |
| US-20100168441-A1 | PROCESS FOR PRODUCTION OF SUBSTITUTED BENZENE | MYB, KCNH2, INTS9 | NPSR1 2893/4885VCP 2707/4885APP 2863/4885 |
| US-20220242844-A1 | CANNABINOID DERIVATIVES | CNR2, CNR1, FAAH | NPSR1 358/4885VCP 1344/4885APP 42/4885 |
| US-20220259221-A1 | CANNABINOID DERIVATIVES | CNR2, CNR1, HTR2A | NPSR1 54/4885VCP 3458/4885APP 2653/4885 |
| US-20030109709-A1 | Processes for the preparation of 1,5-diaryl-3-substituted-pyrazoles | CYP1B1, CYP1A1, CYP2E1 | NPSR1 3188/4885VCP 4369/4885APP 3626/4885 |
| US-20100137196-A1 | HISTONE DEACETYLASES, AND USES RELATED THERETO | HDAC1, HDAC8, HDAC11 | NPSR1 4476/4885VCP 2581/4885APP 4636/4885 |
“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.